龟头神经鞘瘤:一种罕见的临床疾病

Diallo Kadidiatou Folly, Dyatta Mayombo Kévin, A. Gabrielle, Ipouka Doussiemou Sergina, Nguele Ndjota, Afoughe Mayombo Ornela Priscilia, Mpira Yves Marien
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摘要

摘要:龟头神经鞘瘤是一种罕见的临床疾病。病理诊断。治疗是手术,完全切除。作者报告了在利伯维尔大学医院遇到的这一罕见病例,以确定其临床和治疗特点。观察:I.B先生,50岁,无外科病史,因龟头肿胀06年,无法性交就诊。他报告了一个概念,愈合不良的橡子疮后,裤蝇关闭。诊断怀疑是龟头瘢痕疙瘩。完全切除。组织学检查为龟头神经鞘瘤。术后D7愈合良好。勃起功能得以保留。结论:龟头神经鞘瘤少见。手术治疗效果良好。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Glans Schwannoma: A Rare Clinical Entity
Introduction: Schwannoma of the glans is a rare clinical entity. The diagnosis is histological. Treatment is surgical, with complete excision. The authors report this rare case encountered at the University Hospital of Libreville in order to identify its clinical and therapeutic characteristics. Observation: Mr. I.B, 50 years old, with no medical-surgical history, consulted for swelling of the glans evolving for 06 years, preventing coitus. He reported a notion of poor healing from an acorn sore after the trouser fly was closed. The diagnostic suspicion was a glans keloid. A complete resection was performed. Histologic examination favored a glans schwannoma. Healing was effective on D7 postoperatively. Erectile functions have been preserved. Conclusion: The glans schwannoma is rare. Surgical treatment gives good results.
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