Betts C M, Pasquinelli G, Costa A M, Fanti P A, Misciali C, Varotti C
Department of Experimental Pathology, University of Bologna, Italy.
Ultrastruct Pathol. 2001 Nov-Dec;25(6):437-44. doi: 10.1080/019131201753343476.
A case of necrobiotic xanthogranuloma without typical periorbital involvement is described at the ultrastructural level. The patient, a 58-year-old Italian man, presented in 1995 with a brief history of nodulo-papular lesions commencing on the lower limbs, and mild paraproteinemia. During 6 years of follow-up, anemia, neutropenia with marked lymphopenia, and increased ESR were found, while serum cholesterol and triglyceride levels decreased from hyper to hypo values. Systemic diseases, such as diabetes, malignancy, or extracutaneous lesions, often associated with NXG, have not developed. Conventional histology was distinctive for NXG, and immunohistochemistry confirmed that dermal histiocytes were not of Langerhans cell lineage. At ultrastructure, regeneration and degeneration ("regen-degen") features were observed in some individual deep dermal histiocytes, which have not been previously documented in the literature. Identification of giant histiocytes showing 'regen-degen'' aspects might prove to be a useful ultrastructural diagnostic marker for NXG.
本文在超微结构水平描述了一例无典型眶周受累的坏死性黄色肉芽肿病例。患者为一名58岁的意大利男性,于1995年就诊,下肢出现结节性丘疹病变病史较短,伴有轻度副蛋白血症。在6年的随访期间,发现有贫血、中性粒细胞减少伴显著淋巴细胞减少以及血沉加快,而血清胆固醇和甘油三酯水平从高于正常降至低于正常。常与坏死性黄色肉芽肿相关的全身性疾病,如糖尿病、恶性肿瘤或皮肤外病变均未出现。传统组织学表现为坏死性黄色肉芽肿的特征性改变,免疫组化证实真皮组织细胞并非朗格汉斯细胞系。在超微结构上,在一些单个的深部真皮组织细胞中观察到再生和退变(“再退”)特征,这在以往文献中尚未见报道。识别显示“再退”表现的巨大组织细胞可能是坏死性黄色肉芽肿一种有用的超微结构诊断标志物。