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一名乙型血友病患者的下颌骨血友病性假肿瘤

Hemophilic pseudotumor of the mandible in a patient with hemophilia B.

作者信息

Chattopadhyay Probodh K, Nagori Shakil Ahmed, Menon Rahul P, Balasundaram T

机构信息

Department of Oral and Maxillofacial Surgery, Army Dental Centre (Research and Referral), Delhi Cantt-10, New Delhi, India.

出版信息

Oral Maxillofac Surg. 2017 Dec;21(4):467-469. doi: 10.1007/s10006-017-0647-9. Epub 2017 Aug 30.

Abstract

INTRODUCTION

Hemophilic pseudotumor is a rare complication occurring in patients with hemophilia, frequently seen in the femur, tibia, pelvic bones, iliac bones, or rarely in the maxillofacial region.

CASE REPORT

A 7-year-old male reported with a spontaneous extra-oral swelling that was managed with pre-operative transfusion of factor IX along with curettage of the lesion. Our report presents only the fourth case in literature wherein this tumor presented in a patient with hemophilia B.

FINDING

Hemophilic pseudotumor is a rare entity in the maxillofacial region. High degree of suspicion is required for diagnosis, and close coordination between the medical and surgical teams aids in management.

摘要

引言

血友病性假肿瘤是血友病患者中罕见的并发症,常见于股骨、胫骨、骨盆骨、髂骨,很少见于颌面区域。

病例报告

一名7岁男性因自发的口外肿胀前来就诊,术前通过输注IX因子并刮除病变进行治疗。我们的报告是文献中第四例血友病B患者出现这种肿瘤的病例。

发现

血友病性假肿瘤在颌面区域是一种罕见的疾病。诊断需要高度怀疑,医疗团队和外科团队之间的密切协作有助于治疗。

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