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病例报告:一名儿童在轻微创伤后发生前臂非典型急性骨筋膜室综合征,并继发骨髓炎。

Case Report: Atypical acute compartment syndrome of the forearm in a child following minor trauma with consecutive osteomyelitis.

作者信息

Everaert J, Delafontaine A, Juanos Cabanas J, Leclercq G, Jennart H, Baillon B

机构信息

Orthopedics and Traumatology Department, Erasme Hospital, Brussels, Belgium.

Laboratoire D'Anatomie Fonctionnelle, Faculté des Sciences de la Motricité, Université Libre de Bruxelles, Bruxelles, Belgium.

出版信息

Front Surg. 2024 May 15;11:1370558. doi: 10.3389/fsurg.2024.1370558. eCollection 2024.

Abstract

INTRODUCTION

Forearm compartment syndrome (CS) in children is above all a clinical diagnosis whose main cause is traumatic. However, rarer causes such as infection can alter its clinical presentation.

CLINICAL CASE

An 8-year-old boy has been seen in the emergency department complaining of severe forearm pain under a splint in a mild traumatic context. The previous radiological imaging examination three days before had not revealed any fractures. On admission, he presented with major signs of skin inflammation, loss of mobility, paresthesia and a significant biological inflammatory syndrome. The acute CS diagnosis has been made and was treated, but its atypical presentation raised a series of etiological hypotheses, in particular infectious, even if it remains rare. Complementary imaging examinations confirmed the presence of osteomyelitis of the distal radius as well as an occult Salter-Harris II fracture.

DISCUSSION

Beyond the classic "five P's of CS" -pain, paresthesia, paralysis, pallor and pulselessness-, CS's clinical presentations are multiple, especially in pediatric patients. In children, severe pain and increasing analgesic requirement must be indicators of a CS. We hypothesize that this patient sustained a nondisplaced Salter-Harris II fracture with a hematoma colonized by hematogenous osteomyelitis explaining its initial clinical presentation.

CONCLUSION

Hematogenous osteomyelitis complicated by CS is rare and may be accompanied by a traumatic history. It's atypical presentation in pediatric patients requires vigilance and prompt diagnosis given the disastrous and irreversible complications.

摘要

引言

儿童前臂骨筋膜室综合征(CS)首先是一种临床诊断,其主要病因是创伤。然而,感染等较罕见的病因可能会改变其临床表现。

临床病例

一名8岁男孩因轻度创伤后夹板固定下前臂剧痛被送至急诊科。三天前的放射影像学检查未发现任何骨折。入院时,他出现了皮肤炎症、活动受限、感觉异常等主要体征以及明显的生物学炎症综合征。急性CS诊断成立并接受了治疗,但其非典型表现引发了一系列病因假设,尤其是感染性病因,尽管这种情况仍然罕见。补充影像学检查证实存在桡骨远端骨髓炎以及隐匿性Salter-Harris II型骨折。

讨论

除了经典的CS“五P征”(疼痛、感觉异常、麻痹、苍白和无脉)外,CS的临床表现多种多样,尤其是在儿科患者中。在儿童中,严重疼痛和镇痛需求增加必须是CS的指标。我们推测该患者发生了无移位的Salter-Harris II型骨折,伴有血肿,血源性骨髓炎定植于血肿,这解释了其最初的临床表现。

结论

血源性骨髓炎并发CS罕见,可能伴有创伤史。鉴于其灾难性和不可逆的并发症,其在儿科患者中的非典型表现需要警惕并及时诊断。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3365/11133643/2bbf762fefcc/fsurg-11-1370558-g001.jpg

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