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Cytology of Primary Salivary Gland-Type Tumors of the Lower Respiratory Tract: Report of 15 Cases and Review of the Literature

机译:下呼吸道原发唾液腺型肿瘤的细胞学研究:15例报告并文献复习

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摘要

Primary pulmonary salivary gland-type tumors are rare neoplasms arising from the seromucinous submucosal glands of the lower respiratory tract (LRT), the most common of which are mucoepidermoid carcinoma (MEC) and adenoid cystic carcinoma. They are morphologically indistinguishable from their salivary gland counterpart and recognizing them is a challenge, especially on cytological specimens. We analyzed 15 cases of histologically proven primary salivary gland tumors of the LRT to identify cytomorphological features and define potential diagnostic clues that might assist cytopathologists in the preoperative diagnosis of these neoplasias. Three out of the four cases of adenoid cystic carcinomas showed the characteristic tridimensional cell clusters and hyaline globules, whereas the last one did not show malignant cells; only two cases of MEC presented the three characteristic cell types (i.e., squamous, intermediate, and mucin secreting) on cytology. Since these neoplasms are rare and do not have a completely specific set of cytological features, it is important for practicing cytopathologists to be aware of the possibility of encountering them, in specimens from patients with LRT masses, in order to render the correct diagnosis.
机译:原发性肺唾液腺型肿瘤是罕见的肿瘤,由下呼吸道(LRT)的浆液性粘膜下腺产生,其中最常见的是粘液表皮样癌(MEC)和腺样囊性癌。它们在形态上与唾液腺没有区别,并且认识到它们是一个挑战,特别是在细胞学标本上。我们分析了15例经组织学证实为LRT的原发唾液腺肿瘤,以鉴定细胞形态学特征并确定可能的诊断线索,这些线索可能有助于细胞病理学家对这些肿瘤的术前诊断。在四例腺样囊性癌中,三例显示出特征性的三维细胞团和透明性小球,而最后一例则未显示出恶性细胞。仅两例MEC在细胞学上表现出三种特征细胞类型(即鳞状,中间和粘蛋白分泌)。由于这些肿瘤很少见,并且不具有完全特定的细胞学特征,因此对于细胞病理学家来说,重要的是要意识到在LRT肿块患者的标本中遇到这些肿瘤的可能性,以便做出正确的诊断。

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