肺移植患者水痘-带状疱疹病毒再激活的非典型表现:病例报告

Ingrid Hoff, Eivind Rath, Slobodanka Pena-Karan, Elisabeth Sivy Nginamau, A. Holm, T. Thune, Tehmina Mustafa
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摘要

背景。水痘-带状疱疹病毒(VZV)是一种人类神经性病毒,通常在儿童时期引起感染,表现为水痘。日后它可能重新活化为带状疱疹。我们报告了一起罕见的 VZV 感染再活化病例,肺移植受者表现为皮肤血管炎和水痘肺炎。 病例介绍。一名 65 岁的男性因肺气肿接受了双侧肺移植,移植后反复出现胸部感染和铜绿假单胞菌定植。移植后 9 个月,他出现呼吸困难和皮肤血管炎样糜烂,好发于面部、胸部和四肢远端。起初,由于没有典型的水泡状疹子,因此没有怀疑是 VZV 再激活。在对病灶进行皮肤打孔活检后,从溃疡拭子和支气管肺泡灌洗液(BAL)中提取的 VZV PCR 结果证实了诊断。皮肤活检组织学显示上皮损伤和血管损伤,但没有典型的上皮病毒相关改变。患者对抗病毒治疗做出了反应,皮疹完全缓解,经过 29 天的治疗后,在重复的 BAL 中终于检测不到 VZV DNA。然而,由于可能与 VZV 感染无关的原因,肺部放射学特征和呼吸困难仍然存在。 结论如果不是患者提到血管炎皮疹与他的原发性 VZV 感染相似,诊断很容易被忽视。在本病例中,活组织检查并未发现典型的 VZV-血管炎组织病理学结果。导致诊断的是冲孔活检后从伤口拭子中提取的 PCR。本病例提醒人们注意免疫抑制患者常见疾病的非典型表现,在这类患者中可能需要进行广泛的诊断取样。
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Atypical presentation of varicella-zoster virus reactivation in a lung transplant patient: a case report
Background. Varicella-zoster virus (VZV) is a human neurotropic virus which commonly causes infection during childhood, presenting as chickenpox. Later in life it may reactivate as herpes zoster. We report a rare manifestation of reactivation of VZV infection presenting as cutaneous vasculitis and varicella pneumonia in a lung transplant recipient. Case presentation. A 65-year-old man was lung transplanted bilaterally for emphysema and had repeated posttransplant chest infections and colonization with Pseudomonas aeruginosa. Nine months post-transplant he presented with dyspnoea and a cutaneous vasculitis-like eruption with a predilection over face, thorax and distal extremities. Initially, VZV reactivation was not suspected due to absence of the typical vesicular eruptions. The diagnosis was confirmed by VZV PCR from the swabs of the ulcer after skin punch biopsy of a lesion and from bronchoalveolar lavage (BAL). The histology of skin biopsy demonstrated epithelial damage and vascular damage but no typical epithelial virus associated changes. The patient responded to antiviral therapy with total remission of rash and VZV DNA was finally not detectable from repeated BAL after 29 days of therapy. However, the pulmonary radiological features and dyspnoea persisted due to reasons possibly unrelated to the VZV infection. Conclusion. Had it not been for the patient to mention the resemblance of the vasculitic rash with his primary VZV infection, the diagnosis would easily have been overlooked. In this case, the biopsy did not show typical histopathologic findings of VZV-vasculitis. What led the diagnosis was a PCR from the wound swab taken after the punch biopsy. This case serves as a reminder for atypical presentation of common conditions in immunosuppressed patients and that extensive diagnostic sampling may be warranted in this group.
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