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与佩茨-耶格综合征相关的女性化支持细胞肿瘤:青春期前男性乳腺增生症日益被认识的病因。

Feminizing Sertoli cell tumors associated with Peutz-Jeghers syndrome: an increasingly recognized cause of prepubertal gynecomastia.

作者信息

Hertl M C, Wiebel J, Schäfer H, Willig H P, Lambrecht W

机构信息

Department of Pediatric Surgery, University Hospital, Hamburg, Germany.

出版信息

Plast Reconstr Surg. 1998 Sep;102(4):1151-7. doi: 10.1097/00006534-199809040-00036.

Abstract

Testicular sex cord tumors with annular tubules are an increasingly recognized cause of prepubertal gynecomastia typically accompanied by accelerated linear growth and advanced bone maturation. Serum estrogen levels may be elevated. Testicular ultrasound and biopsy are diagnostic, and mastectomy is indicated. Although these tumors can occur independently, causing gynecomastia in 10 percent of cases, they usually occur in patients with Peutz-Jeghers syndrome. In any Peutz-Jeghers syndrome patient developing gynecomastia, a testicular tumor should be sought. Conversely, because a significant proportion of all reported prepubertal gynecomastia patients have Peutz-Jeghers syndrome with testicular tumors, this syndrome must be considered for all young boys in whom the cause of gynecomastia is not otherwise apparent. When Peutz-Jeghers syndrome is suspected, gastroscopy, colonoscopy, and testicular biopsies can be performed under one anesthetic at the time of mastectomy.

摘要

伴有环状小管的睾丸性索肿瘤是青春期前男性乳腺增生症越来越常见的病因,通常伴有线性生长加速和骨成熟提前。血清雌激素水平可能升高。睾丸超声检查和活检具有诊断意义,需行乳房切除术。虽然这些肿瘤可单独发生,在10%的病例中导致男性乳腺增生症,但它们通常发生在患有黑斑息肉综合征的患者中。任何患有黑斑息肉综合征且出现男性乳腺增生症的患者,都应检查是否存在睾丸肿瘤。相反,由于所有报道的青春期前男性乳腺增生症患者中有相当一部分患有伴有睾丸肿瘤的黑斑息肉综合征,因此对于所有病因不明的青春期前男孩,都必须考虑这种综合征。当怀疑患有黑斑息肉综合征时,可在乳房切除术时在一次麻醉下进行胃镜检查、结肠镜检查和睾丸活检。

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