Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Department of Pathology, Henry Ford Hospital, Detroit, MI, USA.
Cancer Cytopathol. 2023 Aug;131(8):526-534. doi: 10.1002/cncy.22709. Epub 2023 Jun 6.
Although alterations in SMARCA4-deficient occur in non-small cell lung carcinoma (SD-NSCLC), thoracic SMARCA4-deficient undifferentiated tumor (TSDUT) is recognized as a distinct entity in the 2021 World Health Organization Classification of Thoracic Tumors because of unique morphologic, immunophenotypic and molecular features, and worse survival compared with SD-NSCLC. Cytologic diagnosis of TSDUT is clinically important because of its aggressive behavior and because it is often diagnosed by fine-needle aspiration because TSDUTs are usually unresectable at presentation. Here, we identify cytologic features that can be used for recognition of TSDUT and distinction from SD-NSCLC.
Cytomorphologic features were investigated in cytology specimens from patients with TSDUT (n = 11) and compared with a control group of patients with SD-NSCLC (n = 20).
The presence of classic rhabdoid morphology, at least focally, was entirely specific for TSDUT (n = 6, 55%) compared with SD-NSCLC (n = 0) in this study. TSDUT more frequently showed tumor necrosis (n = 11, 100% vs. n = 8, 40%; p = .001), dominant single-cell pattern on aspirate smears or touch preparation slides (n = 8 [of 9], 80% vs. n = 3, 15%; p = .010), nuclear molding (n = 5, 45% vs. n = 1, 5%; p = .013), and indistinct cell borders (n = 11, 100% vs. n = 5, 25%; P < .001) compared with SD-NSCLC, respectively.
Cytomorphologic features occurring more frequently in TSDUT include tumor necrosis, dominant single-cell pattern, nuclear molding indistinct cell borders, and focal rhabdoid cells. Presence of these features in a cytology specimen of an undifferentiated tumor, particularly in a patient with a thoracic mass, should raise suspicion for TSDUT and prompt appropriate ancillary workup.
尽管 SMARCA4 缺陷在非小细胞肺癌(SD-NSCLC)中发生改变,但由于其独特的形态、免疫表型和分子特征,以及与 SD-NSCLC 相比生存率更差,2021 年世界卫生组织胸部肿瘤分类将胸内 SMARCA4 缺陷未分化肿瘤(TSDUT)识别为一种独特的实体。由于其侵袭性行为以及 TSDUT 通常在呈现时无法切除,因此细胞学诊断 TSDUT 在临床上非常重要。在这里,我们确定了可用于识别 TSDUT 并将其与 SD-NSCLC 区分开来的细胞学特征。
研究了 11 例 TSDUT 患者的细胞学标本的细胞学特征,并与 20 例 SD-NSCLC 患者的对照组进行了比较。
在这项研究中,至少局灶性存在经典横纹肌样形态是 TSDUT(6 例,55%)与 SD-NSCLC(0 例)完全特异性的(n=6,55%)。与 SD-NSCLC 相比,TSDUT 更常出现肿瘤坏死(n=11,100% vs. n=8,40%;p=0.001),在抽吸涂片或触诊准备幻灯片上显示出优势单细胞模式(n=8 [9 例中的 8 例],80% vs. n=3,15%;p=0.010),核模(n=5,45% vs. n=1,5%;p=0.013)和不清晰的细胞边界(n=11,100% vs. n=5,25%;P<0.001)。
在 TSDUT 中更频繁出现的细胞学特征包括肿瘤坏死、优势单细胞模式、核模、不清晰的细胞边界和局灶性横纹肌样细胞。在未分化肿瘤的细胞学标本中出现这些特征,特别是在胸部肿块的患者中,应怀疑 TSDUT,并提示进行适当的辅助检查。