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Case report: congenital adrenal hyperplasia and malignant Leydig cell tumor.

作者信息

Davis J M, Woodroof J, Sadasivan R, Stephens R

机构信息

Division of Clinical Oncology, University of Kansas Medical Center, Kansas City 66160-7353.

出版信息

Am J Med Sci. 1995 Jan;309(1):63-5. doi: 10.1097/00000441-199501000-00010.

Abstract

Leydig cell tumors are very rarely seen testicular tumors and can be difficult to distinguish from testicular tumors of the adrenogenital syndrome. Testicular tumors of the adrenogenital syndrome are confined to patients with congenital adrenal hyperplasia. The authors report a case of a patient with malignant Leydig cell tumor and a history of congenital adrenal hyperplasia (adrenogenital syndrome). To the authors' knowledge, this has not been reported previously.

摘要

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