Sandbox:Sharmi: Difference between revisions
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| style="padding: 5px 5px; background: #F5F5F5;" |Non-[[caseating]] [[granulomas]] in lungs and other organs, bilateral [[hilar]] [[lymphadenopathy]], mostly in African American females. | | style="padding: 5px 5px; background: #F5F5F5;" |Non-[[caseating]] [[granulomas]] in lungs and other organs, bilateral [[hilar]] [[lymphadenopathy]], mostly in African American females. | ||
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| colspan="2" style="padding: 5px 5px; background: #F5F5F5;" |<small>Adapted from Mandell, Douglas, and Bennett's principles and practice of infectious diseases 2010 | |Caplan syndrome | ||
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| colspan="2" style="padding: 5px 5px; background: #F5F5F5;" |<small>Adapted from Mandell, Douglas, and Bennett's principles and practice of infectious diseases 2010 </small> | |||
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*[[Malignancy]] ([[Lung cancer|Primary lung cance<nowiki/>r]]) | *[[Malignancy]] ([[Lung cancer|Primary lung cance<nowiki/>r]]) | ||
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*Elderly male or female <ref name="pmid4353362">{{cite journal |vauthors=Chaudhuri MR |title=Primary pulmonary cavitating carcinomas |journal=Thorax |volume=28 |issue=3 |pages=354–66 |year=1973 |pmid=4353362 |pmc=470041 |doi= |url=}}</ref> | *Elderly male or female <ref name="pmid4353362">{{cite journal |vauthors=Chaudhuri MR |title=Primary pulmonary cavitating carcinomas |journal=Thorax |volume=28 |issue=3 |pages=354–66 |year=1973 |pmid=4353362 |pmc=470041 |doi= |url=}}</ref> | ||
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*[[Hemoptysis]] is commonly associated with [[bronchogenic carcinoma]] | *[[Hemoptysis]] is commonly associated with [[bronchogenic carcinoma]] | ||
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*A coin-shaped lesion with thick wall(>15mm) is seen on CXR with less ground glass opacities | *A coin-shaped lesion with thick wall(>15mm) is seen on CXR with less ground glass opacities | ||
*[[Bronchoalveolar lavage]] [[cytology]] shows malignant cells | *[[Bronchoalveolar lavage]] [[cytology]] shows malignant cells | ||
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*[[Granulomatosis with polyangiitis]] ([[Wegener's granulomatosis|Wegener's]]) | *[[Granulomatosis with polyangiitis]] ([[Wegener's granulomatosis|Wegener's]]) | ||
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*Women are more commonly effected than man. | *Women are more commonly effected than man. | ||
*Kidneys are also involved | *Kidneys are also involved | ||
*Upper respiratory tract symptoms , perforation of [[nasal septum]], [[chronic sinusitis]], [[otitis media]], [[mastoiditis]]. | *Upper respiratory tract symptoms , perforation of [[nasal septum]], [[chronic sinusitis]], [[otitis media]], [[mastoiditis]]. | ||
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*More common in African-American females | *More common in African-American females | ||
*Often [[asymptomatic]] except for [[Lymphadenopathy|enlarged lymph nodes]] | *Often [[asymptomatic]] except for [[Lymphadenopathy|enlarged lymph nodes]] | ||
*Associated with [[restrictive lung disease]] | *Associated with [[restrictive lung disease]] | ||
*[[Erythema nodosum]] | *[[Erythema nodosum]] | ||
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*On CXR bilateral [[Lymphadenopathy|adenopathy]] and coarse reticular opacities are seen. | *On CXR bilateral [[Lymphadenopathy|adenopathy]] and coarse reticular opacities are seen. | ||
*CT of the chest demonstrates extensive [[Hilar lymphadenopathy|hilar]] and mediastinal adenopathy | *CT of the chest demonstrates extensive [[Hilar lymphadenopathy|hilar]] and mediastinal adenopathy | ||
*Additional findings on CT include [[fibrosis]] (honeycomb, linear, or associated with bronchial distortion), pleural thickening, and ground-glass opacities. | *Additional findings on CT include [[fibrosis]] (honeycomb, linear, or associated with bronchial distortion), pleural thickening, and ground-glass opacities. | ||
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*Biopsy of lung reveals non-[[caseating]] [[granuloma]] | *Biopsy of lung reveals non-[[caseating]] [[granuloma]] | ||
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*[[Bronchiolitis obliterans]] ([[Cryptogenic organizing pneumonia]]) | *[[Bronchiolitis obliterans]] ([[Cryptogenic organizing pneumonia]]) | ||
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*Rare condition and mimics [[asthma]], [[pneumonia]] and [[emphysema]] | *Rare condition and mimics [[asthma]], [[pneumonia]] and [[emphysema]] | ||
*It is due to [[drug]] or [[toxin]] exposure, [[autoimmune diseases]], [[viral infections]], or [[radiation injury]] | *It is due to [[drug]] or [[toxin]] exposure, [[autoimmune diseases]], [[viral infections]], or [[radiation injury]] | ||
*Individuals working in industries are at high risk | *Individuals working in industries are at high risk | ||
*Presents with [[Fever|feve]]<nowiki/>r, [[cough]], [[wheezing]] and [[shortness of breath]] over weeks to months, | *Presents with [[Fever|feve]]<nowiki/>r, [[cough]], [[wheezing]] and [[shortness of breath]] over weeks to months, | ||
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*Common appearance on CT is patchy [[Consolidation (medicine)|consolidation,]]<nowiki/>often accompanied by ground-glass opacities and nodules. | *Common appearance on CT is patchy [[Consolidation (medicine)|consolidation,]]<nowiki/>often accompanied by ground-glass opacities and nodules. | ||
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*Biopsy of the lung <ref name="pmid19561910">{{cite journal |vauthors=Al-Ghanem S, Al-Jahdali H, Bamefleh H, Khan AN |title=Bronchiolitis obliterans organizing pneumonia: pathogenesis, clinical features, imaging and therapy review |journal=Ann Thorac Med |volume=3 |issue=2 |pages=67–75 |year=2008 |pmid=19561910 |pmc=2700454 |doi=10.4103/1817-1737.39641 |url=}}</ref> | *Biopsy of the lung <ref name="pmid19561910">{{cite journal |vauthors=Al-Ghanem S, Al-Jahdali H, Bamefleh H, Khan AN |title=Bronchiolitis obliterans organizing pneumonia: pathogenesis, clinical features, imaging and therapy review |journal=Ann Thorac Med |volume=3 |issue=2 |pages=67–75 |year=2008 |pmid=19561910 |pmc=2700454 |doi=10.4103/1817-1737.39641 |url=}}</ref> | ||
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*[[Langerhans cell histiocytosis|Langerhans]] cell [[Langerhans cell histiocytosis|Histiocytosis]] | *[[Langerhans cell histiocytosis|Langerhans]] cell [[Langerhans cell histiocytosis|Histiocytosis]] | ||
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*Exclusively occurs in smokers, with a peak age of onset 20-40 years. | *Exclusively occurs in smokers, with a peak age of onset 20-40 years. | ||
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*Skin is involved in 80% of the cases, scaly [[erythematous rash]] is typical. | *Skin is involved in 80% of the cases, scaly [[erythematous rash]] is typical. | ||
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*Thin-walled cystic cavities are the usual radiographic manifestation, observed in over 50% of patients by either CXR or CT scans. | *Thin-walled cystic cavities are the usual radiographic manifestation, observed in over 50% of patients by either CXR or CT scans. | ||
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*Biopsy of the lung | *Biopsy of the lung | ||
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|Caplan syndrome | |||
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<references /> |
Revision as of 20:54, 16 June 2021
Disease | Findings |
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Bacterial pneumonia | Sudden onset of symptoms, such as high fever, cough, purulent sputum, chest pain, leukocytosis, chest X-ray shows consolidation. |
Bronchogenic carcinoma | may be asymptomatic, usually at older ages (> 50 years old), cough, hemoptysis, weight loss |
Brucellosis | Fever, anorexia, night sweats, malaise,back pain , headache, and depression. History of exposure to infected animal |
Hodgkin lymphoma | Fever, night sweats, pruritus, painless adenopathy, mediastinal mass |
Mycoplasmal pneumonia | Gradual onset of dry cough, headache, malaise, sore throat. Diffuse bilateral infiltrates on chest X-ray. |
Sarcoidosis | Non-caseating granulomas in lungs and other organs, bilateral hilar lymphadenopathy, mostly in African American females. |
Caplan syndrome | |
Adapted from Mandell, Douglas, and Bennett's principles and practice of infectious diseases 2010 |
Causes of
lung cavities |
Differentiating Features | Differentiating radiological findings | Diagnosis
confirmation |
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Caplan syndrome |
- ↑ Chaudhuri MR (1973). "Primary pulmonary cavitating carcinomas". Thorax. 28 (3): 354–66. PMC 470041. PMID 4353362.
- ↑ Langford CA, Hoffman GS (1999). "Rare diseases.3: Wegener's granulomatosis". Thorax. 54 (7): 629–37. PMC 1745525. PMID 10377211.
- ↑ Al-Ghanem S, Al-Jahdali H, Bamefleh H, Khan AN (2008). "Bronchiolitis obliterans organizing pneumonia: pathogenesis, clinical features, imaging and therapy review". Ann Thorac Med. 3 (2): 67–75. doi:10.4103/1817-1737.39641. PMC 2700454. PMID 19561910.