Spontaneous resolution and bone regeneration in hemophilic pseudotumor: A rare case report and literature review

Author:

Singh Khushboo1ORCID,Gupta Sunita2,Aggarwal Sunita3

Affiliation:

1. Department of Oral Medicine and Radiology Centre for Dental Education and Research, All India Institute of Medical Sciences Ansari Nagar New Delhi India

2. Department of Oral Medicine and Radiology Maulana Azad Institute of Dental Sciences, MAMC Complex New Delhi India

3. Department of Medicine & In‐charge Hemophilia Day Care Centre Lok Nayak Hospital and Maulana Azad Medical College New Delhi India

Abstract

AbstractAimHemophilic pseudotumor (HP) is a very rare complication of hemophilia seen in only 1–2% of the cases. Although it is much more common in long bones, pelvis and small bones of hands and feet and very rarely involving jaw bones.Method and resultIn the present case, the presence of a rare hemophilic pseudotumor of the mandible with the positive history of Hemophilia B justifies that the history, clinical and radiological examinations were sufficient to arrive at conclusive diagnosis precluding invasive diagnostic procedures such as biopsy hence avoiding the risk of hemorrhage, infection, or fistula. This case also highlights that patient was conservatively managed with Factor IX replacement alone with a very good clinical outcome.ConclusionHP should be considered as a differential diagnosis of any progressive swelling of hard and soft tissues occurring in a patient with severe haemophilia.

Publisher

Wiley

Reference39 articles.

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3