Levine Pascale Hummel, Zamuco Ronaldo, Yee Herman T
New York University School of Medicine, New York, New York, USA.
Diagn Cytopathol. 2004 May;30(5):332-40. doi: 10.1002/dc.20070.
Lymphomas of the breast are rare and may mimic carcinoma clinically. We investigated the ability of fine-needle aspiration (FNA) biopsy combined with adjunctive flow cytometry (FC), immunofluorescence microscopy (IFM), and immunocytochemistry (ICH) to diagnose and eventually subclassify lymphomas of the breast according to the Revised European American Lymphoma/World Health Organization classification. We retrieved 21 breast aspirates from 19 patients with a cytologic diagnosis of lymphoma or plasmacytoma over a 10-year period (1992-2002), excluding 98 benign intramammary lymph nodes and 1 atypical lymphohistiocytic proliferation (Rosai Dorfman disease). FC was performed in 15/21 aspirates, IFM in 1/21, ICH in 3/21. Histologic follow-up (HF) was obtained for 10 patients, most of them with primary lymphoma. For the remaining nine patients without HF, flow cytometric analysis, comparative morphology, or remission after chemotherapy regimens supported the cytologic diagnosis. Of 19 patients, 11 patients had a secondary lymphoma (SL) and 8 patients had a primary lymphoma (PL). FNA and FC/IFM/ICH classified 7/8 PLs as B-cell lymphomas and 1/8 PLs as plasmacytoma. However, FNA could only subclassify 3 of 8 PLs. FNA and/or FC subclassified accurately 10/11 SLs. All cases were accurately immunophenotyped as B-, T-cell non-Hodgkin's lymphomas or plasmacytoma. World Health Organization classification was achieved in 3/8 PLs (42%) and 10/11 SLs (91%; P = 0.04). Subclassification (which has an impact on long-term management and prognosis) was significantly better in SL, when a previous histologic diagnosis had already been made, when compared to PL, of which 5/8 cases (62.5%) could not be accurately classified.
乳腺淋巴瘤较为罕见,临床上可能会与癌相混淆。我们研究了细针穿刺(FNA)活检联合辅助流式细胞术(FC)、免疫荧光显微镜检查(IFM)和免疫细胞化学(ICH),根据修订后的欧美淋巴瘤/世界卫生组织分类法诊断并最终对乳腺淋巴瘤进行亚分类的能力。我们在10年期间(1992 - 2002年)从19例经细胞学诊断为淋巴瘤或浆细胞瘤的患者中获取了21份乳腺穿刺样本,排除了98个良性乳腺内淋巴结和1例非典型淋巴组织细胞增生(罗萨伊 - 多夫曼病)。21份样本中15份进行了FC检查,1份进行了IFM检查,3份进行了ICH检查。对10例患者进行了组织学随访(HF),其中大多数为原发性淋巴瘤患者。对于其余9例未进行HF的患者,流式细胞术分析、比较形态学或化疗方案后的缓解情况支持了细胞学诊断。19例患者中,11例为继发性淋巴瘤(SL),8例为原发性淋巴瘤(PL)。FNA和FC/IFM/ICH将8例PL中的7例分类为B细胞淋巴瘤,1例分类为浆细胞瘤。然而,FNA仅能对8例PL中的3例进行亚分类。FNA和/或FC准确地对11例SL中的10例进行了亚分类。所有病例均准确地进行了免疫表型分析,诊断为B细胞、T细胞非霍奇金淋巴瘤或浆细胞瘤。8例PL中的3例(42%)和11例SL中的10例(91%)实现了世界卫生组织分类(P = 0.04)。与PL相比,在SL中,当先前已经做出组织学诊断时,亚分类(这对长期管理和预后有影响)明显更好,PL中有5/8例(62.5%)无法准确分类。