WBR0776: Difference between revisions
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{{WBRQuestion | {{WBRQuestion | ||
|QuestionAuthor={{ | |QuestionAuthor={{SSK}} (Reviewed by Serge Korjian) | ||
|ExamType=USMLE Step 1 | |ExamType=USMLE Step 1 | ||
|MainCategory=Pathophysiology | |MainCategory=Pathophysiology | ||
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|MainCategory=Pathophysiology | |MainCategory=Pathophysiology | ||
|SubCategory=Pulmonology | |SubCategory=Pulmonology | ||
|MainCategory=Pathophysiology | |||
|MainCategory=Pathophysiology | |MainCategory=Pathophysiology | ||
|MainCategory=Pathophysiology | |MainCategory=Pathophysiology | ||
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|MainCategory=Pathophysiology | |MainCategory=Pathophysiology | ||
|SubCategory=Pulmonology | |SubCategory=Pulmonology | ||
|Prompt=A 52 year old African American diabetic woman presents to the chronic care clinic for indurated nodules on her lower extremities. The patient reports that she noticed them just 2 days ago. The nodules were small at first but have been enlarging since. They seem to be warmer and slightly redder than the rest of the skin, and very tender to touch. Upon further questioning the patient reports a dry cough for the past 2 months and a 20 | |Prompt=A 52-year-old African American diabetic woman presents to the chronic care clinic for indurated nodules on her lower extremities. The patient reports that she noticed them just 2 days ago. The nodules were small at first but have been enlarging since. They seem to be warmer and slightly redder than the rest of the skin, and very tender to touch. Upon further questioning, the patient reports a dry cough for the past 2 months and a 9 kg (20 lbs) unintentional weight loss in the same time frame. Concerned with the latter findings, you decide to order a chest CT scan especially given the family history of lung cancer. A cut at the level of the great cardiac vessels is shown below. What would you expect to find on pathology of the observed lesions? | ||
[[Image:WBR0776.jpg|600px]] | [[Image:WBR0776.jpg|600px]] | ||
|Explanation=Sarcoidosis is a systemic disease characterized by the development and accumulation of multiple granulomas | |Explanation=Sarcoidosis is a systemic disease characterized by the development and accumulation of multiple systemic granulomas. Sarcoidosis may involve virtually any organ but is classically most common in the lungs, liver, eyes, and skin. Symptoms of fatigue, night sweats, and weight loss are common at presentation. Löfgren's syndrome, a possible presentation of sarcoidosis consists of arthritis, erythema nodosum, and bilateral hilar adenopathy, and can be seen in up to 35% of patients. Although all racial and ethnic groups can have sarcoidosis, African Americans are 3 times more likely than Caucasians to develop the disease. Diagnosis is usually with a combination of clinical and radiologic findings supported by histopathological evidence of noncaseating epithelioid-cell granulomas with absence of any causative organisms or particles. Granulomas classicaly produce angiotensin-converting enzyme (ACE) with 60% of patients having elevated serum levels (not-diagnostic). Treatment is usually with corticosteroids although therapy is not indicated for everyone. Two thirds of patients recover completely within 10 years of diagnosis. | ||
|AnswerA=Giant cells, granuloma formation with caseating necrosis | |AnswerA=Giant cells, granuloma formation with caseating necrosis | ||
|AnswerAExp=Caseating necrosis within intrathoracic granulomas is usually indicative of a tuberculosis infection. | |AnswerAExp=Caseating necrosis within intrathoracic granulomas is usually indicative of a tuberculosis infection. | ||
|AnswerB=Giant cells, non-caseating granuloma formation | |AnswerB=Giant cells, non-caseating granuloma formation | ||
|AnswerBExp=Patients with sarcoidosis have multiple noncaseating epithelioid-cell (giant cell) granulomas. | |AnswerBExp=Patients with sarcoidosis have multiple noncaseating epithelioid-cell (giant cell) granulomas. | ||
|AnswerC=Inflammatory reaction with molds branching at acute angles | |AnswerC=Inflammatory reaction with molds branching at acute angles | ||
|AnswerCExp=Molds branching at acute angles are seen in aspergillomas usually growing in immunocompromised patients with previous cavitary disease colonized by Aspergillus spp. | |AnswerCExp=Molds branching at acute angles are seen in aspergillomas usually growing in immunocompromised patients with previous cavitary disease colonized by Aspergillus spp. | ||
|AnswerD=Multiplying type II pneumocytes | |AnswerD=Multiplying type II pneumocytes | ||
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|AnswerE=Nests or cords of uniform cells with central nuclei | |AnswerE=Nests or cords of uniform cells with central nuclei | ||
|AnswerEExp=Carcinoid tumors are usually characterized by nests or cords of uniform cells with central nuclei. | |AnswerEExp=Carcinoid tumors are usually characterized by nests or cords of uniform cells with central nuclei. | ||
|EducationalObjectives=Sarcoidosis is characterized by the development of multiple noncaseating epithelioid-cell granulomas. | |||
|References=Iannuzzi MC, Rybicki BA, Teirstein AS. Sarcoidosis. N Engl J Med. 2007;357(21):2153-65. | |||
|RightAnswer=B | |RightAnswer=B | ||
|WBRKeyword=Sarcoidosis, | |WBRKeyword=Sarcoidosis, Granuloma, Lung nodule, Lymph nodes, Perihilar, Autoimmune, Sarcoid, | ||
|Approved= | |Approved=Yes | ||
}} | }} |
Revision as of 13:41, 7 October 2014
Author | [[PageAuthor::Serge Korjian M.D. (Reviewed by Serge Korjian)]] |
---|---|
Exam Type | ExamType::USMLE Step 1 |
Main Category | MainCategory::Pathophysiology |
Sub Category | SubCategory::Pulmonology |
Prompt | [[Prompt::A 52-year-old African American diabetic woman presents to the chronic care clinic for indurated nodules on her lower extremities. The patient reports that she noticed them just 2 days ago. The nodules were small at first but have been enlarging since. They seem to be warmer and slightly redder than the rest of the skin, and very tender to touch. Upon further questioning, the patient reports a dry cough for the past 2 months and a 9 kg (20 lbs) unintentional weight loss in the same time frame. Concerned with the latter findings, you decide to order a chest CT scan especially given the family history of lung cancer. A cut at the level of the great cardiac vessels is shown below. What would you expect to find on pathology of the observed lesions? |
Answer A | AnswerA::Giant cells, granuloma formation with caseating necrosis |
Answer A Explanation | AnswerAExp::Caseating necrosis within intrathoracic granulomas is usually indicative of a tuberculosis infection. |
Answer B | AnswerB::Giant cells, non-caseating granuloma formation |
Answer B Explanation | AnswerBExp::Patients with sarcoidosis have multiple noncaseating epithelioid-cell (giant cell) granulomas. |
Answer C | AnswerC::Inflammatory reaction with molds branching at acute angles |
Answer C Explanation | AnswerCExp::Molds branching at acute angles are seen in aspergillomas usually growing in immunocompromised patients with previous cavitary disease colonized by Aspergillus spp. |
Answer D | AnswerD::Multiplying type II pneumocytes |
Answer D Explanation | AnswerDExp::Type II pneumocytes are seen in the alveolar spaces and multiply during lung injury to restore parenchymal integrity. |
Answer E | AnswerE::Nests or cords of uniform cells with central nuclei |
Answer E Explanation | AnswerEExp::Carcinoid tumors are usually characterized by nests or cords of uniform cells with central nuclei. |
Right Answer | RightAnswer::B |
Explanation | [[Explanation::Sarcoidosis is a systemic disease characterized by the development and accumulation of multiple systemic granulomas. Sarcoidosis may involve virtually any organ but is classically most common in the lungs, liver, eyes, and skin. Symptoms of fatigue, night sweats, and weight loss are common at presentation. Löfgren's syndrome, a possible presentation of sarcoidosis consists of arthritis, erythema nodosum, and bilateral hilar adenopathy, and can be seen in up to 35% of patients. Although all racial and ethnic groups can have sarcoidosis, African Americans are 3 times more likely than Caucasians to develop the disease. Diagnosis is usually with a combination of clinical and radiologic findings supported by histopathological evidence of noncaseating epithelioid-cell granulomas with absence of any causative organisms or particles. Granulomas classicaly produce angiotensin-converting enzyme (ACE) with 60% of patients having elevated serum levels (not-diagnostic). Treatment is usually with corticosteroids although therapy is not indicated for everyone. Two thirds of patients recover completely within 10 years of diagnosis. Educational Objective: Sarcoidosis is characterized by the development of multiple noncaseating epithelioid-cell granulomas. |
Approved | Approved::Yes |
Keyword | WBRKeyword::Sarcoidosis, WBRKeyword::Granuloma, WBRKeyword::Lung nodule, WBRKeyword::Lymph nodes, WBRKeyword::Perihilar, WBRKeyword::Autoimmune, WBRKeyword::Sarcoid |
Linked Question | Linked:: |
Order in Linked Questions | LinkedOrder:: |