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Multiple nodules on the scrotal wall.阴囊壁多发结节。
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本文引用的文献

1
The possible role of dartoic muscle degeneration in the pathogenesis of idiopathic scrotal calcinosis.肉膜肌退变在特发性阴囊钙化症发病机制中的可能作用。
Br J Dermatol. 2003 Apr;148(4):827-9. doi: 10.1046/j.1365-2133.2003.05251.x.
2
Scrotal calcinosis: is it idiopathic?阴囊钙质沉着症:是特发性的吗?
Urology. 2001 Feb;57(2):365. doi: 10.1016/s0090-4295(00)01007-4.
3
Idiopathic scrotal calcinosis: a possible aetiology reaffirmed.特发性阴囊钙化症:一种可能病因的再次确认。
Br J Plast Surg. 1989 May;42(3):324-7. doi: 10.1016/0007-1226(89)90155-0.
4
Idiopathic calcinosis of the scrotum: histopathologic observations of fifty-one nodules.阴囊特发性钙化:51个结节的组织病理学观察
J Am Acad Dermatol. 1988 Dec;19(6):1095-101. doi: 10.1016/s0190-9622(88)70278-9.

特发性阴囊钙化症

Idiopathic Scrotal Calcinosis.

作者信息

Killedar Madhura Milind, Shivani Aslam A, Shinde Usha

机构信息

Bharati Vidyapeeth Deemed University Medical College and Hospital, Sangli, India.

出版信息

Indian J Surg. 2016 Aug;78(4):329-30. doi: 10.1007/s12262-016-1463-4. Epub 2016 Mar 19.

DOI:10.1007/s12262-016-1463-4
PMID:27574356
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4987564/
Abstract

Idiopathic scrotal calcinosis (ISC) is a rare benign condition which presents with multiple, asymptomatic, and painless nodules on the scrotal skin wall. The lesions have been attributed as sebaceous cysts, calcified steatocystoma, fibroma, atheroma, and xanthoma. Shapiro et al. reviewed the histologic data and found no evidence of an epithelial lining, residual cysts, and lipid or organisms, and concluded that the calcification was idiopathic introducing the term "idiopathic scrotal calcinosis." We have studied four cases of idiopathic scrotal calcinosis, one of which had scrotal calcinosis involving the whole of the scrotum. He presented with painless multiple nodules over the scrotum. He was subjected for surgery with SOS skin grafting, but as the scrotal skin is so lax, primary closure is easily possible. In all our four cases, primary closure was easily possible.

摘要

特发性阴囊钙化症(ISC)是一种罕见的良性病症,表现为阴囊皮肤壁上出现多个无症状、无痛的结节。这些病变曾被认为是皮脂腺囊肿、钙化脂囊瘤、纤维瘤、动脉粥样瘤和黄瘤。夏皮罗等人回顾了组织学数据,未发现上皮内衬、残留囊肿、脂质或生物体的证据,并得出结论,钙化是特发性的,从而引入了“特发性阴囊钙化症”这一术语。我们研究了4例特发性阴囊钙化症病例,其中1例阴囊钙化累及整个阴囊。他阴囊上出现无痛性多个结节。他接受了手术及紧急皮肤移植,但由于阴囊皮肤非常松弛,一期缝合很容易实现。在我们所有4例病例中,一期缝合都很容易实现。