Osler-Weber-Rendu综合征或遗传性出血性毛细血管扩张症(HHT)是一种罕见的疾病,报告的病例很少,尤其是在巴基斯坦。作为医护人员,我们在急诊和门诊都会遇到多例复发性鼻出血。然而,患者通常在没有彻底检查的情况下对症治疗。HHT应考虑在复发性鼻出血的差异中,作为临床诊断,可以通过详细的家族史和体格检查。这是一个58岁的男性出现在胃肠病学OPD的案例,联合军事医院,拉合尔,2021年11月,抱怨全身虚弱和大便流血。他有反复发作的鼻出血和毛细血管扩张的病史,进一步的调查显示有类似症状的强烈家族史。他被诊断为奥斯勒-韦伯-伦杜综合症。在撰写手稿之前,已获得患者的知情同意。
Osler-Weber-Rendu syndrome or Hereditary Haemorrhagic Telangiectasia (HHT) is a rare condition, with very few reported cases, especially in Pakistan. As healthcare workers, we encounter multiple cases of recurrent
epistaxis in the emergency as well as outpatient departments. However, patients are usually treated symptomatically without a thorough workup. HHT should be considered among the differentials for recurrent
epistaxis, as a clinical diagnosis can be made with detailed family history and physical examination. Here is the
case of a 58-year-old male who presented to the Gastroenterology OPD, Combined Military Hospital, Lahore, in November 2021, with complaints of generalised weakness and blood in stools. He had a history of recurrent
epistaxis and telangiectasias, and further inquiry revealed a strong family history of similar symptoms. He was diagnosed as a
case of Osler-Weber- Rendu Syndrome. Informed consent was taken from the patient prior to the writing of the manuscript.