Langerhans Cell Histiocytosis of Ocular Region: A Report of Two Cases

Arti Khatri
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Abstract

Langerhans cell histiocytosis (LCH) is a rare monoclonal disorder of dendritic cells originating from bone marrow. We are reporting two cases of isolated involvement of ocular region both of which clinically appeared as soft tissue tumour. A young girl of two and half years presented with swelling of left eyelid. Microscopic examination of biopsy showed collections of round cells which were large having abundant cytoplasm and centrally placed nuclei. Plenty of eosinophils were seen in the background. The final diagnosis of LCH involving eyelid was given after histopathological examination. Second case report is of three-year-old girl presented to ophthalmology outpatient department with the complaints of painless progressive swelling of lateral aspect of left orbital wall for four months which were rapidly increasing in size for the past two months. Fine-needle aspiration (FNA) of both swellings was done and finding was suggestive of LCH. The final diagnosis of LCH was given on histopathological examination of biopsy tissue from both the swellings. Ocular region involvement by Langerhans cell histiocytosis is a very rare presentation.
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眼区朗格汉斯细胞组织细胞增多症2例报告
朗格汉斯细胞组织细胞增生症(LCH)是一种罕见的源自骨髓的树突状细胞单克隆性疾病。我们报告两例孤立受累的眼部区域,这两个临床表现为软组织肿瘤。一个两岁半的小女孩,因左眼睑肿大而就诊。镜下活检显示大量圆形细胞,细胞质丰富,细胞核位于中心。背景可见大量嗜酸性粒细胞。最终诊断为累及眼睑的LCH,需经组织病理学检查。第二例报告是一名三岁女童,以左眶壁外侧无痛性进行性肿胀4个月,近2个月体积迅速增大为主诉就诊于眼科门诊。两处肿胀均行细针穿刺(FNA)检查,提示LCH。LCH的最终诊断是在对两个肿胀的活检组织进行组织病理学检查后得出的。朗格汉斯细胞组织细胞增多症累及眼部是一种非常罕见的表现。
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