Loo C K, Greenberg M L
Department of Cytology, Westmead Hospital, NSW, Australia.
Diagn Cytopathol. 1994;10(2):162-4. doi: 10.1002/dc.2840100214.
Necrotizing lymphadenitis dominated by individual cell necrosis with tingible body macrophages and karyorrhectic nuclear debris is an unusual appearance in smears from fine-needle biopsies (FNB) of lymph nodes (Greenberg et al., Diagn Cytopathol 1993; 9:443-447). These features together with a polymorphous population of lymphocytes, absent epithelioid histiocytes and neutrophils, suggest a possible diagnosis of either histiocytic necrotizing lymphadenitis (HNL) (syn. Kikuchi's Disease) or systemic lupus erythematosus (SLE). These were the cytologic features found in a FNB of a cervical lymph node in a 43-year-old female, treated for a mixed connective tissue disease. A presumptive diagnosis of an acute lupus lymphadenitis was made, based on the above features, and was subsequently confirmed by the presence of raised antinuclear antibodies as well as resolution of the lymphadenopathy on high dose steroids.
以单个细胞坏死为主,伴有吞噬含铁血黄素巨噬细胞和核溶解核碎片的坏死性淋巴结炎,在淋巴结细针穿刺活检(FNB)涂片中是一种不寻常的表现(格林伯格等人,《诊断细胞病理学》1993年;9:443 - 447)。这些特征,连同多形性淋巴细胞群、缺乏上皮样组织细胞和中性粒细胞,提示可能诊断为组织细胞坏死性淋巴结炎(HNL)(同义词:菊池病)或系统性红斑狼疮(SLE)。这些是在一名43岁患有混合性结缔组织病的女性颈部淋巴结FNB中发现的细胞学特征。基于上述特征作出了急性狼疮性淋巴结炎的初步诊断,随后通过抗核抗体升高以及高剂量类固醇治疗后淋巴结病消退得到证实。