WBR0292: Difference between revisions
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YazanDaaboul (talk | contribs) (Created page with "{{WBRQuestion |QuestionAuthor={{YD}} (Reviewed by {{YD}}) |ExamType=USMLE Step 1 |MainCategory=Pathology |SubCategory=Renal |MainCategory=Pathology |SubCategory=Renal |MainCat...") |
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{{WBRQuestion | {{WBRQuestion | ||
|QuestionAuthor={{YD}} (Reviewed by {{YD}}) | |QuestionAuthor= {{YD}} (Reviewed by {{YD}}) | ||
|ExamType=USMLE Step 1 | |ExamType=USMLE Step 1 | ||
|MainCategory=Pathology | |MainCategory=Pathology |
Latest revision as of 00:03, 28 October 2020
Author | [[PageAuthor::Yazan Daaboul, M.D. (Reviewed by Yazan Daaboul, M.D.)]] |
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Exam Type | ExamType::USMLE Step 1 |
Main Category | MainCategory::Pathology |
Sub Category | SubCategory::Renal |
Prompt | [[Prompt::A 68-year-old man presents to his physician for his annual check-up. The patient’s past medical history is significant for hypertension well-controlled on lisinopril and advanced type II diabetes mellitus poorly controlled on daily insulin injections. Routine work-up reveals elevated serum creatinine. A renal biopsy under light microscopy similar to the patient’s biopsy is shown in the image below. The following findings could be best explained by which of the following pathologic processes? |
Answer A | AnswerA::Amorphous pink deposits of amyloid in renal cortex |
Answer A Explanation | [[AnswerAExp::Amyloidosis is characterized by amyloid deposition that is positive for Congo red stain.]] |
Answer B | AnswerB::Immune response mediated by CD4 and CD8 lymphocytes |
Answer B Explanation | [[AnswerBExp::Immune response mediated by CD4 and CD8 lymphocytes describes the mechanism of renal rejection following transplantation.]] |
Answer C | AnswerC::Cystic distribution throughout the renal parenchyma |
Answer C Explanation | [[AnswerCExp::Polycystic kidney disease is characterized by cystic distribution throughout the renal parenchyma.]] |
Answer D | AnswerD::Immune complex deposition activating the complement pathway |
Answer D Explanation | [[AnswerDExp::The pathogenesis of several primary glomerulonephritides, including post-infectious glomerulonephritis and membranoproliferative glomerulonephritis, is characterized by immune complex deposition that activates the complement pathway.]] |
Answer E | AnswerE::Non-enzymatic glycosylation of proteins |
Answer E Explanation | AnswerEExp::Diabetic nephropathy is a common microvascular complication in advanced diabetes mellitus. Renal biopsy under light microscopy would reveal characteristic eosinophilic nodules in the glomerular tuft called “Kimmelsteil-Wilson” lesion. |
Right Answer | RightAnswer::E |
Explanation | [[Explanation::Diabetic nephropathy is a common microvascular complication of advanced diabetes mellitus. Renal biopsy under light microscopy typically demonstrates characteristic eosinophilic nodules in the glomerular tuft called “Kimmelsteil-Wilson” lesions. Chronic hyperglycemia results in accumulation of advanced glycosylation end-products (AGEs) that trap extravasated immunoglobulins, albumin, LDL, and other proteins via cross-linking to the extravascular matrix. Educational Objective: Diabetic nephropathy is a microvascular complication of uncontrolled diabetes mellitus. It is characterized by Kimmelsteil-Wilson lesions, which are eosinophilic nodules in glomerular tufts. The pathogenesis of diabetic nephropathy is thought to be due to accumulation of advanced glycosylation end-products (AGEs). |
Approved | Approved::Yes |
Keyword | WBRKeyword::Diabetic nephropathy, WBRKeyword::Diabetes mellitus, WBRKeyword::Kimmelsteil-Wilson lesion, WBRKeyword::Microvascular complication, WBRKeyword::Renal failure, WBRKeyword::Glomerulonephritis |
Linked Question | Linked:: |
Order in Linked Questions | LinkedOrder:: |