Charles River, Murray Sarah, Gray Eric, Hu Jingjing
Department of Pathology, University of California San Diego, San Diego, California, USA.
Department of Radiology, University of California San Diego, San Diego, California, USA.
Diagn Cytopathol. 2022 Jun;50(6):E156-E162. doi: 10.1002/dc.24936. Epub 2022 Jan 31.
Pulmonary epithelial-myoepithelial carcinoma (P-EMC) is a rare type of salivary gland tumor of the lung. Diagnosis from preoperative biopsies or fine needle aspiration (FNA) cytology specimens is difficult given the rarity of the tumor and overlapping cytomorphology with other entities. These tumors generally have a good prognosis, however prior reports of recurrence and metastasis to lymph nodes have been reported. Further, little is known about the malignant potential of high grade transformation. The molecular characteristics of this entity are unknown, with only a few case reports commenting on molecular findings. Here, we report a case of P-EMC with focal high grade transformation. We present its diagnostic pitfalls on cytology specimens, surgical pathology, immunohistochemistry, and molecular findings.
A 72 year old female presented with an incidentally detected lung mass. A chest computed tomography (CT) demonstrated a left hilar mass measuring 4.1 cm with endobronchial extension into the left upper lobe. On the initial endobronchial core needle biopsy and cytology FNA, the tumor was misinterpreted as squamous cell carcinoma. The patient subsequently underwent a left pneumonectomy along with mediastinal lymph node dissection. Final surgical pathology of the resection specimen indicated a P-EMC with focal high grade transformation. The patient is disease-free 1 year post-surgery.
Due to the rarity of P-EMC, insufficient sampling and histologic heterogeneity, diagnosis of P-EMC on preoperative core needle biopsy or FNA specimen is difficult. Herein, we present a rare case of P-EMC, with a pre-operative FNA cytology specimen that consisted of tumor cells with dense cytoplasm and moderate cytologic atypia, strong positive staining pattern of p40, that was misdiagnosed as squamous cell carcinoma. Follow up surgical resection showed P-EMC with focal high grade transformation. Salivary gland EMCs with high grade transformation have previously been reported to have a worse prognosis, however, little is known about the malignant potential in the lung. Next generation sequencing (NGS) using a 397-gene solid tumor panel identified variants in DNMT3A, APC, STAT3 in both low and high grade components, while KDM5C was present only in the high grade transformation.
肺上皮-肌上皮癌(P-EMC)是一种罕见的肺涎腺肿瘤。鉴于该肿瘤的罕见性以及其细胞形态与其他实体肿瘤的重叠,术前活检或细针穿刺(FNA)细胞学标本的诊断较为困难。这些肿瘤通常预后良好,然而此前已有复发和淋巴结转移的报道。此外,关于高级别转化的恶性潜能知之甚少。该实体的分子特征尚不清楚,仅有少数病例报告提及分子研究结果。在此,我们报告一例伴有局灶性高级别转化的P-EMC病例。我们展示了其在细胞学标本、手术病理、免疫组化及分子研究结果方面的诊断陷阱。
一名72岁女性因偶然发现肺部肿块就诊。胸部计算机断层扫描(CT)显示左肺门肿块,大小为4.1厘米,支气管内延伸至左上叶。在最初的支气管内芯针活检和细胞学FNA检查中,该肿瘤被误诊为鳞状细胞癌。患者随后接受了左肺切除术及纵隔淋巴结清扫术。切除标本的最终手术病理显示为伴有局灶性高级别转化的P-EMC。患者术后1年无疾病复发。
由于P-EMC罕见、取材不足及组织学异质性,术前芯针活检或FNA标本诊断P-EMC较为困难。在此,我们报告一例罕见的P-EMC病例,其术前FNA细胞学标本由细胞质浓密且有中度细胞异型性的肿瘤细胞组成,p40呈强阳性染色模式,被误诊为鳞状细胞癌。后续手术切除显示为伴有局灶性高级别转化的P-EMC。此前报道涎腺EMC伴有高级别转化时预后较差,然而,关于其在肺部的恶性潜能知之甚少。使用397基因实体瘤检测板进行的二代测序(NGS)在低级别和高级别成分中均鉴定出DNMT3A、APC、STAT3的变异,而KDM5C仅存在于高级别转化区域。