Literature DB >> 1362422

Pheochromocytoma: a frequent indicator for MEN 2.

C Calmettes1, M Rosenberg-Gourgin, J Caron, N Feingold.   

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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Year:  1992        PMID: 1362422

Source DB:  PubMed          Journal:  Henry Ford Hosp Med J        ISSN: 0018-0416


  2 in total

Review 1.  Management of medullary thyroid carcinoma and MEN2 syndromes in childhood.

Authors:  Steven G Waguespack; Thereasa A Rich; Nancy D Perrier; Camilo Jimenez; Gilbert J Cote
Journal:  Nat Rev Endocrinol       Date:  2011-08-23       Impact factor: 43.330

2.  "The" pheochromocytoma: a benign, intra-adrenal, hypertensive, sporadic unilateral tumor. Does it exist?

Authors:  C A Proye; M Vix; S Jansson; L E Tisell; H Dralle; W Hiller
Journal:  World J Surg       Date:  1994 Jul-Aug       Impact factor: 3.352

  2 in total

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