WBR0446: Difference between revisions
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|MainCategory=Pathology | |MainCategory=Pathology | ||
|SubCategory=Endocrine | |SubCategory=Endocrine | ||
|MainCategory=Pathology | |||
|MainCategory=Pathology | |MainCategory=Pathology | ||
|MainCategory=Pathology | |MainCategory=Pathology | ||
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|MainCategory=Pathology | |MainCategory=Pathology | ||
|SubCategory=Endocrine | |SubCategory=Endocrine | ||
|Prompt=A 45-year-old female | |Prompt=A 45-year-old female presents to the physician’s office with complaints of severe diarrhea of several days duration. The patient’s medical history is significant for recurrent kidney stones and a parathyroidectomy 8 years ago. Her fasting gastrin level is elevated and endoscopy reveals multiple ulcers in the stomach, duodenum, and jejunum. Which of the following findings is most frequently associated with this patient's condition? | ||
|Explanation= | |Explanation=The patient in this vignette most likely has Multiple Endocrine Neoplasia Type I (MEN 1). We know from the patient's past medical history that she likely had a parathyroid adenoma. Parathyroid adenomas can secrete PTH and thereby increase serum calcium and decrease serum potassium. Increased serum calcium can be lead to elevated calcium passing into the urine, thereby increasing the risk of calcium oxalate kidney stones. The definitive treatment of these tumros is surigcal removal (parathyroidectomy) as in this patient.<br> | ||
The patient now presents with symptoms highly consistent with a gastrinoma.These are gastrin-secreting tumors that form in either the pancreas or the duodenum. | |||
[[MEN I syndrome]] is characterized by [[parathyroid]] tumors, [[pituitary]] tumors, which are usually [[prolactinoma]] or [[GH secreting tumors]], and pancreatic endocrine tumors, such as [[gastrinoma]], [[insulinoma]], [[VIPoma]], or [[glucagonoma]]. | |||
|AnswerA=Oral ganglioneuroma | |AnswerA=Oral ganglioneuroma | ||
|AnswerAExp=Oral ganglioneuromatosis frequently occurs in patients with MEN2B syndrome. | |AnswerAExp=Oral ganglioneuromatosis frequently occurs in patients with MEN2B syndrome. | ||
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|AnswerDExp=Prolactinoma, a pituitary tumor, frequently occurs in MEN I syndrome. | |AnswerDExp=Prolactinoma, a pituitary tumor, frequently occurs in MEN I syndrome. | ||
|AnswerE=Carcinoid tumor | |AnswerE=Carcinoid tumor | ||
|AnswerEExp=Carcinoid tumor is an endocrine tumor, but is not frequently associated with MEN syndrome. | |AnswerEExp=Carcinoid tumor is an endocrine tumor, but is not frequently associated with MEN syndrome. | ||
|EducationalObjectives=MEN I syndrome often manifests with pituitary tumors, parathyroid tumors, or pancreatic endocrine tumors. | |||
|References=First Aid 2014 page 329 | |||
|RightAnswer=D | |RightAnswer=D | ||
|WBRKeyword=Prolactinoma, pheochromocytoma, gastrinoma, neoplasia, MEN I, Wermer syndrome, diarrhea, ulcers | |WBRKeyword=Prolactinoma, pheochromocytoma, gastrinoma, neoplasia, MEN I, Wermer syndrome, diarrhea, ulcers | ||
|Approved=Yes | |Approved=Yes | ||
}} | }} | ||
Revision as of 01:18, 17 January 2015
| Author | [[PageAuthor::Rim Halaby, M.D. [1] (Reviewed by Alison Leibowitz)]] |
|---|---|
| Exam Type | ExamType::USMLE Step 1 |
| Main Category | MainCategory::Pathology |
| Sub Category | SubCategory::Endocrine |
| Prompt | [[Prompt::A 45-year-old female presents to the physician’s office with complaints of severe diarrhea of several days duration. The patient’s medical history is significant for recurrent kidney stones and a parathyroidectomy 8 years ago. Her fasting gastrin level is elevated and endoscopy reveals multiple ulcers in the stomach, duodenum, and jejunum. Which of the following findings is most frequently associated with this patient's condition?]] |
| Answer A | AnswerA::Oral ganglioneuroma |
| Answer A Explanation | AnswerAExp::Oral ganglioneuromatosis frequently occurs in patients with MEN2B syndrome. |
| Answer B | AnswerB::Pheochromocytoma |
| Answer B Explanation | AnswerBExp::Pheochromocytoma frequently occurs in MEN 2A and MEN 2B syndromes. |
| Answer C | AnswerC::Medullary thyroid cancer |
| Answer C Explanation | AnswerCExp::Medullary thyroid cancer frequently occurs in MEN 2A and MEN 2B syndromes. |
| Answer D | AnswerD::Prolactinoma |
| Answer D Explanation | AnswerDExp::Prolactinoma, a pituitary tumor, frequently occurs in MEN I syndrome. |
| Answer E | AnswerE::Carcinoid tumor |
| Answer E Explanation | AnswerEExp::Carcinoid tumor is an endocrine tumor, but is not frequently associated with MEN syndrome. |
| Right Answer | RightAnswer::D |
| Explanation | [[Explanation::The patient in this vignette most likely has Multiple Endocrine Neoplasia Type I (MEN 1). We know from the patient's past medical history that she likely had a parathyroid adenoma. Parathyroid adenomas can secrete PTH and thereby increase serum calcium and decrease serum potassium. Increased serum calcium can be lead to elevated calcium passing into the urine, thereby increasing the risk of calcium oxalate kidney stones. The definitive treatment of these tumros is surigcal removal (parathyroidectomy) as in this patient. The patient now presents with symptoms highly consistent with a gastrinoma.These are gastrin-secreting tumors that form in either the pancreas or the duodenum. MEN I syndrome is characterized by parathyroid tumors, pituitary tumors, which are usually prolactinoma or GH secreting tumors, and pancreatic endocrine tumors, such as gastrinoma, insulinoma, VIPoma, or glucagonoma. |
| Approved | Approved::Yes |
| Keyword | WBRKeyword::Prolactinoma, WBRKeyword::pheochromocytoma, WBRKeyword::gastrinoma, WBRKeyword::neoplasia, WBRKeyword::MEN I, WBRKeyword::Wermer syndrome, WBRKeyword::diarrhea, WBRKeyword::ulcers |
| Linked Question | Linked:: |
| Order in Linked Questions | LinkedOrder:: |