Intracranial hemorrhage in an infant leads to the diagnosis and treatment of severe hemophilia B: a case report.

IF 3.2 3区 医学 Q1 PEDIATRICS Italian Journal of Pediatrics Pub Date : 2024-11-28 DOI:10.1186/s13052-024-01819-2
Giuseppe Lassandro, Valentina Palladino, Paola Giordano
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Abstract

Background: Hemophilia B is a rare bleeding disorder in males, characterized by a deficiency in coagulation factor IX (FIX). Replacement of FIX with a recombinant FIX (rFIX) fusion protein, to sustain therapeutic plasma levels, is recommended as both treatment and prophylaxis to prevent bleeding episodes, particularly intracranial hemorrhage (ICH).

Case presentation: This case report outlines the management of ICH in a 7-month-old infant with severe hemophilia B, following an accidental trauma-related event, resulting in a thin compound fracture of the left occiput. FIX levels were extremely low (˂1.0%) and large deletions of the coagulation F9 gene (including exons 1-6) were identified. Intensive treatment with a rFIX fusion protein conjugated to the immunoglobulin Fc fragment (rFIXFc) continued for 18 days before hospital discharge. A continuous regimen of weekly rFIXFc infusions was implemented. Thirty days after initiating rFIXFc therapy, neutralizing antibodies or FIX inhibitors (common in patients with large F9 gene deletions) were observed, causing a diffuse skin rash. Such allergic reactions typically indicate progression to potentially serious nephrotic syndrome. A unique immunotolerance regimen of oral oxatomide and intravenous hydrocortisone was started to proactively prevent allergic reactions in this patient during rFIXFc prophylaxis. Even though low titers of the inhibitor (0.6-1.0 Bethesda units) were observed occasionally during subsequent follow-up, there were no signs of further allergies or development of nephrotic syndrome.

Conclusion: This is an uncommon case in which rFIXFc was continued despite the appearance of an allergic reaction and the development of FIX inhibitors. Subsequent allergic reactions were prevented with a combination of oral oxatomide and intravenous hydrocortisone given prior to prophylactic rFIXFc. Further studies are recommended to determine the usefulness of this combination with rFIX therapy.

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婴儿颅内出血导致严重血友病B的诊断和治疗:一例报告。
背景:B型血友病是一种罕见的男性出血性疾病,以凝血因子IX (FIX)缺乏为特征。建议用重组FIX (rFIX)融合蛋白替代FIX,以维持治疗血浆水平,作为治疗和预防出血发作的方法,特别是颅内出血(ICH)。病例介绍:本病例报告概述了一名7个月大的患有严重血友病B的婴儿在意外创伤相关事件后发生脑出血的处理,导致左枕部薄复合骨折。FIX水平极低(小于1.0%),并且鉴定出凝血F9基因(包括外显子1-6)的大量缺失。在出院前持续使用结合免疫球蛋白Fc片段的rFIX融合蛋白(rFIXFc)进行强化治疗18天。每周连续输注rFIXFc。开始rFIXFc治疗30天后,观察到中和抗体或FIX抑制剂(常见于F9基因大缺失的患者),引起弥漫性皮疹。这种过敏反应通常表明进展到潜在的严重肾病综合征。在rFIXFc预防期间,该患者开始了口服oxatomide和静脉注射氢化可的松的独特免疫耐受方案,以主动预防过敏反应。尽管在随后的随访中偶尔观察到低滴度抑制剂(0.6-1.0 Bethesda单位),但没有进一步过敏或肾病综合征发展的迹象。结论:这是一个罕见的病例,尽管出现了过敏反应和FIX抑制剂的发展,rFIXFc仍在继续。在预防性rFIXFc之前,通过口服oxatomide和静脉注射氢化可的松来预防随后的过敏反应。建议进一步研究以确定这种联合rFIX疗法的有效性。
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来源期刊
CiteScore
6.10
自引率
13.90%
发文量
192
审稿时长
6-12 weeks
期刊介绍: Italian Journal of Pediatrics is an open access peer-reviewed journal that includes all aspects of pediatric medicine. The journal also covers health service and public health research that addresses primary care issues. The journal provides a high-quality forum for pediatricians and other healthcare professionals to report and discuss up-to-the-minute research and expert reviews in the field of pediatric medicine. The journal will continue to develop the range of articles published to enable this invaluable resource to stay at the forefront of the field. Italian Journal of Pediatrics, which commenced in 1975 as Rivista Italiana di Pediatria, provides a high-quality forum for pediatricians and other healthcare professionals to report and discuss up-to-the-minute research and expert reviews in the field of pediatric medicine. The journal will continue to develop the range of articles published to enable this invaluable resource to stay at the forefront of the field.
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