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一例与霍奇金淋巴瘤相关的朗格汉斯细胞组织细胞增多症:细针穿刺细胞学及组织病理学特征

A case of Langerhans' cell histiocytosis associated with Hodgkin's lymphoma: Fine-needle aspiration cytologic and histopathological features.

作者信息

Das Dilip K, Sheikh Zafar A, Alansary Taiba A, Amir Thasneem, Al-Rabiy Fatma N, Junaid Thamradeen A

机构信息

Department of Pathology, Faculty of Medicine, Kuwait University, Safat, Kuwait.

Mubarak Al-Kabeer Hospital, Cytology Unit, Jabriya, Kuwait.

出版信息

Diagn Cytopathol. 2016 Feb;44(2):128-32. doi: 10.1002/dc.23392. Epub 2015 Nov 26.

Abstract

Langerhans cell histiocytosis (LCH) can be associated with a variety of malignant neoplasms, the most common being malignant lymphoma, especially Hodgkin's lymphoma (HL). In this report, we describe the fine needle aspiration (FNA) cytologic features of a case with concurrent LCH and HL in a lymph node. A 20-year-old man presented with an enlarged left upper cervical lymph node. FNA smears from the swelling revealed numerous CD1a+ and S-100+ Langerhans-type cells (LCs) along with many eosinophils, neutrophils, and lymphocytes; there were also large atypical cells with enlarged nuclei having prominent nucleoli. The cytodiagnosis was LCH and the possibility of association with or trans-differentiation into a lymphoma was suggested. The histopathological diagnosis of the excised left cervical lymph node was classical HL-nodular sclerosis type (CHL-NS) with LCH. The lacunar type Reed-Sternberg (RS) cells were positive for CD30 and CD15, and the LCs were positive for CD1a and S-100 protein. PET/CT imaging demonstrated hypermetabolic lymph nodes in neck, abdomen, thorax and pelvis as well as pulmonary nodules and a splenic mass. The patient received 13 courses of chemotherapy and two years later, the enhanced CT revealed regressive course of the disease.

摘要

朗格汉斯细胞组织细胞增多症(LCH)可与多种恶性肿瘤相关,最常见的是恶性淋巴瘤,尤其是霍奇金淋巴瘤(HL)。在本报告中,我们描述了一例淋巴结同时存在LCH和HL的细针穿刺(FNA)细胞学特征。一名20岁男性因左上颈淋巴结肿大就诊。对肿大部位进行FNA涂片检查,发现大量CD1a+和S-100+朗格汉斯型细胞(LCs),以及许多嗜酸性粒细胞、中性粒细胞和淋巴细胞;还存在核增大且核仁突出的大的非典型细胞。细胞诊断为LCH,并提示有与淋巴瘤相关或转分化为淋巴瘤的可能性。切除的左颈淋巴结的组织病理学诊断为伴有LCH的经典HL-结节硬化型(CHL-NS)。陷窝型里德-斯腾伯格(RS)细胞CD30和CD15呈阳性,LCs CD1a和S-100蛋白呈阳性。PET/CT成像显示颈部、腹部、胸部和骨盆的淋巴结代谢增高,以及肺部结节和脾脏肿块。患者接受了13个疗程的化疗,两年后,增强CT显示病情呈消退过程。

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