严重横纹肌溶解症是人类粒细胞无形体病的罕见并发症

IF 1.1 Q4 INFECTIOUS DISEASES
IDCases Pub Date : 2024-01-01 DOI:10.1016/j.idcr.2024.e01942
Chun-Yu Peng, Prarthana Desai, Mohammed Saleh, Ocheita Daniel
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引用次数: 0

摘要

人类粒细胞无形体病(HGA)是一种由噬细胞无形体感染引起的蜱媒疾病。横纹肌溶解症和急性肾功能衰竭虽然罕见,但却是 HGA 的潜在并发症。我们介绍了一例 86 岁的男性病例,他出现了严重的肌病、横纹肌溶解症和急性肾衰竭,需要进行血液透析。使用强力霉素治疗后,患者的肾功能得到部分改善,8 周后患者可以停止透析。本病例强调了将横纹肌溶解症视为 HGA 一种表现的重要性,尤其是对于居住在地方病流行地区或前往该地区旅行的人。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Severe rhabdomyolysis as a rare complication of human granulocytic anaplasmosis

Human granulocytic anaplasmosis (HGA) is a tick-borne illness caused by infection with Anaplasma phagocytophilum. Although rare, rhabdomyolysis and acute renal failure are potential complications of HGA. We present the case of an 86-year-old male who exhibited severe myopathy, rhabdomyolysis, and acute renal failure necessitating hemodialysis. Treatment with doxycycline resulted in partial renal function improvement, allowing discontinuation of dialysis after 8 weeks. This case underscores the importance of considering rhabdomyolysis as a manifestation of HGA, particularly in individuals residing in or traveling to endemic areas.

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来源期刊
IDCases
IDCases INFECTIOUS DISEASES-
CiteScore
2.60
自引率
6.70%
发文量
300
审稿时长
10 weeks
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