Pathology Unit, Department of Oncology, University of Torino at San Luigi Hospital, Orbassano (Torino), Italy.
Pathology Unit, Department of Oncology, University of Torino at City of Health and Science, Torino, Italy,
Acta Cytol. 2022;66(4):257-268. doi: 10.1159/000519688. Epub 2021 Nov 16.
Small-cell lung carcinoma (SCLC) is a high-grade aggressive disease that belongs to the neuroendocrine (NE) group of lung tumors that also includes typical carcinoid, atypical carcinoid, and large-cell NE carcinoma. SCLC has specific histological diagnostic criteria that are sometimes troublesome to be assessed in cytological samples that indeed represent the most frequent source of diagnostic material due to the typical advanced presentation at the onset of SCLC. However, cytological preparations could be in some instances more reliable than histology due to the better preservation of nuclear details. Cytological criteria for diagnosis of SCLC include high cellularity, small cell size, scant cytoplasm, coarsely granulated chromatin with "salt-and-pepper" appearance, inconspicuous or absent nucleoli, Azzopardi crush effect, and necrotic debris in the background. Despite being distinctive, these features could be incomplete to differentiate SCLC with other small-cell neoplasia. Therefore, immunocytochemical determination of diagnostic biomarkers is crucial to achieve a confident diagnosis. Furthermore, recent findings on molecular and transcriptomic studies of SCLC revealed the potential rise of new predictive and prognostic biomarkers that, whenever validated by immunocytochemistry, may potentially assist to tailor the best therapy, including immune checkpoint inhibition.
小细胞肺癌(SCLC)是一种高级别侵袭性疾病,属于神经内分泌(NE)肿瘤群,其中还包括典型类癌、非典型类癌和大细胞 NE 癌。SCLC 具有特定的组织学诊断标准,在细胞学样本中评估有时比较麻烦,因为 SCLC 通常在发病时就表现为典型的晚期,因此细胞学样本确实是最常见的诊断材料来源。然而,由于核细节的更好保存,细胞学标本在某些情况下可能比组织学更可靠。SCLC 的细胞学诊断标准包括高细胞性、小细胞大小、稀少的细胞质、粗糙颗粒状染色质呈“盐和胡椒”外观、不明显或无核仁、Azzopardi 压碎效应以及背景中的坏死碎片。尽管这些特征具有独特性,但可能不足以区分 SCLC 与其他小细胞肿瘤。因此,免疫细胞化学检测诊断生物标志物对于获得明确的诊断至关重要。此外,最近对 SCLC 的分子和转录组学研究发现,新的预测和预后生物标志物可能会增加,只要通过免疫细胞化学得到验证,它们可能有助于制定最佳治疗方案,包括免疫检查点抑制。