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青少年黄色肉芽肿——细针穿刺细胞学检查的诊断挑战

Juvenile xanthogranuloma-diagnostic challenge on fine-needle aspiration cytology.

作者信息

Bandyopadhyay Arghya, Gangopadhyay Mimi, Chakraborty Subrata

机构信息

Department of Pathology, North Bengal Medical College and Hospital, Darjeeling, India.

出版信息

J Cytol. 2011 Oct;28(4):217-8. doi: 10.4103/0970-9371.86356.

Abstract

Juvenile xanthogranuloma (JXG) is a rare cutaneous lesion with paucity of literature on its cytological features. We report one such case which on fine-needle aspiration cytology yielded a mixed population of foamy histiocytes, multinucleated giant cells and variable admixture of lymphocytes and eosinophils causing diagnostic dilemma with other differentials, especially Langerhans cell histiocytosis. However, clinical correlation followed by histopathology confirmed the diagnosis. Hence, JXG has characteristic and diagnostic cytologic features.

摘要

幼年性黄色肉芽肿(JXG)是一种罕见的皮肤病变,关于其细胞学特征的文献较少。我们报告了这样一例病例,其细针穿刺细胞学检查显示有泡沫状组织细胞、多核巨细胞以及淋巴细胞和嗜酸性粒细胞的不同程度混合,这与其他鉴别诊断,尤其是朗格汉斯细胞组织细胞增多症造成了诊断上的困境。然而,结合临床情况并经组织病理学检查后确诊。因此,JXG具有特征性的诊断性细胞学特征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72b5/3214472/2f0c425361ab/JCytol-28-217-g001.jpg

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