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三例使用利培酮引发的抗精神病药恶性综合征:病例报告及文献综述

Three Episodes of Neuroleptic Malignant Syndrome With Risperidone: A Case Report and Literature Review.

作者信息

Elyasi Forouzan, Alaei Solmaz, Heydari Fatemeh, Zarghami Mehran

机构信息

Sexual and Reproductive Health Research Center, Mazandaran University of Medical Sciences, Sari, Mazandaran, Iran.

Psychiatry and Behavioral Sciences Research Center, Addiction Institute, Mazandaran University of Medical Sciences, Sari, Mazandaran, Iran.

出版信息

Case Rep Psychiatry. 2025 Sep 11;2025:6669246. doi: 10.1155/crps/6669246. eCollection 2025.

DOI:10.1155/crps/6669246
PMID:40979235
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12446600/
Abstract

Neuroleptic malignant syndrome (NMS) is an idiosyncratic and life-threatening side effect that usually occurs in response to dopamine receptor antagonist medications. Despite increased awareness, the diagnosis of NMS remains challenging due to its wide differential diagnoses, which can lead to delayed treatment and increased mortality or premature reinitiation of the causative agent, culminating in recurrent NMS, a phenomenon with limited reports. This case presents a patient who experienced three episodes of NMS within 1 year, all triggered by risperidone. A 58-year-old male patient with schizophrenia presented to the emergency department of a university hospital in Northern Iran, due to decreased consciousness, fever, and rigidity. Initial laboratory results showed elevated creatine phosphokinase (CPK) at 14,949 U/L. He had two previous episodes of rhabdomyolysis and hospitalization in the past year. Review of prior hospital records indicated treatment for rhabdomyolysis with symptoms consistent with NMS, without making this diagnosis. In any patient treated with dopaminergic drugs who suffer from mental status changes, muscle stiffness, high fever, and dysautonomia, especially who have complications such as rhabdomyolysis, kidney failure, seizures, leukocytosis, and increased CPK and lactate dehydrogenase (LDH), the possibility of NMS should be considered.

摘要

神经阻滞剂恶性综合征(NMS)是一种特异质性且危及生命的副作用,通常发生于对多巴胺受体拮抗剂药物的反应中。尽管认识有所提高,但由于NMS的鉴别诊断范围广泛,其诊断仍具有挑战性,这可能导致治疗延迟、死亡率增加或过早重新使用致病药物,最终导致复发性NMS,这一现象的报道有限。本病例介绍了一名在1年内经历三次NMS发作的患者,所有发作均由利培酮引发。一名58岁的男性精神分裂症患者因意识减退、发热和僵硬入住伊朗北部一家大学医院的急诊科。初始实验室结果显示肌酸磷酸激酶(CPK)升高至14,949 U/L。他在过去一年中有两次横纹肌溶解发作并住院治疗。回顾之前的医院记录,发现对横纹肌溶解的治疗症状与NMS一致,但未做出该诊断。在任何接受多巴胺能药物治疗且出现精神状态改变、肌肉僵硬、高热和自主神经功能障碍的患者中,尤其是伴有横纹肌溶解、肾衰竭、癫痫发作、白细胞增多以及CPK和乳酸脱氢酶(LDH)升高的并发症患者,应考虑NMS的可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc3c/12446600/4a07e4e0f3de/CRIPS2025-6669246.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc3c/12446600/c2343db902c7/CRIPS2025-6669246.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc3c/12446600/fbd236980f7a/CRIPS2025-6669246.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc3c/12446600/65758e94dc54/CRIPS2025-6669246.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc3c/12446600/4a07e4e0f3de/CRIPS2025-6669246.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc3c/12446600/c2343db902c7/CRIPS2025-6669246.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc3c/12446600/fbd236980f7a/CRIPS2025-6669246.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc3c/12446600/65758e94dc54/CRIPS2025-6669246.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc3c/12446600/4a07e4e0f3de/CRIPS2025-6669246.004.jpg

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