Gholami Narges
Assistant Professor of Pediatrics, Loghman Hakim Hospital, Shahid Beheshti University of Medical Sciences, Tehran, IR Iran.
Iran Red Crescent Med J. 2016 May 10;18(6):e25604. doi: 10.5812/ircmj.25604. eCollection 2016 Jun.
Langerhans cell histiocytosis (LCH) is a proliferative disorder of histiocytes in multiple organs. Langerhans cell histiocytosis involves bones, skin, lung and other organs.
This study describes a seven-month-old Iranian girl who presented with skin rash and cervical lymphadenopathy. Langerhans cell histiocytosis was suspected when it was associated with anemia, splenomegaly and lytic bone lesions. A skin biopsy confirmed the diagnosis of Langerhans cell histiocytosis. During hospitalization, the patient looked ill with respiratory distress. A chest X-ray showed a ground glass view, and echocardiography showed moderate pericardial effusion.
Pericardial effusion was a rare finding in this case of Langerhans cell histiocytosis. Pericardial effusion in Langerhans cell histiocytosis, which is an unusual presentation, should be considered when the patient experiences respiratory distress.
朗格汉斯细胞组织细胞增多症(LCH)是一种多器官组织细胞的增殖性疾病。朗格汉斯细胞组织细胞增多症累及骨骼、皮肤、肺及其他器官。
本研究描述了一名7个月大的伊朗女孩,她出现皮疹和颈部淋巴结病。当伴有贫血、脾肿大和溶骨性骨病变时,怀疑为朗格汉斯细胞组织细胞增多症。皮肤活检确诊为朗格汉斯细胞组织细胞增多症。住院期间,患者病情危重,伴有呼吸窘迫。胸部X线显示磨玻璃影,超声心动图显示中度心包积液。
心包积液在该例朗格汉斯细胞组织细胞增多症中是一个罕见的发现。当患者出现呼吸窘迫时,应考虑朗格汉斯细胞组织细胞增多症中不常见的心包积液表现。