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Leydig cell tumor of the spermatic cord in an adolescent affected by congenital adrenal hyperplasia
Authors:Matteo Ferrari  Marco Raber  Umberto Capitanio  Gianni Russo  Matilde Ferrario  Nathalie Rizzo  Massimo Freschi  Patrizio Rigatti  Francesco Montorsi
Affiliation:1. Department of Urology and Urological Research Institute;2. Department of Pediatrics, Endocrine Unit, University Vita‐Salute, San Raffaele Hospital;3. Department of Pediatrics, Sant'Anna Hospital, Como, Italy;4. Department of Pathology, Scientific Institute San Raffaele Hospital, Milan
Abstract:We report the first case of a patient with extratesticular Leydig cell tumor associated with congenital adrenal hyperplasia. An 18‐year‐old congenital adrenal hyperplasia patient presented with a palpable and asymptomatic right extratesticular mass. Color Doppler sonography confirmed the presence of a capsulated and vascularised lesion. Sieric tumor markers were negative. The patient underwent surgical scrotal exploration through an inguinal right incision. The mass, 18 mm in size and located within the spermatic cord, was removed and final pathology diagnosed a benign Leydig cell tumor.
Keywords:congenital adrenal hyperplasia  Leydig cell tumor  spermatic cord
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