WBR0446

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Author [[PageAuthor::Rim Halaby, M.D. [1]]]
Exam Type ExamType::USMLE Step 1
Main Category MainCategory::Pathology
Sub Category SubCategory::Endocrine
Prompt [[Prompt::A 45 year old female patient who is previously healthy presents to her physician’s office complaining of severe diarrhea since several days. The patient’s past medical history is also significant for recurrent kidney stones and parathyroidectomy. Fasting gastrin level is elevated. Endoscopy reveals multiple ulcers in the stomach, duodenum, and the jejunum. Which of the following is the most likely additional finding in this patient?]]
Answer A AnswerA::Oral ganglioneuroma
Answer A Explanation AnswerAExp::Oral ganglioneuromatosis is seen in patients with MEN2B syndrome.
Answer B AnswerB::Pheochromocytoma
Answer B Explanation AnswerBExp::Pheochromocytoma can be found in MEN 2A and MEN 2B syndromes.
Answer C AnswerC::Medullary thyroid cancer
Answer C Explanation AnswerCExp::Medullary thyroid cancer can be found in MEN 2A and MEN 2B syndromes.
Answer D AnswerD::Prolactinoma
Answer D Explanation AnswerDExp::Prolactinoma, a pituitary tumor, can be found in MEN I syndrome.
Answer E AnswerE::Carcinoid tumor
Answer E Explanation AnswerEExp::Carcinoid tumor is an endocrine tumor but is not associated with any MEN syndrome.
Right Answer RightAnswer::D
Explanation [[Explanation::Men I syndrome is characterized by parathyroid tumors, pituitary tumors that are usually prolactinoma or GH secreting tumors, and pancreatic endocrine tumors, such as gastrinoma, insulinoma, VIPoma, or glucagonoma.

Educational Objective: MEN I syndrome is characterized by pituitary tumor, parathyroid tumor, and pancreatic endocrine tumor.
Educational Objective:
References: ]]

Approved Approved::No
Keyword WBRKeyword::Prolactinoma, WBRKeyword::pheochromocytoma, WBRKeyword::gastrinoma, WBRKeyword::multiple, WBRKeyword::endocrine, WBRKeyword::neoplasia, WBRKeyword::MEN I, WBRKeyword::syndrome, WBRKeyword::Wermer’s, WBRKeyword::tumor
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Order in Linked Questions LinkedOrder::