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与使用低分子量肝素相关的髂腰肌血肿:一例报告。

Iliopsoas hematoma associated with low-molecular-weight heparin use: A case report.

作者信息

Liu Shangxiang, Mei Chengqing, Zou Hui, Chang Xiaoliang, Ye Zhenglong

机构信息

Intensive Care Unit, Nanjing Jiangbei People's Hospital Affiliated to Nantong University, Nanjing, P.R. China.

出版信息

SAGE Open Med Case Rep. 2020 Jun 13;8:2050313X20931680. doi: 10.1177/2050313X20931680. eCollection 2020.

DOI:10.1177/2050313X20931680
PMID:32587696
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7294477/
Abstract

Iliopsoas hematoma is an uncommon clinical entity that may develop in association with anticoagulation states, coagulopathies and hemodialysis, or anticoagulant therapy. Here, we report a case of unilateral iliopsoas hematoma in a 60-year-old man who received low-molecular-weight heparin for anticoagulation due to continuous veno-venous hemofiltration. The patient presented with fever and productive cough for 2 days. He received continuous veno-venous hemofiltration due to rising blood urea nitrogen (22.7 mmol/L; normal references: 3.2-7.1 mmol) and creatinine (1345 µmol/L; normal references: 53-106 µmol/L). Low-molecular-weight heparin (enoxaparin, 3500-5500 Da, 5-10 IU/kg/h) was delivered continuously by pumps for anticoagulation therapy. At day 12 post heparin treatment, the patient complained left back pain. Platelet count (243 × 10/L) was normal, but both activated partial thromboplastin time (67.5 s) and prothrombin time (17.3 s) were prolonged. Abdominal computed tomography scan revealed left iliopsoas swelling with an indistinct border. Low-molecular-weight heparin was discontinued. Anti-Xa was not monitored throughout the treatment. No improvement was seen, and 3 days later, the patient died after his family decided to terminate therapy. This case highlights the needs for careful anticoagulation as well as close monitoring, and particularly the use of anti-Xa to guide the treatment.

摘要

髂腰肌血肿是一种罕见的临床病症,可能与抗凝状态、凝血障碍、血液透析或抗凝治疗有关。在此,我们报告一例60岁男性单侧髂腰肌血肿病例,该患者因持续静静脉血液滤过接受低分子量肝素抗凝治疗。患者出现发热和咳痰2天。由于血尿素氮(22.7 mmol/L;正常参考值:3.2 - 7.1 mmol)和肌酐(1345 μmol/L;正常参考值:53 - 106 μmol/L)升高,他接受了持续静静脉血液滤过。通过泵持续给予低分子量肝素(依诺肝素,3500 - 5500 Da,5 - 10 IU/kg/h)进行抗凝治疗。肝素治疗后第12天,患者诉左侧背痛。血小板计数(243×10/L)正常,但活化部分凝血活酶时间(67.5 s)和凝血酶原时间(17.3 s)均延长。腹部计算机断层扫描显示左侧髂腰肌肿胀,边界不清。停用低分子量肝素。整个治疗过程中未监测抗Xa水平。未见病情改善,3天后,在患者家属决定终止治疗后患者死亡。该病例强调了谨慎抗凝以及密切监测的必要性,特别是使用抗Xa来指导治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/981a/7294477/49ecd2085f1c/10.1177_2050313X20931680-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/981a/7294477/49ecd2085f1c/10.1177_2050313X20931680-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/981a/7294477/49ecd2085f1c/10.1177_2050313X20931680-fig1.jpg

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本文引用的文献

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Deep Vein Thrombosis Complicated by Spontaneous Iliopsoas Hematoma in Patient with Septic Shock.脓毒性休克患者并发深静脉血栓形成伴自发性髂腰肌血肿
Am J Case Rep. 2017 Oct 30;18:1148-1152. doi: 10.12659/ajcr.905628.
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A case report of idiopathic iliopsoas hematoma which occurred soon after transfer to the wheelchair after total hip arthroplasty.全髋关节置换术后转移至轮椅后不久发生特发性髂腰肌血肿的病例报告。
Nagoya J Med Sci. 2017 Feb;79(1):65-73. doi: 10.18999/nagjms.79.1.65.
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Femoral nerve palsy associated with bilateral spontaneous iliopsoas haematomas: a complication of venous thromboembolism therapy.
双侧自发性髂腰肌血肿相关的股神经麻痹:静脉血栓栓塞治疗的一种并发症
Age Ageing. 2016 Jan;45(1):175-6. doi: 10.1093/ageing/afv176.
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Subsequently occurring bilateral iliopsoas hematoma: a case report.随后发生的双侧髂腰肌血肿:一例报告
J Cardiothorac Surg. 2015 Dec 11;10:183. doi: 10.1186/s13019-015-0386-7.
5
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Surg Endosc. 2014 Jan;28(1):265-70. doi: 10.1007/s00464-013-3183-1. Epub 2013 Sep 6.
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Complete paralysis of the quadriceps secondary to post-traumatic iliopsoas hematoma: a systematic review.创伤后髂腰肌血肿继发股四头肌完全麻痹:一项系统评价
Eur J Orthop Surg Traumatol. 2015 Jan;25(1):39-43. doi: 10.1007/s00590-013-1305-z. Epub 2013 Sep 1.
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Iliopsoas muscle hematoma secondary to alcoholic liver cirrhosis.酒精性肝硬化继发髂腰肌血肿
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