CRANIO CEREBRAL INJURIES FOR MEDICAL STUDENTSwalid maani
This is a simple outline of traumatic injuries which occures to the scalp, skull and brain with some simplified classifications and outlined management
The document discusses several vascular and hereditary retinal diseases:
1. Hypertension affects 15-20% of the population and can lead to complications like ischemic heart disease if not properly treated. Retinal findings in hypertensive retinopathy include arteriolar changes and hemorrhages.
2. Retinal vein occlusion is caused by pressure on the retinal veins and presents with dilated veins, flame-shaped hemorrhages, and retinal edema.
3. Retinal artery occlusion typically results from emboli and presents with sudden vision loss and a cherry red spot at the macula.
4. Retinitis pigmentosa is a group of inherited retinal diseases characterized by night blindness, visual
This document summarizes a case of a 78-year-old female who presented with decreased vision in her right eye. On examination, her vision in the right eye was measured at 20/100 and counting fingers in the left eye. Imaging and labs revealed chronic lacunar infarcts and no signs of infection or inflammation. The patient was diagnosed with anterior ischemic optic neuropathy and started on steroid treatment.
This document provides information on anterior ischemic optic neuropathy (AION), which is the most common cause of acute optic neuropathy in older age groups. It can be divided into two types: arteritic AION, which is due to giant cell arteritis; and non-arteritic AION, which makes up most cases. Both types present with sudden painless vision loss and optic disc swelling. Arteritic AION carries a worse prognosis and requires high-dose steroid treatment to prevent loss of vision in the fellow eye. Non-arteritic AION has a variable course but generally a poor rate of recovery without any proven effective treatments.
Homer is the semi-legendary author of the Iliad and Odyssey, epic poems central to Greek literature. In Greek mythology, Atropos was the Fate who cut the thread of human life, deciding the moment of death. She lends her name to the poisonous plant deadly nightshade. Glaucus was a fisherman transformed into a sea god after eating a magical herb, and may be linked to the treatment of glaucoma symptoms. Don't forget important details about glaucoma types, diagnosis, and treatment complications. Iris is the goddess of the rainbow, and heterochromia iridis can result from various ocular conditions and treatments. Oedipus unwittingly fulfilled a prophecy that
1. Differential diagnosis of disc edema includes conditions like papilledema, optic neuritis, ischemic optic neuropathy, diabetic papillopathy, and hypertensive retinopathy.
2. Papilledema is caused by increased intracranial pressure and presents with bilateral disc swelling and normal vision, while optic neuritis typically causes unilateral vision loss and eye pain.
3. Diabetic papillopathy presents as transient unilateral or bilateral disc edema that resolves within months without vision loss, while malignant hypertension can lead to bilateral disc edema and vision changes as part of hypertensive retinopathy.
CRANIO CEREBRAL INJURIES FOR MEDICAL STUDENTSwalid maani
This is a simple outline of traumatic injuries which occures to the scalp, skull and brain with some simplified classifications and outlined management
The document discusses several vascular and hereditary retinal diseases:
1. Hypertension affects 15-20% of the population and can lead to complications like ischemic heart disease if not properly treated. Retinal findings in hypertensive retinopathy include arteriolar changes and hemorrhages.
2. Retinal vein occlusion is caused by pressure on the retinal veins and presents with dilated veins, flame-shaped hemorrhages, and retinal edema.
3. Retinal artery occlusion typically results from emboli and presents with sudden vision loss and a cherry red spot at the macula.
4. Retinitis pigmentosa is a group of inherited retinal diseases characterized by night blindness, visual
This document summarizes a case of a 78-year-old female who presented with decreased vision in her right eye. On examination, her vision in the right eye was measured at 20/100 and counting fingers in the left eye. Imaging and labs revealed chronic lacunar infarcts and no signs of infection or inflammation. The patient was diagnosed with anterior ischemic optic neuropathy and started on steroid treatment.
This document provides information on anterior ischemic optic neuropathy (AION), which is the most common cause of acute optic neuropathy in older age groups. It can be divided into two types: arteritic AION, which is due to giant cell arteritis; and non-arteritic AION, which makes up most cases. Both types present with sudden painless vision loss and optic disc swelling. Arteritic AION carries a worse prognosis and requires high-dose steroid treatment to prevent loss of vision in the fellow eye. Non-arteritic AION has a variable course but generally a poor rate of recovery without any proven effective treatments.
Homer is the semi-legendary author of the Iliad and Odyssey, epic poems central to Greek literature. In Greek mythology, Atropos was the Fate who cut the thread of human life, deciding the moment of death. She lends her name to the poisonous plant deadly nightshade. Glaucus was a fisherman transformed into a sea god after eating a magical herb, and may be linked to the treatment of glaucoma symptoms. Don't forget important details about glaucoma types, diagnosis, and treatment complications. Iris is the goddess of the rainbow, and heterochromia iridis can result from various ocular conditions and treatments. Oedipus unwittingly fulfilled a prophecy that
1. Differential diagnosis of disc edema includes conditions like papilledema, optic neuritis, ischemic optic neuropathy, diabetic papillopathy, and hypertensive retinopathy.
2. Papilledema is caused by increased intracranial pressure and presents with bilateral disc swelling and normal vision, while optic neuritis typically causes unilateral vision loss and eye pain.
3. Diabetic papillopathy presents as transient unilateral or bilateral disc edema that resolves within months without vision loss, while malignant hypertension can lead to bilateral disc edema and vision changes as part of hypertensive retinopathy.
INTRODUCTION
Optic nerve ischemia most frequently occurs at the optic nerve head, where structural crowding of nerve fibers and reduction of the vascular supply may combine to impair perfusion to a critical degree and produce optic disc edema. The most common such syndrome is termed anterior ischemic optic neuropathy(AION).
Generally, AION is categorized as either arteritic (associated with temporal arteritis) or nonarteritic .
The document discusses various retinal conditions and diseases. It provides information on symptoms, clinical findings, inheritance patterns, pathophysiology and testing results for each condition. These include congenital stationary night blindness, fundus albipunctatus, retinitis pigmentosa, cone dystrophy, Stargardt disease, Best disease, gyrate atrophy, choroideremia, juvenile retinoschisis, Bardet-Biedl syndrome, Tay-Sachs disease, Bietti’s crystalline retinopathy and others. It also covers post-traumatic conditions like commotio retinae, choroidal rupture, intraocular foreign bodies, shaken baby syndrome and Valsalva retinopathy.
This document provides an overview of optic atrophy, including:
1. It defines optic atrophy as degeneration of the optic nerve due to damage to the visual pathways from the retina to the lateral geniculate body.
2. It classifies optic atrophy based on whether damage originates in the retina or more centrally, and by cause. Primary optic atrophy occurs without swelling, while secondary involves prior swelling.
3. Causes of primary optic atrophy include optic neuritis, compression, hereditary conditions, toxins, trauma, and multiple sclerosis. Secondary optic atrophy follows conditions like papilledema.
4. Treatment focuses on the underlying cause, with vitamins sometimes used
This document provides an overview of polypoidal choroidal vasculopathy (PCV), including its history, definitions, pathogenesis, histopathology, demographics, clinical features, investigations, differential diagnosis, classification, treatment and guidelines. PCV is characterized by polyp-like subretinal vascular lesions associated with hemorrhagic detachments of the retinal pigment epithelium. Indocyanine green angiography is the gold standard for diagnosis, showing focal hyperfluorescence arising from the choroidal circulation within minutes. Treatment options include observation, thermal laser photocoagulation, photodynamic therapy, anti-VEGF therapy and combination therapies.
This document discusses pediatric cataract and leucocoria (white pupil). It defines leucocoria as a white reflection seen in the pupil that could indicate an underlying condition like cataract, retinoblastoma, or persistent hyperplastic primary vitreous. The document outlines the causes, presentations, classifications, management, and visual prognosis of pediatric cataracts. It emphasizes the importance of early referral for any detected leucocoria to rule out retinoblastoma or other serious conditions and prevent amblyopia. Overall management of pediatric cataracts aims to restore vision through early surgery and amblyopia treatment for the best possible visual outcomes.
This document provides an overview of congenital cataracts, including:
- The epidemiology, with an incidence of 1-3 per 10,000 births globally. Rates vary by region.
- Classification systems based on age of onset, laterality, morphology, and etiology.
- Descriptions of various morphological types of cataracts like nuclear, lamellar, anterior polar, and their associated etiologies.
- Cataracts can be associated with genetic syndromes, metabolic disorders, infections acquired in utero, and other ocular anomalies.
- Recognition of cataract type provides clues about etiology, timing of surgery, and prognosis.
The document describes a case presentation of a 55-year-old male with a lesion on his left eye that was diagnosed as an apocrine hidrocystoma. Apocrine hidrocystomas are benign cystic proliferations of the apocrine glands that commonly appear as solitary, soft, dome-shaped papules or nodules on the eyelids. Histological examination showed multiple cystic areas lined by apocrine-type secretory epithelium, confirming the diagnosis. Treatment options include incision, drainage, electrosurgical destruction or excision to prevent recurrence.
1) The document provides information on various ophthalmic conditions categorized by number, with each section labeled "1" through "25".
2) Key details are provided for each condition, including associated symptoms, inheritance patterns, relevant imaging/tests, and anatomical associations.
3) Mnemonic devices are presented throughout to help remember details, such as "The Smaller the Mirror, The Peripheral The View" for Goldmann goniolens mirrors.
This document discusses different types of ischemic optic neuropathy, including anterior ischemic optic neuropathy (AION), non-arteritic AION, arteritic AION, and posterior ischemic optic neuropathy. It describes the blood supply of the optic nerve head and risk factors, clinical features, investigations, treatments, and prognosis for each type. The main causes are reduced blood flow to the optic nerve head leading to infarction. AION is the most common cause of acute optic neuropathy in those over 50. Arteritic AION is caused by giant cell arteritis and requires high-dose steroid treatment to prevent blindness.
1. Recurrent central serous chorioretinopathy (CSCR) occurs when there is a new episode of CSCR more than 12 months after resolution of an initial episode. Recurrence rates range from 20-50%.
2. Risk factors for recurrence include subretinal hyperreflective foci, increased subfoveal choroidal thickness, intensity of fluorescein leakage, irregular pigment epithelial detachments, and choroidal hyperpermeability patterns on indocyanine green angiography.
3. Treatment options for recurrent CSCR include focal laser photocoagulation, photodynamic therapy, mineralocorticoid receptor antagonists like eplerenone, and micropulse laser therapy.
The document summarizes a case presentation of a 43-year-old male with blurred vision who underwent LASIK surgery 9 years prior and now presents with worsening vision. Examination found stromal opacities and the patient underwent penetrating keratoplasty (PKP) in the right eye. One year later, vision decreased in both eyes and the patient underwent PKP in the left eye. The document discusses granular dystrophy, a genetic bilateral corneal dystrophy, and reviews the patient's clinical course and management.
This document discusses painful ophthalmoplegia, which presents as periorbital or hemicranial pain, ipsilateral ocular motor palsies, and sensory loss in the trigeminal nerve distribution. Causes include aneurysms, carotid cavernous fistulas, cavernous sinus thrombosis, tumors, and infections. Evaluation involves imaging like MRI/CT/angiography. Management depends on the underlying cause but may include antibiotics, anticoagulation, surgery, or steroids. Prognosis depends on early diagnosis and treatment, with potential for residual neurological deficits.
Depositions and Degenerations of Conjuctiva and Cornea.docxIddi Ndyabawe
This document provides an overview of degenerative changes that can occur in the conjunctiva, cornea, and sclera. It describes age-related changes such as thinning and loss of transparency in the conjunctiva. Specific conditions discussed include pinguecula, pterygium, conjunctival concretions, and conjunctivochalasis. Corneal degenerations covered include Coats white ring, spheroidal degeneration, iron deposition, and calcific band keratopathy. The document also briefly outlines degenerations of the sclera and endothelium and their causes, signs, and treatments.
Angioid streaks are irregular, spoke-like lesions that radiate from the optic disc. They represent cracks in the calcified Bruch's membrane and were first described in 1889. While often asymptomatic, they can be associated with vision loss due to complications like choroidal neovascularization or macular degeneration. The most common systemic associations are pseudoxanthoma elasticum, Paget's disease, and hemoglobinopathies. Treatment may include observation, laser photocoagulation, photodynamic therapy, or surgery depending on complications.
Recovery Of Vision In A Young Patient With Central Retinal Artery ...Dr. Jagannath Boramani
This document describes a case of central retinal artery occlusion in a 21-year-old female patient who presented with sudden painless vision loss in her right eye. Standard treatments were ineffective given her late presentation over 36 hours after onset. She was treated with hyperbaric oxygen therapy which rapidly reduces tissue anoxia and mitigates reperfusion injury. After 3 sessions of HBOT over 3 days, her vision improved significantly from counting fingers to 6/6p. HBOT helps the inner retinal layers obtain oxygen via diffusion from the choroidal circulation when exposed to elevated oxygen pressures until revascularization can restore vision.
Angioid streaks are cracks in Bruch's membrane that were first described in 1889. They are typically bilateral and radiate out from the optic disc in a cruciate pattern. The cracks are caused by calcification and degradation of Bruch's membrane. The most common complication is choroidal neovascularization, which can cause vision loss if untreated. Modern treatments with anti-VEGF agents have shown promise in preventing scarring and vision loss from neovascularization in angioid streaks.
Vitelliform dystrophy, or Best disease,
is a hereditary retinal dystrophy involving the retinal pigment epithelium (RPE), and leads to a characteristic bilateral yellow “egg-yolk” appearance of the macula
Retinitis pigmentosa is a group of inherited retinal diseases characterized by progressive degeneration of the photoreceptors. It initially affects rods, resulting in night blindness and peripheral vision loss, and later involves cones leading to tunnel vision. Symptoms include nyctalopia and peripheral field defects. Signs include bone spicule pigmentation, arteriolar attenuation, and disc pallor. It can be inherited in autosomal dominant, recessive or X-linked patterns. Investigations include electroretinography to detect photoreceptor dysfunction and optical coherence tomography. There is currently no cure or treatment to stop progression.
This document discusses retinal vascular occlusions, including their classification, presentation, investigations, and management. It begins by introducing retinal arterial and venous occlusions as significant causes of blindness. It then covers the anatomy of retinal blood supply and classifies occlusions by anatomical site. The remainder of the document details the characteristics, risk factors, clinical features, investigations, and treatment approaches for various types of retinal arterial occlusions (central retinal artery occlusion, branch retinal artery occlusion, cilioretinal artery occlusion) and venous occlusions (central retinal vein occlusion, branch retinal vein occlusion, hemiretinal vein occlusion).
This document contains mnemonics and summaries on various topics in ophthalmology:
1. It lists the 5 attachments of Whitnall's tubercle using the mnemonic "L".
2. It describes the neuroectoderm derivatives using the mnemonic "MORE".
3. It provides the differential diagnosis of leukocoria using the mnemonic "PREDICT".
4. It summarizes causes of proptosis using the mnemonic "VEIN".
INTRODUCTION
Optic nerve ischemia most frequently occurs at the optic nerve head, where structural crowding of nerve fibers and reduction of the vascular supply may combine to impair perfusion to a critical degree and produce optic disc edema. The most common such syndrome is termed anterior ischemic optic neuropathy(AION).
Generally, AION is categorized as either arteritic (associated with temporal arteritis) or nonarteritic .
The document discusses various retinal conditions and diseases. It provides information on symptoms, clinical findings, inheritance patterns, pathophysiology and testing results for each condition. These include congenital stationary night blindness, fundus albipunctatus, retinitis pigmentosa, cone dystrophy, Stargardt disease, Best disease, gyrate atrophy, choroideremia, juvenile retinoschisis, Bardet-Biedl syndrome, Tay-Sachs disease, Bietti’s crystalline retinopathy and others. It also covers post-traumatic conditions like commotio retinae, choroidal rupture, intraocular foreign bodies, shaken baby syndrome and Valsalva retinopathy.
This document provides an overview of optic atrophy, including:
1. It defines optic atrophy as degeneration of the optic nerve due to damage to the visual pathways from the retina to the lateral geniculate body.
2. It classifies optic atrophy based on whether damage originates in the retina or more centrally, and by cause. Primary optic atrophy occurs without swelling, while secondary involves prior swelling.
3. Causes of primary optic atrophy include optic neuritis, compression, hereditary conditions, toxins, trauma, and multiple sclerosis. Secondary optic atrophy follows conditions like papilledema.
4. Treatment focuses on the underlying cause, with vitamins sometimes used
This document provides an overview of polypoidal choroidal vasculopathy (PCV), including its history, definitions, pathogenesis, histopathology, demographics, clinical features, investigations, differential diagnosis, classification, treatment and guidelines. PCV is characterized by polyp-like subretinal vascular lesions associated with hemorrhagic detachments of the retinal pigment epithelium. Indocyanine green angiography is the gold standard for diagnosis, showing focal hyperfluorescence arising from the choroidal circulation within minutes. Treatment options include observation, thermal laser photocoagulation, photodynamic therapy, anti-VEGF therapy and combination therapies.
This document discusses pediatric cataract and leucocoria (white pupil). It defines leucocoria as a white reflection seen in the pupil that could indicate an underlying condition like cataract, retinoblastoma, or persistent hyperplastic primary vitreous. The document outlines the causes, presentations, classifications, management, and visual prognosis of pediatric cataracts. It emphasizes the importance of early referral for any detected leucocoria to rule out retinoblastoma or other serious conditions and prevent amblyopia. Overall management of pediatric cataracts aims to restore vision through early surgery and amblyopia treatment for the best possible visual outcomes.
This document provides an overview of congenital cataracts, including:
- The epidemiology, with an incidence of 1-3 per 10,000 births globally. Rates vary by region.
- Classification systems based on age of onset, laterality, morphology, and etiology.
- Descriptions of various morphological types of cataracts like nuclear, lamellar, anterior polar, and their associated etiologies.
- Cataracts can be associated with genetic syndromes, metabolic disorders, infections acquired in utero, and other ocular anomalies.
- Recognition of cataract type provides clues about etiology, timing of surgery, and prognosis.
The document describes a case presentation of a 55-year-old male with a lesion on his left eye that was diagnosed as an apocrine hidrocystoma. Apocrine hidrocystomas are benign cystic proliferations of the apocrine glands that commonly appear as solitary, soft, dome-shaped papules or nodules on the eyelids. Histological examination showed multiple cystic areas lined by apocrine-type secretory epithelium, confirming the diagnosis. Treatment options include incision, drainage, electrosurgical destruction or excision to prevent recurrence.
1) The document provides information on various ophthalmic conditions categorized by number, with each section labeled "1" through "25".
2) Key details are provided for each condition, including associated symptoms, inheritance patterns, relevant imaging/tests, and anatomical associations.
3) Mnemonic devices are presented throughout to help remember details, such as "The Smaller the Mirror, The Peripheral The View" for Goldmann goniolens mirrors.
This document discusses different types of ischemic optic neuropathy, including anterior ischemic optic neuropathy (AION), non-arteritic AION, arteritic AION, and posterior ischemic optic neuropathy. It describes the blood supply of the optic nerve head and risk factors, clinical features, investigations, treatments, and prognosis for each type. The main causes are reduced blood flow to the optic nerve head leading to infarction. AION is the most common cause of acute optic neuropathy in those over 50. Arteritic AION is caused by giant cell arteritis and requires high-dose steroid treatment to prevent blindness.
1. Recurrent central serous chorioretinopathy (CSCR) occurs when there is a new episode of CSCR more than 12 months after resolution of an initial episode. Recurrence rates range from 20-50%.
2. Risk factors for recurrence include subretinal hyperreflective foci, increased subfoveal choroidal thickness, intensity of fluorescein leakage, irregular pigment epithelial detachments, and choroidal hyperpermeability patterns on indocyanine green angiography.
3. Treatment options for recurrent CSCR include focal laser photocoagulation, photodynamic therapy, mineralocorticoid receptor antagonists like eplerenone, and micropulse laser therapy.
The document summarizes a case presentation of a 43-year-old male with blurred vision who underwent LASIK surgery 9 years prior and now presents with worsening vision. Examination found stromal opacities and the patient underwent penetrating keratoplasty (PKP) in the right eye. One year later, vision decreased in both eyes and the patient underwent PKP in the left eye. The document discusses granular dystrophy, a genetic bilateral corneal dystrophy, and reviews the patient's clinical course and management.
This document discusses painful ophthalmoplegia, which presents as periorbital or hemicranial pain, ipsilateral ocular motor palsies, and sensory loss in the trigeminal nerve distribution. Causes include aneurysms, carotid cavernous fistulas, cavernous sinus thrombosis, tumors, and infections. Evaluation involves imaging like MRI/CT/angiography. Management depends on the underlying cause but may include antibiotics, anticoagulation, surgery, or steroids. Prognosis depends on early diagnosis and treatment, with potential for residual neurological deficits.
Depositions and Degenerations of Conjuctiva and Cornea.docxIddi Ndyabawe
This document provides an overview of degenerative changes that can occur in the conjunctiva, cornea, and sclera. It describes age-related changes such as thinning and loss of transparency in the conjunctiva. Specific conditions discussed include pinguecula, pterygium, conjunctival concretions, and conjunctivochalasis. Corneal degenerations covered include Coats white ring, spheroidal degeneration, iron deposition, and calcific band keratopathy. The document also briefly outlines degenerations of the sclera and endothelium and their causes, signs, and treatments.
Angioid streaks are irregular, spoke-like lesions that radiate from the optic disc. They represent cracks in the calcified Bruch's membrane and were first described in 1889. While often asymptomatic, they can be associated with vision loss due to complications like choroidal neovascularization or macular degeneration. The most common systemic associations are pseudoxanthoma elasticum, Paget's disease, and hemoglobinopathies. Treatment may include observation, laser photocoagulation, photodynamic therapy, or surgery depending on complications.
Recovery Of Vision In A Young Patient With Central Retinal Artery ...Dr. Jagannath Boramani
This document describes a case of central retinal artery occlusion in a 21-year-old female patient who presented with sudden painless vision loss in her right eye. Standard treatments were ineffective given her late presentation over 36 hours after onset. She was treated with hyperbaric oxygen therapy which rapidly reduces tissue anoxia and mitigates reperfusion injury. After 3 sessions of HBOT over 3 days, her vision improved significantly from counting fingers to 6/6p. HBOT helps the inner retinal layers obtain oxygen via diffusion from the choroidal circulation when exposed to elevated oxygen pressures until revascularization can restore vision.
Angioid streaks are cracks in Bruch's membrane that were first described in 1889. They are typically bilateral and radiate out from the optic disc in a cruciate pattern. The cracks are caused by calcification and degradation of Bruch's membrane. The most common complication is choroidal neovascularization, which can cause vision loss if untreated. Modern treatments with anti-VEGF agents have shown promise in preventing scarring and vision loss from neovascularization in angioid streaks.
Vitelliform dystrophy, or Best disease,
is a hereditary retinal dystrophy involving the retinal pigment epithelium (RPE), and leads to a characteristic bilateral yellow “egg-yolk” appearance of the macula
Retinitis pigmentosa is a group of inherited retinal diseases characterized by progressive degeneration of the photoreceptors. It initially affects rods, resulting in night blindness and peripheral vision loss, and later involves cones leading to tunnel vision. Symptoms include nyctalopia and peripheral field defects. Signs include bone spicule pigmentation, arteriolar attenuation, and disc pallor. It can be inherited in autosomal dominant, recessive or X-linked patterns. Investigations include electroretinography to detect photoreceptor dysfunction and optical coherence tomography. There is currently no cure or treatment to stop progression.
This document discusses retinal vascular occlusions, including their classification, presentation, investigations, and management. It begins by introducing retinal arterial and venous occlusions as significant causes of blindness. It then covers the anatomy of retinal blood supply and classifies occlusions by anatomical site. The remainder of the document details the characteristics, risk factors, clinical features, investigations, and treatment approaches for various types of retinal arterial occlusions (central retinal artery occlusion, branch retinal artery occlusion, cilioretinal artery occlusion) and venous occlusions (central retinal vein occlusion, branch retinal vein occlusion, hemiretinal vein occlusion).
This document contains mnemonics and summaries on various topics in ophthalmology:
1. It lists the 5 attachments of Whitnall's tubercle using the mnemonic "L".
2. It describes the neuroectoderm derivatives using the mnemonic "MORE".
3. It provides the differential diagnosis of leukocoria using the mnemonic "PREDICT".
4. It summarizes causes of proptosis using the mnemonic "VEIN".
I LOVE NEUROSURGERY INITIATIVE: INTRACRANIAL TUMORS.pptwalid maani
This document discusses intracranial tumors, including:
- Their incidence rates, with primary brain tumors occurring in 6 per 100,000 people and metastatic tumors in 30 per 100,000 people.
- Common tumor types like astrocytomas, oligodendrogliomas, ependymomas, medulloblastomas, meningiomas, and pituitary tumors.
- Risk factors, clinical presentation, investigations including CT, MRI, PET and angiography, pathology classification, and management approaches like surgery, radiation and chemotherapy.
I LOVE NEUROSURGERY INITIATIVE: Spinal Tumorswalid maani
A comprehensive presentation about spinal tumors. Some concentration on anatomy. Discussion of presentation, diagnosis and management. Plenty of images.
I LOVE NEUROSURGERY INITIATIVE: Cranio-cerebral Injuries part 1walid maani
A comprehensive presentation about the primary injuries of the scalp, skull and brain occurring in head injuries. Directed to medical students and junior hospital doctors.
A short talk about two of the traumatic intracranial bleeds, namely extra and subdural hematomas. Directed to med students moving from basic into clinical teaching.
A Strategy for Reform of Higher Education in Jordan (16.3.2003)walid maani
The document outlines a vision for reforming Jordan's higher education sector to better align it with economic development needs. It proposes numerous reforms in areas like financing, admissions standards, curriculum, research, governance, and regulation. The goal is to improve quality, relevance, cost recovery, and innovation in higher education so it can better support Jordan's knowledge-based economy.
This document discusses using the Tawjihi exam as an admission test for universities in Jordan. It argues that Tawjihi is not needed as certification of high school completion or for employment, so its only purpose must be as a university entrance exam. The document proposes a new system where students can take exams in 11th-12th grade subjects over multiple sittings each year to qualify for admission to university programs grouped by field of study. A 10th grade exam would direct students to either academic or vocational tracks for 11th-12th grades.
This document provides an overview of the history and current state of neurosurgery in Jordan. It discusses how neurosurgery began in the 1960s with a few pioneering neurosurgeons and has grown significantly since. Today there are over 50 practicing neurosurgeons in Jordan, several residency programs, and Jordan provides neurosurgical care to over 100,000 patients from other countries in the Arab world each year. Infrastructure and supporting facilities for neurosurgery in Jordan have advanced greatly and are now on par with international standards.
This document presents a case study of a 15-year-old girl diagnosed with an extradural cervical myxomatous chordoma with extension beyond the spine and encasement of the vertebral artery. Imaging including CT, MRI, and angiography showed the tumor extending through two intervertebral foramina. The patient underwent a two-stage surgical removal of the tumor, followed by radiation therapy. Follow-up showed no remaining intraspinal tumor and only a small extrapinal nodule. The patient recovered full function and was attending regular checkups.
Travel Clinic Cardiff: Health Advice for International TravelersNX Healthcare
Travel Clinic Cardiff offers comprehensive travel health services, including vaccinations, travel advice, and preventive care for international travelers. Our expert team ensures you are well-prepared and protected for your journey, providing personalized consultations tailored to your destination. Conveniently located in Cardiff, we help you travel with confidence and peace of mind. Visit us: www.nxhealthcare.co.uk
5-hydroxytryptamine or 5-HT or Serotonin is a neurotransmitter that serves a range of roles in the human body. It is sometimes referred to as the happy chemical since it promotes overall well-being and happiness.
It is mostly found in the brain, intestines, and blood platelets.
5-HT is utilised to transport messages between nerve cells, is known to be involved in smooth muscle contraction, and adds to overall well-being and pleasure, among other benefits. 5-HT regulates the body's sleep-wake cycles and internal clock by acting as a precursor to melatonin.
It is hypothesised to regulate hunger, emotions, motor, cognitive, and autonomic processes.
Travel vaccination in Manchester offers comprehensive immunization services for individuals planning international trips. Expert healthcare providers administer vaccines tailored to your destination, ensuring you stay protected against various diseases. Conveniently located clinics and flexible appointment options make it easy to get the necessary shots before your journey. Stay healthy and travel with confidence by getting vaccinated in Manchester. Visit us: www.nxhealthcare.co.uk
These lecture slides, by Dr Sidra Arshad, offer a simplified look into the mechanisms involved in the regulation of respiration:
Learning objectives:
1. Describe the organisation of respiratory center
2. Describe the nervous control of inspiration and respiratory rhythm
3. Describe the functions of the dorsal and respiratory groups of neurons
4. Describe the influences of the Pneumotaxic and Apneustic centers
5. Explain the role of Hering-Breur inflation reflex in regulation of inspiration
6. Explain the role of central chemoreceptors in regulation of respiration
7. Explain the role of peripheral chemoreceptors in regulation of respiration
8. Explain the regulation of respiration during exercise
9. Integrate the respiratory regulatory mechanisms
10. Describe the Cheyne-Stokes breathing
Study Resources:
1. Chapter 42, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 36, Ganong’s Review of Medical Physiology, 26th edition
3. Chapter 13, Human Physiology by Lauralee Sherwood, 9th edition
Cell Therapy Expansion and Challenges in Autoimmune DiseaseHealth Advances
There is increasing confidence that cell therapies will soon play a role in the treatment of autoimmune disorders, but the extent of this impact remains to be seen. Early readouts on autologous CAR-Ts in lupus are encouraging, but manufacturing and cost limitations are likely to restrict access to highly refractory patients. Allogeneic CAR-Ts have the potential to broaden access to earlier lines of treatment due to their inherent cost benefits, however they will need to demonstrate comparable or improved efficacy to established modalities.
In addition to infrastructure and capacity constraints, CAR-Ts face a very different risk-benefit dynamic in autoimmune compared to oncology, highlighting the need for tolerable therapies with low adverse event risk. CAR-NK and Treg-based therapies are also being developed in certain autoimmune disorders and may demonstrate favorable safety profiles. Several novel non-cell therapies such as bispecific antibodies, nanobodies, and RNAi drugs, may also offer future alternative competitive solutions with variable value propositions.
Widespread adoption of cell therapies will not only require strong efficacy and safety data, but also adapted pricing and access strategies. At oncology-based price points, CAR-Ts are unlikely to achieve broad market access in autoimmune disorders, with eligible patient populations that are potentially orders of magnitude greater than the number of currently addressable cancer patients. Developers have made strides towards reducing cell therapy COGS while improving manufacturing efficiency, but payors will inevitably restrict access until more sustainable pricing is achieved.
Despite these headwinds, industry leaders and investors remain confident that cell therapies are poised to address significant unmet need in patients suffering from autoimmune disorders. However, the extent of this impact on the treatment landscape remains to be seen, as the industry rapidly approaches an inflection point.
- Video recording of this lecture in English language: https://youtu.be/Pt1nA32sdHQ
- Video recording of this lecture in Arabic language: https://youtu.be/uFdc9F0rlP0
- Link to download the book free: https://nephrotube.blogspot.com/p/nephrotube-nephrology-books.html
- Link to NephroTube website: www.NephroTube.com
- Link to NephroTube social media accounts: https://nephrotube.blogspot.com/p/join-nephrotube-on-social-media.html
DECLARATION OF HELSINKI - History and principlesanaghabharat01
This SlideShare presentation provides a comprehensive overview of the Declaration of Helsinki, a foundational document outlining ethical guidelines for conducting medical research involving human subjects.
Kosmoderma Academy, a leading institution in the field of dermatology and aesthetics, offers comprehensive courses in cosmetology and trichology. Our specialized courses on PRP (Hair), DR+Growth Factor, GFC, and Qr678 are designed to equip practitioners with advanced skills and knowledge to excel in hair restoration and growth treatments.
Introduction to neurosciences to 4 th year medical students
1. AN INTRODUCTION
TO CLINICAL NEUROSIENCES
WALID MAANI
PROFESSOR OF NEUROSURGERY
08/18/12 FOURTH YEAR LECTURE 1
2. IT IS VERY DIFFICULT TO
DO
THIS IN ONE HOUR
08/18/12 FOURTH YEAR LECTURE 2
3. PRESENTATON OF CENTRAL NERVOUS
SYSTEM PROBLEMS
• HOW DO CRANIAL LESIONS PRESENT?
• HOW DO SPINAL PROBLEMS PRESENT?
08/18/12 FOURTH YEAR LECTURE
3
4. PRESENTATION OF CRANIAL LESIONS
SULCI
THIS IS HOW THE
INTRACRANIAL
CONTENTS ARE VENTRICLE
ARRANGED AS SEEN
ON MAGNETIC CHOROID PLEXUS
RESONANCE MIDLINE
IMAGING (MRI)
T1 WEIGHTED MRI
08/18/12 FOURTH YEAR LECTURE
4
8. INTRACEREBRAL HEMORRHAGE
MAY CAUSE DEATH
MAY CAUSE LOC
DESTRUCTION OF BRAIN AREA
PRESENTS WITH:
SUDDEN HEADACHE
SUDDEN PARALYSIS
SPEECH PROBLEMS
SENSORY DISTURBANCES
VISUAL DISTURBANCES
08/18/12 FOURTH YEAR LECTURE
8
11. SUBARACHNOID HEMORRHAGE
MAY CAUSE DEATH
SUDDEN HEADACHE
LOC
EPILEPSY
NECK RIGIDITY
MAY BE ASSOCITAED
WITH PARALYSIS IF
ACCOMPANIED BY
INTRACEREBRAL
HEMORRHAGE
08/18/12 FOURTH YEAR LECTURE
11
14. INFARCTION
MAY BE ISCHAEMIC
MAY BE HEMORRHAGIC
MAY BE UN-NOTICED
LOC
EPILEPSY
DESTRUCTION OF BRAIN:
PARALYSIS
SPEECH PROBLEMS
VISUAL PROBLEMS
SENSORY PROBLEMS
08/18/12 FOURTH YEAR LECTURE
14
25. NOW IMAGINE IF WE ADD SOMETHING
ELSE TO THE CONTENTS
DISPLACED BRAIN OEDEMA
MIDLINE BRAIN OEDEMA
THE ORIGINAL DEFORMED
MIDLINE VENTRICLE
TUMOR MASS TUMORS
MENINGIOMA ON MRI T2 MULTIPLE LESIONS ON CT
08/18/12 FOURTH YEAR LECTURE
25
26. ADDITION OF NEW CONTENTS
• INCREASE IN THE INTRACRANIAL PRESSURE
• IRRITATION OF THE AREA
• PRESSURE ON THE AFFECTED AREA
• DESTRUCTION OF THE AFFECTED AREA
• OBSTRUCTION OF THE CSF PATHWAYS
• HORMONAL PROBLEMS
08/18/12 FOURTH YEAR LECTURE
26
27. INCREASE IN THE INTRACRANIAL PRESSURE
• SYMPTOMS:
• HEADACHE
• VOMITING
• VISUAL PROBLEMS
• INCREASE IN THE SIZE OF THE HEAD
08/18/12 FOURTH YEAR LECTURE
27
28. INCREASE IN THE INTRACRANIAL PRESSURE
• SYMPTOMS: IS A MORNING
• HEADACHE HEADACHE WHICH
• VOMITING RESPONDS TO
• VISUAL PROBLEMS SIMPLE ANALGESIA. IT
• INCREASE IN THE SIZE DOES NOT INDICATE
OF THE HEAD TYPE OF PROBLEM
08/18/12 FOURTH YEAR LECTURE
28
29. INCREASE IN THE INTRACRANIAL PRESSURE
IS A MORNING
• SYMPTOMS: VOMITING AND IS
• HEADACHE
PROJECTILE IN
• VOMITING
NATURE. IT RESEMBLES
• VISUAL PROBLEMS
•
MIGRAINE VOMITING
INCREASE IN THE SIZE
OF THE HEAD OR THE VOMITING
ASSOCIATED WITH
PREGNANCY
08/18/12 FOURTH YEAR LECTURE
29
30. INCREASE IN THE INTRACRANIAL PRESSURE
COULD BE IN THE
• SYMPTOMS: FORM OF BLURRED
• HEADACHE
VISION OR DECREASED
• VOMITING
ACUITY OR FIELD
• VISUAL PROBLEMS
•
DEFECT IN ONE OR
INCREASE IN THE SIZE
OF THE HEAD BOTH EYES. DEFECTS
CAN INDICATE SITE OF
PATHOLOGY
08/18/12 FOURTH YEAR LECTURE
30
31. INCREASE IN THE INTRACRANIAL PRESSURE
• SYMPTOMS: THIS OCCURS
• HEADACHE
ONLY IN CHILDREN
• VOMITING
BECAUSE THE
• INCREASE IN THE SIZE
OF THE HEAD CRANIAL SUTURES
HAVE NOT UNITED
YET.
08/18/12 FOURTH YEAR LECTURE
31
32. INCREASE IN THE INTRACRANIAL PRESSURE
IS SWELLING OF THE
• SIGNS OPTIC DISC AND
• PAPILLOEDEMA IS SEEN BY
OPHTHALMOSCOPY
NORMAL FUNDUS
08/18/12 PAPILLOEDEMA LECTURE
FOURTH YEAR 32
33. IRRITATION OF THE AREA
THERE ARE MANY FORMS
THIS LEADS TO OF EPILEPSY:
EPILEPSY IF THE GRAND MAL
LESION IS ON THE PETIT MAL
PARTIAL COMPLEX
SURFACE OF THE
ETC.
CEREBRUM. THE CORTEX EPILEPSY MAY LEAD TO:
MUST BE IRRITATED TO SUFFOCATION
PRODUCE EPILEPSY TEMPORARY PARALYSIS
(TODD’S) OR
PERMANENT BRAIN
DAMAGE
08/18/12 FOURTH YEAR LECTURE
33
34. PRESSURE ON THE AFFECTED AREA
or
tum val
e of o
• DEPENDS ON WHETHER: Sit r rem
a fte
• SUPRATENTORIAL
• INFRATENTORIAL
08/18/12 FOURTH YEAR LECTURE
34
35. PRESSURE ON THE AFFECTED AREA
DESTRUCTION OF THE AFFECTED AREA
• SUPRATENTORIAL:
• FRONTAL
• TEMPORAL
• PARIETAL
• OCCIPITAL
• INFRATENTORIAL:
• LATERAL
• MIDLINE
08/18/12 FOURTH YEAR LECTURE
35
36. PRESSURE ON THE AFFECTED AREA
DESTRUCTION OF THE AFFECTED AREA
SUPRA TENTORIAL LESIONS:
FRONTAL LOBE AFFECTION:
DISTURBANCE OF ORIENTATION
BEHAVIORAL CHANGES
SPHINCTER PROBLEMS
MOTOR SYMPTOMS ON THE OPPOSITE SIDE
08/18/12 FOURTH YEAR LECTURE
36
37. PRESSURE ON THE AFFECTED AREA
DESTRUCTION OF THE AFFECTED AREA
TEMPORAL LOBE AFFECTION:
EXPRESSIVE DYSPHASIA OR APHASIA
VISUAL FIELD DEFECTS
SENSORY SYMPTOMS ON THE OPPOSITE
SIDE
MOTOR SYMPTOMS ON THE OPPOSITE SIDE
08/18/12 FOURTH YEAR LECTURE
37
38. PRESSURE ON THE AFFECTED AREA
DESTRUCTION OF THE AFFECTED AREA
PARIETAL LOBE AFFECTION:
RECEPTIVE DYSPHASIA OR APHASIA
SENSORY SYMPTOMS ON THE OPPOSITE SIDE
MOTOR SYMPTOMS ON THE OPPOSITE SIDE
ASTEREOGNOSIS
LACK OF TWO POINT DISCRIMINATION
SPATIAL DISORIENTATION
FINGER AGNOSIA
08/18/12 FOURTH YEAR LECTURE
38
39. PRESSURE ON THE AFFECTED AREA
DESTRUCTION OF THE AFFECTED AREA
OCCIPITAL LOBE AFFECTION:
VISUAL FIELD DEFECTS
(HOMONYMOUS HEMIANOPIA)
08/18/12 FOURTH YEAR LECTURE
39
40. PRESSURE ON THE AFFECTED AREA
DESTRUCTION OF THE AFFECTED AREA
INFRATENTORIAL TUMORS
ATAXIA
NYSTAGMUS
OBSTRUCTION OF CSF
FLOW
TOP:
MEDULLOBLASTOA
BOTTOM:
ASTROCYTOMA
08/18/12 FOURTH YEAR LECTURE
40
41. DESTRUCTION COULD RESULT FROM
OCCLUSION OF A MAJOR ARTERY
INTERNAL CAROTID ARTERY
ANTERIOR CEREBRAL
MIDDLE CEREBRAL
BASILAR ARTERY
POSTERIOR CEREBRAL
08/18/12 FOURTH YEAR LECTURE
41
42. DESTRUCTION COULD RESULT FROM OCCLUSION
OF A MAJOR ARTERY
INTERNAL CAROTID ARTERY
ANTERIOR CEREBRAL
MIDDLE CEREBRAL
BASILAR ARTERY
POSTERIOR CEREBRAL
08/18/12 FOURTH YEAR LECTURE
42
43. DESTRUCTION COULD RESULT FROM
OCCLUSION OF A MAJOR ARTERY
• CONTRALATERAL
INTERNAL CAROTID
HEMIPLEGIA
ARTERY
• MILD SENSORY DEFICIT
ANTERIOR CEREBRAL
MIDDLE CEREBRAL
• MENTAL CONFUSION
BASILAR ARTERY • CLOUDING OF THE
POSTERIOR CEREBRAL CONSCIOUSNESS
08/18/12 FOURTH YEAR LECTURE
43
44. DESTRUCTION COULD RESULT FROM
OCCLUSION OF A MAJOR ARTERY
INTERNAL CAROTID • COMA
ARTERY • CONTRALATERAL
ANTERIOR CEREBRAL
FLACCID HEMIPLEGIA
MIDDLE CEREBRAL
• HEMIANESTHESIA
BASILAR ARTERY
• HEMIANOPIA
POSTERIOR CEREBRAL
• MOTOR APHASIA
• SENSORY APHASIA
08/18/12 FOURTH YEAR LECTURE
44
45. DESTRUCTION COULD RESULT FROM
OCCLUSION OF A MAJOR ARTERY
INTERNAL CAROTID
ARTERY
ANTERIOR CEREBRAL • CONTRALATERAL
MIDDLE CEREBRAL HEMIANESTHESIA
BASILAR ARTERY • CONTRALATERAL
POSTERIOR CEREBRAL HOMONYMOUS
HEMIANOPIA
• SENSORY APHASIA
08/18/12 FOURTH YEAR LECTURE
45
46. OBSTRUCTION OF CSF PATHWAYS
WILL LEAD TO DILATATION OF THE
VENTRICULAR SYSTEM AND SIGNS AND
SYMPTOMS OF
INCREASED INTRACRANIAL PRESSURE.
SEEPAGE
OF CSF DILATED
VENTRICLES
NORMAL ABNORMAL
08/18/12 FOURTH YEAR LECTURE
46
47. OBSTRUCTION OF CSF PATHWAYS
IN INFANTS AND LITTLE
CHILDERN IT WILL
LEAD TO ENLARGMENT OF
THE HEAD DUE TO THE
FACT THAT SUTURES
ARE NOT CLOSED.
HYDROCEPHALUS COULD
BE OBSTRUCTIVE OR
COMMUNICATING
08/18/12 FOURTH YEAR LECTURE
47
48. OBSTRUCTION OF CSF PATHWAYS
BESIDE ENLARGMENT OF THE HEAD,
DILATATION OF THE VENTRICULAR SYSTEM
WILL LEAD TO DETERIORATION OF THE
LEVEL OF CONSCIOUSNESS.
ASSESSMENT OF THE LOC IS DONE GENERALLY
BY THE USE OF THE GLASGOW COMA SCALE
(GCS)
08/18/12 FOURTH YEAR LECTURE
48
49. OBSTRUCTION OF CSF PATHWAYS
THE GLASGOW COMA SCALE
Points Eye Opening Best Verbal Response Best Motor Response
6 Follows command
5 Appropriate Localizes pain
4 Inappropriate Withdraws
3 To voice Moaning Flexion
2 To pain Incomprehensible Extension
08/18/12 FOURTH YEAR LECTURE
49
50. THE GLASGOW COMA SCALE
• A NORMAL PERSON WOULD SCORE 15
• 6 FROM FOLLOWING COMMAND
• 5 FROM APPROPRIATE VERBAL RESPONSE
• 4 FROM SPONTANEOUS EYE OPENING
• A DEAD PERSON SCORES 3
• 1 FROM NO MOTOR RESPONSE
• 1 FROM NO VERBAL REPONSE
• 1 FROM NO EYE OPENING
08/18/12 FOURTH YEAR LECTURE
50
51. HORMONAL PROBLEMS
USUALLY IN PROBLEMS OF THE PITUITARY
GLAND OR THE PINEAL BODY.
INCREASE PITUITARY SECRETION LEADS TO:
ACROMEGALLY
GIGANTISM
GALACTORRHOEA
AMENORRHOEA
DECREASED SECRETION LEADS TO:
HYPOPITUITRISM
08/18/12 FOURTH YEAR LECTURE
51
52. HORMONAL PROBLEMS
USUALLY IN PROBLEMS OF THE PITUITARY
GLAND OR THE PINEAL BODY.
INCREASE PITUITARY SECRETION LEADS TO:
ACROMEGALLY
GIGANTISM
GALACTORRHOEA
AMENORRHOEA
DECREASED SECRETION LEADS TO:
HYPOPITUITRISM
08/18/12 FOURTH YEAR LECTURE
52
53. HORMONAL PROBLEMS
DUE TO THE OVER
SECRETION OF THE
GROWTH HORMONE
AFTER THE EPIPHYSIS
HAD UNITED:
INCREASE NOSE SIZE
INCREASE HAND SIZE
INCREASE FEET SIZE
INCREASE JAW SIZE
08/18/12 FOURTH YEAR LECTURE
53
54. HORMONAL PROBLEMS
USUALLY IN PROBLEMS OF THE PITUITARY
GLAND OR THE PINEAL BODY.
INCREASE PITUITARY SECRETION LEADS TO:
ACROMEGALLY
GIGANTISM
GALACTORRHOEA
AMENORRHOEA
DECREASED SECRETION LEADS TO:
HYPOPITUITRISM
08/18/12 FOURTH YEAR LECTURE
54
55. HORMONAL PROBLEMS
DUE TO THE OVER
SECRETION OF THE
GROWTH HORMONE
BEFORE THE EPIPHYSIS
HAD UNITED.
08/18/12 FOURTH YEAR LECTURE
55
56. HORMONAL PROBLEMS
USUALLY IN PROBLEMS OF THE PITUITARY
GLAND OR THE PINEAL BODY.
INCREASE PITUITARY SECRETION LEADS TO:
ACROMEGALLY
GIGANTISM
GALACTORRHOEA
AMENORRHOEA
DECREASED SECRETION LEADS TO:
HYPOPITUITRISM
08/18/12 FOURTH YEAR LECTURE
56
59. PRESENTATION OF SPINAL LESIONS
SPINAL CORD LESIONS
LOSS OF POWER BELOW THE LEVEL
LOSS OF SENSATION BELOW THE LEVEL
LOSS OF SPHINCTERIC CONTROL
ROOT LESIONS
PAIN ALONG A ROOT
LOSS OF POWER IN A MUSCLE OR GROUP
LOSS OF SENSATION IN A DERMATOME
LOSS OF A REFLEX OR REFLEXES
LOSS OF SPHINCTERIC CONTROL
08/18/12 FOURTH YEAR LECTURE
59
60. PRESENTATION OF SPINAL LESIONS
ACUTE PRESENTATION CHRONIC PRESENTATION
LOSS OF POWER LOSS OF POWER
LOSS OF SENSATION LOSS OF SENSATION
HYPOTONIA HYPERTONIA
DECREASED REFLEXES INCREASED REFLEXES
MUTE PLANTER REFLEX EXTENSOR PLANTER
REFLES ( BABINISKI)
08/18/12 FOURTH YEAR LECTURE
60
61. PRESENTATION OF CORD LESIONS
EXAMPLE OF A
SPINAL CORD LESION
(TUMOUR)
INTRADURAL SPINAL
CORD TUMOR ON T2
WEIGHTED
MRI
08/18/12 FOURTH YEAR LECTURE
61
62. PRESENTATION OF ROOT LESIONS
EXAMPLE OF A
SPINAL ROOT LESION
(PROLAPSED DISC)
PROLAPSED DISC ON
T1
WEIGHTED MRI
08/18/12 FOURTH YEAR LECTURE
62