The Association of Neurofibromatosis, Bilateral Pheochromocytoma and Primary Hyperparathyroidism

A. E. Altinova; F. Toruner; A. R. Cimen; A. Karakoc; T. Atasever; I. Yetkin; G. Ayvaz; N. Cakir; M. Arslan

doi:10.1055/s-2007-981661

Experimental and Clinical Endocrinology & Diabetes, Table of Contents

Exp Clin Endocrinol Diabetes 2007; 115(7): 468-470
DOI: 10.1055/s-2007-981661

Case Report

The Association of Neurofibromatosis, Bilateral Pheochromocytoma and Primary Hyperparathyroidism

A. E. Altinova¹ , F. Toruner¹ , A. R. Cimen² , A. Karakoc¹ , T. Atasever³ , I. Yetkin¹ , G. Ayvaz¹ , N. Cakir¹ , M. Arslan¹

¹Department of Endocrinology and Metabolism, Gazi University Faculty of Medicine, Ankara, Turkey
²Department of Internal Medicine, Gazi University Faculty of Medicine, Ankara, Turkey
³Department of Nuclear Medicine, Gazi University Faculty of Medicine, Ankara, Turkey

Abstract

Neurofibromatosis (NF) is a hereditary disease and carries increased risk of both benign and malignant tumor development. Pheochromocytoma or hyperparathyroidism have been reported to be associated with NF type 1 (NF1). However, the coexistance of pheochromocytoma and parathyroid adenoma in a patient with NF1 is very rare. We report a case of a 37-year-old male with NF1, bilateral pheochromocytoma and parathyroid adenoma. This association sould be kept in mind in patients with NF1 in initial evaluation as well as during follow-up.

Key words

Neurofibromatosis - pheochromocytoma - hyperparathyroidism - parathyroid adenoma

Full Text

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Correspondence

Dr. A. E. Altinova

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