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朗格汉斯细胞组织细胞增多症中的心包积液:一例报告

Pericardial Effusion in Langerhans Cell Histiocytosis: A Case Report.

作者信息

Gholami Narges

机构信息

Assistant Professor of Pediatrics, Loghman Hakim Hospital, Shahid Beheshti University of Medical Sciences, Tehran, IR Iran.

出版信息

Iran Red Crescent Med J. 2016 May 10;18(6):e25604. doi: 10.5812/ircmj.25604. eCollection 2016 Jun.

Abstract

INTRODUCTION

Langerhans cell histiocytosis (LCH) is a proliferative disorder of histiocytes in multiple organs. Langerhans cell histiocytosis involves bones, skin, lung and other organs.

CASE PRESENTATION

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.

CONCLUSIONS

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.

摘要

引言

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。

病例介绍

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。

结论

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b969/5004507/213ce6580f8b/ircmj-18-06-25604-g001.jpg

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