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5岁男孩莱迪希细胞瘤表现为同性性早熟假性青春期,未触及睾丸肿块

Leydig Cell Testicular Tumour Presenting as Isosexual Precocious Pseudopuberty in a 5 Year-old Boy with No Palpable Testicular Mass.

作者信息

Méndez-Gallart Roberto, Bautista Adolfo, Estevez Elina, Barreiro Jesús, Evgenieva Elena

机构信息

Department of Pediatric Surgery, Complexo Hospitalario Universitario de Santiago, Santiago de Compostela, Spain.

出版信息

Clin Pediatr Endocrinol. 2010 Jan;19(1):19-23. doi: 10.1297/cpe.19.19. Epub 2010 Mar 11.

Abstract

Leydig cell testicular tumors are very rare in children and cause isosexual precocious puberty. Palpable testicular mass or asymmetric testes are common findings on routine examination. We report on a 5-yr-old boy with a Leydig cell tumor of the testis presented with isosexual precocious puberty but no scrotal palpable mass. To our knowledge, this is the first reported Leydig cell tumor in a boy without palpable scrotal mass.

摘要

睾丸间质细胞瘤在儿童中非常罕见,可导致同性性早熟。常规检查中常见的体征是可触及的睾丸肿块或睾丸不对称。我们报告一例5岁男孩,患有睾丸间质细胞瘤,表现为同性性早熟,但阴囊未触及肿块。据我们所知,这是首例报道的无阴囊可触及肿块的男孩睾丸间质细胞瘤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/371b/3687613/e00456817872/cpe-19-019-g001.jpg

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