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一名患有精神分裂症女性患者的成人斯蒂尔病:病例报告及文献综述

Adult-onset Still's Disease in a Female Patient with Schizophrenia: A Case Report and Literature Review.

作者信息

Golchin Nasim, Sharifzadeh Mohaddeseh, Fransawy Alkomos Mina, Sachmechi Issac

机构信息

Endocrinology, Icahn School of Medicine at Mount Sinai/Queens Hospital Center, New York, USA.

Internal Medicine, Icahn School of Medicine at Mount Sinai Queen Hospital Center, New York, USA.

出版信息

Cureus. 2018 Jul 21;10(7):e3019. doi: 10.7759/cureus.3019.

Abstract

Adult-onset Still's disease (AOSD) is a rare diagnosis. In small percentage of cases, AOSD is associated with other autoimmune diseases including schizophrenia. Despite the lack of sufficient studies, both conditions may share similar autoimmune pathogenic pathways. Herein we describe a 36-year-old woman with the past medical history of schizophrenia who presented with spiking fevers, arthralgia, evanescent rash and pleural chest pain. She reported developing these symptoms a while after poor compliance with her antipsychotic medication. On admission, physical examination was remarkable for high-grade fever, maculopapular rash, oligo arthralgia, hepatomegaly and lymphadenopathy. Laboratory investigation revealed leukocytosis with neutrophilia and markedly elevated ferritin. The patient met four out of four major, and three out of five minor Yamaguchi criteria for AOSD. The patient started on therapy with corticosteroid. Soon after, her symptoms resolved and most of her biochemical markers went back to normal. We review the literature on co-existence of AOSD with other autoimmune diseases, we also discuss that there may be a correlation between ceasing antipsychotic medication (with known immunomodulatory effect) in a schizophrenic patient and triggering an auto-inflammatory process such as AOSD in a susceptible host. In addition, we discussed the possible similar autoimmune pathway of schizophrenia to pathogenesis of AOSD.

摘要

成人斯蒂尔病(AOSD)是一种罕见的诊断。在一小部分病例中,AOSD与包括精神分裂症在内的其他自身免疫性疾病有关。尽管缺乏充分的研究,但这两种疾病可能共享相似的自身免疫致病途径。在此,我们描述了一名36岁有精神分裂症病史的女性,她出现了高热、关节痛、一过性皮疹和胸膜胸痛。她报告称在不依从抗精神病药物治疗一段时间后出现了这些症状。入院时,体格检查显示有高热、斑丘疹、少关节痛、肝肿大和淋巴结病。实验室检查显示白细胞增多伴中性粒细胞增多以及铁蛋白显著升高。该患者符合AOSD的四条主要山口标准中的四条以及五条次要标准中的三条。患者开始使用皮质类固醇治疗。不久后,她的症状缓解,大部分生化指标恢复正常。我们回顾了关于AOSD与其他自身免疫性疾病共存的文献,我们还讨论了在精神分裂症患者中停用具有已知免疫调节作用的抗精神病药物与在易感宿主中引发如AOSD这样的自身炎症过程之间可能存在的相关性。此外,我们讨论了精神分裂症与AOSD发病机制可能相似的自身免疫途径。

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