نتایج جستجو برای: adrenocortical carcinoma
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Myxoid changes have been rarely reported both in adrenocortical adenomas and carcinomas. The recent observation by our group of an adrenal myxoid tumor with morphologically borderline features, but aggressive clinical behavior prompted us to review a series of 196 adrenocortical lesions, comprising 122 carcinomas and 74 adenomas, to define the morphologic, phenotypical and clinical characterist...
Adrenal rest tumor in liver is a very rare tumor. It originates from an adrenal rest, which is derived from the aberrant adrenocortical tissue. Adrenal rest tumor is an ectopic collection of adrenocortical cells in extra-adrenal sites. This tumor may be hormonally active and manifest endocrine syndromes. But, most tumors are non-functioning and benign. Histologically, hepatic adrenal rest tumor...
Cushing syndrome is rare in infancy and usually due to an adrenocortical tumor (ACT). We report an infant with Cushing syndrome due to adrenocortical carcinoma. The patient presented at six months of age with a three-month history of growth failure, rapid weight gain, acne, and irritability. Physical examination showed obesity, hypertension, and Cushingoid features. Biochemical evaluation showe...
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