血管性埃勒-丹洛斯综合征和粘性血小板综合征共存:一名年轻的血栓和出血性素质患者的致命组合。

Q3 Medicine
European journal of case reports in internal medicine Pub Date : 2024-11-28 eCollection Date: 2024-01-01 DOI:10.12890/2024_005018
Manuel De Miguel-Escribano, Manuel Garrido-Montes, Pablo Astudillo-Ortega, Roberto Pertusa-Mataix, Andrea Rodríguez-Trigueros, Jorge Corchero-Gijón, Jose-Salvador Garcia-Morillo
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引用次数: 0

摘要

背景:同一患者同时存在高凝性和出血性素质,由于其复杂的治疗,这是一种潜在的致命组合。血管性ehers - danlos综合征(vEDS)和粘性血小板综合征(SPS)因其发病率低而被归类为罕见病。vEDS与血管壁脆弱引起的出血倾向有关,而SPS的特点是不典型的动脉和静脉血栓形成。病例报告:我们报告了一名27岁的女性,吸烟和经常饮用能量饮料,有亚临床甲状腺功能减退、轻度地中海贫血、复发性关节扭伤、高度近视和前二尖瓣脱垂的病史,被诊断为vEDS和SPS i型。患者在短时间内经历了灾难性的进展,表现为多次血栓和出血发作,最终导致致命的结果。结论:本报告记录了首例vEDS和SPS并发病例,强调了这两种罕见疾病同时治疗的复杂性和挑战。这些症状之间的相互作用需要仔细的临床考虑和制定量身定制的管理策略,以减轻相关风险。这强调了内科医生在监督此类病例中的关键作用。需要进一步的研究来探索新的治疗策略,旨在提高这种独特疾病组合患者的生存率和预后。学习要点:血管性ehers - danlos综合征(vEDS)和粘性血小板综合征(SPS)的共存创造了一种独特的临床场景,其中潜在的结缔组织虚弱和血小板高聚集性协同增加了血栓和出血事件的风险,使管理策略复杂化。内科医生必须在vEDS和SPS患者的综合管理中发挥关键作用,促进多学科策略,不仅解决血栓栓塞和出血性并发症的双重风险,而且强调个性化治疗算法和持续监测的重要性,以优化长期结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Coexistence of Vascular Ehlers-Danlos Syndrome and Sticky Platelet Syndrome: A Lethal Combination in A Young Patient with Thrombophilia and Haemorrhagic Diathesis.

Background: The coexistence of hypercoagulability and bleeding diathesis in the same patient represents a potentially lethal combination due to its complex management. Vascular Ehlers-Danlos syndrome (vEDS) and sticky platelet syndrome (SPS) are classified as rare diseases due to their low prevalence. vEDS is associated with bleeding tendencies caused by vascular wall fragility, while SPS is characterized by atypical arterial and venous thrombosis.

Case report: We report a 27-year-old woman, smoker and regular consumer of energy drinks, with a medical history of subclinical hypothyroidism, minor thalassemia, recurrent joint sprains, high myopia, and anterior mitral valve prolapse, who was diagnosed with both vEDS and SPS type I. The patient experienced a catastrophic progression over a short time period, marked by numerous thrombotic and bleeding episodes, ultimately leading to a fatal outcome.

Conclusions: This report documents the first known case of concurrent vEDS and SPS, highlighting the complexity and challenges in the management of these two rare conditions together. The interplay between these syndromes necessitates careful clinical consideration and the development of tailored management strategies to mitigate associated risks. This underscores the crucial role of the internist in overseeing such cases. Further studies are needed to explore new therapeutic strategies aimed at improving survival rates and outcomes for patients with this unique combination of disorders.

Learning points: The coexistence of vascular Ehlers-Danlos syndrome (vEDS) and sticky platelet syndrome (SPS) creates a unique clinical scenario where the underlying connective tissue weakness and platelet hyperaggregability synergistically increase the risk of both thrombotic and haemorrhagic events, complicating management strategies.Internists must assume a pivotal role in the integrated management of patients with vEDS and SPS, facilitating a multidisciplinary strategy that not only addresses the dual risk of thromboembolic and haemorrhagic complications but also emphasizes the importance of personalized treatment algorithms and ongoing surveillance to optimize long-term outcomes.

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来源期刊
CiteScore
2.10
自引率
0.00%
发文量
166
审稿时长
8 weeks
期刊介绍: The European Journal of Case Reports in Internal Medicine is an official journal of the European Federation of Internal Medicine (EFIM), representing 35 national societies from 33 European countries. The Journal''s mission is to promote the best medical practice and innovation in the field of acute and general medicine. It also provides a forum for internal medicine doctors where they can share new approaches with the aim of improving diagnostic and clinical skills in this field. EJCRIM welcomes high-quality case reports describing unusual or complex cases that an internist may encounter in everyday practice. The cases should either demonstrate the appropriateness of a diagnostic/therapeutic approach, describe a new procedure or maneuver, or show unusual manifestations of a disease or unexpected reactions. The Journal only accepts and publishes those case reports whose learning points provide new insight and/or contribute to advancing medical knowledge both in terms of diagnostics and therapeutic approaches. Case reports of medical errors, therefore, are also welcome as long as they provide innovative measures on how to prevent them in the current practice (Instructive Errors). The Journal may also consider brief and reasoned reports on issues relevant to the practice of Internal Medicine, as well as Abstracts submitted to the scientific meetings of acknowledged medical societies.
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