Faculty of Medicine, Department of Pathology, Kuwait University, Safat, Kuwait.
Cytology Unit, Mubarak Al-Kabeer Hospital, Jabriya, Kuwait.
Diagn Cytopathol. 2020 Nov;48(11):1115-1120. doi: 10.1002/dc.24477. Epub 2020 Jun 3.
Anaplastic large cell lymphoma (ALCL) is a non-Hodgkin lymphoma of T-cell or null-cell lineage with variable cytomorphology. We report two rare ALCL cases with carcinomatous and sarcomatous patterns, respectively, in fine needle aspiration (FNA) cytology and histopathology. The first case was a 56-year-old man with enlarged left inguinal lymph node. FNA smears showed a malignant small round cell tumor with nuclear molding. In addition, there were large bi-nucleated and multinucleated cells with wreath-like arrangement of nuclei. ALCL and small cell (neuroendocrine) carcinoma were the possibilities considered. Immunocytochemical studies on FNA smears showed positive reaction for leukocyte common antigen (LCA) and negative results for cytokeratin (CK) and chromogranin. Histopathological examination of the lymph node showed features of ALCL with following immunohistochemical staining results: LCA+, CD30+, CD45RO+, CD20-, CD3+ (weak), and Alk1-. During review of sections, areas resembling a small cell anaplastic carcinoma were observed. The second case was a 24-year-old woman with right cervical lymphadenopathy. FNA smears showed an ALCL with highly atypical large cells including bi-nucleated and donut shaped cells, which were positive for CD30, EMA, and Alk-1 protein, and negative for CD20, CD3, and CK. Histopathological examination corroborated the cytodiagnosis of ALCL, and with positive immunohistochemical staining for CD30, EMA, Alk-1 protein+, BCL6+, and Ki67+ (40% cells) and negative results for CD20, CD10, CD3, CD5, CD15, BCl2, CD79a, and CD68. Sarcomatous components were noticed during review of cytologic and histopathological specimen. Awareness about these unusual cytomorphological patterns in ALCL may be of help in proper diagnosis of this neoplasm.
间变大细胞淋巴瘤(ALCL)是一种 T 细胞或无细胞谱系的非霍奇金淋巴瘤,具有不同的细胞形态学特征。我们报告了两例罕见的 ALCL 病例,它们分别在细针抽吸(FNA)细胞学和组织病理学中具有癌性和肉瘤性模式。
第一个病例是一名 56 岁男性,左侧腹股沟淋巴结肿大。FNA 涂片显示恶性小圆细胞肿瘤,核有塑形。此外,还有大的双核和多核细胞,具有轮状排列的核。考虑的可能性包括 ALCL 和小细胞(神经内分泌)癌。FNA 涂片的免疫细胞化学研究显示白细胞共同抗原(LCA)阳性反应,细胞角蛋白(CK)和嗜铬粒蛋白阴性。淋巴结的组织病理学检查显示具有以下免疫组织化学染色结果的 ALCL 特征:LCA+,CD30+,CD45RO+,CD20-,CD3+(弱阳性)和 Alk1-。在复习切片时,观察到类似于小细胞间变大细胞癌的区域。
第二个病例是一名 24 岁女性,右侧颈部淋巴结病。FNA 涂片显示 ALCL,具有高度非典型的大细胞,包括双核和环形细胞,这些细胞对 CD30、EMA 和 Alk-1 蛋白阳性,对 CD20、CD3 和 CK 阴性。组织病理学检查证实了 ALCL 的细胞学诊断,并对 CD30、EMA、Alk-1 蛋白+、BCL6+和 Ki67+(40%细胞)呈阳性免疫组织化学染色,对 CD20、CD10、CD3、CD5、CD15、BCL2、CD79a 和 CD68 呈阴性。在细胞学和组织病理学标本的复习中注意到肉瘤成分。了解 ALCL 中这些不寻常的细胞形态模式可能有助于正确诊断这种肿瘤。