Nguyen Khang D, Lee Eunice E, Yue Yangbo, Stork Jiri, Pock Lumir, North Jeffrey P, Vandergriff Travis, Cockerell Clay, Hosler Gregory A, Pastrana Diana V, Buck Christopher B, Wang Richard C
Department of Dermatology, University of Texas Southwestern Medical Center, Dallas, Texas.
Dermatohistopathological Laboratory, Charles University in Prague, Prague, Czech Republic.
J Am Acad Dermatol. 2017 May;76(5):932-940.e3. doi: 10.1016/j.jaad.2016.11.035. Epub 2016 Dec 29.
Human polyomavirus (HPyV)6 and HPyV7 are shed chronically from human skin. HPyV7, but not HPyV6, has been linked to a pruritic skin eruption of immunosuppression.
We determined whether biopsy specimens showing a characteristic pattern of dyskeratosis and parakeratosis might be associated with polyomavirus infection.
We screened biopsy specimens showing "peacock plumage" histology by polymerase chain reaction for HPyVs. Cases positive for HPyV6 or HPyV7 were then analyzed by immunohistochemistry, electron microscopy, immunofluorescence, quantitative polymerase chain reaction, and complete sequencing, including unbiased, next-generation sequencing.
We identified 3 additional cases of HPyV6 or HPyV7 skin infections. Expression of T antigen and viral capsid was abundant in lesional skin. Dual immunofluorescence staining experiments confirmed that HPyV7 primarily infects keratinocytes. High viral loads in lesional skin compared with normal-appearing skin and the identification of intact virions by both electron microscopy and next-generation sequencing support a role for active viral infections in these skin diseases.
This was a small case series of archived materials.
We have found that HPyV6 and HPyV7 are associated with rare, pruritic skin eruptions with a distinctive histologic pattern and describe this entity as "HPyV6- and HPyV7-associated pruritic and dyskeratotic dermatoses."
人多瘤病毒(HPyV)6和HPyV7可长期从人皮肤中排出。HPyV7而非HPyV6与免疫抑制性瘙痒性皮疹有关。
我们确定显示特征性角化不良和不全角化模式的活检标本是否可能与多瘤病毒感染有关。
我们通过聚合酶链反应对显示“孔雀羽毛”组织学的活检标本进行HPyV筛查。然后对HPyV6或HPyV7阳性的病例进行免疫组织化学、电子显微镜、免疫荧光、定量聚合酶链反应和全序列分析,包括无偏差的二代测序。
我们又发现了3例HPyV6或HPyV7皮肤感染病例。病变皮肤中T抗原和病毒衣壳表达丰富。双重免疫荧光染色实验证实HPyV7主要感染角质形成细胞。与外观正常的皮肤相比,病变皮肤中的病毒载量高,并且通过电子显微镜和二代测序均鉴定出完整病毒颗粒,这支持了活跃病毒感染在这些皮肤病中的作用。
这是一个关于存档材料的小病例系列。
我们发现HPyV6和HPyV7与罕见的、瘙痒性皮疹有关,具有独特的组织学模式,并将此实体描述为“HPyV6和HPyV7相关的瘙痒性和角化不良性皮肤病”。