Woszczyna-Mleczko Katarzyna, Kowalik Artur, Harazin-Lechowska Agnieszka, Bobkiewicz Piotr, Marszałek Andrzej, Ryś Janusz
Pol J Pathol. 2016;67(4):415-420. doi: 10.5114/pjp.2016.65877.
We report a case of 40-year-old Caucasian man presented with an asymptomatic nodule localized on his arm. The puzzle histiocytosis composed of juvenile xanthogranuloma and Langerhans cell histiocytosis was diagnosed. The results of immunohistochemical studies confirm the dual character of histological texture of the lesion.
我们报告一例40岁的白种男性病例，其手臂上出现一个无症状结节。经诊断为混合组织细胞增多症，由幼年性黄色肉芽肿和朗格汉斯细胞组织细胞增多症组成。免疫组化研究结果证实了病变组织学结构的双重特征。
