与 COVID-19 和 COVID-19 疫苗相关的下肢皮肤溃疡:病例报告和文献综述。

Paul Beaineh, Ayman El-Bsat, Bassel Hafez, Abdul Rahman Bizri, Abdul-Ghani Kibbi, Mira Merashli, Fady Haddad
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摘要

病例一名 53 岁的男性患者到皮肤科门诊就诊,他的左右脚踝外侧踝骨出现疼痛性坏死斑块,已有三周病史。病史可追溯到患者接种第二针辉瑞生物技术公司生产的 COVID-19 疫苗(BNT162b2)两周后出现瘙痒性丘疹。穿刺活检结果与白细胞凝集性血管炎一致。根据培养结果,他接受了为期四周的全身皮质类固醇和抗生素治疗。血管评估证实外周动脉和静脉系统正常。两个月后,患者因发烧和下肢溃疡恶化再次就诊。他接受了伤口清创术。术中培养发现了耐多药细菌。几天后,他需要再进行一次清创,并接受为期 14 天的哌拉西林-他唑巴坦治疗。患者随后服用皮质类固醇和硫唑嘌呤出院,并在血管外科和风湿病诊所接受了随访。在四个月的随访中,患者的伤口几乎完全愈合:本文重点介绍了一例严重的新发 COVID-19 疫苗相关性白细胞坏死性血管炎并发感染性溃疡的病例,患者除了需要长期服用抗生素和免疫抑制剂外,还需要进行两次清创。据我们所知,文献中报道的病例均未达到如此严重的程度。在这个大流行后的时代,它必须在鉴别病例名单上保持高位,医疗专家在评估无明显病因的突发新发皮损时应保持高度怀疑。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
COVID-19 and COVID-19 Vaccine-Related Skin Ulcerations in the Lower Extremities: A Case Report and Literature Review.

Case: A 53-year-old male patient presented to the dermatology clinics with a three-week history of painful necrotic patches coalescent of the lateral malleolus of the right and left ankles. History goes back to when the patient reported developing pruritic papules two weeks after receiving his second shot of the Pfizer BioNTech COVID-19 vaccine (BNT162b2). Punch biopsy was consistent with leukocytoclastic vasculitis. He was prescribed a four-week course of systemic corticosteroids and antibiotics as per cultures. Vascular assessment confirmed normal peripheral arterial and venous system. Two months later, the patient re-presented with fever and worsening of his lower extremity ulcers. He underwent debridement of his wounds. Intra-operative cultures revealed multidrug resistant bacteria. He required an additional debridement session a few days later and a 14-day course of Piperacillin-Tazobactam. The patient was subsequently discharged on corticosteroids and Azathioprine and followed up in the vascular surgery and rheumatology clinics. At four months follow-up, the patient's wounds were almost completely healed.

Conclusion: This article highlights a case of severe new-onset COVID-19 vaccine-associated leukocytoclastic vasculitis complicated with infected ulcers that required debridement twice in addition to a prolonged course of antibiotics and immunosuppression therapy. To our knowledge, none of the cases reported in the literature were this severe in nature. In this post-pandemic era, it must remain high on the differential list, and healthcare specialists should maintain a high index of suspicion when evaluating sudden new-onset skin lesions that do not have an immediately apparent etiology.

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