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嗜酸性粒细胞性多肌炎:前臂非创伤性骨筋膜室综合征的罕见病因。

Eosinophilic Polymyositis: A Rare Cause of Atraumatic Compartment Syndrome of the Forearm.

作者信息

Boyajian Michael K, Roussel Lauren O, Khan Galam, Stopa Edward, Bhatt Reena

机构信息

Warren Alpert Medical School of Brown University, Providence, Rhode Island, United States.

Division of Plastic and Reconstructive Surgery, Brown University, Providence, Rhode Island, United States.

出版信息

J Hand Microsurg. 2020 Oct;12(Suppl 1):S67-S69. doi: 10.1055/s-0039-1694288. Epub 2019 Nov 2.

DOI:10.1055/s-0039-1694288
PMID:33335377
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7735544/
Abstract

Eosinophilic polymyositis is a rare disorder in which eosinophils infiltrate muscle and supporting connective tissue structures, resembling autoimmune or immunologically mediated disease. This disorder can be associated with muscle inflammation and death, and can be a cause of atraumatic compartment syndrome.  This is a retrospective chart review of a case report as well as review of pertinent literature.  This report presents a rare case of atraumatic compartment syndrome of the forearm caused by eosinophilic polymyositis. It provides a case summary and histological examination of this patient.  This is an important case to report because it highlights eosinophilic polymyositis as a unique etiology of compartment syndrome. In appropriate clinical situations where patients do not improve despite standard interventions, one should consider the rare and unusual etiology of compartment syndrome due to eosinophilic polymyositis. Furthermore, primary surgical intervention should not be delayed while waiting to ascertain a definitive diagnosis.

摘要

嗜酸性粒细胞性多肌炎是一种罕见的疾病,其中嗜酸性粒细胞浸润肌肉和支持性结缔组织结构,类似于自身免疫性或免疫介导性疾病。这种疾病可伴有肌肉炎症和坏死,并可导致非创伤性骨筋膜室综合征。

这是一份对病例报告的回顾性图表分析以及相关文献综述。

本报告介绍了一例由嗜酸性粒细胞性多肌炎引起的前臂非创伤性骨筋膜室综合征的罕见病例。报告提供了该患者的病例总结和组织学检查结果。

报告这一病例很重要,因为它凸显了嗜酸性粒细胞性多肌炎作为骨筋膜室综合征的一种独特病因。在适当的临床情况下,若患者尽管接受了标准干预仍无改善,应考虑嗜酸性粒细胞性多肌炎导致骨筋膜室综合征这种罕见且不寻常的病因。此外,在等待明确诊断时不应延迟进行初次手术干预。

相似文献

1
Eosinophilic Polymyositis: A Rare Cause of Atraumatic Compartment Syndrome of the Forearm.嗜酸性粒细胞性多肌炎:前臂非创伤性骨筋膜室综合征的罕见病因。
J Hand Microsurg. 2020 Oct;12(Suppl 1):S67-S69. doi: 10.1055/s-0039-1694288. Epub 2019 Nov 2.
2
Forearm compartment syndrome as a result of eosinophilic fasciitis: case report.嗜酸性筋膜炎导致的前臂骨筋膜室综合征:病例报告
J Hand Surg Am. 2015 Apr;40(4):707-10. doi: 10.1016/j.jhsa.2015.01.003. Epub 2015 Mar 4.
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Severe Rhabdomyolysis without Systemic Involvement: A Rare Case of Idiopathic Eosinophilic Polymyositis.无全身累及的严重横纹肌溶解症:一例罕见的特发性嗜酸性粒细胞性多肌炎病例
Case Rep Rheumatol. 2015;2015:908109. doi: 10.1155/2015/908109. Epub 2015 Jul 1.
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Multiple organ involvement in eosinophilic polymyositis: an autopsy report.嗜酸性粒细胞性多肌炎的多器官受累:一份尸检报告。
Hum Pathol. 2006 Feb;37(2):231-5. doi: 10.1016/j.humpath.2005.10.006. Epub 2005 Dec 27.
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Eosinophilic myositis: an updated review.嗜酸性粒细胞性肌炎:更新综述。
Autoimmun Rev. 2014 Apr-May;13(4-5):375-8. doi: 10.1016/j.autrev.2014.01.018. Epub 2014 Jan 11.
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Atraumatic gluteal compartment syndrome-an unusual presentation of a rare syndrome.非创伤性臀肌间室综合征——一种罕见综合征的不寻常表现
J Wound Care. 2022 Dec 2;31(12):1046-1047. doi: 10.12968/jowc.2022.31.12.1046.
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A Curious Case of Proximal Muscle Weakness with Eosinophilic Polymyositis.一例伴有嗜酸性粒细胞性多发性肌炎的近端肌无力的罕见病例。
Case Rep Rheumatol. 2016;2016:7810916. doi: 10.1155/2016/7810916. Epub 2016 Sep 14.
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Focal Eosinophilic Myositis of the Hand Presenting as a Refractory Pyogenic Infection.表现为难治性化脓性感染的手部局灶性嗜酸性肌炎
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Recurrent, atraumatic acute compartment syndrome secondary to IgA vasculitis: A case report.继发于IgA血管炎的复发性、非创伤性急性骨筋膜室综合征:一例报告
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[A case of Ki-1 lymphoma-associated eosinophilic polymyositis].[1例Ki-1淋巴瘤相关嗜酸性粒细胞性多发性肌炎]
Rinsho Shinkeigaku. 1997 Apr;37(4):314-8.

本文引用的文献

1
Clinicopathologic and immunophenotypic features of eosinophilic fasciitis and morphea profunda: A comparative study of 27 cases.嗜酸粒细胞性筋膜炎和深部硬皮病的临床病理和免疫表型特征:27 例对比研究。
J Am Acad Dermatol. 2018 Jan;78(1):121-128. doi: 10.1016/j.jaad.2017.06.148. Epub 2017 Aug 31.
2
Acute idiopathic compartment syndrome of the forearm in an adolescent.一名青少年的急性特发性前臂骨筋膜室综合征
West J Emerg Med. 2015 Jan;16(1):158-60. doi: 10.5811/westjem.2014.9.23019. Epub 2014 Nov 11.
3
Eosinophilic myositis: an updated review.嗜酸性粒细胞性肌炎:更新综述。
Autoimmun Rev. 2014 Apr-May;13(4-5):375-8. doi: 10.1016/j.autrev.2014.01.018. Epub 2014 Jan 11.
4
Eosinophilia-associated muscle disorders: an immunohistological study with tissue localisation of major basic protein in distinct clinicopathological forms.嗜酸性粒细胞增多相关肌肉疾病:一项针对主要碱性蛋白在不同临床病理形式中的组织定位的免疫组织学研究。
J Clin Pathol. 2009 May;62(5):442-7. doi: 10.1136/jcp.2008.060616. Epub 2009 Jan 12.
5
Multiple organ involvement in eosinophilic polymyositis: an autopsy report.嗜酸性粒细胞性多肌炎的多器官受累:一份尸检报告。
Hum Pathol. 2006 Feb;37(2):231-5. doi: 10.1016/j.humpath.2005.10.006. Epub 2005 Dec 27.
6
Becker muscular dystrophy presenting as eosinophilic inflammatory myopathy in an infant.贝克尔肌营养不良症在一名婴儿中表现为嗜酸性粒细胞性炎性肌病。
J Child Neurol. 1997 Feb;12(2):146-7. doi: 10.1177/088307389701200214.