This document discusses various fungal infections of the chest and their imaging appearances. It provides an overview of 9 main fungal organisms (Histoplasmosis, Coccidioidomycosis, Blastomycosis, Paracoccidioidomycosis, Candidiasis, Pneumocystis, Cryptococcosis, Mucormycosis, Aspergillosis) and summarizes their typical radiographic or CT findings. These include calcified nodules, cavitating lesions, consolidations, ground glass opacities, and halo signs which help differentiate the fungal pathogens.
This document discusses several common interstitial lung diseases. It begins with an overview and then focuses on sarcoidosis, describing its typical radiological presentation including small nodules in a perilymphatic distribution and stages of disease. Other diseases discussed include silicosis, lymphangitic carcinomatosis, pulmonary edema, hypersensitivity pneumonitis, tuberculosis, and chronic eosinophilic pneumonia. For each disease, the document outlines key radiological findings on HRCT and chest x-ray and provides differential diagnoses.
This document discusses various radiological manifestations of cerebral tuberculosis. It describes that approximately 10% of tuberculosis patients have central nervous system involvement. Imaging plays an important role in the diagnosis and evaluation of various intracranial manifestations of tuberculosis including tuberculous meningitis, tuberculoma, miliary tuberculosis, tuberculous encephalopathy and others. Characteristic radiological findings of each condition are outlined along with recommendations for appropriate imaging modalities. Spinal tuberculosis is also discussed with descriptions of typical radiographic and MRI findings.
This document discusses the imaging and characterization of solitary pulmonary nodules (SPNs). It defines an SPN and lists potential benign and malignant causes. Key imaging features that can help differentiate benign from malignant SPNs are described, including size, shape, edge characteristics, internal textures like calcification, fat and cavitation. The roles of CT, MRI, PET and other modalities are outlined. Determining the growth rate over time and performing biopsies are important for indeterminate nodules. Common benign entities like granulomas, hamartomas and infarcts are shown as examples.
This document discusses various pulmonary infections including lobar pneumonia, round pneumonia, bronchopneumonia, atypical pneumonia, tuberculosis, and lung abscess. It provides definitions, etiologies, clinical presentations, and radiographic features of each condition. For tuberculosis specifically, it describes features of primary tuberculosis, post-primary tuberculosis, and miliary tuberculosis. It also discusses complications of pneumonia and differential diagnoses for various pulmonary findings.
Describes the basic radiology of diffuse interstitial disease ,with differential diagnosis of nodular interstitial pattern and how to approach HRCT findings .
Presentation1.pptx, radiological signs in thoracic radiology.Abdellah Nazeer
The document discusses various radiological signs seen in thoracic diseases. It describes signs such as the silhouette sign, air bronchogram sign, signet ring sign, popcorn calcification, tram-track sign, tree-in-bud sign, CT angiogram sign, finger-in-glove sign, halo sign, reverse halo sign, coin lesion, miliary shadowing, Monod's sign, fallen lung sign, bulging fissure sign, flat waist sign, Golden S sign, bat wing appearance, ground glass pattern, crazy paving sign, mosaic pattern, sandstorm appearance, and honeycomb lung. Each sign is accompanied by an illustration and description of associated diseases.
This document provides an overview of CT chest imaging, including the different types of CT chest scans, chest anatomy visualized on CT, and common abnormalities seen on CT chest exams. It discusses standard CT chest, HRCT, low dose CT, CT angiography, and combined PET/CT scans. It details the mediastinal compartments and lung segments seen on CT. It also provides examples of abnormalities such as pulmonary nodules/masses, pulmonary embolism, interstitial lung disease patterns, emphysema, atelectasis, pneumothorax, pleural effusions, and cardiomegaly. Virtual bronchoscopy and CT-guided biopsy procedures are also summarized.
Radiological imaging of pleural diseases Pankaj Kaira
The document discusses the anatomy, imaging, and common diseases of the pleura. It begins by describing the normal anatomy of the pleural layers and thickness. Common pleural diseases are then reviewed, including pleural effusions, pneumothorax, hemothorax, and empyema. Imaging findings on chest x-ray, ultrasound, CT, and MRI are provided for diagnosing and characterizing various pleural conditions. Key signs that help differentiate pleural, pulmonary, and extra-pleural masses are also outlined.
This document discusses several common interstitial lung diseases. It begins with an overview and then focuses on sarcoidosis, describing its typical radiological presentation including small nodules in a perilymphatic distribution and stages of disease. Other diseases discussed include silicosis, lymphangitic carcinomatosis, pulmonary edema, hypersensitivity pneumonitis, tuberculosis, and chronic eosinophilic pneumonia. For each disease, the document outlines key radiological findings on HRCT and chest x-ray and provides differential diagnoses.
This document discusses various radiological manifestations of cerebral tuberculosis. It describes that approximately 10% of tuberculosis patients have central nervous system involvement. Imaging plays an important role in the diagnosis and evaluation of various intracranial manifestations of tuberculosis including tuberculous meningitis, tuberculoma, miliary tuberculosis, tuberculous encephalopathy and others. Characteristic radiological findings of each condition are outlined along with recommendations for appropriate imaging modalities. Spinal tuberculosis is also discussed with descriptions of typical radiographic and MRI findings.
This document discusses the imaging and characterization of solitary pulmonary nodules (SPNs). It defines an SPN and lists potential benign and malignant causes. Key imaging features that can help differentiate benign from malignant SPNs are described, including size, shape, edge characteristics, internal textures like calcification, fat and cavitation. The roles of CT, MRI, PET and other modalities are outlined. Determining the growth rate over time and performing biopsies are important for indeterminate nodules. Common benign entities like granulomas, hamartomas and infarcts are shown as examples.
This document discusses various pulmonary infections including lobar pneumonia, round pneumonia, bronchopneumonia, atypical pneumonia, tuberculosis, and lung abscess. It provides definitions, etiologies, clinical presentations, and radiographic features of each condition. For tuberculosis specifically, it describes features of primary tuberculosis, post-primary tuberculosis, and miliary tuberculosis. It also discusses complications of pneumonia and differential diagnoses for various pulmonary findings.
Describes the basic radiology of diffuse interstitial disease ,with differential diagnosis of nodular interstitial pattern and how to approach HRCT findings .
Presentation1.pptx, radiological signs in thoracic radiology.Abdellah Nazeer
The document discusses various radiological signs seen in thoracic diseases. It describes signs such as the silhouette sign, air bronchogram sign, signet ring sign, popcorn calcification, tram-track sign, tree-in-bud sign, CT angiogram sign, finger-in-glove sign, halo sign, reverse halo sign, coin lesion, miliary shadowing, Monod's sign, fallen lung sign, bulging fissure sign, flat waist sign, Golden S sign, bat wing appearance, ground glass pattern, crazy paving sign, mosaic pattern, sandstorm appearance, and honeycomb lung. Each sign is accompanied by an illustration and description of associated diseases.
This document provides an overview of CT chest imaging, including the different types of CT chest scans, chest anatomy visualized on CT, and common abnormalities seen on CT chest exams. It discusses standard CT chest, HRCT, low dose CT, CT angiography, and combined PET/CT scans. It details the mediastinal compartments and lung segments seen on CT. It also provides examples of abnormalities such as pulmonary nodules/masses, pulmonary embolism, interstitial lung disease patterns, emphysema, atelectasis, pneumothorax, pleural effusions, and cardiomegaly. Virtual bronchoscopy and CT-guided biopsy procedures are also summarized.
Radiological imaging of pleural diseases Pankaj Kaira
The document discusses the anatomy, imaging, and common diseases of the pleura. It begins by describing the normal anatomy of the pleural layers and thickness. Common pleural diseases are then reviewed, including pleural effusions, pneumothorax, hemothorax, and empyema. Imaging findings on chest x-ray, ultrasound, CT, and MRI are provided for diagnosing and characterizing various pleural conditions. Key signs that help differentiate pleural, pulmonary, and extra-pleural masses are also outlined.
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.
This document summarizes various patterns seen on imaging in interstitial lung diseases. It describes the reticulated, ground glass, nodular, cystic and mosaic patterns. For each pattern it provides examples of diseases that may cause it and key radiographic features. It also discusses specific interstitial lung diseases like UIP, NSIP, COP, RB-ILD and DIP that demonstrate characteristic patterns on imaging. The cystic diseases LAM and LCH are outlined. The document serves as a guide to interpreting interstitial lung disease imaging findings.
This document discusses pulmonary collapse, also known as atelectasis. It defines collapse as a partial or complete loss of lung volume. Collapse can occur through different mechanisms such as relaxation, cicatrization, or adhesion. Common causes include endobronchial obstruction from tumors, infections, or foreign bodies. Radiographic signs of collapse include loss of aeration, fissure displacement, and compensatory hyperinflation. CT scans can reveal additional details like mucus plugging. The document reviews signs of collapse involving each lung lobe.
A solitary pulmonary nodule is a rounded opacity less than 3 cm in diameter surrounded by lung parenchyma. Differentiating between benign and malignant nodules is important for prognosis and treatment. CT is the preferred imaging method and can evaluate nodule characteristics like size, shape, margin, attenuation and the presence of calcification which provide clues to benign or malignant etiology. Benign nodules often demonstrate smooth margins and characteristic calcification patterns while malignant nodules tend to have spiculated margins, irregular shapes and other concerning imaging features requiring biopsy for diagnosis.
This document discusses various types of cavitary lung lesions seen on imaging. It includes 18 figures showing examples of cavitary lesions caused by conditions such as bacterial abscesses, tuberculosis, fungal infections, metastases, pulmonary emboli, bronchiectasis, emphysema, cystic fibrosis, and papillomatosis. The cavities vary in appearance depending on the etiology, with differences in size, wall thickness, presence of air-fluid levels, and associated findings. Proper diagnosis relies on correlating the clinical history and imaging appearance.
This document discusses pulmonary vasculature abnormalities including pulmonary artery hypertension, pulmonary edema, pulmonary embolism, and venous abnormalities. It provides definitions, classifications, risk factors, and radiographic findings for each condition. For pulmonary artery hypertension, the document describes the definition, etiology, classification systems, and findings on plain radiography, CT, and MRI. It also discusses pulmonary edema, pulmonary embolism, pulmonary arteriovenous malformations, pulmonary varices, and pulmonary venoocclusive disease.
This document provides an overview of various demyelinating diseases of the central nervous system. It begins by defining demyelinating diseases as those involving disruption of myelin, which forms an insulating sheath around axons. It then classifies and describes several specific diseases, including acute disseminated encephalomyelitis (ADEM), inflammatory demyelinating pseudotumor, multiple sclerosis (MS), neuromyelitis optica, central pontine myelinolysis, HIV encephalopathy, progressive multifocal leukoencephalopathy (PML), and others. For each disease, it discusses clinical features, magnetic resonance imaging (MRI) findings, differential diagnoses, and pathology where relevant.
This document describes the various types and radiographic appearances of lobar and segmental lung collapse. It discusses intrinsic and extrinsic causes of collapse and describes the typical findings for each lobe, including displacement of fissures, loss of volume, and compensatory changes. Specific signs are outlined to help identify collapse of the different lung lobes based on chest x-ray and CT imaging. Rarer forms of collapse including complete opacification and shifting atelectasis are also covered.
Presentation1.pptx, radiological imaging of sarcoidosis.Abdellah Nazeer
Sarcoidosis is an inflammatory disease characterized by non-caseating granulomas that can affect multiple organs. Pulmonary involvement occurs in up to 90% of patients and includes lymph node enlargement, micronodules with a perilymphatic distribution, fibrotic changes, and bilateral perihilar opacities. Extrapulmonary involvement such as skin and eye lesions is present in 25% of cases. HRCT is useful for evaluating the pulmonary manifestations which can vary significantly between patients.
The document discusses lung collapse (atelectasis) and consolidation. Collapse is a loss of lung volume while consolidation involves fluid filling the alveoli. Collapse can be caused by obstruction of airways or loss of contact between the lungs and chest wall. Consolidation is seen in conditions like pneumonia. Specific patterns of collapse and consolidation are seen on chest x-rays depending on the affected lung lobe. Signs like fissure shifts and volume changes in the unaffected lobes help identify the collapsed lobe.
The document discusses the radiological findings of tuberculosis based on 7 patient case presentations. It summarizes common findings seen on chest x-rays such as miliary shadows, cavities, consolidation, lymphadenopathy, pleural effusions and changes. Specific findings are described for different stages of TB including primary infection, post-primary infection, and complications such as tuberculoma, pleural thickening and airway involvement. Radiological images are included to demonstrate various manifestations of pulmonary and pleural TB.
Cavitary lung lesions can have various causes including cancer, infection, autoimmune disease, vascular embolism, and trauma. On imaging, characteristics like wall thickness, inner contour, location, and other associated findings provide clues to the underlying etiology. Malignant processes tend to have thicker walls over 15mm while benign lesions usually have thinner walls under 4mm. Infectious cavities often have irregular inner walls and may contain fluid levels. Autoimmune diseases typically cause multiple bilateral nodules. The clinical context is also important for determining the most likely diagnosis.
Segmental anatomy of lungs , anatomy of mediastinum and secondary lobuleGamal Agmy
The document discusses the segmental anatomy of the lungs and secondary lobule. It notes that there are approximately 23 generations of dichotomous branching from the trachea to the alveolar sacs. The secondary lobule is described as the basic anatomic unit of pulmonary structure and function, measuring 1-2 cm and containing 5-15 pulmonary acini. It is supplied by a terminal bronchiole in the center and surrounded by connective tissue septa and two lymphatic systems. Diseases typically manifest in either the centrilobular or perilymphatic areas based on how they enter the lungs.
Presentation1.pptx, radiological imaging of diffuse lung disease.Abdellah Nazeer
This document discusses radiological imaging techniques for evaluating diffuse interstitial lung disease. It begins by describing diffuse interstitial lung disease as a group of conditions that cause inflammation and scarring of the lung tissue supporting the air sacs. Common symptoms include shortness of breath and cough. The document then outlines the various tests and imaging modalities used to diagnose interstitial lung diseases, including blood tests, spirometry, pulse oximetry, chest x-rays, CT scans, and biopsies. CT scans are highlighted as particularly useful for identifying patterns of lung damage and assessing disease progression and severity. Specific interstitial lung diseases like idiopathic pulmonary fibrosis, hypersensitivity pneumonitis, and sarco
1. The initial assessment of a pediatric chest x-ray should include evaluation of technique, tubes/lines, mediastinum, airways, lungs, and pulmonary vasculature. Inspiration level and thymic tissue should not be mistaken for pathology.
2. Causes of neonatal respiratory distress are categorized as medical or surgical. Common medical causes include transient tachypnea of the newborn, pneumonia, respiratory distress syndrome, and meconium aspiration syndrome. Surgical causes include diaphragmatic hernia and congenital lung malformations.
3. Complications of respiratory distress treatment include barotrauma manifestations like pneumothorax and pulmonary interstitial emphysema. Other
This document defines non-resolving pneumonia and discusses its causes and diagnostic evaluation. Non-resolving pneumonia is defined as persistence of clinical symptoms and radiographic abnormalities for longer than expected despite adequate antibiotic therapy. Common causes include inappropriate antibiotic therapy, complications of the initial infection, host factors, and presence of resistant or unusual pathogens. A thorough diagnostic evaluation includes assessing treatment response, looking for complications or superinfections, evaluating for unusual organisms, and examining host immune function. Radiological imaging, bronchoscopy with protected specimen brushing or biopsy, and CT-guided biopsies can help identify causative organisms or underlying conditions.
The document discusses abnormalities that may appear on a chest x-ray and how to interpret them. It describes findings related to the lung parenchyma including consolidations, interstitial diseases, nodules, cavities, and calcifications. It also covers pleural abnormalities such as effusions, thickening, and plaques. Key signs are explained like air bronchograms, silhouetting, and Kerley lines which provide clues to diagnose conditions like pneumonia.
Imaging in pulmonary infections (non bacterial)devrajkandel1
This document provides an overview of imaging features of non-bacterial pulmonary infections. It begins by describing the mechanisms of pulmonary infections and then discusses various types of infections including viral, fungal, protozoal and helminthic origins. For each type of infection, examples of specific pathogens are given along with their typical radiographic and CT imaging appearances. Common findings include areas of consolidation, ground-glass opacities, nodules and reticulation. The document emphasizes how imaging can help identify and characterize different pulmonary infections.
This document provides information on systemic mycoses, including Blastomycosis, Coccidioidomycosis, and Histoplasmosis. It begins with an introduction to systemic mycoses and then discusses the epidemiology, pathogenesis, clinical presentation, and laboratory diagnosis of each individual fungus. For Blastomycosis, it describes its endemic regions in North America, how it is acquired via inhalation of spores and can cause pulmonary or disseminated disease. For Coccidioidomycosis, it outlines its occurrence in semi-arid regions of the Americas and how inhalation of windborne spores from disturbed soil causes symptoms ranging from asymptomatic to influenza-like illness. The document
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.
This document summarizes various patterns seen on imaging in interstitial lung diseases. It describes the reticulated, ground glass, nodular, cystic and mosaic patterns. For each pattern it provides examples of diseases that may cause it and key radiographic features. It also discusses specific interstitial lung diseases like UIP, NSIP, COP, RB-ILD and DIP that demonstrate characteristic patterns on imaging. The cystic diseases LAM and LCH are outlined. The document serves as a guide to interpreting interstitial lung disease imaging findings.
This document discusses pulmonary collapse, also known as atelectasis. It defines collapse as a partial or complete loss of lung volume. Collapse can occur through different mechanisms such as relaxation, cicatrization, or adhesion. Common causes include endobronchial obstruction from tumors, infections, or foreign bodies. Radiographic signs of collapse include loss of aeration, fissure displacement, and compensatory hyperinflation. CT scans can reveal additional details like mucus plugging. The document reviews signs of collapse involving each lung lobe.
A solitary pulmonary nodule is a rounded opacity less than 3 cm in diameter surrounded by lung parenchyma. Differentiating between benign and malignant nodules is important for prognosis and treatment. CT is the preferred imaging method and can evaluate nodule characteristics like size, shape, margin, attenuation and the presence of calcification which provide clues to benign or malignant etiology. Benign nodules often demonstrate smooth margins and characteristic calcification patterns while malignant nodules tend to have spiculated margins, irregular shapes and other concerning imaging features requiring biopsy for diagnosis.
This document discusses various types of cavitary lung lesions seen on imaging. It includes 18 figures showing examples of cavitary lesions caused by conditions such as bacterial abscesses, tuberculosis, fungal infections, metastases, pulmonary emboli, bronchiectasis, emphysema, cystic fibrosis, and papillomatosis. The cavities vary in appearance depending on the etiology, with differences in size, wall thickness, presence of air-fluid levels, and associated findings. Proper diagnosis relies on correlating the clinical history and imaging appearance.
This document discusses pulmonary vasculature abnormalities including pulmonary artery hypertension, pulmonary edema, pulmonary embolism, and venous abnormalities. It provides definitions, classifications, risk factors, and radiographic findings for each condition. For pulmonary artery hypertension, the document describes the definition, etiology, classification systems, and findings on plain radiography, CT, and MRI. It also discusses pulmonary edema, pulmonary embolism, pulmonary arteriovenous malformations, pulmonary varices, and pulmonary venoocclusive disease.
This document provides an overview of various demyelinating diseases of the central nervous system. It begins by defining demyelinating diseases as those involving disruption of myelin, which forms an insulating sheath around axons. It then classifies and describes several specific diseases, including acute disseminated encephalomyelitis (ADEM), inflammatory demyelinating pseudotumor, multiple sclerosis (MS), neuromyelitis optica, central pontine myelinolysis, HIV encephalopathy, progressive multifocal leukoencephalopathy (PML), and others. For each disease, it discusses clinical features, magnetic resonance imaging (MRI) findings, differential diagnoses, and pathology where relevant.
This document describes the various types and radiographic appearances of lobar and segmental lung collapse. It discusses intrinsic and extrinsic causes of collapse and describes the typical findings for each lobe, including displacement of fissures, loss of volume, and compensatory changes. Specific signs are outlined to help identify collapse of the different lung lobes based on chest x-ray and CT imaging. Rarer forms of collapse including complete opacification and shifting atelectasis are also covered.
Presentation1.pptx, radiological imaging of sarcoidosis.Abdellah Nazeer
Sarcoidosis is an inflammatory disease characterized by non-caseating granulomas that can affect multiple organs. Pulmonary involvement occurs in up to 90% of patients and includes lymph node enlargement, micronodules with a perilymphatic distribution, fibrotic changes, and bilateral perihilar opacities. Extrapulmonary involvement such as skin and eye lesions is present in 25% of cases. HRCT is useful for evaluating the pulmonary manifestations which can vary significantly between patients.
The document discusses lung collapse (atelectasis) and consolidation. Collapse is a loss of lung volume while consolidation involves fluid filling the alveoli. Collapse can be caused by obstruction of airways or loss of contact between the lungs and chest wall. Consolidation is seen in conditions like pneumonia. Specific patterns of collapse and consolidation are seen on chest x-rays depending on the affected lung lobe. Signs like fissure shifts and volume changes in the unaffected lobes help identify the collapsed lobe.
The document discusses the radiological findings of tuberculosis based on 7 patient case presentations. It summarizes common findings seen on chest x-rays such as miliary shadows, cavities, consolidation, lymphadenopathy, pleural effusions and changes. Specific findings are described for different stages of TB including primary infection, post-primary infection, and complications such as tuberculoma, pleural thickening and airway involvement. Radiological images are included to demonstrate various manifestations of pulmonary and pleural TB.
Cavitary lung lesions can have various causes including cancer, infection, autoimmune disease, vascular embolism, and trauma. On imaging, characteristics like wall thickness, inner contour, location, and other associated findings provide clues to the underlying etiology. Malignant processes tend to have thicker walls over 15mm while benign lesions usually have thinner walls under 4mm. Infectious cavities often have irregular inner walls and may contain fluid levels. Autoimmune diseases typically cause multiple bilateral nodules. The clinical context is also important for determining the most likely diagnosis.
Segmental anatomy of lungs , anatomy of mediastinum and secondary lobuleGamal Agmy
The document discusses the segmental anatomy of the lungs and secondary lobule. It notes that there are approximately 23 generations of dichotomous branching from the trachea to the alveolar sacs. The secondary lobule is described as the basic anatomic unit of pulmonary structure and function, measuring 1-2 cm and containing 5-15 pulmonary acini. It is supplied by a terminal bronchiole in the center and surrounded by connective tissue septa and two lymphatic systems. Diseases typically manifest in either the centrilobular or perilymphatic areas based on how they enter the lungs.
Presentation1.pptx, radiological imaging of diffuse lung disease.Abdellah Nazeer
This document discusses radiological imaging techniques for evaluating diffuse interstitial lung disease. It begins by describing diffuse interstitial lung disease as a group of conditions that cause inflammation and scarring of the lung tissue supporting the air sacs. Common symptoms include shortness of breath and cough. The document then outlines the various tests and imaging modalities used to diagnose interstitial lung diseases, including blood tests, spirometry, pulse oximetry, chest x-rays, CT scans, and biopsies. CT scans are highlighted as particularly useful for identifying patterns of lung damage and assessing disease progression and severity. Specific interstitial lung diseases like idiopathic pulmonary fibrosis, hypersensitivity pneumonitis, and sarco
1. The initial assessment of a pediatric chest x-ray should include evaluation of technique, tubes/lines, mediastinum, airways, lungs, and pulmonary vasculature. Inspiration level and thymic tissue should not be mistaken for pathology.
2. Causes of neonatal respiratory distress are categorized as medical or surgical. Common medical causes include transient tachypnea of the newborn, pneumonia, respiratory distress syndrome, and meconium aspiration syndrome. Surgical causes include diaphragmatic hernia and congenital lung malformations.
3. Complications of respiratory distress treatment include barotrauma manifestations like pneumothorax and pulmonary interstitial emphysema. Other
This document defines non-resolving pneumonia and discusses its causes and diagnostic evaluation. Non-resolving pneumonia is defined as persistence of clinical symptoms and radiographic abnormalities for longer than expected despite adequate antibiotic therapy. Common causes include inappropriate antibiotic therapy, complications of the initial infection, host factors, and presence of resistant or unusual pathogens. A thorough diagnostic evaluation includes assessing treatment response, looking for complications or superinfections, evaluating for unusual organisms, and examining host immune function. Radiological imaging, bronchoscopy with protected specimen brushing or biopsy, and CT-guided biopsies can help identify causative organisms or underlying conditions.
The document discusses abnormalities that may appear on a chest x-ray and how to interpret them. It describes findings related to the lung parenchyma including consolidations, interstitial diseases, nodules, cavities, and calcifications. It also covers pleural abnormalities such as effusions, thickening, and plaques. Key signs are explained like air bronchograms, silhouetting, and Kerley lines which provide clues to diagnose conditions like pneumonia.
Imaging in pulmonary infections (non bacterial)devrajkandel1
This document provides an overview of imaging features of non-bacterial pulmonary infections. It begins by describing the mechanisms of pulmonary infections and then discusses various types of infections including viral, fungal, protozoal and helminthic origins. For each type of infection, examples of specific pathogens are given along with their typical radiographic and CT imaging appearances. Common findings include areas of consolidation, ground-glass opacities, nodules and reticulation. The document emphasizes how imaging can help identify and characterize different pulmonary infections.
This document provides information on systemic mycoses, including Blastomycosis, Coccidioidomycosis, and Histoplasmosis. It begins with an introduction to systemic mycoses and then discusses the epidemiology, pathogenesis, clinical presentation, and laboratory diagnosis of each individual fungus. For Blastomycosis, it describes its endemic regions in North America, how it is acquired via inhalation of spores and can cause pulmonary or disseminated disease. For Coccidioidomycosis, it outlines its occurrence in semi-arid regions of the Americas and how inhalation of windborne spores from disturbed soil causes symptoms ranging from asymptomatic to influenza-like illness. The document
This chapter discusses several types of systemic mycoses including blastomycosis, coccidioidomycosis, paracoccidioidomycosis, and histoplasmosis. It describes the epidemiology, pathogenesis, clinical presentation, and laboratory diagnosis of each infection. The laboratory diagnosis sections explain how to identify the fungi microscopically in clinical specimens and cultures through their morphological characteristics and growth patterns. Serological tests are also used to aid diagnosis and indicate disease activity. The chapter aims to describe the pathogens that cause systemic mycoses and the techniques used to diagnose these infections.
This document discusses HIV and its effects on the ENT system. It begins by explaining what HIV is and how it attacks the immune system. It then discusses the epidemiology of HIV and current global statistics. Various opportunistic infections that can affect the ENT system are described, including fungal infections of the ear, sinusitis, neoplasms like Kaposi's sarcoma, and lymphomas of the nose and oral cavity. Manifestations in different areas like the ear, nose, oral cavity and airways are summarized. Risk groups, disease progression, and treatment approaches are also briefly covered.
This document provides an overview of tuberculosis (TB), including its definition, causes, pathogenesis, clinical presentation, investigations, types, treatment regimens, and relationship to HIV/AIDS. TB is caused by mycobacteria, commonly Mycobacterium tuberculosis, which can affect any organ but typically affects the lungs. It is transmitted via airborne droplets from someone with active pulmonary TB. Primary infection may result in latent TB or active TB, depending on immune response. Symptoms vary based on location of infection. Diagnosis involves chest x-ray, sputum smear, and Mantoux test. Treatment involves a combination of bactericidal and bacteriostatic drugs. Multi-drug resistant TB can develop if treatment is not completed
This document discusses various types of pulmonary infections (pneumonias). It begins by defining pneumonia as inflammation and consolidation of the lung parenchyma. It then describes different types of pneumonia including community-acquired bacterial pneumonia, atypical pneumonia, hospital-acquired pneumonia, aspiration pneumonia, and fungal and viral pneumonias. For each type, it discusses causative organisms, pathogenesis, clinical presentation, pathology, diagnosis and treatment. It provides detailed descriptions and microscopic images of different stages of lobar pneumonia, bronchopneumonia, and infectious processes like histoplasmosis, aspergillosis, and cryptococcosis.
Infeksi Jamur pada Paru dapat disebabkan oleh berbagai jenis jamur, seperti Candida, Aspergillus, Cryptococcus, dan Pneumocystis. Candida albicans adalah penyebab utama kandidiasis paru yang menyebabkan gejala batuk berdahak, sesak napas, dan demam. Aspergillus dapat menyebabkan aspergilloma, ABPA, atau aspergilosis invasif yang ditandai dengan nodul paru dan bronkiektazis. Diagnosis didasarkan pada pemer
Dimorphic systemic mycoses are caused by fungal pathogens that can change morphology to overcome host defenses. The diseases are geographically restricted and commonly involve inhalation of spores leading to pulmonary infection. Histopathological examination is important for identifying potential pathogens by revealing characteristic tissue morphologies like spherules in coccidioidomycosis or broad-budding yeasts in blastomycosis. Laboratory diagnosis involves microscopy, culture and serology of clinical specimens but cultures require special handling due to their pathogenicity.
Pulmonary tuberculosis is caused by the bacterium Mycobacterium tuberculosis. It is transmitted via airborne droplets when people with active TB cough, sneeze or spit. Primary tuberculosis occurs when someone is initially infected, usually resulting in a self-limited infection. Post-primary tuberculosis occurs after a latent period and is usually due to reinfection or reactivation of a latent infection. Diagnosis involves microbiological testing of sputum samples, chest imaging, and tuberculin skin testing or interferon-gamma release assays. Radiographic findings can help determine if a case is active or inactive.
This document discusses surgical infections of the thorax, including pathology, investigations, treatments, and specific conditions. It covers topics such as the stages of empyema (exudative, fibrino purulent, organizing), classifications of inflammatory diseases of the thorax (infections of the container vs contents), and treatments for specific infections like tuberculosis of the ribs and actinomycosis. Empyema treatment options discussed include antibiotics, tube thoracostomy, fibrinolytic therapy, VATS, rib resection, decortication, and thoracoplasty.
The document discusses several fungal diseases including mycetoma, candidiasis, cutaneous superficial mycosis, and viral haemorrhagic fevers. Mycetoma is a chronic infection of the limbs characterized by draining sinuses discharging grains. Candidiasis is an opportunistic infection most commonly caused by Candida albicans. Cutaneous superficial mycosis includes infections caused by dermatophytes like Microsporum and Trichophyton. Viral haemorrhagic fevers covered are yellow fever, dengue fever, chikungunya virus infection, and influenza virus infections.
The document discusses several infectious diseases including measles, rubella, chickenpox, diphtheria, meningitis, and dengue hemorrhagic fever. It provides details on the causative agents, modes of transmission, signs and symptoms, diagnostic tests, and treatment for each disease. For dengue hemorrhagic fever specifically, it notes that reported cases in the Philippines were over 24,000 lower in 2011 compared to the previous year, with fewer deaths. Prevention strategies discussed include immunization and controlling the mosquito vector.
1. The document describes four systemic mycoses caused by dimorphic fungi: histoplasmosis, blastomycosis, coccidioidomycosis, and paracoccidioidomycosis.
2. It provides details on the causative agents, pathogenesis, clinical manifestations, laboratory diagnosis including histopathology, culture, and serology, and treatment recommendations for each fungal infection.
3. Key diagnostic methods include histopathological staining of tissue samples to identify characteristic fungal structures, culture of samples to demonstrate the dimorphic nature of the fungi, and serological tests to detect antibodies.
This document discusses lymphangitis and lymphadenitis. Lymphangitis is defined as inflammation of the lymphatic channels that occurs as a result of infection at a site distal to the channel. Common causes include streptococcal bacteria. Symptoms include red streaks on the skin extending from the infection site toward lymph nodes. Treatment involves antibiotics. Lymphadenitis is inflammation of lymph nodes, which can be caused by various bacteria, viruses, fungi or other pathogens. Evaluation may involve imaging and biopsy to determine the cause and guide treatment.
Meningococci are a type of bacteria that cause serious infections. The most common infection is meningitis, which is an inflammation of the thin tissue that surrounds the brain and spinal cord. Meningococci can also cause other problems, including a serious bloodstream infection called sepsis. In its early stages, you may have flu-like symptoms and a stiff neck. But the disease can progress quickly and can be fatal. Early diagnosis and treatment are extremely important. Lab tests on your blood and cerebrospinal fluid can tell if you have it. Treatment is with antibiotics. Since the infection spreads from person to person, family members may also need to be treated.
A vaccine can prevent meningococcal infections.
Neuroradiology of cns funfal infectionsNeurologyKota
This document discusses the neuroradiology of central nervous system (CNS) fungal infections. It covers the common fungal pathogens that can cause CNS infections such as Cryptococcus neoformans and Aspergillus fumigatus. Imaging findings for various fungal infections like cryptococcosis, aspergillosis, and mucormycosis are described. Cryptococcal meningitis most commonly presents as leptomeningeal enhancement on MRI. Aspergillosis can cause hemorrhagic or infarcted lesions. Mucormycosis often involves paranasal sinus infection with intracranial extension. The document also briefly discusses spinal fungal infections and references
This document provides information on cryptococcosis, caused by the fungi Cryptococcus neoformans and Cryptococcus gattii. It discusses the clinical case of a 31-year-old HIV+ female presenting with confusion and other symptoms. The diagnosis was determined to be cryptococcal meningitis based on CSF analysis showing yeast cells and a positive India ink test. Background information is then given on the microbiology, epidemiology, pathogenesis, clinical presentation and investigations for cryptococcosis. Standard treatment in Botswana involves initial intravenous amphotericin B and fluconazole followed by oral fluconazole consolidation therapy.
Lung abscess is a localized area of lung destruction caused by infection, typically by aspiration of oropharyngeal bacteria. It appears on imaging as a cavity containing air-fluid levels. The infection can start as necrotizing pneumonia that progresses to microabscesses and larger cavitary lesions over time. Risk factors include dental/sinus infections, impaired swallowing, or pre-existing lung disease. Treatment involves antibiotics targeting common aerobic and anaerobic bacteria. Therapy typically lasts 4-6 weeks until imaging shows resolution, though surgery may be needed for large or resistant abscesses. Complications can include empyema, bronchopleural fistula, or distant infections if not properly treated.
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Imaging in fungal infection of chest
1. Imaging in
Fungal Infections of Chest
Dr. Gobardhan Thapa
Resident, First year
Radiodiagnosis,
NAMS, Bir Hospital
Nepal
2. Outline of Presentation
• Introduction
• Classification of Fungal Infections
• Overview of specific Fungal organism and the
current Imaging modalities
• Summary
• references
3. A case report
• A 71-year-old Chinese male was admitted with complaint of
chronic cough and malaise for two months. He had been in
Tucson, Arizona, USA, visiting for four months right before
the symptoms occurred. He had transient low-grade fever,
but denied hemoptysis, night sweats, skin rashes, or
headache. He did not smoke or abuse drugs. Physical
examination revealed no abnormalities. Lab tests showed
an elevated erythrocyte sedimentation rate (ESR) of 46
mm/h, while complete blood count (CBC), eosinophil count,
serum chemistry, and tumor biomarkers were all in normal
range. Human immunodeficiency virus (HIV) antibody was
found to be negative. Sputum culture showed normal flora
growth.
4. • Chest computed tomographic (CT) scan revealed
an irregular-margined opacity measuring 3.0
cm×3.8 cm in diameter in the sub-pleura region of
right middle lobe. Right hilar and mediastinal
lymphadenopathy was noted. Lung cancer was
considered as the most likely diagnosis.
Subsequent bronchoscopy and brush cytology
were negative. The patient received a procedure
of right middle lobe and lower lobectomy on the
eighth day after admission.
6. -Journal of Zhejiang university science, April, 2014
• Histopathological examination of lung specimen
showed focal necrotic granulomatous
inflammation with multinucleated giant cells
containing fungal spherules and infiltrations of
massive neutrophils, eosinophils, and
lymphocytes.. The final diagnosis thus was
confirmed pathologically as pulmonary
Coccidioides infection. The patient was totally free
from discomfort in the course of two years follow-
up after the lobectomy
7. Introduction
• Fungal Pneumonia
– Are now seen with increased frequency
• Increase in the incidence of disease caused by pathogenic
fungi in healthy hosts
• Emergence of opportunistic species in immuno-
compromsied hosts
9. 1. Histoplasmosis
• Histoplasma capsulatum
• In moist soil and bird/bat excreta
• Mostly subclinical infection:
– Heals spontaneously
– CXR: may be normal
• Or sometimes well-defined, calcific nodules <1 mm in size
• Calcified hilar of mediastinal nodes
• Multiple miliary calcified nodules
10. • Progression of the infective foci:
– Leading to a larger nodule
– Hilar nodes enlargement is common
– Locally progressive: may have consolidative changes,
later associated with Fibrosis and cavitation.
• Massive inhalation of organisms:
– May show fairly discrete, nodular opacities 3-4 mm in
diameter with hilar adenopathy
14. • Histoplasmoma:
– A solitary, sharply defined nodule <3 cm
– Most common in lower lobes-frequently calcify
• Fibrosing Mediastinitis (chronic pulmonary disease):
– Uncommon late manifestation
– Stenosis of venacava, oesophagus, trachea, bronchi or
central pulmonary vessels
– CXR: widened mediastinum
17. • blood-borne dissemination
– Asymptomatic blood-borne dissemination is common
– Eg calcified granulomas in patients of endemic area
– Clinically apparent disseminated histoplasmosis
• Extremely rare
18. 2. Coccidioidomycosis
• Coccidioides immitis
• Found in soil in arid/semi-arid areas
• 4 types of clinical and radiographic pulmonary
infections:
a) Acute Coccidioidomycosis
b) Persistent Coccidioidomycosis
c) Chronic progressive disease
d) Disseminated (Miliary) Coccidioidomycosis
19. a) Acute coccidioidomycosis
• Develops in 40% of infected adults
• Self-limiting viral type illness: Valley fever
• Associated with erythema nodosum and Arthralgia
• CXR: may be normal or
Focal or multifocal segmental air-space opacities
Associated with Hilar and mediastinal adenopathy and pleural
effusion
b) Persistent coccidioidomycosis (infection beyond 6-8
weeks)
• Coccidioidal masses or nodules (coccidioidomas)
• Areas of round pneumonia- subpleural regions of upper lobes
• Cavitate rapidly-produce characteristic thin-walled cavities
20. c) Chronic progressive disease
• Upper lobe fibro-cavitatory disease
– Thin-walled cyst : Grape-skin sign
• Similar to Post-primary TB and Histoplasmosis
d) Disseminated (Miliary) coccidioidomycosis
• Relatively rare
• Affects the immuno-compromised patients
22. Fig. primary coccidioides infection
frontal radiograph in a female with a clinical diagnosis of
valley fever reveals a mass like opacity in the right lower
lung with enlarged right hilar nodes
23. Fig. primary coccidioides infection
coronal reformatted CT of same patient
confirms a right middle lobe nodule
24. Fig. Chest x-ray showing Grape-skin sign
thin-walled grape-skin cyst
over time cavity may deflate and acquire slightly thicker wall
25. 3. Blastomycois
• Caused by Blastomyces dermatidis
• Chronic systemic disease
• Primarily affects the lungs and the skin
• Pulmonary infections often asymptomatic
• Symptomatic infection:
– Resembles that of an Acute bacterial pneumonia
26. • Radiographically:
– Usually non-specific
• Most common presentation:
– Homogeneous non-segmental air space opacification with
propensity for upper lobes
• Less common presentation:
– Single or multiple masses
– Cavitate in 15% of cases
– Tend to occur in patients with prolonged symptoms (1
months)-may mimic Bronchogenic Ca
27. • Less common presentation:
– Diffuse reticulo-nodular opacities
• Pleural effusion and lymph node enlargement –
uncommon
• Disseminated miliary form
– In immunocompromised hosts
28. Fig. Blastomyces dermatidis infection
chest radiograph shows an ill-defined mass in the left upper
lobe. CT scan through the upper lobes shows an irregular mass
in the left upper lobe with surrounding ground glass opacity.
Biopsy revealed Blastomyces dermatidis infection
29. 4. Paracoccidioidomycosis(PCM)
• Also known as South American Blastomycosis
• Endemic disease caused by dimorphic fungi
– Paracoccidioides brasiliensis
• Most frequent systemic mycosis in Latin America
esp. in Brazil
• HRCT:
– Areas of ground-glass opacities, nodules, interlobular
septal thickening, air-space consolidation, cavitation
and fibrosis
30. 5. Candidiasis
• Candida albicans
• Important pathogen esp. in Immunocompromised
patients:
– Particularly in patients with underlying malignancy, IV
drugs abuser, AIDS, following Bone marrow transplant
• Lung infection is usually due to hematogeneous
spread
31. • Radiographically, may present as
– Chronic pneumonia
– Abscess formation
– Mycetoma formation
• CT
– Multiple bilateral nodular opacities often associated with
areas of consolidation and ground glass opacities-CT halo
sign
• Less common presentations:
– Pleural effusion, thickening of bronchial walls, cavitation
33. 6. Pneumocystis jiroveci
• Opportunistic fungal pathogen
• Cause pneumonia in patients with
– AIDs
– Organ transplant
– Undergoing chemotherapy
– Immunosuppressive treatment
– Long term corticosteroids
34. • Radiographically,
– May have normal findings
– Classic features: diffuse, bilateral interstitial infiltrates in
peri-hilar distribution
• CT:
– Done in a highly suspicious case for confirming the
diagnosis
– Peri-hilar ground glass opacities, in a patchy or geographic
distribution with areas of superimposed interlobular septal
thickening: Crazy Paving pattern
– May rapidly progress to involve entire lung
37. 7. Cryptococcosis (Torulosis)
• Cryptococcus neoformans (yeast form fungi)
• Found in soil or bird droppings
• Mostly asymptomatic
• Cryptococcal pneumonia
– Common in AIDS (when CD4 <100/cu. mm)
38. • Chest radiography:
– Homogeneous, segmental or lobar opacifications
– Miliary, reticular or reticulo-nodular interstitial
patterns
– Pulmonary masses-5 mm to large (usually pleura-
based) with ill-defined edge known as Torulosis
• May show Halo sign
• May cavitate
– Lymph node enlargement and calcification is unusual
39. Fig. cryptococcus
a pleurally based mass like area of consolidation in the left
upper lobe is present in a patient who also had cryptococcal
meningitis
40. 8. Mucormycosis
• Opportunistic fungal infection of order Mucorales
• Broad, non-septated hyphae that randomly branch
at right angles
• Spreading destructive infections in Diabetics and
immuno-compromised
41. • Radiographically,
– Lobar or multi-lobar areas of consolidation and solitary or
pulmonary nodules and masses with Cavitation in 26-40 %
cases-air crescent sign suggestive of invasive fungal
infection in 5-12.5 % cases
• Dense cavitating bronchopneumonia
• CT:
– Non-specific
– Solitary or multiple areas of consolidation or
– solitary of multiple nodules surrounded by a Halo of
ground-glass attenuation and cavitation
42. Fig. pulmonary mucormycosis in a patient
reverse halo or bird nest or Atoll sign
axial (left) and coronal (right) images show peripheral rim of consolidation
surrounding central ground glass opacity, reticulation and nodularity
43. 9. Aspergillus infection
• Caused by Aspergillus species, usually A.
fumigatus
• Can take different forms, depending on an
individual’s immune response to the organism,
classically:
– Aspergilloma or Mycetoma formation or Saprophytic
forms
– Invasive forms
– Allergic forms
44. Aspergilloma
• Also known as fungus ball
• a ball of hyphae, mucus and cellular debris that
colonizes a pre-existing bulla or a parenchymal cavity
created by some other pathogen or destructive
process
• Invasion into lung parenchyma does not occur unless
the host defense mechanisms are compromised
• Usually asymptomatic
• May cause Hemoptysis-which can be massive
45. • Radiographs or CT findings:
– Solid round mass within an upper
lobe cavity, with an area of Air-
crescent separating the mycetoma
from the cavity wall- roll
dependently on decubitus
radiographs
– Progressive apical pleural
thickening adjacent to a cavity is
common
• should prompt a search for a
complicating mycetoma
46. Fig. Air-crescent or Monad sign of Aspergillus
gravity dependence of fungus ball
47. Semi-invasive or Chronic necrotizing Aspergillosis
• In patients with mildly impaired immunity e.g.
Chronic illness, Diabetes, malnutrition, alcoholism,
advanced age, steroid administration, chronic
obstructive disease
• Radiographically- variable appearance
– Most common:
• One or more rounded, poorly marginated areas of homogeneous
opacification with or without Air-bronchograms and or cavitation
• With time, the lesions margins may become discrete
– May resemble a mass
49. Invasive Aspergillosis
• Angio-invasive:
– Occlusion of small-to-medium pulmonary arteries
– Developing necrotic hemorrhagic nodules or infarcts
– CT:
• Multiple nodules surrounded by a Halo of ground glass
attenuation CT HALO sign or
• Pleural-based wedge-shaped areas of consolidation
50. Halo sign: Angio-Invasive aspergillosis
PA radiograph and axial CT image show right upper lobe mass with
peripheral ground glass opacity constituting Halo sign
51. • Broncho-invasive:
– In patients with severe
neutropenia and in patients
with AIDS
– Chest X-ray: large nodular
opacities to diffuse
parenchymal consolidation
52. Allergic Bronchopulmonary Aspergillosis
(ABPA)
• A hypersensitivity reaction-occurring in major airways
• Associated with asthma, elevated serum IgE levels,
positive precipitins and skin reactivity to aspergillus
• Chest X-ray:
– Non-segmental areas of opacities most common in upper
lobes
– Lobar collapse
– thick tubular opacities due to bronchi distended with
mucus and fungus- Finger-in-gloves sign
– Occasional cavitation
53. Fig. chest x-ray PA view:
branching tubular opacities emanating from the hila -
FINGER-IN-GLOVE appearance
56. Fig. allergic bronchopulmonary aspergillosis
HRCT scan demonstrating finger-like opacities due
to dilated mucus-filled bronchi
57. Summary
Fungal pneumonia Specific imaging findings
1 Histoplasmosis • Central, lamellated or diffuse calcification of a nodule
< 3 cm virtually diagnostic
• Acute histoplasma pneumonia: Airspace opacities
any lobe, solitary or multiple; usually lower lungs
• Ipsilateral hilar mediastinal lymphadenopathy
• Fibrosing mediastinitis
2 Coccodioidomycosis Cavitating segmental or lobar consolidation in an
endemic area
Solitary or multifocal segmental or lobar consolidation
Solitary or multiple lung nodules
Mediastinal and hilar nodes
3 Blastomycosis • Airspace disease or mass in an outdoorsman from an
endemic area
• Cavitation
58. Fungal pneumonia Specific imaging findings
4 Paracoccidioidomycosis • Areas of ground glass opacities, interlobular septal
thickening, consolidation, cavitation and fibrosis
5 Candidiasis Chronic pneumonia, abscess, mycetoma formation
Multiple bilateral nodular opacities with areas of
consolidation and ground glass opacities
6 Pneumocystis Peri-hilar ground-glass opacited in a patchy or
geographic distribution with thickened septa
59. Fungal pneumonia Specific imaging findings
7 Cryptococcosis Homogeneous segmental or lobar opacifications
Miliary, reticular or reticulo-nodular interstitial patterns
8 Mucormycosis Lobar or multilobar areas of consolidation
cavitation
9 Aspergillus Aspergilloma of mycetoma formation
Chronic necrotizing aspergillosis
Broncho-invasive with diffuse parenchymal
consolidation
Necrotic nodules surrounded by ground glass
attenuaiton- halo sign
ABPA with non-segmental areas of opacities mainly in
upper lobes, branching thick tubular opacities due to
bronchi distended with mucus- finger-in-glove
appearance
60. Role of the radiologists
• Integrating the clinical data and the radiological
data enables in substantial narrowing of the
differential diagnosis
• Need of guided biopsy in selected cases for
providing a presumptive final diagnosis, especially
when dealing with immuno-compromised patients
61. References
• Text book of Imaging and radiology, David sutton
• Fundamentals of diagnostic radiology, Brant and
Helms
• Grainger and Allison’s Diagnostic radiology
• Christopher M. et al, Imaging Pulmonary Infection:
classic signs and patterns (2014) American journal
of radiology
• Images from Various websites