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[骨筋膜室综合征:作为过敏性紫癜病因的一种非典型表现]

[Compartment syndrome: an atypical presentation as a cause of Henoch-Schönlein purpura].

作者信息

Botero-Bermúdez M, Briceño-Rodríguez L, Quiñonez-Yepes T, Taborda-Aitken J C

机构信息

Facultad de Medicina, Pontificia Universidad Javeriana. Bogotá, Colombia.

Departamento de Ortopedia y Traumatología, Hospital Universitario San Ignacio. Bogotá, Colombia.

出版信息

Acta Ortop Mex. 2022 Sep-Oct;36(5):324-328.

PMID:37402500
Abstract

INTRODUCTION

there are few case reports available that describe compartment syndrome as a complication of Henoch-Schönlein purpura.

CASE REPORT

we report the case of a 17-year-old patient with bilateral compartment syndrome of the foot as an atypical presentation of Henoch-Schönlein purpura. A case like this has not been reported before.

CONCLUSION

although the patient had an extremely rare clinical presentation, the viability and functionality of the limbs was preserved even after six months of follow-up thanks to an early diagnosis and surgical treatment.

摘要

引言

关于将骨筋膜室综合征描述为过敏性紫癜并发症的病例报告很少。

病例报告

我们报告一例17岁患者,其足部双侧骨筋膜室综合征为过敏性紫癜的非典型表现。此前尚未报道过这样的病例。

结论

尽管该患者临床表现极为罕见,但由于早期诊断和手术治疗,即使在随访六个月后,肢体的生存能力和功能仍得以保留。

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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
J Am Coll Emerg Physicians Open. 2024 Aug 5;5(4):e13270. doi: 10.1002/emp2.13270. eCollection 2024 Aug.