Role of flow cytometric immunophenotyping in the diagnosis of breast implant-associated anaplastic large cell lymphoma: A 6-year, single-institution experience
Alexander Chan, Romany Auclair, Qi Gao, Paola Ghione, Steven Horwitz, Ahmet Dogan, Mikhail Roshal, Oscar Lin
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引用次数: 0
Abstract
Breast implant-associated anaplastic large cell lymphoma (BIA-ALCL) is an uncommon mature T-cell neoplasm occurring in patients with textured breast implants, typically after 7–10 years of exposure. Although cytopathologic or histopathologic assessment is considered the gold standard diagnostic method for BIA-ALCL, flow cytometry (FC)-based immunophenotyping is recommended as an adjunct test. However, the diagnostic efficacy of FC is not well reported. We reviewed 290 FC tests from breast implant pericapsular fluid and capsule tissue from 182 patients, including 16 patients with BIA-ALCL over a 6-year period, calculating diagnostic rates and test efficacy. FC showed an overall sensitivity of 75.9%, specificity of 100%, and negative and positive predictive values of 95.4% and 100%, respectively. Blinded expert review of false-negative cases identified diagnostic pitfalls, improving sensitivity to 96.6%. Fluid samples had better rates of adequate samples for FC testing compared with tissue samples. Paired with FC testing of operating room (OR)-acquired fluid samples, capsulectomy FC specimens added no diagnostic value in patients with concurrent fluid samples; no cases had positive capsule FC with negative fluid FC. Fluid samples are adequate for FC testing more often than tissue. Capsule tissue FC specimens do not improve FC efficacy when paired with OR-acquired fluid FC samples and are often inadequate samples. FC is 100% specific for BIA-ALCL and can serve as a confirmatory test but should not be the sole diagnostic method. Awareness of sample-specific diagnostic pitfalls greatly improves the sensitivity of BIA-ALCL testing by FC.
乳房植入物相关性无性大细胞淋巴瘤(BIA-ALCL)是一种不常见的成熟T细胞肿瘤,多发于有纹理的乳房植入物患者,通常在植入物暴露7-10年后发病。虽然细胞病理学或组织病理学评估被认为是 BIA-ALCL 的金标准诊断方法,但建议将基于流式细胞术(FC)的免疫分型作为辅助检查。然而,有关 FC 诊断效果的报道并不多。我们对 182 名患者(包括 16 名 BIA-ALCL 患者)的乳房植入物包囊液和包囊组织进行了 290 次 FC 检测,计算诊断率和检测效果。FC的总体灵敏度为75.9%,特异性为100%,阴性和阳性预测值分别为95.4%和100%。专家对假阴性病例的盲法复查发现了诊断误区,使灵敏度提高到 96.6%。与组织样本相比,体液样本的FC检测合格率更高。在对手术室(OR)获得的液体样本进行FC检测的同时,对同时获得液体样本的患者来说,胶囊切除术FC标本没有增加诊断价值;没有病例出现胶囊FC阳性而液体FC阴性的情况。液体样本比组织样本更适于 FC 检测。胶囊组织 FC 标本与手术室获得的体液 FC 标本配对时并不能提高 FC 的疗效,而且往往是不充分的标本。FC对BIA-ALC具有100%的特异性,可作为确诊试验,但不应作为唯一的诊断方法。对样本特异性诊断误区的认识可大大提高 FC 检测 BIA-ALCL 的灵敏度。