1. A 50-year-old woman presents with progressive shortness of breath, cough, and low-grade fever after working in maintenance jobs around boats for many years. Chest x-ray shows bilateral lower lung zone reticular infiltrates and hazy angles.
2. The most likely diagnosis is silicosis given her occupational exposure history involving inorganic dust. Silicosis is associated with decreased diffusion on pulmonary function tests.
3. Key findings include bilateral lower lung zone reticular infiltrates on chest x-ray, occupational exposure history involving inorganic dust, and decreased diffusion capacity expected on pulmonary function tests.
The patient has a history consistent with cystic fibrosis. The chest x-ray shows bilateral cystic lesions in the upper zones. Physical exam will likely reveal clubbing and spirometry will show a mixed obstructive and restrictive pattern. Treatment should include starting an anti-pseudomonas antibiotic regimen.
CXR-2 is most likely to belong to this patient based on the clinical scenario provided. The patient presents with shortness of breath, fever, and crackles on lung exam suggestive of pneumonia. CXR-2 shows bilateral infiltrates consistent with pneumonia.
1. The chest X-ray shows a cavitary lesion in the right upper lobe containing a dense ball within an air crescent, indicative of a mycetoma likely caused by Aspergillus colonizing a preexisting cavity from the patient's history of tuberculosis.
2. Common causes of cavitary lung lesions include infections, tumors, and sequelae of conditions like tuberculosis that can result in cavitation.
3. This patient presented with massive hemoptysis, a potential complication of mycetoma that may require bronchial embolization for control of bleeding.
This document provides a guide for summarizing chest x-rays. It outlines key areas to examine including position, quality, lesions, masses, cavitary findings, linear patterns, and mediastinal anatomy. Key items to note include opacity, margins, calcification, location, associated abnormalities, and comparison to prior x-rays. Common pathologies are described based on appearance including nodules, infiltrates, fibrosis, and more.
1. The document provides guidance on interpreting chest CT scans by describing common patterns seen in interstitial lung diseases.
2. It outlines different types of nodules seen on CT scans including dot-like, ill-defined centrilobular, and tree-in-bud nodules and associates each with specific conditions.
3. The document also discusses the distribution of nodules and how this can provide clues to different diseases, such as perilymphatic nodules suggesting sarcoidosis.
The patient has a history consistent with cystic fibrosis. The chest x-ray shows bilateral cystic lesions in the upper zones. Physical exam will likely reveal clubbing and spirometry will show a mixed obstructive and restrictive pattern. Treatment should include starting an anti-pseudomonas antibiotic regimen.
CXR-2 is most likely to belong to this patient based on the clinical scenario provided. The patient presents with shortness of breath, fever, and crackles on lung exam suggestive of pneumonia. CXR-2 shows bilateral infiltrates consistent with pneumonia.
1. The chest X-ray shows a cavitary lesion in the right upper lobe containing a dense ball within an air crescent, indicative of a mycetoma likely caused by Aspergillus colonizing a preexisting cavity from the patient's history of tuberculosis.
2. Common causes of cavitary lung lesions include infections, tumors, and sequelae of conditions like tuberculosis that can result in cavitation.
3. This patient presented with massive hemoptysis, a potential complication of mycetoma that may require bronchial embolization for control of bleeding.
This document provides a guide for summarizing chest x-rays. It outlines key areas to examine including position, quality, lesions, masses, cavitary findings, linear patterns, and mediastinal anatomy. Key items to note include opacity, margins, calcification, location, associated abnormalities, and comparison to prior x-rays. Common pathologies are described based on appearance including nodules, infiltrates, fibrosis, and more.
1. The document provides guidance on interpreting chest CT scans by describing common patterns seen in interstitial lung diseases.
2. It outlines different types of nodules seen on CT scans including dot-like, ill-defined centrilobular, and tree-in-bud nodules and associates each with specific conditions.
3. The document also discusses the distribution of nodules and how this can provide clues to different diseases, such as perilymphatic nodules suggesting sarcoidosis.
1) Ground-glass opacity and consolidation are the main patterns of increased lung attenuation seen on chest CT.
2) Ground-glass opacity indicates mild decrease in airspace or mild increase in soft tissue and is potentially treatable, while consolidation obscures vessels/airways and indicates more severe disease.
3) The distribution, associated patterns, and clinical context can help determine if an interstitial lung disease is acute/potentially treatable versus chronic/not treatable.
The document describes several idiopathic interstitial pneumonias including idiopathic pulmonary fibrosis, nonspecific interstitial pneumonia, acute interstitial pneumonia, organizing pneumonia, respiratory bronchiolitis, desquamative interstitial pneumonia, and lymphocytic interstitial pneumonia. It provides information on clinical features such as age, gender predominance, survival rates, treatments, and radiologic/pathologic findings for each condition. Differential diagnoses are also listed.
This document discusses various patterns seen on high-resolution computed tomography (HRCT) of the lungs. It describes linear and reticular opacities, nodules and nodular opacities, increased lung attenuation, parenchymal opacification including consolidation and ground glass opacities, cystic lesions, emphysema, bronchietasis, mosaic attenuation and perfusion patterns, and decreased lung attenuation with air trapping on expiratory scans. It also discusses the appearances of miliary tuberculosis and how it can be categorized as random, centrilobular, or perilymphatic distributions.
The document describes imaging patterns and histopathological findings related to lung cysts and diseases that cause cyst formation. It includes descriptions of:
- Langerhans cell histiocytosis, which presents with small nodular opacities in early stages and bizarrely-shaped cysts in late stages, typically in the upper lobes.
- Lymphangioleiomyomatosis, characterized by multiple, rounded and uniformly distributed thin-walled cysts throughout the lungs in women of child-bearing age.
- Differential diagnoses and distinguishing features between diseases that can cause lung cysts such as Langerhans cell histiocytosis, lymphangioleiomyomatosis, and centril
This document provides guidance on interpreting chest CT scans by summarizing common appearance patterns, distributions, and what various patterns may indicate. Appearance patterns include increased or decreased lung attenuation, nodular or linear opacities. Distribution patterns include upper/lower lung involvement or diffuse/central/peripheral localization. Together, appearance and distribution patterns can provide clues to conditions like infections, interstitial lung disease, or tumors.
1. The document discusses several chest CT and histology cases showing abnormalities including nodules, consolidation, and ground-glass opacity.
2. One case shows centrilobular nodules connected by linear structures, known as a tree-in-bud pattern, indicative of endobronchial infection.
3. Histology slides illustrate granulomas with necrosis, palisading histiocytes, and aerated alveolar parenchyma consistent with tuberculosis. Differential diagnoses include fungal infection and Wegener's granulomatosis.
This document discusses patterns seen on HRCT that can help characterize different lung diseases. It describes the nodular, reticulation, cystic and airway patterns seen in conditions such as sarcoidosis, lymphoma, metastases, pulmonary fibrosis, bronchiectasis and others. Key findings include perilymphatic nodules in sarcoidosis, random nodules in metastases, honeycombing and reticulation in idiopathic pulmonary fibrosis, and cysts in lymphangioleiomyomatosis. Differentiating these patterns on HRCT can provide clues to diagnose underlying lung abnormalities.
2012 noroozi-carotid sinus syndrome as the presenting symptom of cystadenolym...Klinikum Lippe GmbH
This case report describes a 45-year-old woman who presented with a one-week history of swelling in her left mandibular angle and symptoms of vertigo, loss of consciousness, and sinus arrest. Testing revealed she had carotid sinus syndrome caused by a cystadenolymphoma tumor in her left parotid gland. Surgical removal of the 31x17mm tumor resulted in complete resolution of her symptoms and electrocardiogram abnormalities. To the authors' knowledge, this is the first reported case of carotid sinus syndrome secondary to cystadenolymphoma.
The document discusses various patterns seen on HRCT scans of the lungs. It begins by describing the basic anatomical structure of the secondary pulmonary lobule. It then discusses numerous findings seen on HRCT scans including interlobular septal thickening, ground glass opacities, nodules, parenchymal opacification, low attenuation areas such as cysts and honeycombing. It also covers emphysema patterns, mosaic perfusion, bronchiectasis and other findings. The document provides details on the appearance and potential causes of each type of finding to aid in radiological interpretation.
This document provides information about interpreting HRCT scans of the chest. It describes bronchial and lobar anatomy, Hounsfield units, and patterns seen on HRCT such as ground glass opacity, consolidation, reticulation, nodules, honeycombing, and vascular anatomy. Common diseases that can cause each pattern are listed, such as sarcoidosis presenting with perilymphatic nodules or pulmonary edema seen as smooth septal thickening. The document emphasizes using patterns and distributions to narrow the differential diagnosis on HRCT scans.
The document discusses the basic interpretation of HRCT scans of the lungs. It describes the anatomy of the secondary lobule and how diseases can affect the centrilobular or perilymphatic areas. Common patterns seen on HRCT like reticular, nodular, ground glass and consolidations are explained. The distribution of abnormalities within the lungs and specific signs like tree-in-bud are also covered.
Approach To Diffuse Parenchymal Lung DiseasesGamal Agmy
This document provides an overview of interstitial lung diseases (ILD), also known as diffuse parenchymal lung diseases (DPLD). It begins by defining the pulmonary interstitium and reviewing the spectrum of ILD. Common clinical presentations are discussed. The document then reviews approaches to diagnosis, including history, physical exam, imaging like chest x-ray and CT, pulmonary function tests, and lung sampling. Common radiographic patterns seen in ILD like ground glass, reticulation, nodules and cysts are also summarized.
This document describes and shows images of various pathologies that can cause calcification or ossification within the bronchi, a condition known as broncholithiasis. It includes images showing calcified lymph nodes, foreign bodies, tumors, and other conditions that have led to intraluminal calcification within the bronchi visible on CT scans. The images demonstrate how different diseases can produce similar appearances of intraluminal calcifications or ossifications that are visible on radiographs.
The Role Of Corticosteroids In The Perioperative Management Of Endobronchial ...Bassel Ericsoussi, MD
This case study describes a 31-year-old woman who presented with chronic cough and recurrent pneumonia. Imaging revealed a foreign body obstructing her right lower lobe bronchus, which was encased in bulky granulation tissue. The foreign body, a chicken wishbone fragment measuring 2.5 cm, was removed with forceps during bronchoscopy. Corticosteroids were given before and after removal to reduce inflammation and granulation tissue, facilitating removal of the object and improving the patient's symptoms. She had complete resolution of symptoms after treatment.
Pitfalls in chest CT can usually be easily avoided, if the reader is aware of them.
Technical issues, artifacts, error of perception and error of interpretation, if not recognized, can result in >>>>>>>>inappropriate treatment.
This document discusses ground-glass opacities seen on CT scans. It defines ground-glass opacities as a hazy increase in lung opacity while preserving bronchial and vascular markings. Various pathologies can cause ground-glass opacities by partially filling the airspaces. The document then describes different patterns of ground-glass opacities including diffuse, patchy, focal, halo, and peripheral distributions. For each pattern, common diseases that may present with that appearance are listed and briefly characterized.
1) HRCT shows reticular pattern involving subpleural areas of the superior segment of lower lobes with some interlobular septal thickening, suggestive of usual interstitial pneumonia.
2) There is also a reticular pattern with tractional bronchiectasis and subpleural sparing with surrounding areas of fibrosis, consistent with fibrotic nonspecific interstitial pneumonia.
3) Small multifocal areas show the "atoll sign" with central ground glass opacity and thick-walled cysts, seen in conditions like bronchiolitis obliterans organizing pneumonia, especially in an immune compromised patient.
Describes the basic radiology of diffuse interstitial disease ,with differential diagnosis of nodular interstitial pattern and how to approach HRCT findings .
HRCT in Diffuse Lung Diseases - I (Techniques and Quality)Bhavin Jankharia
The first part of a series on HRCT in diffuse lung diseases. This covers how to obtain good quality scans, which are the basis of learning how to interpret HRCT studies in the setting of diffuse lung diseases.
Based on the clinical history of excessive secretions, elevated pressures, and fever, aspiration pneumonia with right upper lobe atelectasis is the most likely diagnosis. An important next step in management would be fiberoptic bronchoscopy, antibiotic therapy, and chest physiotherapy.
1. This document provides guidance on how to read chest x-rays and summarizes 5 case examples.
2. Key elements to evaluate on a CXR are described such as position, quality, lesions, mediastinal structures, and other findings.
3. The case examples demonstrate different pathologies such as pneumonia, pulmonary edema, and infiltrates. Each case provides the patient history and radiographic findings.
1) Ground-glass opacity and consolidation are the main patterns of increased lung attenuation seen on chest CT.
2) Ground-glass opacity indicates mild decrease in airspace or mild increase in soft tissue and is potentially treatable, while consolidation obscures vessels/airways and indicates more severe disease.
3) The distribution, associated patterns, and clinical context can help determine if an interstitial lung disease is acute/potentially treatable versus chronic/not treatable.
The document describes several idiopathic interstitial pneumonias including idiopathic pulmonary fibrosis, nonspecific interstitial pneumonia, acute interstitial pneumonia, organizing pneumonia, respiratory bronchiolitis, desquamative interstitial pneumonia, and lymphocytic interstitial pneumonia. It provides information on clinical features such as age, gender predominance, survival rates, treatments, and radiologic/pathologic findings for each condition. Differential diagnoses are also listed.
This document discusses various patterns seen on high-resolution computed tomography (HRCT) of the lungs. It describes linear and reticular opacities, nodules and nodular opacities, increased lung attenuation, parenchymal opacification including consolidation and ground glass opacities, cystic lesions, emphysema, bronchietasis, mosaic attenuation and perfusion patterns, and decreased lung attenuation with air trapping on expiratory scans. It also discusses the appearances of miliary tuberculosis and how it can be categorized as random, centrilobular, or perilymphatic distributions.
The document describes imaging patterns and histopathological findings related to lung cysts and diseases that cause cyst formation. It includes descriptions of:
- Langerhans cell histiocytosis, which presents with small nodular opacities in early stages and bizarrely-shaped cysts in late stages, typically in the upper lobes.
- Lymphangioleiomyomatosis, characterized by multiple, rounded and uniformly distributed thin-walled cysts throughout the lungs in women of child-bearing age.
- Differential diagnoses and distinguishing features between diseases that can cause lung cysts such as Langerhans cell histiocytosis, lymphangioleiomyomatosis, and centril
This document provides guidance on interpreting chest CT scans by summarizing common appearance patterns, distributions, and what various patterns may indicate. Appearance patterns include increased or decreased lung attenuation, nodular or linear opacities. Distribution patterns include upper/lower lung involvement or diffuse/central/peripheral localization. Together, appearance and distribution patterns can provide clues to conditions like infections, interstitial lung disease, or tumors.
1. The document discusses several chest CT and histology cases showing abnormalities including nodules, consolidation, and ground-glass opacity.
2. One case shows centrilobular nodules connected by linear structures, known as a tree-in-bud pattern, indicative of endobronchial infection.
3. Histology slides illustrate granulomas with necrosis, palisading histiocytes, and aerated alveolar parenchyma consistent with tuberculosis. Differential diagnoses include fungal infection and Wegener's granulomatosis.
This document discusses patterns seen on HRCT that can help characterize different lung diseases. It describes the nodular, reticulation, cystic and airway patterns seen in conditions such as sarcoidosis, lymphoma, metastases, pulmonary fibrosis, bronchiectasis and others. Key findings include perilymphatic nodules in sarcoidosis, random nodules in metastases, honeycombing and reticulation in idiopathic pulmonary fibrosis, and cysts in lymphangioleiomyomatosis. Differentiating these patterns on HRCT can provide clues to diagnose underlying lung abnormalities.
2012 noroozi-carotid sinus syndrome as the presenting symptom of cystadenolym...Klinikum Lippe GmbH
This case report describes a 45-year-old woman who presented with a one-week history of swelling in her left mandibular angle and symptoms of vertigo, loss of consciousness, and sinus arrest. Testing revealed she had carotid sinus syndrome caused by a cystadenolymphoma tumor in her left parotid gland. Surgical removal of the 31x17mm tumor resulted in complete resolution of her symptoms and electrocardiogram abnormalities. To the authors' knowledge, this is the first reported case of carotid sinus syndrome secondary to cystadenolymphoma.
The document discusses various patterns seen on HRCT scans of the lungs. It begins by describing the basic anatomical structure of the secondary pulmonary lobule. It then discusses numerous findings seen on HRCT scans including interlobular septal thickening, ground glass opacities, nodules, parenchymal opacification, low attenuation areas such as cysts and honeycombing. It also covers emphysema patterns, mosaic perfusion, bronchiectasis and other findings. The document provides details on the appearance and potential causes of each type of finding to aid in radiological interpretation.
This document provides information about interpreting HRCT scans of the chest. It describes bronchial and lobar anatomy, Hounsfield units, and patterns seen on HRCT such as ground glass opacity, consolidation, reticulation, nodules, honeycombing, and vascular anatomy. Common diseases that can cause each pattern are listed, such as sarcoidosis presenting with perilymphatic nodules or pulmonary edema seen as smooth septal thickening. The document emphasizes using patterns and distributions to narrow the differential diagnosis on HRCT scans.
The document discusses the basic interpretation of HRCT scans of the lungs. It describes the anatomy of the secondary lobule and how diseases can affect the centrilobular or perilymphatic areas. Common patterns seen on HRCT like reticular, nodular, ground glass and consolidations are explained. The distribution of abnormalities within the lungs and specific signs like tree-in-bud are also covered.
Approach To Diffuse Parenchymal Lung DiseasesGamal Agmy
This document provides an overview of interstitial lung diseases (ILD), also known as diffuse parenchymal lung diseases (DPLD). It begins by defining the pulmonary interstitium and reviewing the spectrum of ILD. Common clinical presentations are discussed. The document then reviews approaches to diagnosis, including history, physical exam, imaging like chest x-ray and CT, pulmonary function tests, and lung sampling. Common radiographic patterns seen in ILD like ground glass, reticulation, nodules and cysts are also summarized.
This document describes and shows images of various pathologies that can cause calcification or ossification within the bronchi, a condition known as broncholithiasis. It includes images showing calcified lymph nodes, foreign bodies, tumors, and other conditions that have led to intraluminal calcification within the bronchi visible on CT scans. The images demonstrate how different diseases can produce similar appearances of intraluminal calcifications or ossifications that are visible on radiographs.
The Role Of Corticosteroids In The Perioperative Management Of Endobronchial ...Bassel Ericsoussi, MD
This case study describes a 31-year-old woman who presented with chronic cough and recurrent pneumonia. Imaging revealed a foreign body obstructing her right lower lobe bronchus, which was encased in bulky granulation tissue. The foreign body, a chicken wishbone fragment measuring 2.5 cm, was removed with forceps during bronchoscopy. Corticosteroids were given before and after removal to reduce inflammation and granulation tissue, facilitating removal of the object and improving the patient's symptoms. She had complete resolution of symptoms after treatment.
Pitfalls in chest CT can usually be easily avoided, if the reader is aware of them.
Technical issues, artifacts, error of perception and error of interpretation, if not recognized, can result in >>>>>>>>inappropriate treatment.
This document discusses ground-glass opacities seen on CT scans. It defines ground-glass opacities as a hazy increase in lung opacity while preserving bronchial and vascular markings. Various pathologies can cause ground-glass opacities by partially filling the airspaces. The document then describes different patterns of ground-glass opacities including diffuse, patchy, focal, halo, and peripheral distributions. For each pattern, common diseases that may present with that appearance are listed and briefly characterized.
1) HRCT shows reticular pattern involving subpleural areas of the superior segment of lower lobes with some interlobular septal thickening, suggestive of usual interstitial pneumonia.
2) There is also a reticular pattern with tractional bronchiectasis and subpleural sparing with surrounding areas of fibrosis, consistent with fibrotic nonspecific interstitial pneumonia.
3) Small multifocal areas show the "atoll sign" with central ground glass opacity and thick-walled cysts, seen in conditions like bronchiolitis obliterans organizing pneumonia, especially in an immune compromised patient.
Describes the basic radiology of diffuse interstitial disease ,with differential diagnosis of nodular interstitial pattern and how to approach HRCT findings .
HRCT in Diffuse Lung Diseases - I (Techniques and Quality)Bhavin Jankharia
The first part of a series on HRCT in diffuse lung diseases. This covers how to obtain good quality scans, which are the basis of learning how to interpret HRCT studies in the setting of diffuse lung diseases.
Based on the clinical history of excessive secretions, elevated pressures, and fever, aspiration pneumonia with right upper lobe atelectasis is the most likely diagnosis. An important next step in management would be fiberoptic bronchoscopy, antibiotic therapy, and chest physiotherapy.
1. This document provides guidance on how to read chest x-rays and summarizes 5 case examples.
2. Key elements to evaluate on a CXR are described such as position, quality, lesions, mediastinal structures, and other findings.
3. The case examples demonstrate different pathologies such as pneumonia, pulmonary edema, and infiltrates. Each case provides the patient history and radiographic findings.
This document provides a guide for reading chest x-rays. It outlines key areas to examine including position, quality, lesions, masses, consolidation, and other findings. Specific features to evaluate for solitary pulmonary nodules and cavitary lesions are described such as appearance, size, location, and associated abnormalities. Causes of common chest x-ray findings are listed for conditions like pneumonia, lymphoma, and sarcoidosis.
The document summarizes the causes, evaluation, and management of epistaxis (nosebleeds). Key points include:
- The most common causes are local trauma, dry air, and hypertension. Weather has a proven association with incidence.
- Evaluation involves examination of the nasal cavity to identify the bleeding site. Imaging and labs may be needed to investigate underlying causes.
- Management begins with first aid and may involve cautery, nasal packing, medications, or surgery to control active bleeding and address its cause. Continued or severe bleeding may require embolization or ligation of arteries supplying the nasal cavity.
mastoidectomy
Follow up: long term antibiotics
Prognosis: depends on size,location,duration before treatment
Mortality: 10-20%
Morbidity: neurological deficits
Recurrence: 5-10%
Prevention: early treatment of ear infection
Education: personal hygiene
Socioeconomic: improved living standards
Problem oriented approach in pediatric radiologyAhmed Bahnassy
This document provides an introduction to the problem-oriented approach in pediatric radiology. It discusses 5 clinical presentations: [1] a chest mass, [2] upper airway obstruction, [3] chest infection, [4] recurrent/chronic pulmonary problems, and [5] respiratory distress in a neonate. For each presentation, the document discusses etiology, role of imaging, and specific radiologic findings. The goal is to use a problem-oriented approach to tailor imaging techniques to the clinical problem and reach a diagnosis with minimal radiation exposure.
This document provides an overview of different types of CT imaging of the chest, including standard CT, high resolution CT, low dose CT, and CT angiography. It discusses the anatomy visible on chest CT scans and common disease patterns seen, such as air bronchograms, bronchiectasis, ground glass opacities, and pulmonary nodules. References are provided for further reading on CT signs of lung disease.
This document provides an overview of acute respiratory distress syndrome (ARDS). It defines ARDS and differentiates it from acute lung injury. The pathophysiology of ARDS involves diffuse lung inflammation from neutrophils and proteinaceous fluid in the alveoli, reducing gas exchange. Management focuses on low tidal volume ventilation to prevent further lung injury while allowing permissive hypercapnia. Diuretics may help lung function if used conservatively. Pulmonary artery catheters are no longer routinely recommended as they do not improve outcomes and carry risk of complications.
The document provides information about Acute Respiratory Distress Syndrome (ARDS) including its definition, pathophysiology, diagnosis, management, and prognosis. ARDS is defined as rapid onset hypoxemia and diffuse pulmonary infiltrates leading to respiratory failure. It is caused by direct lung injury from conditions like pneumonia or indirect injury from sepsis or trauma. Diagnosis involves criteria of acute onset, hypoxemia with PaO2/FiO2 ≤200, and no heart failure. Management focuses on treating the underlying cause and providing ventilator support using low tidal volumes per the ARDSNet protocol to reduce ventilator-induced lung injury. Prognosis depends on risk factors and mortality ranges from 26-44%.
This document provides a detailed summary of various patterns seen on HRCT scans of the lungs including reticular, nodular, ground glass, mosaic and honeycombing patterns. It describes the characteristic radiological features of different interstitial lung diseases such as UIP, NSIP, COP, RB-ILD, DIP, LIP, AIP and others. Key diagnostic criteria and differentiating features between these conditions are discussed. HRCT images demonstrating examples of the described patterns are also included.
1. The document discusses idiopathic interstitial pneumonias (IIPs), a group of rare lung diseases that can be distinguished from other lung diseases based on clinical features, imaging, and pathology.
2. A new classification is proposed that includes idiopathic pulmonary fibrosis (IPF), nonspecific interstitial pneumonia (NSIP), cryptogenic organizing pneumonia (COP), acute interstitial pneumonia (AIP), respiratory bronchiolitis-associated interstitial lung disease (RB-ILD), desquamative interstitial pneumonia (DIP), and lymphoid interstitial pneumonia (LIP).
3. Achieving an accurate diagnosis is a dynamic process
Intracranial complication of chronic suppurative otitis mediaAbino David
The document discusses several potential intracranial complications that can arise from chronic suppurative otitis media (CSOM), including:
1. Extradural abscess - pus collects between the bone and dura, often caused by bone erosion or thrombophlebitis.
2. Subdural abscess - pus collects against the brain surface, causing symptoms and becoming loculated.
3. Meningitis - inflammation of the meninges and bacterial invasion of CSF, presenting with fever, headache, neck stiffness.
4. Otogenic brain abscess - develops in the temporal lobe or cerebellum, presenting with headaches, seizures, and focal neurological deficits depending on
This document discusses the interpretation of interstitial lung diseases based on CT imaging patterns. It describes various CT findings including linear and reticular opacities, nodules, ground glass opacities, consolidations, cystic lesions, mosaic attenuation, and air trapping. It provides examples of different diseases that can present with each pattern and discusses approaches to narrow the differential diagnosis based on distribution and characteristics of the opacities seen on CT. Key points such as the differences between ground glass opacities and consolidations are highlighted. Differential diagnoses are provided for common presentations.
This document provides an overview of chest trauma, including:
- Common injuries like pneumothorax, hemothorax, flail chest and their signs and symptoms.
- Assessment involves clinical exam, chest x-ray and ultrasound to detect injuries. Chest tube insertion can be both therapeutic and diagnostic.
- "Deadly dozen" life-threatening injuries from chest trauma include tension pneumothorax, cardiac tamponade, aortic disruption and others that often require emergency procedures or surgery.
- Management involves airway control, ventilation, chest tube drainage, analgesia and monitoring for complications like respiratory failure. Operative treatment is indicated for severe injuries or those not responding to initial management.
This document discusses juvenile nasopharyngeal angiofibroma (JNA), a rare benign but invasive tumor that arises in adolescent males near the sphenopalatine foramen. JNA presents with nasal obstruction and epistaxis. Diagnosis involves imaging like CT and MRI to determine the extent of involvement. Treatment depends on staging and may include preoperative embolization, surgery such as endoscopic resection, or radiation for advanced cases. Complete resection aims to prevent recurrence while minimizing complications like bleeding, infection, and nerve damage.
This document discusses cardiopulmonary disease and provides information on:
1. The causes of shortness of breath including pulmonary and cardiac issues as well as systemic illnesses.
2. The indications and uses of chest x-rays which can help diagnose lung, heart, skeletal and soft tissue problems.
3. The components of respiratory examination including inspection, palpation, percussion, and auscultation and what each technique evaluates.
4. Common breath sounds like vesicular, whistling, and crepitus and their characteristics.
KMA Annual Meeting 2010 - Allergy - Wheeze, Crackle, POP: When its not Asthma...KSAAI
Are the spirometry maneuvers acceptable?
Uof L Division of Pulmonary, Critical Care, and Sleep Disorders Medicine
Minimally acceptable criteria ‐
Spirometry
• Have the patient assume the correct posture.
• Attach the nose clip, place mouthpiece in mouth and instruct patient to
close lips around the mouthpiece and breathe quietly.
• Instruct the patient to inhale completely and rapidly with little or no pause
(< 1 sec) at TLC.
• Instruct patient to exhale maximally until no more air can be expelled.
• Repeat instructions as necessary, coaching vigorously during the
expiratory maneuver.
• Repeat for a minimum of
1) The document provides guidance on how to read a chest x-ray, including assessing technical quality, determining if it is a PA or AP view, and evaluating penetration and inspiration.
2) It describes how to analyze the lungs by comparing vascular markings in different regions, identifying fissures and localizing lesions.
3) Three case studies are presented and summarized, showing examples of right upper lobe atelectasis, left upper lobe atelectasis, and left lower lobe atelectasis. Key findings are described for each case.
A 46-year-old woman is referred for a possible thyroidectomy due to a tender neck swelling. Blood tests show hyperthyroidism and elevated ESR. A thyroid scan shows decreased uptake globally. This suggests subacute thyroiditis, characterized by hyperthyroidism, painful goiter, elevated ESR, and globally reduced uptake on scan. This condition is usually self-limiting and does not require surgery.
Step up to bat and practice dictating complex cases a residents guide to effe...TriMed Media Group
Findings:
There is a normal appendix
visualized in the RLQ. The
small bowel appears normal
without evidence of
diverticulum.
The document provides guidelines for effective radiology reporting, noting that residency training focuses
Impression:
little on dictation skills. It highlights the importance of concise, clinically relevant reports that answer the
No evidence of Meckel
diverticulum. Normal exam.
clinical question. The guidelines emphasize organizing findings logically, providing a clear impression, and
focusing reports on the clinical history and diagnosis rather than just describing images.
1) The document defines key terms related to venous thromboembolism (VTE) such as Wells score, provoked and unprovoked DVT/PE, and defines the Wells clinical prediction rules.
2) It then presents three case scenarios (Susan, Nita, Harry) and walks through evaluating each patient for suspected DVT or PE using the Wells criteria, performing appropriate tests, and determining next steps in management.
3) Tables are included defining the two-level Wells score for DVT and PE to estimate probability of each.
Based on the information provided, elemental mercury best explains this patient's clinical presentation and exposure history. Elemental mercury was inhaled from broken thermometers, allowing rapid absorption and distribution throughout the body, including the brain. The neurological and respiratory symptoms are consistent with elemental mercury toxicity.
This document contains information about various chest radiograph and CT scan cases. It includes 10 chest CT cases with images and descriptions of findings such as parenchymal bands, subpleural lines, centrilobular nodules, lobular remodeling, architectural distortion, and more advanced disease. It also provides 2 chest clinical cases describing patients with progressive dyspnea and worsening radiographic findings consistent with coal workers' pneumoconiosis and progressive massive fibrosis.
The document discusses various chest X-ray, clinical case, and CT scan cases related to respiratory diseases. It includes images and descriptions of cases involving conditions like lymphoma, sarcoidosis, lung metastases, radiation pneumonitis, and sarcoidosis. The document also presents clinical cases on recurrent pneumothoraces and catamenial pneumothorax and includes related questions and discussions.
This document outlines various pulmonary issues that can affect women, including those related to pregnancy. It discusses topics like tuberculosis and pneumonia in pregnancy, acute respiratory failure during pregnancy covering things like sepsis, mechanical ventilation concerns, amniotic fluid embolism, and venous air embolism. It also briefly touches on tobacco-related lung diseases in women and catamenial pneumothorax and hemoptysis. For many of the conditions, it provides details on presentation, management considerations, and treatment approaches.
Based on the discussion, the best therapeutic management for this patient is E) Aggressive antibiotic therapy and airway clearance maneuvers. The goals of treatment for PCD are to treat pulmonary infections aggressively with antibiotics tailored to sputum cultures and regular airway clearance to help maintain lung function.
The blood gas results show a respiratory acidosis with a pH of 7.25 and a PCO2 of 7.5 kPa. This is consistent with type I respiratory failure due to an acute process like pneumonia. Bronchopulmonary dysplasia and asthma are chronic conditions unlikely to cause such an acute deterioration. While intubation may be required, the immediate priority should be supportive care and treating the underlying cause rather than intubation alone. Bicarbonate is usually not required to correct a respiratory acidosis as the kidney can compensate.
The best answer is:
B - Blood gases suggest type 1 respiratory failure.
The abnormality seen on this HRCT image is predominantly subpleural and basal. There are bilateral reticular opacities in the subpleural regions extending into the bases posteriorly. The lung apices and upper lobes appear relatively spared.
Here are the answers to the multiple choice questions about respiratory topics:
1. A, B, E - Streptococcus pneumoniae is the most common cause of community acquired pneumonia in older children and adults, not infants. It can be caused by Staphylococcus aureus or Mycoplasma pneumoniae in infants. Ciprofloxacin would not be appropriate for presumed bacterial pneumonia without a confirmed pathogen. Bordatella pertussis is not usually mild.
2. C, D - 10% of cystic fibrosis patients may not require pancreatic enzyme supplementation. 10-15% of neonates present with meconium ileus. The other statements are false.
3. A, D, E -
This document discusses a case of a 64-year-old female patient with chronic obstructive pulmonary disease (COPD). It provides her medical history, physical exam findings, diagnostic test results including pulmonary function tests and imaging, and discusses gender differences in COPD presentations. It also includes two multiple choice questions about gender differences in COPD and indices used to evaluate COPD severity and mortality.
This document contains information from Dr. Anas Sahle regarding chest CT cases and a collicum exam. For the chest CT cases, there are images and descriptions of findings for HRCT-1, including linear opacities, centrilobular nodules, tree-in-bud patterns and bronchial wall thickening. After treatment, there is marked resolution of the findings. Histology shows a bronchiole with lymphoid follicles, consistent with chronic follicular bronchiolitis. The collicum exam contains 12 multiple choice questions on various respiratory topics like teratomas, Hounsfield units, findings associated with ARDS, and appropriate treatments for conditions like lung abscesses. Contact information
The characteristic presentations of cystic fibrosis include:
A- A 26 week gestation infant with x-ray appearance of meconium ileus.
B- An 8 month old girl admitted the second time with lower respiratory tract changes on chest x- ray.
C- A 9 month old Indian girl with failure to thrive.
The key presentations are meconium ileus in a preterm infant, and recurrent or chronic lung infections leading to changes on chest x-ray in an infant or child. Failure to thrive can also be seen. Prolonged jaundice and nasal obstruction are not characteristic of cystic fibrosis.
The chest x-ray shows bilateral hazy opacities and a peripherally located ill-defined opacity, suggesting adenocarcinoma as the likely diagnosis given its common peripheral presentation as an incidental finding; a CT-guided biopsy revealed malignant cells consistent with adenocarcinoma, which is often an incidentally detected peripheral carcinoma on chest x-ray in smokers.
The normal chest CT shows an aortic arch landmark in the mediastinum window. The brachiocephalic trunk and left common carotid artery are seen originating from the arch. In the lung window, the trachea provides a landmark and the lungs are divided into three sections based on the carina: above is the upper lobe, at the carina is the anterior and superior segments, and below is the lingula (left) and middle lobe (right).
1. Look at the technical quality of the chest x-ray including whether it is centered, properly exposed, and taken in inspiration.
2. Examine the lungs for any opacities, consolidation, or atelectasis which can be localized using the zones and identifying fissure lines on lateral view.
3. Check the mediastinum, heart, and diaphragm for any shifts or distortions that may indicate underlying lung pathology such as atelectasis.
Integrating Ayurveda into Parkinson’s Management: A Holistic ApproachAyurveda ForAll
Explore the benefits of combining Ayurveda with conventional Parkinson's treatments. Learn how a holistic approach can manage symptoms, enhance well-being, and balance body energies. Discover the steps to safely integrate Ayurvedic practices into your Parkinson’s care plan, including expert guidance on diet, herbal remedies, and lifestyle modifications.
Rasamanikya is a excellent preparation in the field of Rasashastra, it is used in various Kushtha Roga, Shwasa, Vicharchika, Bhagandara, Vatarakta, and Phiranga Roga. In this article Preparation& Comparative analytical profile for both Formulationon i.e Rasamanikya prepared by Kushmanda swarasa & Churnodhaka Shodita Haratala. The study aims to provide insights into the comparative efficacy and analytical aspects of these formulations for enhanced therapeutic outcomes.
Basavarajeeyam is a Sreshta Sangraha grantha (Compiled book ), written by Neelkanta kotturu Basavaraja Virachita. It contains 25 Prakaranas, First 24 Chapters related to Rogas& 25th to Rasadravyas.
share - Lions, tigers, AI and health misinformation, oh my!.pptxTina Purnat
• Pitfalls and pivots needed to use AI effectively in public health
• Evidence-based strategies to address health misinformation effectively
• Building trust with communities online and offline
• Equipping health professionals to address questions, concerns and health misinformation
• Assessing risk and mitigating harm from adverse health narratives in communities, health workforce and health system
Knee anatomy and clinical tests 2024.pdfvimalpl1234
This includes all relevant anatomy and clinical tests compiled from standard textbooks, Campbell,netter etc..It is comprehensive and best suited for orthopaedicians and orthopaedic residents.
Muktapishti is a traditional Ayurvedic preparation made from Shoditha Mukta (Purified Pearl), is believed to help regulate thyroid function and reduce symptoms of hyperthyroidism due to its cooling and balancing properties. Clinical evidence on its efficacy remains limited, necessitating further research to validate its therapeutic benefits.
Adhd Medication Shortage Uk - trinexpharmacy.comreignlana06
The UK is currently facing a Adhd Medication Shortage Uk, which has left many patients and their families grappling with uncertainty and frustration. ADHD, or Attention Deficit Hyperactivity Disorder, is a chronic condition that requires consistent medication to manage effectively. This shortage has highlighted the critical role these medications play in the daily lives of those affected by ADHD. Contact : +1 (747) 209 – 3649 E-mail : sales@trinexpharmacy.com
NVBDCP.pptx Nation vector borne disease control programSapna Thakur
NVBDCP was launched in 2003-2004 . Vector-Borne Disease: Disease that results from an infection transmitted to humans and other animals by blood-feeding arthropods, such as mosquitoes, ticks, and fleas. Examples of vector-borne diseases include Dengue fever, West Nile Virus, Lyme disease, and malaria.
ABDOMINAL TRAUMA in pediatrics part one.drhasanrajab
Abdominal trauma in pediatrics refers to injuries or damage to the abdominal organs in children. It can occur due to various causes such as falls, motor vehicle accidents, sports-related injuries, and physical abuse. Children are more vulnerable to abdominal trauma due to their unique anatomical and physiological characteristics. Signs and symptoms include abdominal pain, tenderness, distension, vomiting, and signs of shock. Diagnosis involves physical examination, imaging studies, and laboratory tests. Management depends on the severity and may involve conservative treatment or surgical intervention. Prevention is crucial in reducing the incidence of abdominal trauma in children.
These lecture slides, by Dr Sidra Arshad, offer a quick overview of the physiological basis of a normal electrocardiogram.
Learning objectives:
1. Define an electrocardiogram (ECG) and electrocardiography
2. Describe how dipoles generated by the heart produce the waveforms of the ECG
3. Describe the components of a normal electrocardiogram of a typical bipolar lead (limb II)
4. Differentiate between intervals and segments
5. Enlist some common indications for obtaining an ECG
6. Describe the flow of current around the heart during the cardiac cycle
7. Discuss the placement and polarity of the leads of electrocardiograph
8. Describe the normal electrocardiograms recorded from the limb leads and explain the physiological basis of the different records that are obtained
9. Define mean electrical vector (axis) of the heart and give the normal range
10. Define the mean QRS vector
11. Describe the axes of leads (hexagonal reference system)
12. Comprehend the vectorial analysis of the normal ECG
13. Determine the mean electrical axis of the ventricular QRS and appreciate the mean axis deviation
14. Explain the concepts of current of injury, J point, and their significance
Study Resources:
1. Chapter 11, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 9, Human Physiology - From Cells to Systems, Lauralee Sherwood, 9th edition
3. Chapter 29, Ganong’s Review of Medical Physiology, 26th edition
4. Electrocardiogram, StatPearls - https://www.ncbi.nlm.nih.gov/books/NBK549803/
5. ECG in Medical Practice by ABM Abdullah, 4th edition
6. Chapter 3, Cardiology Explained, https://www.ncbi.nlm.nih.gov/books/NBK2214/
7. ECG Basics, http://www.nataliescasebook.com/tag/e-c-g-basics
3. POSITION
PA AP
QUALITY
ROTATION PENETRATION INSPIRATION
LESION
OPACIT
OPACITY
Homo
Heterogenous Wellill defined Zone
Centralperipher
Silhouet sign
al
Y Necrotic
PATCHY
HILUMMEDIASTINAL
NODULE Central deviasionwided
MASS
COSTO-PHRENIC ANGEL
Freeoblitern
CAVITARY
OTHER
INFILTIRATION
Bone soft tissuediaphragm
5. Solitary Pulmonary Nodule(SPN)
Appearance
Margin Calcification cavitation
Comparison with a
Size
previous x-ray to >8mm
<8mm
Assess growth over
time. Location
Upperhillar zone Lowerbasesup-pleural
Associated abnormalities
Lymph node enlargement Rib destruction/erosion
6. Cavitary lesion
Air +
Air-fluid level Air only
tissue
Wall thickness
Straight Wavy Thick Thin
1. Fungal ball.
2. Rupture hydatid cyct site
3. Necrotic tumor
ruptured
4. Blood glot Hydatid
Abscess Irregular Regular
Peripheral Central
inner wall inner wall
cyst
Emphesemato
Cavitating Chronic us pneumatoc
neoplasm abscess ele
bulla
7. LINEAR PATTERN
1) Linear (reticular) abnormality is due to
pathology involving:
• airways,
• lymphatics,
• veins,
• interstitium of the lung.
2) Volume loss is a key finding in fibrosis.
8. LINEAR PATTERN
LINEAR PATTERN
LEFT VENTRICULAR FAILURE Perihilar and peripheral basal septal lines,
changes acutely and resolves with diuretics
Normal ageing Coarsening of lung markings in lower zones, no
change on review of recent films
Lymphangitis Coarse nodular and linear thickening of
markings, known malignancy, often associated
with pleural effusion, rapid clinical
deterioration of patient
9. LINEAR PATTERN
LINEAR PATTERN
Atelectasis Short thin lines, often basal, new on review of
previous films
Subsegmental Longer thicker bands, often perihilar or basal,
collapse suggest recent infection or infarction
Scarring Any length, persist over time unchanged
Fibrosis Volume loss is key, persists over time
10. Causes of fibrosis
Mid zone lung Lower zone lung Upper zone lung
tuberculosis Drug indused fibrosis sarcoidosis
(most common)
Chronic extrinsic allergic UIP
alveolitis
Radio-therapy Asbestose-related fibrosis
Ankylosing spondylitis
Progressive massive
fibrosis
histoplasmosis
11. Case-1
• A 49-year-old white woman presents with progressive
cough and dyspnea.
• She denies any history of arthritis, skin lesions, or eye
complaints.
• On physical examination, vital signs are:
– pulse 90 bpm;
– temperature 98°F;
– respirations 32/min;
– blood pressure 119/76 mm Hg.
• General exam: patient is in moderate distress, and
pertinent physical findings reveal clubbing of the fingers
and bilateral “Velcro” rales on lung auscultation.
• ABGs on room air: pH 7.47; PCO2 32 mm Hg; PO2 60 mm
Hg with further de-saturation on mild exertion
13. POSITION •PA CXR
QUALITY •Good Technical Quality
•Bilateral reticular infitration
•At lower zone and left mid zone
LESION
•Central trachea and mediasteinal.
MEDIASTINALHilum
ANGELS •Hazy left angle .
•No
OTHER
14. Case-1
1-Least likely to be associated with this condition is
a. Positive antinuclear antigen
b. Positive rheumatoid factor
c. Increased erythrocyte sedimentation rate
d. Increased IgE
2- What is the most likely diagnosis?
a. Idiopathic pulmonary fibrosis
b. Langerhans granulomatosis/histiocytosis-X disorders
c. Rheumatoid lung
d. Sarcoidosis
3- PFTS would be expected to show
a. An obstructive pattern
b. A restrictive pattern
c. A normal pattern
d. A reversible obstructive pattern
15. Case-2
• A 65-year-old woman from Honduras complains of arthralgias
and difficulty getting out of a chair and doing her daily chores
at home.
• She has muscle aches and generalized
weakness, dyspnea, and cough.
• On physical
• examination, vital signs are:
– pulse 98 bpm;
– temperature normal;
– Respirations 23/min
– bilateral crackles on lung exam.
• Neuro exam reveals proximal muscular weakness with no
sensory deficit.
• CPK and aldolase are increased:
• sedimentation rate is 120 mm/min.
• PFT: restrictive pattern.
17. POSITION •PA CXR
QUALITY •Poor Technical Quality
•Bilateral reticular infitration
•Diffuse bilateral lung especially left
LESION lower zone.
•Central trachea and mediasteinal.
MEDIASTINALHilum
ANGELS •Free .
•Right hemi-diaphragm elevated
OTHER
18. Case-2
1. What is the most likely diagnosis?
a. Paraneoplastic syndrome
b. Polymyositis
c. Sjgren syndrome
d. Scleroderma
2. There is an increased association of one
of the following with this condition
a. Carcinoma of the pancreas
b. Diabetes mellitus
c. Diabetes insipidus
d. Alzheimer’s disease
19. Case-3
• A 48-year-old female nurse is seen with
complaints of cough.
• She has been treated for “bronchitis”
without much improvement.
• On exam, she is afebrile and has crackles
in the upper zones of the lung field.
• PPD is negative and sputum for AFB is
negative.
21. POSITION •PA CXR
QUALITY •Good Technical Quality
•Bilateral reticular infitration
LESION •Diffuse bilateral lung especially
middle,upper zone.
•Central trachea and mediasteinal.
MEDIASTINALHilum •Bilateral hilar enlargementparathraceal
ANGELS •Disappear.
•No
OTHER
22. Case-3
• 1. The most likely diagnosis is:
• a. Tuberculosis
• b. Blastomycosis
• c. Sarcoidosis
• d. Silicosis
• 2. All of the following findings may be seen in
this patient except
• a. Uveitis
• b. Skin lesion
• c. Bony cysts
• d. Hypocalcemia
23. Case-4
• A 56-year-old black male non-smoker is seen with a history of dyspnea
• on walking two blocks and chronic chest congestion and cough.
• He has been followed for progressive shortness of breath after his CABG.
• Recently, he was ill with a flulike illness, but he denies any fever or chills
presently.
• Past history: reveals a GI clinic follow-up for inflammatory bowel disease for
• which he has been on chronic steroid therapy off and on.
• On physical examination, vital signs are:
• pulse 110 bpm;
• temperature normal;
• respirations24/min;
• blood pressure 120/78 mm Hg.
• General exam: patient appears frail but in no distress.
• Pertinent findings:
• coarse rhonchi and scattered expiratory wheeze with squeaks.
• Heart exam reveals normal S1-S2 with no gallop.
• There is no hepatomegaly or pedal edema.
24. Case-4
• Laboratory data:
• Hb 11 g; Hct 33%;
• WBCs 15.0/μL; differential normal.
• PFTs/spirometry:
• FVC 3.43 L (78% of predicted);
• FEV1: 2.15 L (63% of predicted);
• FEV1/FVC% 72%;
• TLC 5.34 L (69% of predicted);
• DLCO 14 cc/min/mm Hg (57% of predicted).
• Echocardiogram shows an:
• ejection fraction of 55%.
• no focal dyskinesia.
26. POSITION •PA CXR
QUALITY •Poor Technical Quality
•Bilateral reticular infitration
•Diffuse bilateral lung especially
LESION peripherial lower right zone.
•Central trachea and mediasteinal.
MEDIASTINALHilum
ANGELS •Free .
•No
OTHER
27. Case-4
• 1. What is the most likely diagnosis?
• a. Congestive heart failure
• b. COPD
• c. Nonspecific pneumonitis
• d. Bronchiolitis obliterans with organizing pneumonia
(BOOP)
• 2. There may be an increased risk of one of the
following during therapy in this patient:
• a. Pulmonary embolism
• b. Staphylococcal infection
• c. Mycobacterial infection
• d. HIV infection
28. Case-5
• A 50-year-old woman is admitted with progressive
shortness of breath.
• She was well until about 2 mo ago, when she noted
that she was getting tired and fatigued easily.
• She gives a history of working as a domestic worker
and “cleaning lady” for many years.
• Recently, she was working for a company that did
maintenance work on boats in a marina area.
• She now has cough, shortness of breath, and low-grade
fever with malaise.
• This has continued despite symptomatic treatment.
29. Case-5
• On exam she is found to be in:
• mild to moderate distress
• with harsh vesicular breath sounds,
• Diffuse rhonchi
• bilateral basilar crackles on lung exam, more
on the right.
• Routine labs are normal,
• PPD is 5 mm.
• sputum is negative for fungal.
• AFB smear with cultures pending.
31. POSITION •AP CXR
QUALITY •Poor Technical Quality
•Bilateral reticular (linar) infitration
•bilateral lower lung zone.
LESION
•Central trachea and mediasteinal.
MEDIASTINALHilum
ANGELS •Bilateral hazy angels .
•No
OTHER
32. Case-5
• 1. The most likely diagnosis is
• a. Silicosis
• b. Asbestosis
• c. Extrinsic allergic alveolitis
• d. Nontuberculous mycobacterial infection
• 2. Associated with this condition is
• a. Increased lung volumes
• b. Decreased diffusion
• c. Peripheral eosinophilia
• d. Inorganic dust exposure