Heiner Syndrome Mimicking Pneumonia with Iron Deficiency Anemia

Priyabrata Panda, Anil Kumar Sapare, R. Aggarwal
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Abstract

Heiner Syndrome is an unusual form of pulmonary hemosiderosis mostly caused by cow milk. It presents as iron deficiency anemia,and hypoproteinemia. This clinical case describes a female infant with failure to thrive presenting with cough, low grade fever , fastbreathing with refusal to feed. On examination severe anemia with congestive cardiac failure was found, the cause of which wa sevaluated. Chest X ray showed bilateral fluffy infiltrates mimicking pneumonia. Investigations revealed microcytic hypochromicanemia with normal corrected reticulocyte count. Iron deficiency anemia (IDA) was diagnosed. However, the etiology of bilater alfluffy lung infiltrates could not be established in this child. Hence Broncho Alveolar Lavage (BAL) for hemosiderin ladenmacrophages and immunoglobulin for cow milk precipitin was done to establish the diagnosis.
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模拟肺炎伴缺铁性贫血的海纳综合征
海纳综合征(Heiner Syndrome)是一种不寻常的肺血细胞增多症,主要由牛奶引起。它表现为缺铁性贫血和低蛋白血症。本临床病例描述了一名发育不良的女婴,表现为咳嗽、低烧、呼吸急促和拒绝进食。检查时发现婴儿严重贫血,并伴有充血性心力衰竭,需要对病因进行评估。胸部 X 光片显示双侧绒毛状浸润,疑似肺炎。检查发现小红细胞低色素血症,校正网织红细胞计数正常。诊断结果为缺铁性贫血(IDA)。然而,该患儿肺部双侧白细胞浸润的病因无法确定。因此,对该患儿进行了支气管肺泡灌洗液(BAL)检查,以检测含血色素的巨噬细胞和牛乳沉淀蛋白的免疫球蛋白,从而确定诊断。
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