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以口腔底部肿胀为表现的获得性因子 VIII 缺乏症。

Acquired factor VIII deficiency presenting as a floor of the mouth swelling.

作者信息

Al-Hilou Ahmed, Reid Johnny, Kelly Richard, Ong T K

机构信息

Department of Oral and Maxillofacial Surgery, Leeds General Infirmary, Leeds, UK.

出版信息

BMJ Case Rep. 2011 Aug 4;2011:bcr0520114235. doi: 10.1136/bcr.05.2011.4235.

Abstract

The authors report the case of a patient with previously undiagnosed acquired haemophilia A who presented to the accident and emergency department with a swollen tongue and difficulty in swallowing. There were no signs of trauma or obvious dental infection. She was admitted onto a high dependency unit for observation. Over the course of the day, the floor of her mouth and neck became increasingly swollen to the extent that she developed breathing difficulties. She was transferred to an intensive care unit, where she was intubated to protect her airway from further compromise. Acquired factor VIII deficiency was diagnosed and appropriate treatment commenced. Despite intervention, her respiratory and cardiovascular functions deteriorated. Following discussions between the medical specialities involved in her care and her family, the decision was made to withdraw support. The patient passed away 96 h after admission.

摘要

作者报告了一例既往未诊断出的获得性血友病A患者的病例,该患者因舌头肿胀和吞咽困难就诊于急诊室。没有创伤迹象或明显的牙齿感染。她被收治到高依赖病房进行观察。在一天当中,她的口腔底部和颈部肿胀越来越严重,以至于出现了呼吸困难。她被转至重症监护病房,在那里进行了插管以保护气道免受进一步损害。诊断出获得性因子VIII缺乏症并开始进行适当治疗。尽管进行了干预,她的呼吸和心血管功能仍恶化。在参与其治疗的医学专科与她的家人进行讨论后,决定停止支持治疗。患者在入院96小时后去世。

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