Anemia of unknown etiology in a young child: Pulmonary hemosiderosis the real culprit

Aleena Naushad, Pramod Ravi
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Abstract

Pulmonary hemosiderosis (PH) is characterized by a triad of iron-deficiency anemia, hemoptysis, and pulmonary infiltrates. We report a case of idiopathic PH diagnosed in a 6-year-old female child who initially presented with anemia of unknown etiology for about 2 years, with all the workups for the etiology of anemia being negative. When she presented to us, she had severe respiratory distress with hemoptysis. Chest X-ray showed diffuse infiltrates. Contrast-enhanced computed tomography showed ground-glass opacity. Bronchoalveolar lavage and lung cryobiopsy were performed, which showed hemosiderin-laden macrophages and confirmed the diagnosis of PH. After exclusion of cardiac, infective, immunological, and glomerular causes, a diagnosis of idiopathic PH was made. The child had recurrent exacerbations of lower respiratory tract infection thereafter, hence started on steroid inhalers. Even after starting inhalers, recurrent episodes continued and hence changed to oral steroids. Now, the frequency of episodes reduced, and the child had good symptom control.
病因不明的儿童贫血:肺含铁血黄素沉着是真正的罪魁祸首
肺含铁血黄素沉着症(PH)的特征是缺铁性贫血、咯血和肺浸润。我们报告一例特发性PH诊断为一名6岁女童,最初表现为不明原因的贫血约2年,所有贫血病因检查均为阴性。当她出现在我们面前时,她有严重的呼吸窘迫和咯血。胸部x线显示弥漫性浸润。增强计算机断层扫描显示磨玻璃样不透明。支气管肺泡灌洗及肺低温活检显示含铁血黄素巨噬细胞,确诊为PH。排除心源性、感染性、免疫性、肾小球性原因后,诊断为特发性PH。此后患儿下呼吸道感染复发加重,开始使用类固醇吸入器。即使在开始使用吸入器后,复发性发作仍在继续,因此改为口服类固醇。现在,发作的频率减少了,孩子的症状得到了很好的控制。
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