Non functional adrenocortical carcinoma

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Non functional adrenocortical carcinoma A case report

Adrenocortical carcinoma is a rare disease with an incidence of approximately 1-2 per million populations per year. The main symptoms are abdominal mass with or without endocrine dysfunction. However, there are difficulties in the diagnosis and treatment of this case due to its unspecific clinical presentation which sometimes require additional diagnostic methods such as immunohistochemistry. T...

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A Primary non-functional extra-adrenal adrenocortical carcinoma

endocrine tumor, which is more common in women than in men with an incidence of approximately 0.5-2 cases per million per year.1 It tends to occur in bimodal age distribution with peaks in the first and fifth decades.2,3 The tumors are classified as functional or nonfunctional, depending on tumor production of corticosteroid, mineralocorticoid, androgen, or estrogen. In children functional tumo...

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A rare coexistence of non-functional adrenocortical carcinoma and multicentric papillary thyroid microcarcinoma: a case report

INTRODUCTION In this report, we describe a rare case of papillary thyroid carcinoma with adrenocortical carcinoma without excess hormone production. CASE PRESENTATION A 40-year-old Turkish man was admitted to our institution with a large left adrenal mass that was identified during the work-up for shortness of breath. The patient did not have specific signs and symptoms of hormone excess. The...

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Scintigraphic patterns of adrenocortical carcinoma: morpho-functional correlates.

OBJECTIVE Adrenocortical scintigraphy has demonstrated clinical utility in the morpho-functional characterization of adrenal tumors. The aim of this study was to identify possible relationships between the scintigraphic pattern and endocrine and/or morphological data in a series of adrenocortical carcinomas. DESIGN AND METHODS Twenty-one patients with adrenocortical carcinoma (11 nonfunctioni...

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Cutaneous metastasis in a patient with adrenocortical carcinoma

Adrenocortical carcinoma is an uncommon and aggressivemalignancy. Despite a high frequency of metastasis, cutaneousmetastasis of adrenocortical carcinoma is rare with only isolatedcase reports. Its diagnosis can be challenging based solely onhistopathological findings. Yet, the clinical history in combinationwith an immunohistochemical panel consisting of inhibin,vimentin, chromogranin, synapto...

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ژورنال

عنوان ژورنال: Medical Journal of Indonesia

سال: 2008

ISSN: 2252-8083,0853-1773

DOI: 10.13181/mji.v17i3.316