Lee J S, Lee M C, Park C S, Juhng S W
Department of Pathology, Chonnam University Medical School, Kwangju, Seoul, Korea.
Acta Cytol. 1997 Nov-Dec;41(6):1793-6. doi: 10.1159/000333188.
Lymph node involvement in Langerhans cell (LC) histiocytosis (LCH) can be seen as a component of the systemic form, or it may be the initial and sometimes exclusive manifestation of the disease. Descriptions of patients with LCH whose disease is confined to lymph nodes are rare.
We present a case of LCH confined to lymph nodes initially diagnosed by fine needle aspiration (FNA) cytology in a 43-year-old male. The cytologic findings in LCH included high cellularity, isolated LCs with prominent nuclear indentations and grooves, multinucleate giant cells, eosinophils and lymphocytes. Confirmation of LCH was obtained by positive S-100 protein immunohistochemical staining and the demonstration of Birbeck granules on electron microscopy.
The presence of LCs with prominent nuclear indentations and grooves is characteristic of LCH confined to lymph nodes and serves as a key point in suggesting the diagnosis of LCH.
朗格汉斯细胞(LC)组织细胞增多症(LCH)中的淋巴结受累可被视为系统性形式的一个组成部分,或者它可能是该疾病的初始表现,有时甚至是唯一表现。关于疾病局限于淋巴结的LCH患者的描述很少见。
我们报告一例LCH局限于淋巴结的病例,该病例最初由细针穿刺(FNA)细胞学在一名43岁男性中诊断出来。LCH的细胞学表现包括细胞密度高、孤立的LC伴有明显的核凹陷和沟、多核巨细胞、嗜酸性粒细胞和淋巴细胞。通过S-100蛋白免疫组化染色阳性以及电子显微镜下显示Birbeck颗粒确诊为LCH。
存在伴有明显核凹陷和沟的LC是局限于淋巴结的LCH的特征,也是提示LCH诊断的关键点。