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[阴囊特发性钙化:一例报告]

[Idiopathic calcinosis of the scrotum: a case report].

作者信息

Kumagai K, Amemiya H, Muramatsu H, Kariba T, Matsuse K, Toyoshima A, Yazaki T, Waku M, Okada N

机构信息

Department of Urology, Teikyo University School of Medicine.

出版信息

Hinyokika Kiyo. 1987 Aug;33(8):1289-91.

PMID:3425527
Abstract

A 25-year-old man complained of painless, firm scrotal nodules which increased in number and size for the last 7 years. Physical examination was unremarkable except for many, firm painless nodules near the scrotal raphe. Preoperative diagnosis was multiple scrotal tumors of unknown etiology. Surgical excision was performed under epidural anesthesia. On microscopic examination, the nodules were located in the dermis and composed of calcified material which was positive with the von Kossa calcium stain. There were numerous foreign giant cells and dense fibrosis at the margins of the lesions. Idiopathic calcinosis of the scrotum was the final diagnosis. Although its etiology is unknown, the literature reviewed supported the view that the mast cell accumulation and its degranulation are related to idiopathic calcinosis of the scrotum.

摘要

一名25岁男性主诉阴囊出现无痛性、质地坚硬的结节,在过去7年里结节数量和大小均有所增加。体格检查未见明显异常,仅在阴囊中缝附近有多个质地坚硬的无痛性结节。术前诊断为病因不明的多发性阴囊肿瘤。在硬膜外麻醉下进行了手术切除。显微镜检查显示,结节位于真皮层,由钙化物质组成,经冯·科萨钙染色呈阳性。病变边缘有大量异物巨细胞和致密纤维化。最终诊断为特发性阴囊钙化症。尽管其病因不明,但文献综述支持肥大细胞聚集及其脱颗粒与特发性阴囊钙化症有关的观点。

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