Virilizing Adrenal Oncocytoma

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Aldosterone Excretion in Virilizing Adrenal

Sodium depletion with concomitant dehydration occurs as a complicating factor in approximately one-third of patients with virilizing adrenal hyperplasia (1). A number of writers have discussed certain differences between the electrolyte disturbance occurring in this syndrome and that of Addison's disease (2-5) and several hypotheses have been offered to explain the sodium loss and potassium ret...

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Virilizing Adrenocortical Oncocytoma in a Child: A Case Report

Functioning adrenocortical oncocytomas are extremely rare and most reported patients are 40-60 yr of age. To our knowledge, only 2 cases of functioning adrenocortical oncocytomas have been reported in childhood. We report a case of functioning adrenocortical oncocytoma in a 14-yr-old female child presenting with virilization. She presented with deepening of the voice and excessive hair growth, ...

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Adrenal cortical oncocytoma mimicking pheochromocytoma.

OBJECTIVE Adrenal tumors present with clinical features and signs unique to their specific hormonal hypersecretion. However, there have been cases in which the clinical expression has been in conflict with the histologic features of the tumor. In this communication we report an unusual clinical presentation of an adrenal cortical tumor with histologic features of an oncocytoma that clinically m...

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Birthweight in congenital virilizing adrenal hyperplasia.

The deficiency of C-21-hydroxylation in adrenocorticosteroid synthesis is the commonest cause of congenital virilizing adrenal hyperplasia (CVAH). Abnormal secretory activity in CVAH begins about the third month of gestation before the differentiation of external genitalia (Bierich, 1963). The masculinization of the female external genitalia noted at birth in almost all cases is thought to resu...

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Virilizing Tumor Relieves Adrenal Insufficiency in CAH

75 Received June 11, 2013; revised and accepted September 17, 2013. Published online September 28, 2013; doi: 10.1620/tjem.231.75. Correspondence: Masayuki Hayashi, Department of Endocrinology and Metabolism, Chukyo Hospital, 1-1-10, Sanjo, Minami-ku, Nagoya, Aichi 457-8510, Japan. e-mail: [email protected] A 68-Year-Old Phenotypically Male Patient with 21-Hydroxylase Deficiency a...

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ژورنال

عنوان ژورنال: Journal of Clinical Imaging Science

سال: 2012

ISSN: 2156-7514

DOI: 10.4103/2156-7514.104309