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青年女性佩吉特-施罗氏综合征。

Paget-Schroetter Syndrome in a Young Female.

机构信息

Quantum HC, Navicent Health, Macon, GA, USA.

University of Toledo and Promedica Toledo Hospital, Toledo, OH, USA.

出版信息

J Investig Med High Impact Case Rep. 2021 Jan-Dec;9:23247096211003263. doi: 10.1177/23247096211003263.

Abstract

Paget-Schroetter syndrome or effort thrombosis is a relatively rare primary spontaneous thrombosis of upper extremity deep veins secondary to entrapment of axillary subclavian veins from an abnormality of the thoracic outlet. It is commonly seen in young adults who lift heavy weights or strenuous use of the upper extremities during athletic activities. Repetitive microtrauma to the subclavian vein secondary to narrow costoclavicular space and strenuous activities leads to intimal layer inflammation, hypertrophy, fibrosis, and coagulation cascade activation. Management of Paget-Schroetter syndrome differs from the venous thrombosis of the lower extremity as treatment includes anticoagulation, thrombolysis, and surgical decompression. Early recognition and timely management are required to prevent significant disability from post-thrombotic syndrome and long-term morbidity from recurrent thromboembolism and pulmonary embolism. Internists and emergency physicians should be aware of the disease's presentation, treatment options, and early referral to vascular surgeons since prompt initiation of appropriate treatment will have better outcomes than delayed treatment. We discussed a case of a 31-year-old female who lifts heavyweight at work, presented with right arm swelling and pain for 2 weeks, and diagnosed with axillary subclavian vein thrombosis secondary to thoracic outlet obstruction. She received a high-dose heparin drip followed by catheter-directed thrombolysis and underwent surgical decompression of axillary subclavian vein via resection of the first rib, subclavius muscle resection, partial anterior scalenectomy, and venolysis. In our review of the literature, randomized controlled studies lack the efficacy and safety of surgical decompression. However, the results are promising based on accumulated experience from vascular surgery experts and small case series. Extensive studies are needed further to delineate the protocol for the management of Paget-Schroetter syndrome.

摘要

佩吉特-施罗氏病或劳力性血栓形成是一种相对罕见的上肢深静脉原发性自发性血栓形成,继发于腋窝锁骨下静脉在胸廓出口处受压。它常见于举重或在运动活动中剧烈使用上肢的年轻成年人。由于锁骨下静脉狭窄和剧烈活动导致的重复微创伤,会引起内膜层炎症、肥大、纤维化和凝血级联激活。佩吉特-施罗氏病的治疗方法与下肢静脉血栓形成不同,包括抗凝、溶栓和手术减压。需要早期识别和及时治疗,以防止血栓后综合征引起的显著残疾和复发性血栓栓塞和肺栓塞引起的长期发病。内科医生和急诊医生应该了解该病的表现、治疗选择,并及早转介给血管外科医生,因为及时开始适当的治疗将比延迟治疗有更好的结果。我们讨论了一个 31 岁女性的病例,她在工作中举重,出现右臂肿胀和疼痛 2 周,诊断为继发于胸廓出口阻塞的腋-锁骨下静脉血栓形成。她接受了高剂量肝素滴注,随后进行了导管引导下溶栓,并通过切除第一肋骨、锁骨下肌切除术、部分前斜角肌切除术和静脉溶解术进行了腋-锁骨下静脉减压手术。在我们对文献的回顾中,随机对照研究缺乏手术减压的疗效和安全性。然而,基于血管外科专家的积累经验和小病例系列,结果是有希望的。需要进一步进行广泛的研究,以阐明佩吉特-施罗氏病的管理方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/583d/7983469/76733109d800/10.1177_23247096211003263-fig1.jpg

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