Author/Authors
almuradova, elvina ege üniversitesi - tıp fakültesi - iç hastalıkları anabilim dalı, Türkiye , şimşir, ilgın yıldırım ege üniversitesi - tıp fakültesi - iç hastalıkları anabilim dali, Turkey , erdoğan, mehmet ege üniversitesi - tıp fakültesi - iç hastalıkları anabilim dalı, Turkey , çetinkalp, şevki ege üniversitesi - tıp fakültesi - iç hastalıkları anabilim dalı, Turkey , saygılı, füsun ege üniversitesi - tıp fakültesi - iç hastalıkları anabilim dalı, Turkey , özgen, ahmet gökhan ege üniversitesi - tıp fakültesi - iç hastalıkları anabilim dalı, Türkiye
Title Of Article
A case of medullary thyroid carcinoma presenting with diarrhea: MEN 2B syndrome
شماره ركورد
15035
Abstract
Multiple endocrine neoplasia type 2B (MEN 2B) is a rare autosomal dominant process characterized by medullary thyroid carcinoma, pheochromocytoma, physical features such as presence of marfanoid habitus and mucosal neuromas. Clinical features are hypertension, episodic sweating, diarrhea, pruritic skin lesions or compressive symptoms from a neck mass. Patients with hypercalcemia may present with constipation, polyuria, polydipsia, memory problems, depression, nephrolithiasis, glucose intolerance, gastroesophageal reflux and fatigue, or they may have no symptoms. Herein we present a case of a patient who was hospitalised several times due to diarrhea but did not diagnosed, but when he referred to our clinic diagnosed as MEN 2B, on the basis of bilateral pheochromocytoma, medullary thyroid carcinoma, multiple paragangliomas located along the spine, marfanoid features of body habitus and mucosal neuromas.
From Page
160
NaturalLanguageKeyword
Multiple endocrine neoplasia type 2B , meduller thyroid carcinom
JournalTitle
Ege Journal Of Medicine
To Page
161
JournalTitle
Ege Journal Of Medicine
Link To Document