M Botero-Bermúdez, L Briceño-Rodríguez, T Quiñonez-Yepes, J C Taborda-Aitken
{"title":"[Compartment syndrome: an atypical presentation as a cause of Henoch-Schönlein purpura].","authors":"M Botero-Bermúdez, L Briceño-Rodríguez, T Quiñonez-Yepes, J C Taborda-Aitken","doi":"","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>there are few case reports available that describe compartment syndrome as a complication of Henoch-Schönlein purpura.</p><p><strong>Case report: </strong>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.</p><p><strong>Conclusion: </strong>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.</p>","PeriodicalId":7081,"journal":{"name":"Acta ortopedica mexicana","volume":"36 5","pages":"324-328"},"PeriodicalIF":0.0000,"publicationDate":"2022-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Acta ortopedica mexicana","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
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.