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非典型基底细胞痣综合征

Atypical gorlin's syndrome.

作者信息

Yesudian D, Krishnan S G, Jayaraman M, Janaki V R, Yesudian P

机构信息

Department of Dermatology, Madras Medical College and Goverenment General Hospital, Madras, India, .

出版信息

Indian J Dermatol Venereol Leprol. 1995 Sep-Oct;61(5):314-6.

PMID:20953003
Abstract

A 21-year-old woman presented with complaints of skin lesions on her face, palms and soles. On examination, 8 to 10 well-defined, pigmented nodules with raised and pearly borders were seen on the face. Multiple pits were present on the palms and soles. Biopsy of both lesions revealed the presence of basal cell epitheliomas. The patient also gave history of removal of a keratocyst of mandible 10 years back. The case was diagnosed as Gorlin's syndrome. It is atypical due to the low number of basal cell epitheliomas, the occurrence of only a single odontogenic cyst and the absence of other features usually associated with this condition.

摘要

一名21岁女性因面部、手掌和足底出现皮肤病变前来就诊。检查发现,面部有8至10个边界清晰、色素沉着的结节,边界隆起呈珍珠样。手掌和足底有多个凹坑。两处病变的活检均显示存在基底细胞上皮瘤。患者还述及10年前曾切除下颌骨的一个角化囊肿。该病例被诊断为戈林综合征。由于基底细胞上皮瘤数量较少、仅出现单个牙源性囊肿且缺乏通常与该疾病相关的其他特征,故该病例为非典型病例。

相似文献

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Atypical gorlin's syndrome.非典型基底细胞痣综合征
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Hypoplastic thumb in Gorlin's syndrome.戈林综合征中的发育不全拇指。
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Delayed diagnosis of Gorlin's syndrome in a renal transplant recipient.一名肾移植受者的戈林综合征延迟诊断。
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Multiple keratoacanthomas in a young woman: report of a case emphasizing medical management and a review of the spectrum of multiple keratoacanthomas.一名年轻女性的多发性角化棘皮瘤:病例报告,着重于医疗管理及多发性角化棘皮瘤谱系的综述
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Gorlin-Goltz syndrome: An often missed diagnosis.戈林-戈尔茨综合征:一种常被漏诊的疾病。
Ann Maxillofac Surg. 2016 Jan-Jun;6(1):120-4. doi: 10.4103/2231-0746.186148.
2
Gorlin-Goltz syndrome: A case series of 5 patients in North Indian population with comparative analysis of literature.戈林-戈尔茨综合征:北印度人群中5例患者的病例系列及文献对比分析
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Gorlin-Goltz Syndrome: Case report and literature review.戈林-戈尔茨综合征:病例报告与文献综述。
J Oral Maxillofac Pathol. 2015 May-Aug;19(2):267. doi: 10.4103/0973-029X.164557.
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Gorlin-Goltz syndrome.戈林-戈尔茨综合征。
J Oral Maxillofac Pathol. 2009 Jul;13(2):89-92. doi: 10.4103/0973-029X.57677.