病例报告:四名 1 型纤溶酶原缺乏症患者通过静脉注射人-tvmh 纤溶酶原替代疗法成功治疗了呼吸系统病变。

IF 2.1 3区 医学 Q2 PEDIATRICS Frontiers in Pediatrics Pub Date : 2024-09-20 eCollection Date: 2024-01-01 DOI:10.3389/fped.2024.1465166
Charles Nakar, Heather McDaniel, Joseph M Parker, Karen Thibaudeau, Neelam Thukral, Amy D Shapiro
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引用次数: 0

摘要

Plasminogen deficiency type 1(PLGD-1,低蛋白血症)是一种超罕见的终身性疾病,与多个器官系统的纤维蛋白病变有关。根据病变部位的不同,PLGD-1 的临床表现可导致急性和/或慢性呼吸道疾病,从而损害呼吸功能,危及生命。及早识别和有效治疗纤维蛋白病变引起的气道阻塞对于防止因呼吸功能受损而导致的发病至关重要。然而,医生可能并不熟悉 PLGD-1 的临床表现和治疗方法,从而延误了诊断和治疗,并可能导致发病。本文介绍了一个病例系列,其中包括一名成人患者和三名儿童患者,他们都患有 PLGD-1 的严重呼吸系统并发症,通过输注纤溶酶原、人-tvmh 替代疗法成功得到了控制。患者的呼吸系统症状得到了缓解或极大改善,治疗的耐受性普遍良好。在所有患者中,纤溶酶原替代疗法的基线纤溶酶原活性都得到了大幅提高,最初每隔一到两天给药一次,随后随着症状得到控制或缓解而延长给药间隔时间。所有这四例病例都证明了使用人纤溶酶原替代治疗对缓解与 PLGD-1 相关的危及生命的呼吸系统并发症有临床益处。除呼吸系统病变外,其他临床表现也在持续治疗后得到改善或缓解。
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Case Report: Respiratory lesions successfully treated with intravenous plasminogen, human-tvmh, replacement therapy in four patients with plasminogen deficiency type 1.

Plasminogen deficiency type 1 (PLGD-1, hypoplasminogenemia) is an ultra-rare, lifelong disease associated with development of fibrinous lesions in multiple organ systems. Depending on lesion location, clinical manifestations of PLGD-1 can result in acute and/or chronic respiratory airway disease which can compromise respiratory function leading to life-threatening events. Early recognition and effective treatment of airway obstruction caused by fibrinous lesions are critical to prevent morbidity due to respiratory compromise. However, physicians may not be familiar with the clinical presentation and management of PLGD-1, causing delays in diagnosis and treatment and potentially contributing to morbidity. Presented here is a case series of one adult and three pediatric patients with severe respiratory complications of PLGD-1 successfully managed by infusions of plasminogen, human-tvmh replacement therapy. Patients' respiratory symptoms were resolved or greatly improved, and treatment was generally well tolerated. In all patients, baseline plasminogen activity was substantially increased with plasminogen replacement therapy administered initially every one to two days followed by extended interval dosing as symptoms were controlled or resolved. All four described cases support the clinical benefit of replacement therapy with plasminogen, human-tvmh in the resolution of life-threatening respiratory complications associated with PLGD-1. Clinical manifestations in addition to respiratory lesions were also improved or resolved with continued treatment.

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来源期刊
Frontiers in Pediatrics
Frontiers in Pediatrics Medicine-Pediatrics, Perinatology and Child Health
CiteScore
3.60
自引率
7.70%
发文量
2132
审稿时长
14 weeks
期刊介绍: Frontiers in Pediatrics (Impact Factor 2.33) publishes rigorously peer-reviewed research broadly across the field, from basic to clinical research that meets ongoing challenges in pediatric patient care and child health. Field Chief Editors Arjan Te Pas at Leiden University and Michael L. Moritz at the Children''s Hospital of Pittsburgh are supported by an outstanding Editorial Board of international experts. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide. Frontiers in Pediatrics also features Research Topics, Frontiers special theme-focused issues managed by Guest Associate Editors, addressing important areas in pediatrics. In this fashion, Frontiers serves as an outlet to publish the broadest aspects of pediatrics in both basic and clinical research, including high-quality reviews, case reports, editorials and commentaries related to all aspects of pediatrics.
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