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双下肢快速进展性、对称性、急性皮肤坏死:结节性多动脉炎的罕见表现

Rapidly Progressive, Symmetrical, Acute Cutaneous Necrosis of Bilateral Lower Limbs: A Rare Presentation of Polyarteritis Nodosa.

作者信息

Wettasinghe Indika, Puthra Shiran, Sugathapala Hemal A, Mendis Suresh

机构信息

Internal Medicine, Colombo South Teaching Hospital, Colombo, LKA.

出版信息

Cureus. 2024 Apr 20;16(4):e58649. doi: 10.7759/cureus.58649. eCollection 2024 Apr.

DOI:10.7759/cureus.58649
PMID:38770516
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11103124/
Abstract

Acute cutaneous necrosis is a rare presentation of polyarteritis nodosa (PAN). In this study, we report a presentation with symmetrical cutaneous necrosis of the lower limbs, which ascended upward at a rapid rate. A 47-year-old man presented with a fever of one day and pain in the feet for six days. He had no history of claudication. Upon examination, he was febrile, and subtle bluish discoloration was observed on the sole of his foot. There was a bilateral stocking-type paresthesia up to the ankle joint. His blood pressure on admission was 210/120 mmHg. Eight hours later, the pain subsided, but a left-sided foot drop was noted along with the paresthesia extending up both feet to approximately 10 cm above the medial malleolus. The feet turned black, and dark discoloration spread rapidly upward over the next 16 hours, and the skin became necrosed. A clinical diagnosis of vasculitis was established, and the patient received IV methylprednisolone at a daily dosage of 1 g for three days, effectively stopping the advancement of necrosis. This was followed by treatment with IV cyclophosphamide. A conclusive diagnosis of PAN was made, and the patient underwent wound debridement. After three months of physiotherapy, a successful skin graft was performed. Prompt identification of the underlying etiology is crucial to prevent the advancement of necrosis and save the limbs. When vasculitis is suspected, ruling out infectious causes is essential before starting early immunosuppressive treatment.

摘要

急性皮肤坏死是结节性多动脉炎(PAN)的一种罕见表现。在本研究中,我们报告了一例以下肢对称性皮肤坏死为表现的病例,坏死迅速向上蔓延。一名47岁男性,发热1天,足部疼痛6天。他无间歇性跛行病史。检查时,他发热,足底可见轻微的 bluish 变色。双侧袜套样感觉异常至踝关节。入院时血压为210/120 mmHg。8小时后,疼痛缓解,但出现左侧足下垂,感觉异常向上蔓延至双足内踝上方约10 cm处。足部变黑,在接下来的16小时内,深色变色迅速向上蔓延,皮肤坏死。确诊为血管炎,患者接受每日1 g剂量的静脉注射甲泼尼龙治疗3天,有效阻止了坏死进展。随后进行静脉注射环磷酰胺治疗。最终确诊为PAN,患者接受了伤口清创术。经过三个月的物理治疗,成功进行了皮肤移植。及时识别潜在病因对于防止坏死进展和挽救肢体至关重要。当怀疑血管炎时,在开始早期免疫抑制治疗之前排除感染性病因至关重要。 (注:文中“bluish”未准确对应中文词汇,可根据语境灵活处理,这里暂保留英文)

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f18/11103124/b82966d7420a/cureus-0016-00000058649-i04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f18/11103124/58b64443094a/cureus-0016-00000058649-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f18/11103124/c6c4a29d7bde/cureus-0016-00000058649-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f18/11103124/aed035bf3df3/cureus-0016-00000058649-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f18/11103124/b82966d7420a/cureus-0016-00000058649-i04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f18/11103124/58b64443094a/cureus-0016-00000058649-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f18/11103124/c6c4a29d7bde/cureus-0016-00000058649-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f18/11103124/aed035bf3df3/cureus-0016-00000058649-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f18/11103124/b82966d7420a/cureus-0016-00000058649-i04.jpg

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