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诊断细胞学中胸 SMARCA4 缺陷型未分化肿瘤。

Diagnosis of thoracic SMARCA4-deficient undifferentiated tumor in cytology.

机构信息

Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Department of Pathology, Henry Ford Hospital, Detroit, MI, USA.

出版信息

Cancer Cytopathol. 2023 Aug;131(8):526-534. doi: 10.1002/cncy.22709. Epub 2023 Jun 6.

Abstract

INTRODUCTION

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.

MATERIALS AND METHODS

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).

RESULTS

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.

CONCLUSIONS

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.

摘要

简介

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。

材料和方法

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。

结果

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)。

结论

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。

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