Holzer Aton M, Hughey Lauren C
J Am Acad Dermatol. 2009 Jan;60(1):169-72. doi: 10.1016/j.jaad.2008.07.051.
Trichodysplasia of immunosuppression (TOI) is a newly described rare clinicopathologic entity usually found in transplant patients on chronic immunosuppressive medications or with hematologic malignancies. TOI consists of a cutaneous eruption of spiny papules predominantly affecting the face and arms. The distinct histopathologic picture includes abnormally maturing anagen follicles with hyperkeratotic infundibula and excessive inner root sheath differentiation. Given that intranuclear viral particles have been noted on electron microscopy of skin biopsy in several patients, a viral etiology is suspected. These viral particles are similar in shape and size to a polyoma virus, however, the virus has not been identified to date. There are reports of improvement of TOI with topical cidofovir or tazarotene 0.5% gel, but to our knowledge there has not been a report of near-complete resolution with oral valganciclovir. We report a case of TOI in a heart transplant patient on a chronic immunosuppressive regimen of sirolimus, mycophenolic acid and prednisone that demonstrated almost complete response to treatment with systemic valganciclovir.
免疫抑制性毛发发育异常(TOI)是一种新描述的罕见临床病理实体,通常见于接受慢性免疫抑制药物治疗的移植患者或患有血液系统恶性肿瘤的患者。TOI表现为以面部和手臂为主的棘状丘疹皮肤疹。独特的组织病理学表现包括生长期毛囊异常成熟,伴有角化过度的漏斗部和内根鞘过度分化。鉴于在数例患者的皮肤活检电子显微镜检查中发现了核内病毒颗粒,怀疑其病因与病毒有关。这些病毒颗粒在形状和大小上与多瘤病毒相似,然而,迄今为止尚未鉴定出该病毒。有报道称局部使用西多福韦或0.5%他扎罗汀凝胶可改善TOI,但据我们所知,尚无口服缬更昔洛韦使病情几乎完全缓解的报道。我们报告1例心脏移植患者发生TOI,该患者接受西罗莫司、霉酚酸和泼尼松的慢性免疫抑制方案治疗,使用全身性缬更昔洛韦治疗后几乎完全缓解。