Hand and Foot Subungual Haematomas in Haemophilia: A Report of Six Cases.

IF 3 2区 医学 Q2 HEMATOLOGY
Haemophilia Pub Date : 2025-06-02 DOI:10.1111/hae.70059
Jessica Pearce, Luke Visscher, Natalie Karlovic, Brett Halliday, Jane Mason
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Abstract

Aim: Subungual haematomas are a collection of blood underneath the nail subsequent to trauma. Whilst a commonly recognised injury in the general population, there is limited literature and no guidelines for management in haemophilia patients. This case series aims to provide insight into the clinical characteristics, management and sequelae of subungual haematomas in the haemophilia group.

Methods: A retrospective case series was performed of patients with haemophilia presenting with subungual haematomas between July 2018 and June 2024, and the background literature reviewed. Data were collected from electronic medical records and analysis was purely descriptive given the small cohort included.

Results: Six individual cases were identified with traumatic subungual haematomas. Five patients were male (83.3%), there was an event split between haemophilia A and B cases, with severity ranging from mild to moderate. One patient with mild haemophilia A also had concurrent type 1 von Willebrand disease. Most cases (83.3%) had a 48-72 h delay before hospital presentation. Five cases (83.3%) required either nail trephination or removal. Two moderate haemophilia B patients (33.3%), had recurrent bleeding within the first 2 weeks post injury.

Conclusion: Haemophilia patients presenting with subungual haematomas should be considered for nail trephination or surgical intervention as per standard of care following factor replacement. Larger patient series may provide more insight into comparative outcomes in haemophilia patients versus the general population. Early collaboration between haematology and surgical teams is important. Inclusion of this site-specific bleed into patient education resources and haemophilia guidelines warrants consideration.

血友病致手足掌下血肿6例报告。
目的:甲下血肿是外伤后甲下的血肿。虽然在一般人群中是一种公认的损伤,但对于血友病患者的治疗,文献有限,也没有指导方针。本病例系列旨在提供深入了解血友病组的临床特征,管理和蹄下血肿的后遗症。方法:回顾性分析2018年7月至2024年6月期间以甲下血肿为表现的血友病患者的病例系列,并对背景文献进行复习。数据是从电子病历中收集的,由于纳入的队列较小,分析纯粹是描述性的。结果:外伤性甲下血肿6例。男性5例(83.3%),血友病A型和B型有事件分裂,严重程度从轻度到中度不等。一名轻度A型血友病患者同时患有1型血管性血友病。大多数病例(83.3%)在就诊前延迟48-72小时。5例(83.3%)需要穿甲或拔除。2例中度B型血友病患者(33.3%)在损伤后2周内出现复发性出血。结论:血友病患者表现为甲下血肿,应考虑在因素置换后按照护理标准进行指甲穿刺或手术干预。更大的患者系列可以提供血友病患者与一般人群比较结果的更多见解。血液学和外科团队之间的早期合作很重要。将这种部位特异性出血纳入患者教育资源和血友病指南值得考虑。
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来源期刊
Haemophilia
Haemophilia 医学-血液学
CiteScore
6.50
自引率
28.20%
发文量
226
审稿时长
3-6 weeks
期刊介绍: Haemophilia is an international journal dedicated to the exchange of information regarding the comprehensive care of haemophilia. The Journal contains review articles, original scientific papers and case reports related to haemophilia care, with frequent supplements. Subjects covered include: clotting factor deficiencies, both inherited and acquired: haemophilia A, B, von Willebrand''s disease, deficiencies of factor V, VII, X and XI replacement therapy for clotting factor deficiencies component therapy in the developing world transfusion transmitted disease haemophilia care and paediatrics, orthopaedics, gynaecology and obstetrics nursing laboratory diagnosis carrier detection psycho-social concerns economic issues audit inherited platelet disorders.
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