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鼻型NK/T细胞淋巴瘤的结内表现。两例细针穿刺细胞学检查结果报告。

Nodal presentation of nasal-type NK/T-cell lymphoma. Report of two cases with fine needle aspiration cytology findings.

作者信息

Ng Wai-Kuen, Lee Chris Y, Li Albert S, Cheung Leslie K

机构信息

Department of Pathology, Pamela Youde Nethersole Eastern Hospital, 3 Lok Man Road, Chai Wan, Hong Kong SAR, China.

出版信息

Acta Cytol. 2003 Nov-Dec;47(6):1063-8. doi: 10.1159/000326648.

Abstract

BACKGROUND

Epstein-Barr virus (EBV)-associated NK/T-cell lymphoma typically occurs in extranodal sites, such as nasal cavity, nasopharynx, gastrointestinal tract, skin, testis and salivary gland. Secondary lymph node involvement is rarely encountered until late in the disease course. The fine needle aspiration cytology of NK/T-cell lymphoma with a nodal presentation has not been described before.

CASES

Two cases of nasal-type (extranasal) NK/T-cell lymphoma with a nodal presentation were seen at Pamela Youde Nethersole Eastern Hospital, Hong Kong. Both patients presented with submandibular lymph node enlargement but unremarkable peripheral blood and bone marrow findings. Fine needle aspiration cytology was available in both cases, showing a heterogeneous population of small to medium-sized lymphoid cells, follicular center cells, plasma cells, eosinophils and some histiocytes. The medium-sized lymphoid cells showed readily discernible nuclear atypia with an irregular nuclear outline. Cell block sections revealed occasional lymphoid cells with pleomorphic nuclei. Immunocytochemical study confirmed the presence of CD56-positive lymphoma cells. In situ hybridization for EBV-encoded RNA also revealed positive nuclear signals. Histologic examination of the surgical biopsies showed interfollicular expansion by malignant lymphoid cells. Immunoglobulin heavy chain gene and T-cell receptor gene rearrangement studies demonstrated a germline pattern, confirming the putative NK (natural killer cell), non-B and non-T lineage of the lymphoma cells.

CONCLUSION

Nodal presentation of NK/T-cell lymphoma, though rare, is diagnosable on the basis of fine needle aspiration biopsy alone, especially in view of its distinctive immunophenotype and EBV association. Recognition of the subtle but definite cytologic atypia of malignant lymphoid cells and presence of an appropriate background (including more eosinophils than usual), together with proper application of ancillary techniques, is crucial to arriving at a correct diagnosis.

摘要

背景

爱泼斯坦-巴尔病毒(EBV)相关的NK/T细胞淋巴瘤通常发生于结外部位,如鼻腔、鼻咽、胃肠道、皮肤、睾丸和唾液腺。疾病晚期才很少出现继发性淋巴结受累。此前尚未有关于结节型NK/T细胞淋巴瘤细针穿刺细胞学的描述。

病例

香港东区尤德夫人那打素医院收治了2例结节型鼻型(鼻外)NK/T细胞淋巴瘤患者。2例患者均表现为下颌下淋巴结肿大,但外周血和骨髓检查无异常。2例均进行了细针穿刺细胞学检查,显示为小至中等大小淋巴细胞、滤泡中心细胞、浆细胞、嗜酸性粒细胞和一些组织细胞组成的异质性细胞群。中等大小淋巴细胞显示出易于辨认的核异型性,核轮廓不规则。细胞块切片显示偶尔有核多形性的淋巴细胞。免疫细胞化学研究证实存在CD56阳性淋巴瘤细胞。EBV编码RNA的原位杂交也显示核阳性信号。手术活检的组织学检查显示恶性淋巴细胞在滤泡间浸润。免疫球蛋白重链基因和T细胞受体基因重排研究显示为胚系模式,证实淋巴瘤细胞为假定的NK(自然杀伤细胞)、非B和非T细胞系。

结论

NK/T细胞淋巴瘤的结节型表现虽罕见,但仅凭细针穿刺活检即可诊断,尤其是考虑到其独特的免疫表型和与EBV的关联。识别恶性淋巴细胞细微但明确的细胞学异型性以及存在适当背景(包括比通常更多的嗜酸性粒细胞),并正确应用辅助技术,对于做出正确诊断至关重要。

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