This document discusses various non-neoplastic diseases of the salivary glands. It covers common and uncommon infectious diseases like viral and bacterial sialadenitis. It also discusses specific infections like mumps which causes parotid gland swelling. Other conditions covered include Sjögren's syndrome, sialolithiasis (salivary stones), drug-induced salivary gland disorders, sialosis (non-inflammatory swelling) and bulimia nervosa related salivary gland enlargement. The document provides details on clinical features, investigations, diagnosis and treatment of these salivary gland conditions.
HIV is a retrovirus that causes AIDS by destroying CD4+ T cells. It is transmitted through bodily fluids and can be occupational hazard for surgeons. Universal precautions like proper protective equipment and disposal of contaminated waste are important to prevent transmission. Current antiretroviral therapy uses combination of three or more drugs like nucleoside analogs that inhibit reverse transcriptase and protease inhibitors. This effectively suppresses the virus and prevents opportunistic infections associated with AIDS.
This document discusses various surgical aspects related to HIV infection. It covers common perianal conditions seen in HIV patients like abscesses, fistulae, and ulcers. GI manifestations involving the esophagus, stomach, intestines, liver and biliary tract are described. Tumors associated with HIV like Kaposi's sarcoma and lymphomas are also outlined. Staging of HIV based on WHO criteria and perioperative management of HIV patients undergoing surgery are briefly touched upon.
This document provides an overview of Behcet's disease, including its characteristics, diagnostic criteria, clinical manifestations, and treatment approaches. Some key points:
- Behcet's disease is a chronic, relapsing inflammatory vasculitis that can affect multiple organ systems. It is characterized by oral and genital ulcers, skin lesions, uveitis, and vascular, gastrointestinal, and neurological involvement.
- Diagnosis is based on recurrent oral ulcers plus two of the following: genital ulcers, eye inflammation, skin lesions. Major organ involvement like the eyes or CNS also indicate Behcet's disease.
- Treatment involves local therapies for ulcers and lesions as well as systemic corticosteroids
This document discusses sexually transmitted infections (STIs) caused by Treponema pallidum (syphilis), Neisseria gonorrhoeae (gonorrhea), and Chlamydia trachomatis (chlamydia). It describes the clinical manifestations of primary, secondary, and late syphilis. It also discusses gonococcal and chlamydial infections in males and females, including urethritis, cervicitis, pelvic inflammatory disease, and disseminated gonococcal infection. The document provides details on laboratory testing, treatment, and clinical presentation of these common STIs.
Sarcoidosis is a multisystem granulomatous disorder of unknown etiology characterized by non-caseating granulomas. It most commonly affects the lungs presenting as bilateral hilar lymphadenopathy and pulmonary infiltrates. Extrapulmonary involvement can include the skin, eyes, liver and musculoskeletal system. Diagnosis involves clinical features and exclusion of other causes. Treatment involves corticosteroids while prognosis depends on organ involvement with lung fibrosis carrying the worst prognosis.
This document provides information on sarcoidosis, including:
1) It is a chronic granulomatous disease characterized by noncaseating granuloma formation of unknown cause, often affecting the lungs and lymph nodes.
2) It has a higher prevalence in African Americans and Japanese populations. The disease often affects people aged 20-40 and has a female predominance.
3) Granulomas form as a result of an abnormal cellular immune response potentially triggered by infectious agents. This leads to the formation of noncaseating granulomas containing giant cells.
4) The disease can have acute or chronic presentations and involve multiple organs, with lungs and lymph nodes most commonly affected. Corticost
This document discusses ocular manifestations of HIV/AIDS. It begins by describing HIV/AIDS etiology, noting that HIV-1 is the most common type worldwide. It then discusses various ocular manifestations associated with different CD4 counts, including Kaposi's sarcoma, CMV retinitis, and HIV retinopathy. Specific conditions of the anterior segment like molluscum contagiosum and of the posterior segment like CMV retinitis are then described in more detail, including characteristics, treatment options, and images. The document emphasizes that CMV retinitis is the most common opportunistic infection and discusses antiviral treatments for it like ganciclovir and foscarnet. It concludes by noting
1. HLA-associated uveitis refers to intraocular inflammation involving the uvea, retina, and retinal vessels that has been linked to certain HLA genes.
2. Specific HLA genes may predispose individuals to developing uveitis in response to infectious agents through molecular mimicry or an inability to distinguish self from non-self.
3. Many autoimmune and inflammatory diseases have shown associations with particular HLA genes, including ankylosing spondylitis (HLA-B27), Behcet's disease (HLA-B51), and birdshot retinochoroidopathy (HLA-A29).
HIV is a retrovirus that causes AIDS by destroying CD4+ T cells. It is transmitted through bodily fluids and can be occupational hazard for surgeons. Universal precautions like proper protective equipment and disposal of contaminated waste are important to prevent transmission. Current antiretroviral therapy uses combination of three or more drugs like nucleoside analogs that inhibit reverse transcriptase and protease inhibitors. This effectively suppresses the virus and prevents opportunistic infections associated with AIDS.
This document discusses various surgical aspects related to HIV infection. It covers common perianal conditions seen in HIV patients like abscesses, fistulae, and ulcers. GI manifestations involving the esophagus, stomach, intestines, liver and biliary tract are described. Tumors associated with HIV like Kaposi's sarcoma and lymphomas are also outlined. Staging of HIV based on WHO criteria and perioperative management of HIV patients undergoing surgery are briefly touched upon.
This document provides an overview of Behcet's disease, including its characteristics, diagnostic criteria, clinical manifestations, and treatment approaches. Some key points:
- Behcet's disease is a chronic, relapsing inflammatory vasculitis that can affect multiple organ systems. It is characterized by oral and genital ulcers, skin lesions, uveitis, and vascular, gastrointestinal, and neurological involvement.
- Diagnosis is based on recurrent oral ulcers plus two of the following: genital ulcers, eye inflammation, skin lesions. Major organ involvement like the eyes or CNS also indicate Behcet's disease.
- Treatment involves local therapies for ulcers and lesions as well as systemic corticosteroids
This document discusses sexually transmitted infections (STIs) caused by Treponema pallidum (syphilis), Neisseria gonorrhoeae (gonorrhea), and Chlamydia trachomatis (chlamydia). It describes the clinical manifestations of primary, secondary, and late syphilis. It also discusses gonococcal and chlamydial infections in males and females, including urethritis, cervicitis, pelvic inflammatory disease, and disseminated gonococcal infection. The document provides details on laboratory testing, treatment, and clinical presentation of these common STIs.
Sarcoidosis is a multisystem granulomatous disorder of unknown etiology characterized by non-caseating granulomas. It most commonly affects the lungs presenting as bilateral hilar lymphadenopathy and pulmonary infiltrates. Extrapulmonary involvement can include the skin, eyes, liver and musculoskeletal system. Diagnosis involves clinical features and exclusion of other causes. Treatment involves corticosteroids while prognosis depends on organ involvement with lung fibrosis carrying the worst prognosis.
This document provides information on sarcoidosis, including:
1) It is a chronic granulomatous disease characterized by noncaseating granuloma formation of unknown cause, often affecting the lungs and lymph nodes.
2) It has a higher prevalence in African Americans and Japanese populations. The disease often affects people aged 20-40 and has a female predominance.
3) Granulomas form as a result of an abnormal cellular immune response potentially triggered by infectious agents. This leads to the formation of noncaseating granulomas containing giant cells.
4) The disease can have acute or chronic presentations and involve multiple organs, with lungs and lymph nodes most commonly affected. Corticost
This document discusses ocular manifestations of HIV/AIDS. It begins by describing HIV/AIDS etiology, noting that HIV-1 is the most common type worldwide. It then discusses various ocular manifestations associated with different CD4 counts, including Kaposi's sarcoma, CMV retinitis, and HIV retinopathy. Specific conditions of the anterior segment like molluscum contagiosum and of the posterior segment like CMV retinitis are then described in more detail, including characteristics, treatment options, and images. The document emphasizes that CMV retinitis is the most common opportunistic infection and discusses antiviral treatments for it like ganciclovir and foscarnet. It concludes by noting
1. HLA-associated uveitis refers to intraocular inflammation involving the uvea, retina, and retinal vessels that has been linked to certain HLA genes.
2. Specific HLA genes may predispose individuals to developing uveitis in response to infectious agents through molecular mimicry or an inability to distinguish self from non-self.
3. Many autoimmune and inflammatory diseases have shown associations with particular HLA genes, including ankylosing spondylitis (HLA-B27), Behcet's disease (HLA-B51), and birdshot retinochoroidopathy (HLA-A29).
This document discusses various infectious causes of uveitis, including viruses, fungi, protozoa, helminths, and bacteria. It covers specific infectious etiologies such as herpesviridae family members, toxoplasmosis, toxocariasis, syphilis, Lyme disease, tuberculosis, and endogenous infectious endophthalmitis. For each condition, it describes clinical features, diagnostic testing, treatment approaches, and prognosis. Infectious uveitis remains an important consideration in uveitis evaluation and management.
Vasculitis refers to inflammation of blood vessels. It can present with a variety of clinical manifestations depending on the size of vessels involved. The Chapel Hill Consensus Conference created a classification system for major types of vasculitis including Wegener's granulomatosis, Churg-Strauss syndrome, and microscopic polyangiitis. Henoch-Schönlein purpura is the most common vasculitis in children, characterized by a vasculitis involving small vessels of the skin, GI tract, kidneys, joints, and rarely lungs and CNS, with IgA deposits in vessel walls. Granulomatosis with polyangiitis is a multisystem disease involving vasculitis of small to medium
This document provides information on Behcet's syndrome and Sjogren's syndrome. It discusses the diagnostic criteria for Behcet's syndrome according to the 1990 International Study Group. It describes the common oral, skin, eye, neurological, and other manifestations of Behcet's syndrome. It also discusses the etiology, pathogenesis, epidemiology, and management of Sjogren's syndrome.
Lupus pernio is a specific cutaneous manifestation of sarcoidosis that presents as violaceous, indurated plaques on the ears, nose, cheeks, lips, hands and feet. It is more common in African Americans and women with longstanding pulmonary sarcoidosis. Histopathology shows noncaseating granulomas. Treatment involves potent topical steroids, intralesional steroids, or systemic steroids and immunosuppressants like methotrexate. Refractory cases may require TNF-alpha antagonists or thalidomide. Lupus pernio can indicate significant pulmonary involvement and has a chronic course, sometimes causing disfigurement.
Generalized lymphadenopathy is a common presenting symptom of HIV infection. The patient's medical history and physical exam revealed unprotected sex, multiple partners, and sexually transmitted infections which increased their risk of contracting HIV. Laboratory tests such as CD4 count and serological testing can help diagnose HIV infection and monitor disease progression. Generalized lymphadenopathy in early stage HIV typically presents as symmetrical and non-tender lymph node enlargement.
1. Behcet's disease is a systemic autoimmune vasculitis characterized by recurrent oral and genital ulcers. It can affect multiple organ systems including eyes, skin, joints, gastrointestinal tract, and nervous system.
2. The disease is named after Turkish dermatologist Hulusi Behcet who first described the triple symptom complex in 1937. It is more common in countries along the Silk Road. Genetic factors like HLA-B51 are associated with increased risk.
3. Pathogenesis involves inflammation of blood vessels due to immune dysregulation. Diagnosis is based on clinical criteria including oral/genital ulcers, skin lesions, eye inflammation, and positive pathergy test. Treatment focuses on
Sarcoidosis is a multisystem granulomatous disorder of unknown origin characterized by non-caseating granulomas. It most commonly affects the lungs, skin and eyes of young adults. The cause is believed to be an abnormal immune response triggered by an environmental antigen in genetically susceptible individuals. Diagnosis involves compatible clinical features and histological evidence of non-caseating granulomas. Treatment focuses on suppressing granuloma formation and inflammation, with corticosteroids being the mainstay. Other immunosuppressants may be used for resistant or severe disease.
Sarcoidosis is a chronic multisystem inflammatory disorder characterized by non-caseating granulomas in affected tissues. Common organs involved are the lungs, lymph nodes, eyes, skin and heart. Ocular involvement occurs in 40% of sarcoidosis patients, most commonly presenting as uveitis. Uveitis manifestations include anterior uveitis, intermediate uveitis, posterior uveitis, scleritis, conjunctivitis, keratopathy and optic nerve involvement. Treatment involves topical, periocular or intraocular corticosteroids. Systemic corticosteroids or immunosuppressive drugs are used for more severe or treatment resistant disease.
This document discusses drugs used to treat uveitis. It describes three main groups of drugs: steroids, immunosuppressants, and mydriatics. Steroids are the mainstay of initial therapy and can be administered topically or via injection. Immunosuppressants like methotrexate, azathioprine, and cyclosporine work to modulate the immune system and are used when steroids are not effective or cause intolerable side effects. Mydriatics are used to dilate the pupil and relieve pain. The document provides details on specific drugs, their mechanisms of action, indications for use, and potential adverse effects.
Ocular involvement in HIV could be caused by opportunistic infections, vascular abnormalities, neoplasms, neuro-ophthalmic conditions, and adverse effects of medications.
Ocular involvement in HIV infection occurs most commonly due to opportunistic infections and neoplasms. But also can be due to drug related and direct infections.
Opportunistic infections like CMV retinitis occur with a significantly reduced CD4 T-cell count and are one of the common causes of blindness in HIV patients.
Unlike other diseases, ocular infection in these immunosuppressed patients is associated with minimal inflammatory signs.
HIV has been isolated from tears, cornea, vitreous, and chorioretinal tissue in affected persons.
The ocular structures affected by HIV include the adnexa, anterior segment, posterior segment, and orbit.
Neuro ophthalmological manifestations also may be seen.
The institution of highly active antiretroviral therapy (HAART) has caused a dramatic improvement in the immune status of HIV-infected individuals and a change in the clinical presentation and course of opportunistic infections.
Sarcoidosis is a multisystem disorder characterized by non-caseating granulomas that commonly affect the lungs and lymph nodes. It most often occurs in adults under 40 years old and has a higher prevalence in African Americans. While the exact cause is unknown, it involves an abnormal immune response in genetically predisposed individuals. Lung involvement is present in 90% of cases and lymph node involvement in 70% of cases. Pulmonary sarcoidosis ranges from asymptomatic hilar lymphadenopathy to progressive pulmonary fibrosis. Skin and eye involvement also occurs in a significant portion of patients.
In 1937, Prof. Hulusi Behçet described a syndrome characterized by recurrent oral and genital ulcers as well as eye inflammation. Known as Behçet's Disease, it is more common in people from the Mediterranean, Middle East and Asia. The cause is unknown but likely involves a genetic predisposition interacting with environmental triggers. Symptoms vary but can include oral, genital and eye lesions as well as skin, joint, gastrointestinal, neurological and vascular involvement. Treatment depends on symptoms and may include steroids, immunosuppressants and monoclonal antibodies. Prognosis is variable with mucocutaneous and ocular symptoms often worst early on and mortality increased if pulmonary artery lesions lead to hemoptysis
This document summarizes the presentation and management of a patient with HIV who presented with vision loss in the right eye. Examination found severe vision loss and retinal necrosis in the right eye. Labs showed positive syphilis serology. The patient was diagnosed with syphilitic retinitis and treated with IV penicillin. Vision improved after treatment.
Ocular Manifestations of HIV outlines common eye diseases seen in patients with HIV/AIDS. A study in Ethiopia found 60% of HIV patients had at least one ocular manifestation, most commonly retinal microvasculopathy (24%). Posterior segment manifestations include opportunistic infections like cytomegalovirus retinitis (30-40% of patients) and varicella zoster virus retinitis. Neuro-ophthalmic manifestations occur in 10-15% of patients and include optic neuritis, optic atrophy, and cranial nerve palsies. Children with HIV have fewer ocular manifestations than adults.
Lymphadenopathy refers to abnormal lymph nodes in size, number, or consistency. It can be generalized, affecting more than two lymph node groups, or localized to a single group. Generalized lymphadenopathy has many potential causes, including viral, bacterial, and fungal infections, metabolic disorders, hypersensitivity reactions, and cancers like Hodgkin's disease or non-Hodgkin's lymphoma. Regionally localized lymphadenopathy may be caused by infections or diseases affecting the local area, such as oral infections leading to submandibular lymph node enlargement. A dentist can examine for extraoral lymphadenopathy and make appropriate referrals for testing and diagnosis. Treatment focuses on the underlying cause rather than the lymphaden
This document discusses syphilis, a bacterial infection caused by Treponema pallidum. It begins by describing the etiology, epidemiology, signs and symptoms, and laboratory evaluation of syphilis. It then discusses the stages of syphilis in more detail, including primary, secondary, latent, tertiary, and congenital syphilis. The stages are characterized by different clinical manifestations such as chancres, rashes, neurological symptoms, and cardiovascular involvement. The document also covers the pathology of syphilis, its transmission routes, relationship to HIV, and laboratory tests for diagnosis.
This document discusses HIV and its effects in orthopaedics. It provides statistics on HIV deaths and hospitalizations. It describes the structure and life cycle of the HIV virus, how it attacks the immune system, and the stages of HIV infection. It discusses various orthopaedic problems seen in HIV patients like arthritis and fractures. It also outlines strategies to diagnose and manage HIV, including antiretroviral drug therapies, and precautions orthopaedic surgeons should take when operating on HIV patients.
Sarcoidosis is a multisystem disorder characterized by the formation of noncaseating granulomas in multiple organs. It most commonly involves the lungs, lymph nodes, skin, and eyes. The cause is unknown but believed to be due to an abnormal immune response to unknown antigens in genetically predisposed individuals. Diagnosis is based on clinical features and identification of granulomas on biopsy, and exclusion of other conditions. While often asymptomatic, it can cause respiratory symptoms as well as involvement of other organs. Treatment involves corticosteroids, with hydroxychloroquine or methotrexate as steroid-sparing options. Prognosis is generally good, though some degree of permanent organ dysfunction occurs in about half of
This document discusses the evaluation of lymphadenopathy. It outlines the key steps in evaluation which include determining the size and characteristics of palpable lymph nodes, identifying accompanying symptoms, examining the distribution of enlarged lymph nodes, and considering epidemiological factors. A variety of diagnostic tests are described based on the location and suspected causes of lymphadenopathy including blood tests, imaging studies, biopsies and cultures. The goal of evaluation is to arrive at an accurate diagnosis and guide further treatment.
This document provides an overview of salivary gland disorders, including their presentation, diagnosis, and treatment. It discusses the major salivary glands and their functions. Common salivary gland disorders mentioned include obstructive salivary diseases, infections, Sjogren's syndrome, xerostomia, sialolithiasis, mucoceles, ranulas, pleomorphic adenomas, Warthin's tumor, and mucoepidermoid carcinoma. The document outlines the steps for clinical examination of the salivary glands and describes the various investigative tools that can be used to diagnose salivary gland disorders.
Here are the answers to your questions:
1. Common types of salivary gland benign tumors with origin of each:
- Pleomorphic adenoma - originates from the intercalated duct cells and myoepithelial cells.
- Oncocytic tumors - originate from the striated duct cells.
- Acinous cell tumors - originate from the acinar cells.
- Mucoepidermoid tumors and squamous cell carcinomas develop in the excretory duct cells.
2. The histological features of mucoepidermoid carcinoma include:
- Containing mucin-producing cells and epithelial cells of the epidermoid variety.
- Divided into
This document discusses various infectious causes of uveitis, including viruses, fungi, protozoa, helminths, and bacteria. It covers specific infectious etiologies such as herpesviridae family members, toxoplasmosis, toxocariasis, syphilis, Lyme disease, tuberculosis, and endogenous infectious endophthalmitis. For each condition, it describes clinical features, diagnostic testing, treatment approaches, and prognosis. Infectious uveitis remains an important consideration in uveitis evaluation and management.
Vasculitis refers to inflammation of blood vessels. It can present with a variety of clinical manifestations depending on the size of vessels involved. The Chapel Hill Consensus Conference created a classification system for major types of vasculitis including Wegener's granulomatosis, Churg-Strauss syndrome, and microscopic polyangiitis. Henoch-Schönlein purpura is the most common vasculitis in children, characterized by a vasculitis involving small vessels of the skin, GI tract, kidneys, joints, and rarely lungs and CNS, with IgA deposits in vessel walls. Granulomatosis with polyangiitis is a multisystem disease involving vasculitis of small to medium
This document provides information on Behcet's syndrome and Sjogren's syndrome. It discusses the diagnostic criteria for Behcet's syndrome according to the 1990 International Study Group. It describes the common oral, skin, eye, neurological, and other manifestations of Behcet's syndrome. It also discusses the etiology, pathogenesis, epidemiology, and management of Sjogren's syndrome.
Lupus pernio is a specific cutaneous manifestation of sarcoidosis that presents as violaceous, indurated plaques on the ears, nose, cheeks, lips, hands and feet. It is more common in African Americans and women with longstanding pulmonary sarcoidosis. Histopathology shows noncaseating granulomas. Treatment involves potent topical steroids, intralesional steroids, or systemic steroids and immunosuppressants like methotrexate. Refractory cases may require TNF-alpha antagonists or thalidomide. Lupus pernio can indicate significant pulmonary involvement and has a chronic course, sometimes causing disfigurement.
Generalized lymphadenopathy is a common presenting symptom of HIV infection. The patient's medical history and physical exam revealed unprotected sex, multiple partners, and sexually transmitted infections which increased their risk of contracting HIV. Laboratory tests such as CD4 count and serological testing can help diagnose HIV infection and monitor disease progression. Generalized lymphadenopathy in early stage HIV typically presents as symmetrical and non-tender lymph node enlargement.
1. Behcet's disease is a systemic autoimmune vasculitis characterized by recurrent oral and genital ulcers. It can affect multiple organ systems including eyes, skin, joints, gastrointestinal tract, and nervous system.
2. The disease is named after Turkish dermatologist Hulusi Behcet who first described the triple symptom complex in 1937. It is more common in countries along the Silk Road. Genetic factors like HLA-B51 are associated with increased risk.
3. Pathogenesis involves inflammation of blood vessels due to immune dysregulation. Diagnosis is based on clinical criteria including oral/genital ulcers, skin lesions, eye inflammation, and positive pathergy test. Treatment focuses on
Sarcoidosis is a multisystem granulomatous disorder of unknown origin characterized by non-caseating granulomas. It most commonly affects the lungs, skin and eyes of young adults. The cause is believed to be an abnormal immune response triggered by an environmental antigen in genetically susceptible individuals. Diagnosis involves compatible clinical features and histological evidence of non-caseating granulomas. Treatment focuses on suppressing granuloma formation and inflammation, with corticosteroids being the mainstay. Other immunosuppressants may be used for resistant or severe disease.
Sarcoidosis is a chronic multisystem inflammatory disorder characterized by non-caseating granulomas in affected tissues. Common organs involved are the lungs, lymph nodes, eyes, skin and heart. Ocular involvement occurs in 40% of sarcoidosis patients, most commonly presenting as uveitis. Uveitis manifestations include anterior uveitis, intermediate uveitis, posterior uveitis, scleritis, conjunctivitis, keratopathy and optic nerve involvement. Treatment involves topical, periocular or intraocular corticosteroids. Systemic corticosteroids or immunosuppressive drugs are used for more severe or treatment resistant disease.
This document discusses drugs used to treat uveitis. It describes three main groups of drugs: steroids, immunosuppressants, and mydriatics. Steroids are the mainstay of initial therapy and can be administered topically or via injection. Immunosuppressants like methotrexate, azathioprine, and cyclosporine work to modulate the immune system and are used when steroids are not effective or cause intolerable side effects. Mydriatics are used to dilate the pupil and relieve pain. The document provides details on specific drugs, their mechanisms of action, indications for use, and potential adverse effects.
Ocular involvement in HIV could be caused by opportunistic infections, vascular abnormalities, neoplasms, neuro-ophthalmic conditions, and adverse effects of medications.
Ocular involvement in HIV infection occurs most commonly due to opportunistic infections and neoplasms. But also can be due to drug related and direct infections.
Opportunistic infections like CMV retinitis occur with a significantly reduced CD4 T-cell count and are one of the common causes of blindness in HIV patients.
Unlike other diseases, ocular infection in these immunosuppressed patients is associated with minimal inflammatory signs.
HIV has been isolated from tears, cornea, vitreous, and chorioretinal tissue in affected persons.
The ocular structures affected by HIV include the adnexa, anterior segment, posterior segment, and orbit.
Neuro ophthalmological manifestations also may be seen.
The institution of highly active antiretroviral therapy (HAART) has caused a dramatic improvement in the immune status of HIV-infected individuals and a change in the clinical presentation and course of opportunistic infections.
Sarcoidosis is a multisystem disorder characterized by non-caseating granulomas that commonly affect the lungs and lymph nodes. It most often occurs in adults under 40 years old and has a higher prevalence in African Americans. While the exact cause is unknown, it involves an abnormal immune response in genetically predisposed individuals. Lung involvement is present in 90% of cases and lymph node involvement in 70% of cases. Pulmonary sarcoidosis ranges from asymptomatic hilar lymphadenopathy to progressive pulmonary fibrosis. Skin and eye involvement also occurs in a significant portion of patients.
In 1937, Prof. Hulusi Behçet described a syndrome characterized by recurrent oral and genital ulcers as well as eye inflammation. Known as Behçet's Disease, it is more common in people from the Mediterranean, Middle East and Asia. The cause is unknown but likely involves a genetic predisposition interacting with environmental triggers. Symptoms vary but can include oral, genital and eye lesions as well as skin, joint, gastrointestinal, neurological and vascular involvement. Treatment depends on symptoms and may include steroids, immunosuppressants and monoclonal antibodies. Prognosis is variable with mucocutaneous and ocular symptoms often worst early on and mortality increased if pulmonary artery lesions lead to hemoptysis
This document summarizes the presentation and management of a patient with HIV who presented with vision loss in the right eye. Examination found severe vision loss and retinal necrosis in the right eye. Labs showed positive syphilis serology. The patient was diagnosed with syphilitic retinitis and treated with IV penicillin. Vision improved after treatment.
Ocular Manifestations of HIV outlines common eye diseases seen in patients with HIV/AIDS. A study in Ethiopia found 60% of HIV patients had at least one ocular manifestation, most commonly retinal microvasculopathy (24%). Posterior segment manifestations include opportunistic infections like cytomegalovirus retinitis (30-40% of patients) and varicella zoster virus retinitis. Neuro-ophthalmic manifestations occur in 10-15% of patients and include optic neuritis, optic atrophy, and cranial nerve palsies. Children with HIV have fewer ocular manifestations than adults.
Lymphadenopathy refers to abnormal lymph nodes in size, number, or consistency. It can be generalized, affecting more than two lymph node groups, or localized to a single group. Generalized lymphadenopathy has many potential causes, including viral, bacterial, and fungal infections, metabolic disorders, hypersensitivity reactions, and cancers like Hodgkin's disease or non-Hodgkin's lymphoma. Regionally localized lymphadenopathy may be caused by infections or diseases affecting the local area, such as oral infections leading to submandibular lymph node enlargement. A dentist can examine for extraoral lymphadenopathy and make appropriate referrals for testing and diagnosis. Treatment focuses on the underlying cause rather than the lymphaden
This document discusses syphilis, a bacterial infection caused by Treponema pallidum. It begins by describing the etiology, epidemiology, signs and symptoms, and laboratory evaluation of syphilis. It then discusses the stages of syphilis in more detail, including primary, secondary, latent, tertiary, and congenital syphilis. The stages are characterized by different clinical manifestations such as chancres, rashes, neurological symptoms, and cardiovascular involvement. The document also covers the pathology of syphilis, its transmission routes, relationship to HIV, and laboratory tests for diagnosis.
This document discusses HIV and its effects in orthopaedics. It provides statistics on HIV deaths and hospitalizations. It describes the structure and life cycle of the HIV virus, how it attacks the immune system, and the stages of HIV infection. It discusses various orthopaedic problems seen in HIV patients like arthritis and fractures. It also outlines strategies to diagnose and manage HIV, including antiretroviral drug therapies, and precautions orthopaedic surgeons should take when operating on HIV patients.
Sarcoidosis is a multisystem disorder characterized by the formation of noncaseating granulomas in multiple organs. It most commonly involves the lungs, lymph nodes, skin, and eyes. The cause is unknown but believed to be due to an abnormal immune response to unknown antigens in genetically predisposed individuals. Diagnosis is based on clinical features and identification of granulomas on biopsy, and exclusion of other conditions. While often asymptomatic, it can cause respiratory symptoms as well as involvement of other organs. Treatment involves corticosteroids, with hydroxychloroquine or methotrexate as steroid-sparing options. Prognosis is generally good, though some degree of permanent organ dysfunction occurs in about half of
This document discusses the evaluation of lymphadenopathy. It outlines the key steps in evaluation which include determining the size and characteristics of palpable lymph nodes, identifying accompanying symptoms, examining the distribution of enlarged lymph nodes, and considering epidemiological factors. A variety of diagnostic tests are described based on the location and suspected causes of lymphadenopathy including blood tests, imaging studies, biopsies and cultures. The goal of evaluation is to arrive at an accurate diagnosis and guide further treatment.
This document provides an overview of salivary gland disorders, including their presentation, diagnosis, and treatment. It discusses the major salivary glands and their functions. Common salivary gland disorders mentioned include obstructive salivary diseases, infections, Sjogren's syndrome, xerostomia, sialolithiasis, mucoceles, ranulas, pleomorphic adenomas, Warthin's tumor, and mucoepidermoid carcinoma. The document outlines the steps for clinical examination of the salivary glands and describes the various investigative tools that can be used to diagnose salivary gland disorders.
Here are the answers to your questions:
1. Common types of salivary gland benign tumors with origin of each:
- Pleomorphic adenoma - originates from the intercalated duct cells and myoepithelial cells.
- Oncocytic tumors - originate from the striated duct cells.
- Acinous cell tumors - originate from the acinar cells.
- Mucoepidermoid tumors and squamous cell carcinomas develop in the excretory duct cells.
2. The histological features of mucoepidermoid carcinoma include:
- Containing mucin-producing cells and epithelial cells of the epidermoid variety.
- Divided into
The document describes the anatomy and surgical features of the major salivary glands - the parotid gland, submandibular gland, and sublingual gland. It also discusses common benign diseases of the salivary glands including sialolithiasis (salivary stones), mumps parotitis, bacterial parotitis, chronic sialadenitis, and salivary fistulas. Treatment options involve manual removal of stones, incision and drainage of abscesses, or sialadenectomy for certain inflammatory conditions.
This document provides information on salivary gland diseases. It begins with the anatomy of the major salivary glands (parotid, submandibular, sublingual) and minor salivary glands. It then discusses the embryology, microanatomy, and functions of saliva. The document outlines various non-neoplastic salivary gland disorders including sialectasis, ranulas, mucoceles, irradiation reactions, and necrotizing sialometaplasia. It provides details on diagnostic tests and treatments for conditions affecting the salivary glands.
Salivary gland diseases , Dr.Syed Alam ZebSyed Alam Zeb
This document summarizes key information about salivary gland diseases. There are four main salivary glands: the parotid glands, submandibular glands, and two sublingual glands. Disorders of the sublingual glands are rare and include retention cysts and tumors. Ranulas are mucous cysts that can occur in the sublingual or submandibular glands. Submandibular gland disorders include infections, stones, and tumors. The parotid gland can develop infections, tumors, or stones, with pleomorphic adenoma being the most common tumor. Surgeries for these glands aim to remove pathology while protecting nearby nerves.
The document provides information on salivary glands including their embryology, anatomy, functions, blood supply, nerve supply, and common disorders. It describes the three major salivary glands - parotid, submandibular, and sublingual glands. The parotid gland is the largest salivary gland and is located in front of ear. The submandibular gland is below the mandible. The sublingual glands are numerous small glands under the tongue. Saliva contains water and electrolytes and helps with swallowing, speech, and digestion. The glands are supplied by parasympathetic and sympathetic fibers. Common disorders include infections, stones, cysts and Sjog
This document provides an overview of the anatomy of the major salivary glands - the parotid, submandibular, and sublingual glands. It describes the location, structure, relations, blood supply, nerve supply, and clinical implications of each gland. The parotid gland is the largest salivary gland and is located below and in front of the external ear. The submandibular gland is situated in the submandibular triangle below the mandible. The sublingual glands are the smallest salivary glands and are located under the tongue in the floor of the mouth. The document also briefly discusses surgical approaches like the Blair and facelift incisions for parot
The document discusses the major salivary glands - parotid, submandibular, and sublingual glands. It notes that the submandibular gland has superficial and deep portions separated by the mylohyoid muscle. Diagnosing submandibular gland swelling involves checking for transillumination and palpating for movement during swallowing. Parotid calculi can be identified through plain radiographs or CT scans. The facial nerve branch at risk during submandibular gland surgery is the marginal mandibular nerve.
This document summarizes the anatomy and surgical approaches related to the major salivary glands. It describes the location and relations of the parotid, submandibular, and sublingual glands. For each gland, it details the blood supply, lymphatic drainage, and nerve supply. It also outlines the surgical approaches for removing or accessing portions of each gland, including superficial and total parotidectomy, and intraoral, extraoral, and transoral approaches for the submandibular and sublingual glands. Key anatomical structures addressed include the facial nerve branches in the parotid and relations to the lingual and hypoglossal nerves for the submandibular and sublingual g
This document provides an overview of non-neoplastic salivary gland disorders. It discusses various classifications of these disorders and then describes specific conditions in detail under categories such as developmental disorders, infections, traumatic/ischemic disorders, and autoimmune disorders. Key points include descriptions of common developmental disorders like ductal atresia and polycystic disease of the parotid. Infectious disorders covered include viral sialadenitis from mumps virus and bacterial sialadenitis. Conditions resulting from trauma or ischemia like cheilitis glandularis and necrotizing sialometaplasia are also summarized.
The document summarizes the anatomy of the parotid and submandibular salivary glands. It describes the location, structure, relations to surrounding tissues, blood supply, nerve supply, and duct system of each gland. Key details include that the parotid gland is the largest salivary gland located near the ear, and the submandibular gland has superficial and deep parts located under the mandible in the digastric triangle region.
Salivary glands secrete saliva, which plays an important role in maintaining oral health. There are three major salivary glands - the parotid gland, submandibular gland, and sublingual gland. The parotid gland is the largest salivary gland and is located below the external ear. The submandibular gland is located beneath the mandible. The sublingual gland is the smallest salivary gland and is located under the tongue. Saliva contains enzymes and minerals that protect teeth from decay and support digestion. The salivary glands and saliva play an essential role in oral health.
The document discusses salivary gland diseases, focusing on sialadenitis (inflammation of the salivary glands) and salivary gland tumors. Sialadenitis can be caused by viruses, bacteria, or autoimmune disorders. The most common viral cause is mumps. Bacterial sialadenitis often results from ductal obstruction. Chronic sialadenitis is usually caused by Sjögren's syndrome. Common benign salivary gland tumors include pleomorphic adenoma, Warthin's tumor, and monomorphic adenomas. Malignant tumors include mucoepidermoid carcinoma and adenoid cystic carcinoma.
The document summarizes salivary gland diseases. The major salivary glands are the parotid, submandibular, and sublingual glands. Common presentations of salivary gland disease include dry mouth, swelling, and masses in the glands. Causes can include Sjogren's syndrome, infections, tumors, medications, and systemic diseases. Diagnosis involves evaluating dry mouth, imaging, and biopsy of masses. Treatment focuses on managing dry mouth symptoms and surgical removal of tumors.
The parotid gland is the largest major salivary gland. It is located below and in front of the external ear. The parotid gland develops early in the fourth week of prenatal development. It has multiple surfaces and borders that relate to surrounding structures like the mandible, masseter muscle, and facial nerve which branches within the gland. The parotid gland secretes saliva through the parotid duct which travels anteriorly to open in the mouth. It receives nerve supply from both the parasympathetic and sympathetic nervous systems. Lymph from the gland drains to local and deep cervical lymph nodes.
This document discusses salivary gland diseases. It begins by describing the normal anatomy and function of the major and minor salivary glands. It then discusses various diseases affecting the salivary glands including inflammatory conditions like sialadenitis, infections, salivary stones, cysts, tumors, and dysfunction. Specific conditions covered in more detail include mumps, sialolithiasis, Sjogren's syndrome, mucocele, necrotizing sialometaplasia, pleomorphic adenoma, Warthin's tumor, mucoepidermoid carcinoma, and adenoid cystic carcinoma. The document provides information on clinical features, diagnosis, and treatment for each condition.
This document discusses evaluation of salivary glands. It begins with an introduction to salivary glands and saliva. It then describes methods for clinical examination of salivary glands including visual examination, palpation, and measuring salivary flow rates. It also discusses various radiological techniques used in evaluation of salivary glands such as sialography, ultrasonography, scintigraphy and MRI. Finally, it briefly covers classification and descriptions of common salivary gland diseases.
Diagnostic Imaging of Salivary, Parathyroid and Thyroid GlandsMohamed M.A. Zaitoun
This document provides an overview of salivary gland, parathyroid gland, and thyroid gland diseases. It discusses several common salivary gland conditions including sialolithiasis, sialosis, sialoadenitis, Sjogren's disease, and cystic lesions. For each condition, it describes the incidence, etiology, location, and radiographic features as seen on imaging like CT, MRI, ultrasound, and sialography. It provides examples of images showing the characteristic findings of each disease. In summary, the document is a radiologist's guide to recognizing and differentiating various head and neck gland diseases based on their imaging appearance.
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Salivary gland infections are usually viral but can also be bacterial or fungal. The parotid glands are most commonly infected. Mumps is a viral infection that causes parotitis and is transmitted through airborne droplets. It has an incubation period of 2-3 weeks and causes bilateral swelling of the parotid glands. Diagnosis is made through viral serology and treatment is usually supportive. Complications can include orchitis, meningitis, and hearing loss. Vaccination has reduced mumps cases.
This document discusses HIV/AIDS and considerations for surgery in HIV-infected patients. It covers the epidemiology and transmission of HIV, surgical procedures commonly performed in HIV patients like draining abscesses, anorectal surgeries, and managing acute abdominal issues. Occupational risks for surgeons are addressed, including post-exposure prophylaxis guidelines. Universal precautions like barriers, vaccination, and waste disposal are emphasized to prevent transmission during procedures.
The document discusses the anatomy, development, disorders, and tumors of the parotid gland. It begins by describing the location and structures of the parotid gland. It then discusses various inflammatory and infectious disorders that can affect the gland such as mumps, bacterial infections, and HIV-associated sialadenitis. Obstructive disorders from stones, strictures, or papillary obstruction are also reviewed. The majority of the document focuses on tumors of the parotid gland, describing the classification and most common tumor types as well as their presentation, investigations, and surgical management.
The document discusses diseases of the salivary glands including sialadenitis, obstruction and traumatic lesions, sialadenosis, and salivary gland tumors. Sialadenitis can be acute or chronic and is usually caused by bacterial or viral infection. Obstruction can be due to calculi, strictures, or trauma. Sialadenosis involves non-inflammatory swelling and is associated with various systemic conditions. Tumors include pleomorphic adenoma, Warthin's tumor, and carcinomas. Treatment involves surgery with potential adjuvant radiation or chemotherapy depending on tumor type, size, grade, and involvement of surrounding structures.
1. Oral ulcers, or oral ulcerations, are breaks in the oral mucosa that are a common feature of stomatitis. Important causes of oral ulcers include infectious diseases like herpes and tuberculosis, as well as non-infectious conditions like pemphigus vulgaris.
2. Traumatic ulcers are usually caused by ill-fitting dentures and take the form of tender ulcers with red margins. Recurrent aphthous stomatitis is the most common oral mucosal disease, affecting 10-25% of the population. Its exact cause is unclear but may involve genetic or immunological factors.
3. Treatment for oral ulcers focuses on pain relief and
1. Sweet's syndrome is an uncommon skin condition characterized by abrupt onset of tender red skin lesions and systemic symptoms. Histopathology shows a dense neutrophilic infiltrate without evidence of infection.
2. Treatment involves oral corticosteroids which provide excellent response within days to weeks. Recurrences may occur in about 30% of cases.
3. Pyoderma gangrenosum is a rare neutrophilic dermatosis presenting as painful cutaneous ulcers with undermined, irregular borders and purulent bases that may enlarge. About half of cases are associated with underlying systemic disease. Treatment focuses on controlling underlying conditions and using high-dose corticosteroids or immunosuppressants.
Typhoid fever is a severe illness caused by the bacteria Salmonella typhi. It is characterized by prolonged fever and can invade the liver, spleen, and other organs if untreated. It occurs primarily in developing countries with poor sanitation. Persons are infected by consuming food or water contaminated by the feces or urine of infected individuals. Diagnosis involves isolating the bacteria from blood or bone marrow cultures. Antibiotics are the primary treatment and help reduce complications if started early. Vaccines can help prevent infection but hygiene practices are also important for those in endemic areas.
This document discusses sexually transmitted infections including syphilis, gonorrhea, chlamydia, and HSV. It provides details on the pathogenesis, transmission, clinical manifestations, diagnosis, and treatment of each STI. For syphilis, gonorrhea and chlamydia, it outlines the recommended screening, diagnostic tests including NAAT and culture, and CDC-recommended treatment regimens for pregnant and non-pregnant patients. Complications of untreated STIs for both mother and fetus are also discussed.
Syphilis is a sexually transmitted infection caused by the bacterium Treponema pallidum. It has four stages - primary, secondary, latent, and tertiary - and can also be transmitted from mother to fetus. Diagnosis involves tests to detect antibodies against T. pallidum such as RPR and TPPA. Treatment is with penicillin, though dose and duration varies by stage. Without treatment, later complications can include neurosyphilis, cardiovascular disease, and gummatous lesions. Ongoing research aims to develop vaccines and better understand disease progression and response to infection.
The liver is commonly injured in abdominal trauma, with blunt injuries more frequent than penetrating injuries. Liver trauma can cause contusions, lacerations, or avulsions. Management involves addressing associated injuries, resuscitation, injury assessment with imaging, and treatment such as correcting coagulopathy, suturing lacerations, or resection for major vascular injuries. Complications include hematoma, abscess, bile collections, or fistulas.
The document discusses several ulcerative sexually transmitted infections (STIs), including genital herpes, syphilis, chancroid, lymphogranuloma venereum, and granuloma inguinale. For each STI, it provides information on the causative pathogen, pathogenesis, epidemiology, clinical presentation, diagnostic workup, management, and prognosis. The document aims to give healthcare providers a comprehensive overview of these important ulcerative STIs.
This document discusses sexually transmitted infections (STIs), including their causes, symptoms, and treatments. It focuses on gonorrhea, caused by Neisseria gonorrhoeae. Gonorrhea symptoms vary between males and females and can include discharge and dysuria. Complications include pelvic inflammatory disease and disseminated gonococcal infection. Treatment involves ceftriaxone or other cephalosporins. The document also briefly outlines Chlamydia trachomatis, lymphogranuloma venereum, syphilis, and neurosyphilis.
The document discusses various salivary gland disorders including infections, inflammatory conditions, cysts, tumors and other pathologies. It provides details on:
- Acute and chronic bacterial sialadenitis, most commonly caused by retrograde infection from the mouth. Acute infections more often affect the parotid gland.
- Viral infections like mumps can cause acute non-suppurative sialadenitis. Mumps is spread through droplets and involves the parotid glands.
- Sjögren's syndrome is an autoimmune condition characterized by lymphocytic destruction of exocrine glands causing dry mouth and eyes. Diagnosis involves labial biopsy.
- Common benign sal
Syphilis is a sexually transmitted infection caused by the bacterium Treponema pallidum. It has four stages - primary, secondary, latent, and tertiary. It is most commonly spread through sexual activity but can also be transmitted from mother to baby. Diagnosis involves blood tests and microscopy. While treatable with antibiotics, syphilis remains a global health problem.
This document provides an overview of acute pelvic inflammatory disease (PID). It discusses the definition, epidemiology, risk factors, microbiology, pathogenesis, stages, clinical features, diagnostic criteria, investigations, management, complications, prevention of reinfection, and follow up of PID. PID is caused by the ascending spread of microorganisms from the cervix to the upper genital tract organs. It is commonly caused by sexually transmitted organisms like N. gonorrhoeae and C. trachomatis. Clinical features include lower abdominal and pelvic pain, fever, abnormal vaginal discharge. Management involves antibiotic therapy based on CDC guidelines to treat infection and prevent complications like infertility.
This document discusses communicable diseases that commonly affect the elderly population. It summarizes that geriatrics refers to healthcare for elderly people, noting that the elderly population is growing rapidly. Some common communicable diseases that impact the elderly include pneumonia, influenza, herpes zoster, urinary tract infections, and gastrointestinal infections such as H. pylori and C. difficile infections. Prevention strategies include vaccination, hygiene practices, and early treatment of infections to prevent worsening and spread.
STD by Dr Rajesh Sarkar, PhD in Medical Microbiology with PostdoctoratesDrRajeshSarkarPhDMed
STD (excluding HIV)
I am an Academic and Scientist in Medical Microbiology and Immunology and no business owned by me.
I do not know Indian cities very well. Definitely not Chennai!
I need to mention this as identity theft is a serious issue in my career! All glory's goes to others of my handworks.
Everyone's child's are not born by me.
This document provides a summary of key information about primary care approaches to treating HIV patients, including:
1) It discusses the history and epidemiology of HIV, modes of transmission, clinical presentations to different specialists, treatment with HAART, and baseline evaluations prior to treatment initiation.
2) Primary care providers should offer ART to patients with CD4 counts <200 or symptoms, consider treatment for counts 200-350, and can defer for asymptomatic patients with counts >350 and low viral loads.
3) When initiating ART, providers should evaluate readiness, ensure adherence, perform baseline testing, and select preferred first-line regimens consisting of 2 NRTIs combined with an NNRTI or PI.
This document summarizes Behcet's disease (BD), a multisystem inflammatory vasculitis affecting blood vessels of all sizes. It is characterized by recurrent oral and genital ulcers, skin lesions, and eye inflammation. It can also involve other organ systems like the arteries, veins, intestines, and brain. The cause is unknown but may involve genetic and infectious factors. Diagnosis is based on clinical features and pathergy testing can support the diagnosis. Prognosis depends on organ involvement and treatment aims to reduce inflammation and prevent complications.
Similar to @ Non neoplasitc salivary gland diseases (20)
The Pure Tone Audiometry (PTA) test is used to determine a person's hearing threshold levels using pure tone pulses presented at standardized frequencies from 125-8000Hz. The threshold is the lowest sound level at which a person detects 50% of tones. Specific test conditions include the type and presentation of tones. Tones are presented one ear at a time through earphones to determine if hearing loss is present and what type based on the audiogram configuration. Sources of error in PTA tests include physiological, psychological, methodological, physical/acoustic factors, and ambient noise levels.
This document summarizes different types of vertigo and nystagmus. It describes 7 causes of vertigo: 1) Benign Paroxysmal Positional Vertigo, 2) Meniere's disease, 3) Vestibular Neuronitis, 4) Perilymph Fistula, 5) Vestibulotoxic drugs, 6) Labyrinthitis, and 7) Acoustic Neuroma. It also defines nystagmus as involuntary eye movements and classifies the degree of nystagmus into three levels based on the components of eye movement involved.
Stridor is an abnormal noise caused by partial airway obstruction. The document discusses different types of stridor and common causes of stridor in children, including croup (laryngotracheobronchitis), epiglottitis, and spasmodic croup. Croup most often affects children ages 3 months to 3 years and is caused by influenza viruses. Epiglottitis typically affects children ages 3 to 6 years and can cause drooling, muffled voice, and stridor. Management of airway obstruction may include oxygen, humidification, steroids, nebulizers, and intubation or tracheostomy in severe cases.
Obstructive sleep apnea in children is defined as cessation of breathing for 6 seconds or more during sleep, which can lead to hypoxia and hypercapnia, disrupting normal sleep patterns. The severity of obstructive sleep apnea is classified based on the number of apneas per hour as mild, moderate, or severe. Obstructive sleep apnea can be caused by blockages at four levels - the adenoid pad, tonsils, tongue base, or supraglottic area. Treatment depends on the site of obstruction and may include adenoidectomy, tonsillectomy, use of nasal airways or mandibular advancement devices, or laser procedures. Adenotonsillectomy c
The nose has important anatomical structures that allow it to carry out its key physiological functions. Externally, the nose is made up of bone and cartilage, including the nasal bones and lateral cartilages. Internally, the nasal cavity contains three turbinates that divide it into air passages. The osteomeatal complex includes structures like the agger nasi and ethmoid bulla that are involved in drainage and ventilation of the paranasal sinuses. Physiologically, the nose conditions inhaled air by warming, humidifying and filtering it. It also plays a role in respiration and protects the lower airways through mucociliary clearance.
This document discusses diseases of the tonsils, including recurrent acute tonsillitis and chronic tonsillitis. It outlines indications for tonsillectomy in cases of recurrent tonsillitis. The normal flora found on the tonsils is described, as are complications of tonsillitis like scarlet fever and rheumatic fever. Treatment approaches for acute and chronic tonsillitis are discussed. The role of the tonsils in immunity is covered. Finally, potential transmission of prion diseases like Creutzfeldt-Jakob disease via contaminated tonsillectomy instruments is mentioned.
The tonsils are lymphoid tissues located in the throat that help protect the respiratory and digestive tracts from infection. Common pathogens found in the tonsils include streptococcus and other bacteria. Acute tonsillitis is usually caused by streptococcus and presents with fever, sore throat, and painful swallowing. It is generally self-limiting but complications can include abscesses or spread of the infection. Chronic or recurrent tonsillitis may require treatment like antibiotics or tonsillectomy.
Corticosteroids readily diffuse into cells and bind with glucocorticoid receptors to form complexes that interact with proteins and act as transcription factors, reducing inflammation. Intranasal corticosteroids become effective within 3 hours and are most effective for symptoms like itching and sneezing, while systemic corticosteroids are more effective for blockage and anosmia. Methylprednisolone and dexamethasone are preferred for intravenous use due to their minimal mineralocorticoid effects. Prednisone is converted to prednisolone in the liver, while dexamethasone has minimal mineralocorticoid effects.
The document discusses several viruses that cause respiratory infections including influenza, respiratory syncytial virus, parainfluenza, adenovirus, rhinovirus, and coronaviruses. It notes that respiratory tract infections are very common worldwide and responsible for many lost work days. Diagnosis methods include enzyme immunoassays, immunofluorescent antibody tests, and PCR tests. Treatment depends on the virus but may include antivirals like acyclovir, oseltamivir, ribavirin, and interferon. Herpes simplex virus, Epstein-Barr virus, human papillomavirus, and others are described in relation to various diseases. Conditions with possible viral etiologies include Bell's p
The document discusses several types of tumors that can occur in the head and neck region of children. Lymphoma, rhabdomyosarcoma, medullary carcinoma of the thyroid, and neuroblastoma are some of the tumors mentioned. For lymphoma, the most common presentation is cervical lymphadenopathy, while rhabdomyosarcoma often presents with pain and swelling in locations like the orbit or paranasal sinuses. Diagnosis involves biopsy along with imaging and lab tests. Treatment depends on the specific tumor but may involve chemotherapy, radiation, and surgery. All childhood cancer cases should be referred to a specialist center.
The document discusses the adenoid and adenoidectomy procedure. It covers the anatomy and function of the adenoid, including its role in immunity. It describes pathological effects like otitis media, upper airway obstruction, and rhinosinusitis. The assessment, management, and complications of adenoidectomy are outlined. While adenoidectomy is effective for upper airway obstruction and otitis media with effusion, its efficacy for other issues like recurrent ear infections, sleep apnea, and sinusitis requires more research. Mild adenoid hypertrophy does not always require surgery.
This document provides information on otitis media with effusion (OME), including its definition, causes, characteristics, diagnosis, and epidemiology. Specifically:
- OME is the chronic accumulation of fluid in the middle ear for at least 12 weeks, usually presenting as hearing impairment. It is often preceded by acute otitis media or upper respiratory infection.
- The fluid results from inflammation of the Eustachian tube epithelium that prevents drainage of the middle ear. Histological examination shows replacement of normal epithelium with mucus-secreting cells.
- Diagnosis involves otoscopy, pneumatic otoscopy, and tympanometry which can classify effusions. Type B
This document defines and discusses gastro-oesophageal reflux, aspiration, their causes, symptoms, diagnostic tests and treatments. It notes that reflux is common in infants and usually physiological, but can become pathological if harming the child. Aspiration risks include impaired swallowing coordination or laryngeal protection. Diagnostic tests are videofluoroscopy and fibreoptic evaluation of swallowing. Treatments include positioning, thickened feeds, acid suppression, and sometimes surgery to control severe reflux or reduce saliva production for aspiration.
1) Mycotic diseases of the paranasal sinuses range from indolent infections in healthy individuals to lethal infections in immunocompromised people.
2) Fungal sinusitis is classified into invasive, noninvasive, and allergic types based on histopathology and clinical presentation. Invasive types can spread to nearby structures like the orbit and brain.
3) Diagnosis involves imaging like CT scans to assess bone destruction, biopsy and culture of tissue to confirm infection and identify the fungal species. Treatment depends on the type but may include antifungal drugs, surgery, and improving immune function.
The tonsils are lymphoid tissue located in the throat that help the immune system. Acute tonsillitis is usually caused by viruses or bacteria like Streptococcus and is typically self-limiting. Treatment focuses on pain relief and hydration. Antibiotics may help if symptoms persist after 2-3 days. Complications are rare but include peritonsillar abscesses, which are treated with antibiotics and needle aspiration. The tonsils can also present lymphomas or cancers.
This document discusses chronic otitis media, including the histology and pathogenesis. It notes that chronic inflammation is characterized by both tissue destruction and attempts at healing. Repeated infections from the nasopharynx or external ear canal can prevent resolution of otitis media. Persistent bacterial biofilms and chronic perforations of the tympanic membrane also contribute. Chronic retraction of the pars tensa portion of the eardrum can lead to atrophy and complications like cholesteatoma formation over time if not addressed. Early intervention may be warranted for more advanced retractions to prevent future problems.
This document discusses the embryology and presentation of several congenital anomalies of the head and neck region, including branchial arch fistulae, thyroglossal duct anomalies, preauricular sinuses, and lymphangioma. It describes how these structures develop from the branchial arches and pouches during embryogenesis. Common locations and presentations of each anomaly are provided, along with diagnostic evaluation and treatment approaches. Surgical excision is often needed but can be challenging due to the relationship of these structures to nearby nerves and vessels.
The document discusses the use of antimicrobial therapy and various classes of antibiotics. It provides details on the mechanisms of action, spectra of activity, indications for use, and side effects of different classes of antibiotics including beta-lactams (penicillins, cephalosporins, carbapenems), glycopeptides, quinolones, sulfonamides/trimethoprim, metronidazole, tetracyclines, chloramphenicol, macrolides, aminoglycosides, streptogramins, and oxazolidinones. It also discusses Clostridium difficile infection as a common gastrointestinal side effect caused by antibiotic use.
Acute otitis media (AOM) is an inflammation of the middle ear caused by bacterial or viral infection. It is common in young children and causes symptoms like ear pain, fever, and hearing loss. While most cases clear up without treatment, antibiotics are usually prescribed to reduce symptoms and risk of complications. For recurrent cases, management involves identifying and addressing risk factors, medical or surgical prophylaxis including ventilation tubes, and vaccination when available. AOM poses a significant burden as it is one of the most frequent reasons children receive antibiotics.
Swallowing involves three phases - oral, pharyngeal, and esophageal. In the oral phase, food is mixed with saliva and moved to the back of the throat by the tongue. The soft palate then elevates to protect the nasal airway. In the pharyngeal phase, the larynx and pharynx elevate to allow food to pass while protecting the airway, and a series of muscle contractions propel the food over the epiglottis and into the esophagus. In the esophageal phase, the upper esophageal sphincter relaxes to allow the food to pass into the esophagus for peristalsis down to the stomach.
1. Non-neoplastic salivary gland diseases
Infections of the salivary gland
Viral & bacterial infection are the the most common infectious disorders of the salivary glands,
although very rarely other infectious agents can be involved. In addition, the salivary glands may be
the site of asymptomatic viral infection- particularly some of the herpes group( human herpes 6,
CMV & human herpes 8,while saliva can be a vehicle for a wide range of infectious agents including
hepatitis B virus, hepatitis C, Humane herpes virus-8, & HIV.
Infections of the salivary glands.
Common Uncommon
Acute suppurative sialadenititis
Mumps
Human immunodeficiency virus associated
salivary gland disease;
Hepatitis C virus-associated sialoadenitis
Human T-lymphocytic virus 1(HTLV-1)
Epstein-Barr virus
CMV
Mycobacteria tuberculosis
Non-tuberculous mycobacteria
Haemophilus infleuenzae
E.coli
Treponema pallidum
Actionmycosis
Salmonella
Histoplasma
Candidia sp.
Cysticercosis
Mumps (epidemic parotitis)
Mumps is an acute generalized paramyxovirus infection of children & young adults. Mumps typically
affects the major salivary glands, although involvement of the other structures can occur including
the pancrease, testes , ovaries, brain, breast, liver, joints, &heart.
Mumps is transmitted via the droplet route & has an incubation time of approximately 14-18 days.
2. Clinical features
Patient with initial pyrexia, chills 7 facial pain. The parotid is typically bilateral enlarged, although
this may be unilateral. There is often swelling of the submandibular glands together with
lymphadenopathy, giving rise to profound facial & neck swelling.
Orchitis may develop approximately four to five days ofter the onset of parotitis, typically one testis
but both testis can be involved. Orchitis tends to arise in post-pubertal boys.
Mumps can give rise to a viral meningitis(lymphocytic). Other neurological manifestation include
retrobulbar neuritis& encephalitis. Likewise cardiac hepatic & joint can occur.
Diagnosis of mumps is typically based on clinical picture; it may be confirmed by detection of viral
IgG &IgA
Treatment:
Analgesic & appropriate fluid intake is tha main stay of treatment.
Corticosteroids may be effective for severe parotitis & other organ involvement like orchitis.
Mumps can be prevented with vaccination (Mumps/measles/rubella(MMR)).
HIV salivary gland disease
HIV salivary gland disease is a distinct disorder characterized by recurrent or persistent major
salivary gland enlargement & xerostomia, tends to arise late in HIV infection, although can be first
manifestation. A variety of lesions can underlie the salivary gland disease of HIV infection includes
bacterial sialadenitis, intraparotid lymphadenopathy, primary or metastatic non-Hodgkin’s
lymphoma or Kaposi’s sarcoma.
Salivary gland disease in HIV infection.
Disease Clinical features
HIV salivary gland disease
Kaposi’s sarcoma
No-Hodgkin lymphoma
Lymphadenopathy
Acute suppurative sialadenitis
Xerostomia
Salivary gland enlargement
HIV salivary gland disease more generalized termed diffuse infiltrated lymphocytosis syndrome
characterized by CD8 T cell infiltration of the lungs ,salivary glands, & lacrimal glands.
Clinical picture mimics that of Sjogren’s syndrome however, there are distinct histopathological &
serological differences between two disorders. Patient with HIV do not have anti-Ro & anti-La
antibodies but do have hypergammaglobulinaemia.
3. Histologically ; perivascular, periacinar & periductal lymphocytic infiltration. Majority CD8 T cells.
Multicystic lymphoepithelial lesions may also occur due to intraductal obstruction by
hyperplastic/infiltrating lymphoid tissue.
Diagnosis
FNAC to exclude malignancy;
Similar to Sjogren’s syndrome.
Treatment
Antiretroviral therapy may cause at least some short-term resolution of the swelling.
Others therapies are repeared aspiration, tetracycline sclerosis or surgical removal of an enlarged
gland.
External beam radiation (8-10 Gy) can cause transient improvement, although higher dose (24Gy)
can cause resolution of the disease for at least for 24 months- without causing severe xerostomia.
Hepatitis c virus infection
Unlike other hepatotropic hepatitis viruses, hepatitis C virus (HCV) gives rise to a wide spectrum of
extrahepatic manifestation that include salivary gland. Hepatitis C virus-associated salivary gland
disease arises as many as 80% of the infected patients.
Xerostomia is the predominant symptom of HCV-associated salivary gland disease.
The histopathological features of HCV-associated sialoadenitis not identical to Sjogren’s syndrome.
In HCV-associated sialoadenitis, there is a pericapillary lymphocytic infiltration within salivary gland.
Occasionally HCV infection give rise to non-Hodgkin’s lymphoma but not Sjogren’s syndrome.
Suppurative sialadenitis (suppurative parotitis)
Acute suppurative sialadenitis is an uncommon disorder, usually of childhood, characterized by
recurrent or persistent enlargement of one major salivary gland. The parotid are more commonly
affected than the submadibular glands. Patient can have episodes of disease akin to acute
suppurative sialoadenitis. Affected patients are generally well & have no disease likely to cause
sialoadenitis, although they may have a history of recurrent parotitis of childhood or previous
sialolithiasis.
In most instances, chronic non-specific sialoadenitis reflects abnormalities of the ductal system- the
recurrent infection having caused or worsen any ductal strictures. Primary cause of this disorder are
small stone sialoliths, less commonly denture induced ductal defect, congenital ductal edfects,
radiotherapy-induced salivary gand damage.
Investigations
Sialography & ultrasonogrphy are the principal investigation.
4. Sialography will reveal stricture & distortion of the major ducts. There can be variable sialectasis.
Clinical feature of the chronic non-specific sialoadenitis is highly varied, about 50% of the patients
have eventual spontaneous resulotion of symptoms after upto 5years & 40 % needs surgical
intervention.
Treatment
-management of acute infection with chronic non-specific sialoadenitis follows that of acute
suppurative disease.(hydration & appropriate antibiotics).
-in addition, sialagogues such as chewing gum, duct& glandular massage, improved oral
hygiene,& therapeutic sialography have been suggested to be useful.
- unless the cause is likely to be a sialolith, subtotal or total surgical removal of the affected
gland may be the only useful treatment.( chronic , non-infected state unless calculi can be
identified.)
Recurrent parotitis of childhood(juvenile recurrent parotitis)
Recurrent parotitis of childhood is characterized by recurrent parotid inflammation usually
associated with non-obstructive sialectasis of the parotid gland.
Recurrent parotitis can occur at any age but usually occur at 3 to 6 years of age. Childhood onset
usually in male but adult onset in female.
The disease is characterized by localized pain & swelling that may last upto 14days. Fever &
overlying erythema are common. Occasionally white mucopus can express from the duct. Usually
unilateral but may be bilateral. The number of attack vary from one to five episodes per year but
may be upto 20 episodes.
The frequency of recurrence tends to peak between 5 to 7 years of age & about 90% of the patients
have resolution of the disease by puberty.
Sialography & ultrasonography reveal sialectasis( this feature can be observed in the non-affected
gland of the opposite side.
Treatment
Analgesic is the mainstay of therapy. Antibiotic do not shorten attacks. In general , disease tends to
resolve and there is no need for surgical intervention.
Sialolithiasis
5. Clinical features
Sialolithiasis is a common disorder characterized by the formation of a calculus usually within the
ductal system of a gland. Sialoliths can arise in both the major & minor salivary glands.
Sialolith are more common in the submandular glands 83%, parotid 10%, sublingual 7%. More
common in female,& much more likely in adult than children.
Sialolithiasis presents as pain & swelling, typically in the submandibular gland with gestation or
eating. The swelling is diffuse, develops rapidly & is often associated with a burning-like local pain.
The swelling is nontender & gradually resolves over a few hours.
Long-standing sialolithiasis may give rise to acute suppurative sialolithiasis or chronic non-specific
sialolithiasis.
The cause of sialolithiasis ; defect migration of autophaogsomes through the ductal system or the
calcification of the mucous plugs. Sialolithiasis may be associated with DM,HTN,& chronic liver
disease & possibly nephrolithiasis but not to water hardness.
Investigations
Plain x-ray may reveal a sialolith- provided it is large & radiopague.
Ultrasonography can detect both radiopaque & radiolucent sialoliths while sialography may also be
helpful. Panoral tomograms are not helpful.
Treatment
When small & accessible, it may be possible to express a sialolith from the submandibular duct by
manual palpation. Or surgically, this carry a risk of stricture formation.
Surgical removal of an affected gland may often be only effective treatment for calculi in the
posterior aspect of the duct or within the gland.
Lithotripsy is most effective for calculi less than 7mm in diameter.
Drug-associated salivary gland disease
A wide range of drug-related salivary disorders can arise, these predominantly comprise salivary
gland swelling, xerostomia, salivary gland pain.
1.Salivary gland swelling
Painless, usually bilateral, salivary gland enlargement may be an occasional side effect
phenylbutazone, chlorhexidine, iodine, radioactive iodine usage. Mild acute sialoadenitis( iodine
mumps) can arise in response to iodine based contrast media for angioplasty. Insulin & interferon &
sulphonamides also causes salivary gland enlargement.
2.Xerostomia
Over 500 drugs can cause dry mouth, common complaints of many elderly people.
6. Principal mechanism of action to cause xerostomia is anticholinergic & sympathomimetic. Therefore,
tricylic , benzodiapines, atropine, betablockers & antihstamin are the most common culprits.
3.Salivary gland pain
Salivary gland enlargement due to sialosis may be associated with DM, hypothyroidism,
malnutrition, hepatic cirrhosis puberty, menopause& antihypertensive drugs.
Treatment of often difficult with endocrine & hepatic causes if sialosis being particularly resistant
even if the underlying disorder is addressed.
Sialosis
Sialosis is an uncommon nonneoplastic & non-inflammatory disorder giving rise to bilateral non-painful
enlargement of the major salivary glands. Sialosis tends to arise in middle to late life with
peak incidence in the fifth & sixth decades. There is a slight female predominace. The parotid glands
are typically affected, indeed often the enlargement is profound. The enlargement develops slowly
& there may be some decrease in salivary flow.
Aetiology is unknown, but may be neuropathy. There is association with DM,
hypothyroidism,malnutrition, alcoholic, & hepatic cirrohsis. Puberty , menopause, reaction to anti
hypertensive drugs.
Sialosis is histopathologically chacterized by acinar cel hypertrophy, atrophy of striated ducts with
oedema of the interstitial connective tissue. Ultimately , widespread fatty replacement of acini.
Treatment
Treatment of the underlying cause.
Rarely surgical reduction of the parotids glands may be necessary.
Pilocarpine successfully resolving sialosis associated with bulimia nervosa.
Bulimia nervosa
Salivary gland enlargement can occur with bulimia nervosa. Functional hypertrophy of the salivary
glands.(autonomic neuropathy, endocrine disease or past alcohol) with high level of serum amylase.
Treatment local application of heat, salivary substitutes & use of pilocarpine may result in reduction
in the size of the parotid gland. Superficial parotidectomy may rarely required.
7. Principal mechanism of action to cause xerostomia is anticholinergic & sympathomimetic. Therefore,
tricylic , benzodiapines, atropine, betablockers & antihstamin are the most common culprits.
3.Salivary gland pain
Salivary gland enlargement due to sialosis may be associated with DM, hypothyroidism,
malnutrition, hepatic cirrhosis puberty, menopause& antihypertensive drugs.
Treatment of often difficult with endocrine & hepatic causes if sialosis being particularly resistant
even if the underlying disorder is addressed.
Sialosis
Sialosis is an uncommon nonneoplastic & non-inflammatory disorder giving rise to bilateral non-painful
enlargement of the major salivary glands. Sialosis tends to arise in middle to late life with
peak incidence in the fifth & sixth decades. There is a slight female predominace. The parotid glands
are typically affected, indeed often the enlargement is profound. The enlargement develops slowly
& there may be some decrease in salivary flow.
Aetiology is unknown, but may be neuropathy. There is association with DM,
hypothyroidism,malnutrition, alcoholic, & hepatic cirrohsis. Puberty , menopause, reaction to anti
hypertensive drugs.
Sialosis is histopathologically chacterized by acinar cel hypertrophy, atrophy of striated ducts with
oedema of the interstitial connective tissue. Ultimately , widespread fatty replacement of acini.
Treatment
Treatment of the underlying cause.
Rarely surgical reduction of the parotids glands may be necessary.
Pilocarpine successfully resolving sialosis associated with bulimia nervosa.
Bulimia nervosa
Salivary gland enlargement can occur with bulimia nervosa. Functional hypertrophy of the salivary
glands.(autonomic neuropathy, endocrine disease or past alcohol) with high level of serum amylase.
Treatment local application of heat, salivary substitutes & use of pilocarpine may result in reduction
in the size of the parotid gland. Superficial parotidectomy may rarely required.