Pheochromocytoma: a frequent indicator for MEN 2.

Henry Ford Hospital medical journal Pub Date : 1992-01-01
C Calmettes, M Rosenberg-Gourgin, J Caron, N Feingold
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Abstract

Pheochromocytoma is a frequent indicator of multiple endocrine neoplasia type 2A (MEN 2A); in the 35 French MEN 2A families in which a pheochromocytoma occurred first in some affected members, 30% of the patients had a pheochromocytoma as the first manifestation constituting 45% of all patients with pheochromocytomas. The finding of a pheochromocytoma is a strong indication for a search for medullary thyroid carcinoma and for initiating family screening.

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嗜铬细胞瘤:men2的常见指标。
嗜铬细胞瘤是2A型多发性内分泌瘤(MEN 2A)的常见指标;在35个法国MEN 2A家族中,嗜铬细胞瘤首先发生在一些受影响的成员中,30%的患者以嗜铬细胞瘤为首发表现,占所有嗜铬细胞瘤患者的45%。嗜铬细胞瘤的发现是一个强烈的迹象,以寻找甲状腺髓样癌和启动家庭筛查。
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Extracellular Ca2+ sensing in C-cells and parathyroid cells. Proceedings of the Urban Health Care Symposium II. June 2-4, 1991. Characterization of the clinical features of five families with hereditary primary cutaneous lichen amyloidosis and multiple endocrine neoplasia type 2. Unusual features of multiple endocrine neoplasia. Long-term follow-up in four large MEN 2 families in The Netherlands.
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