朗格汉斯细胞组织细胞增多症罕见病例

G. Sailabala, D. Kalyani
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引用次数: 0

摘要

朗格汉斯细胞组织细胞增生症(LCH)是一组以单核吞噬系统细胞增生为特征的疾病。本研究发现罕见的朗格汉斯细胞组织细胞增多症(LCH)。其中1例出现骨缺损、突出、双侧颈淋巴肿大。第2例出现面颊肿胀、肝脾肿大、颅骨及面颊肿胀伴突出。两例的细胞学检查均可见特征性朗格汉斯细胞。基于临床、放射学和细胞学特征,诊断为朗格汉斯细胞组织细胞增多症(LCH)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Rare cases of Langerhans cell histiocytosis
Langerhans cell histiocytosis (LCH) is a group of disorders character-ized by proliferation of cells of mononuclear phagocytic system. In this study rare cases of Langerhans cell histiocytosis (LCH) were diagnosed. These patients had bony defects, proptosis, bilateral cervical lymphadenopathy in one case. The second case had cheek swelling, hepatosplenomegaly, skull and cheek swellings along with proptosis. The characteristic Langerhans cells were present on cytology for both cases. Hence these cases were diagnosed in both cases as Langerhans cell histiocytosis (LCH) based on clinical, radiological and cytological features.
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