Myxoid adrenal cortical carcinoma - A rare variant of adrenocortical carcinoma

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منابع مشابه

Myxoid adrenal cortical carcinoma--a rare variant of adrenocortical carcinoma.

1. Schoenberg BS, Mellinger JF, Schoenberg DG. Cerebrovascular disease in infants and children:A study of incidence, clinical features and survival. Neurology 1978; 28:763-8. 2. Mitra S, Ghosh D, Puri R, Parmar VR. Top-ofthe-basi lar-ar tery stroke. Indian Pediatr 2001;38:83-7. 3. Nagaraja D, Verma A, Taly AB, Kumar MV, Jayakumar PN. Cerebrovascular disease in children. Acta Neurol Scand 1994;9...

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Myxoid and Sarcomatoid Variants of Adrenocortical Carcinoma: Analysis of Rare Variants in Single Tertiary Care Center

The aim of this study is to describe rare variants of adrenocortical carcinoma (ACC) and to compare the prognosis with that of conventional ACC. We retrospectively reviewed 8 cases of myxoid variant, 1 sarcomatoid variant, and 14 cases of conventional ACC, who underwent surgical resection at the Asan Medical Center between 1996 and 2014. An analysis of the clinicopathological characteristics, i...

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An infant with rare adrenocortical carcinoma

Adrenocortical tumors (ACT) include both adrenocortical adenomas (ACA) and adrenocortical carcinomas (ACC). Carcinomas are rare in children and adolescents. In the United States, Surveillance Epidemiology and End Results (SEER) data from the National Cancer Institute show that the proportion of adrenocortical tumors (ACT) in childhood carcinoma is only about 1.3%, and the proportion of ACT in c...

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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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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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ژورنال

عنوان ژورنال: Indian Journal of Medical Sciences

سال: 2005

ISSN: 0019-5359

DOI: 10.4103/0019-5359.18970