Acute promyelocytic leukemia complicated by osteofascial compartment syndrome.

IF 0.9 4区 医学 Q2 Medicine
Acta Clinica Belgica Pub Date : 2026-04-01 Epub Date: 2025-12-21 DOI:10.1080/17843286.2025.2606872
Xiaojuan Li, Min Liu, Zhan Su, Xiaojun Zou
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引用次数: 0

Abstract

Background: Osteofascial compartment syndrome (OCS) refers to a series of clinical syndromes caused by acute ischemia and hypoxia of the tissues inside a fascial compartment. OCS secondary to acute leukemia is extremely rare. Coagulopathy is a common phenomenon in acute promyelocytic leukemia (APL), which often leads to various bleeding complications.

Clinical presentation: We report the first case of APL complicated by OCS. The elderly female experienced differentiation syndrome, left forearm OCS, and rhabdomyolysis during the induction treatment. The coagulopathy ultimately resulted in a fatal cerebral hemorrhage.

Conclusion: Compared to the more commonly reported OCS associated with chronic leukemias, OCS secondary to APL is particularly perilous.

急性早幼粒细胞白血病合并骨筋膜室综合征。
背景:骨筋膜间室综合征(OCS)是指由于筋膜间室内组织急性缺血和缺氧引起的一系列临床综合征。急性白血病继发的OCS极为罕见。凝血功能障碍是急性早幼粒细胞白血病(APL)的常见现象,常导致各种出血并发症。临床表现:我们报告第一例APL合并OCS。老年女性在诱导治疗期间出现分化证、左前臂OCS和横纹肌溶解。凝血功能障碍最终导致了致命的脑出血。结论:与更常见的与慢性白血病相关的OCS相比,继发于APL的OCS尤其危险。
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来源期刊
Acta Clinica Belgica
Acta Clinica Belgica 医学-医学:内科
CiteScore
2.90
自引率
0.00%
发文量
44
审稿时长
6-12 weeks
期刊介绍: Acta Clinica Belgica: International Journal of Clinical and Laboratory Medicine primarily publishes papers on clinical medicine, clinical chemistry, pathology and molecular biology, provided they describe results which contribute to our understanding of clinical problems or describe new methods applicable to clinical investigation. Readership includes physicians, pathologists, pharmacists and physicians working in non-academic and academic hospitals, practicing internal medicine and its subspecialties.
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