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病例报告:4例1型纤溶酶原缺乏症患者经静脉注射人组织型纤溶酶原激活剂替代治疗,呼吸病变成功治愈。

Case Report: Respiratory lesions successfully treated with intravenous plasminogen, human-tvmh, replacement therapy in four patients with plasminogen deficiency type 1.

作者信息

Nakar Charles, McDaniel Heather, Parker Joseph M, Thibaudeau Karen, Thukral Neelam, Shapiro Amy D

机构信息

Indiana Hemophilia & Thrombosis Center, Indianapolis, IN, United States.

Vanderbilt University Medical Center, Nashville, TN, United States.

出版信息

Front Pediatr. 2024 Sep 20;12:1465166. doi: 10.3389/fped.2024.1465166. eCollection 2024.

DOI:10.3389/fped.2024.1465166
PMID:39372655
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11449724/
Abstract

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.

摘要

1型纤溶酶原缺乏症(PLGD-1,低纤溶酶原血症)是一种极为罕见的终身疾病,与多器官系统纤维蛋白性病变的发生有关。根据病变位置,PLGD-1的临床表现可导致急性和/或慢性呼吸道疾病,这可能会损害呼吸功能,导致危及生命的事件。早期识别并有效治疗由纤维蛋白性病变引起的气道阻塞对于预防呼吸功能受损导致的发病至关重要。然而,医生可能不熟悉PLGD-1的临床表现和管理,导致诊断和治疗延迟,并可能导致发病。本文介绍了一例成人和三例儿童PLGD-1严重呼吸并发症患者,通过输注纤溶酶原(人-tvmh替代疗法)成功治疗的病例系列。患者的呼吸道症状得到缓解或显著改善,治疗总体耐受性良好。在所有患者中,初始每1至2天给予纤溶酶原替代疗法,随着症状得到控制或缓解,给药间隔延长,基线纤溶酶原活性大幅增加。所描述的所有四例病例均支持使用纤溶酶原(人-tvmh)替代疗法在解决与PLGD-1相关的危及生命的呼吸并发症方面的临床益处。随着持续治疗,除呼吸道病变外的临床表现也得到改善或缓解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7405/11449724/4683c8805cd0/fped-12-1465166-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7405/11449724/ab7e98f2f0d9/fped-12-1465166-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7405/11449724/7a7abe8b60ed/fped-12-1465166-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7405/11449724/4683c8805cd0/fped-12-1465166-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7405/11449724/ab7e98f2f0d9/fped-12-1465166-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7405/11449724/7a7abe8b60ed/fped-12-1465166-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7405/11449724/4683c8805cd0/fped-12-1465166-g003.jpg

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本文引用的文献

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2
Ligneous conjunctivitis and use of human plasminogen eyedrops: The Italian experience.木质化性结膜炎与人纤溶酶原滴眼液的使用:意大利的经验。
Haemophilia. 2023 Mar;29(2):681-684. doi: 10.1111/hae.14745. Epub 2023 Jan 19.
3
Treatment of Ligneous Conjunctivitis with Plasminogen Eyedrops.用纤溶酶原滴眼液治疗木样结膜炎。
Ophthalmology. 2022 Aug;129(8):955-957. doi: 10.1016/j.ophtha.2022.03.019. Epub 2022 Mar 26.
4
Type 1 Plasminogen Deficiency With Pulmonary Involvement: Novel Treatment and Novel Mutation.1型纤溶酶原缺乏伴肺部受累:新的治疗方法和新的突变
J Pediatr Hematol Oncol. 2021 May 1;43(4):e558-e560. doi: 10.1097/MPH.0000000000001951.
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An international registry of patients with plasminogen deficiency (HISTORY).国际纤维蛋白溶酶原缺乏症患者注册登记(HISTORY)。
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Replacement Therapy with Glu-Plasminogen for the Treatment of Severe Respiratory and Auditory Complications of Congenital Plasminogen Deficiency.
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