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在一名患棘状毛发发育异常的患者的皮肤和肾移植组织中对棘状毛发发育异常相关多瘤病毒DNA进行特异性检测。

Specific detection of trichodysplasia spinulosa–associated polyomavirus DNA in skin and renal allograft tissues in a patient with trichodysplasia spinulosa.

作者信息

Fischer Max K, Kao Grace F, Nguyen Harrison P, Drachenberg Cinthia B, Rady Peter L, Tyring Stephen K, Gaspari Anthony A

机构信息

Department of Pathology, University of Maryland Medical Center, MD, USA.

出版信息

Arch Dermatol. 2012 Jun;148(6):726-33. doi: 10.1001/archdermatol.2011.3298.

DOI:10.1001/archdermatol.2011.3298
PMID:22351786
Abstract

BACKGROUND

Trichodysplasia spinulosa (TS) is a rare, disfiguring skin condition that affects immunosuppressed patients, universally involving the central face. New data point to the recently discovered TS-associated polyomavirus (TSPyV) as the causative agent.

OBSERVATIONS

We report a case of TS in a 48-year-old African American man after renal transplant; via polymerase chain reaction and sequencing, confirm the detection of TSPyV in lesional skin; and report the novel detection of TSPyV DNA in renal allograft tissue. Results of polymerase chain reaction analysis were negative for Merkel cell polyomavirus in lesional skin. Fifteen months later, urine cytologic findings showed morphologic evidence of a urinary tract polyomavirus infection. Results of SV40 immunohistochemical analysis were negative in lesional skin, renal allograft, and urine specimens.

CONCLUSIONS

To our knowledge, this is the first reported case in which TSPyV DNA has been detected in extracutaneous tissues and the third with combined ultrastructural and molecular confirmation of the presence of TSPyV in lesional skin. Lack of detection of other pathogenic human polyomaviruses in this patient's skin supports the specific role of this polyomavirus in the genesis of TS. Further basic science studies are needed to determine the exact pathomechanisms of this polyomavirus and to explore possible tumorigenic roles in other skin diseases.

摘要

背景

棘状毛囊发育异常(TS)是一种罕见的、毁容性的皮肤疾病,影响免疫抑制患者,普遍累及面部中央。新数据表明,最近发现的与TS相关的多瘤病毒(TSPyV)是病原体。

观察结果

我们报告了一例肾移植后48岁非裔美国男性的TS病例;通过聚合酶链反应和测序,证实病变皮肤中检测到TSPyV;并报告在同种异体肾移植组织中首次检测到TSPyV DNA。病变皮肤中默克尔细胞多瘤病毒的聚合酶链反应分析结果为阴性。15个月后,尿液细胞学检查结果显示有尿路多瘤病毒感染的形态学证据。病变皮肤、同种异体肾移植和尿液标本的SV40免疫组织化学分析结果均为阴性。

结论

据我们所知,这是第一例在皮肤外组织中检测到TSPyV DNA的报告病例,也是第三例通过超微结构和分子方法联合证实病变皮肤中存在TSPyV的病例。在该患者皮肤中未检测到其他致病性人类多瘤病毒,支持了这种多瘤病毒在TS发病机制中的特定作用。需要进一步开展基础科学研究,以确定这种多瘤病毒的确切发病机制,并探索其在其他皮肤疾病中可能的致瘤作用。

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