首页> 美国卫生研究院文献>BMJ Case Reports >Rare disease: A female soccer player with recurrent haemoptysis and iron deficiency anaemia: idiopathic pulmonary haemosiderosis (IPH)—case report and literature review
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Rare disease: A female soccer player with recurrent haemoptysis and iron deficiency anaemia: idiopathic pulmonary haemosiderosis (IPH)—case report and literature review

机译:罕见疾病:一名患有复发性验血和缺铁性贫血的女足球运动员:特发性肺血铁质病(IPH)—病例报告和文献复习

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摘要

A 19-year-old woman presented with repeated episodes of haemoptysis and shortness of breath. Blood tests revealed iron deficiency anaemia and chest imaging studies showed bilateral lung opacities. In further laboratory tests and technical examination including bronchoalveolar lavage and transbronchial lung biopsy, pulmonary embolism, cardiac disease, and pulmonary vasculitis due to autoimmune disease were ruled out. Finally, a diagnosis of idiopathic pulmonary haemosiderosis (IPH) was made in January 2008. The patient was treated with prednisone, azathioprine, and oral iron supplementation. Subsequently, the patient’s condition and haemoglobin value improved notably. In May 2009, the patient was in full disease remission including a normal blood count and normal iron parameters. IPH is a rare cause of diffuse alveolar haemorrhage of unknown origin. It occurs most frequently in children and adolescents and typically presents with recurrent haemoptysis due to alveolar bleeding. However, pulmonary signs and symptoms often are obscure in children. In these cases iron deficiency anaemia is the prominent clinical finding. The purpose of this case report is to increase awareness of IPH as a possible cause of recurrent haemoptysis and anaemia.
机译:一名19岁的女性反复出现咯血和呼吸急促。验血显示缺铁性贫血,胸部影像学检查显示双侧肺部混浊。在进一步的实验室检查和技术检查中,排除了支气管肺泡灌洗和经支气管肺活检,肺栓塞,心脏病和自身免疫性疾病引起的肺血管炎。最后,于2008年1月诊断为特发性肺血铁质病(IPH)。该患者接受了泼尼松,硫唑嘌呤和口服铁的补充治疗。随后,患者的病情和血红蛋白值明显改善。在2009年5月,患者的疾病完全缓解,包括血液计数正常和铁参数正常。 IPH是原因不明的弥漫性肺泡出血的罕见原因。它在儿童和青少年中最常见,由于肺泡出血通常会出现复发性咯血。但是,儿童的肺部体征和症状通常不明显。在这些情况下,缺铁性贫血是主要的临床发现。该病例报告的目的是提高人们对IPH的认识,因为IPH是反复出现的验血和贫血的可能原因。

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