Brooke-Spiegler Syndrome: A rare cause of skin appendageal tumor
N. Suganthan, S Pirasath, Dikowita Dd
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引用次数: 0
Abstract
A 51-year-old women presented with asymptomatic multiple polypoidal nodules over scalp with simultaneous papularnodular skin eruptions involving nose, nasolabial folds and forehead for 40 years duration. Her daughter also noted to be having multiple papularnodular skin eruptions involving nose, nasolabial folds and forehead which raised curiosity of possible familial condition. The punch biopsy of polypoidal nodule indicating histological evidence of spiradenoma was favour in diagnosis of Brook Spienger Syndrome. We report this case as this is a rare clinical entity. Case Report Brooke-Spiegler Syndrome: A rare cause of skin appendageal tumor N Suganthan1*, S Pirasath2 and DD Dikowita2 1Consultant, Physician and Senior Lecturer, University Medical Unit, Teaching Hospital, Jaffna, Sri Lanka 2Registrar, University Medical Unit, Teaching Hospital, Jaffna, Sri Lanka *Address for Correspondence: Dr. N Suganthan, Consultant, Physician and Senior Lecturer, University Medical Unit, Teaching Hospital, Jaffna, Sri Lanka, Email: drn.suganthan@yahoo.com Submitted: 12 October 2018 Approved: 31 October 2018 Published: 01 November 2018 Copyright: © 2018 Suganthan N, et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited
布鲁克-斯皮格勒综合征:一种罕见的皮肤附件肿瘤的原因
一位51岁的女性,在无症状的多发性息肉样结节的头皮,同时丘疹结节性皮肤爆发涉及鼻子,鼻唇襞和前额持续40年。她的女儿也注意到鼻子、鼻唇沟和前额有多处丘疹样皮肤疹,这引起了人们对可能的家族性疾病的好奇。息肉样结节穿刺活检提示螺旋腺瘤的组织学证据,有利于布鲁克-斯宾格综合征的诊断。我们报告这个病例,因为这是一个罕见的临床实体。病例报告Brooke-Spiegler综合征:一种罕见的皮肤附件肿瘤N Suganthan1*, S Pirasath2和DD Dikowita2 1斯里兰卡贾夫纳教学医院大学医疗部门顾问,医师和高级讲师2斯里兰卡贾夫纳教学医院大学医疗部门注册主任*通信地址:N Suganthan1博士,顾问,医师和高级讲师,斯里兰卡贾夫纳教学医院大学医疗部门,电子邮件:drn.suganthan@yahoo.com2018年10月12日批准:2018年10月31日发布:2018年11月01日版权所有:©2018 Suganthan N, et al。这是一篇在知识共享署名许可下发布的开放获取文章,该许可允许在任何媒体上不受限制地使用、分发和复制,只要原始作品被适当引用
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