Department of Pathology, Massachusetts General Hospital, Boston, Massachusetts, USA.
Department of Pathology, John Hopkins Hospital, Baltimore, Maryland, USA.
Diagn Cytopathol. 2021 Jan;49(1):83-95. doi: 10.1002/dc.24602. Epub 2020 Sep 14.
Salivary gland lymphadenoma (LAD) is a rare benign neoplasm comprising sebaceous (SLAD) and nonsebaceous (NSLAD) types. Despite established histologic criteria, limited data on cytomorphology, tumor heterogeneity, and overlap with other entities make the diagnosis of LAD by fine needle aspiration (FNA) challenging. We describe a multi-institutional cohort of 14 LADs with cytology, clinical, radiologic, and histopathologic data.
Our cohort included nine SLAD and five NSLAD with corresponding histopathology. Mean patient age and M:F ratio were 60.4 years (range 45-86 years) and 1:2 for SLADs and 57.4 years (range 42-80 years) and 1:1.5 for NSLADs, respectively. One NSLAD patient had a germline predisposition for Cowden syndrome. Glass slides and whole slide images of air-dried Diff-Quik (DQ), alcohol-stained Papanicolaou smears (Pap) and cellblocks were reviewed for key cytomorphologic findings.
FNAs from SLAD and NSLADs demonstrated vacuolated and basaloid epithelial clusters within a lymphoid background. Vacuolated cells from SLAD showed sebaceous cells with microvesicular cytoplasm indenting a central nucleus. Vacuolated cells from NSLAD were columnar with eccentric nuclei, corresponding to abluminal glandular cells. SLADs were classified using the Milan System for Reporting Salivary Gland Cytopathology as nondiagnostic (11.1%), nonneoplastic (44.4%), atypia of uncertain significance (AUS) (22.2%), and salivary gland neoplasm of uncertain malignant potential (SUMP) (22.2%). NSLADs were classified as AUS (40%), SUMP (40%) and Benign Neoplasm (20%).
Although rare, knowing the cytologic features of salivary LAD is important to avoid diagnostic pitfalls. Vacuolated cells can be prominent in both SLAD and NSLAD aspirates. Diagnostic issues arise from insufficient sampling of all tumor components leading to marked variation in diagnostic classification of LAD.
唾液腺淋巴上皮瘤(LAD)是一种罕见的良性肿瘤,包括皮脂腺(SLAD)和非皮脂腺(NSLAD)两种类型。尽管有明确的组织学标准,但关于细胞形态学、肿瘤异质性以及与其他实体之间的重叠的有限数据使得通过细针抽吸(FNA)诊断 LAD 具有挑战性。我们描述了一个由 14 例 LAD 组成的多机构队列,这些 LAD 具有细胞学、临床、影像学和组织病理学数据。
我们的队列包括 9 例 SLAD 和 5 例 NSLAD,并有相应的组织病理学。SLAD 的平均患者年龄和男女比例为 60.4 岁(范围 45-86 岁)和 1:2,NSLAD 分别为 57.4 岁(范围 42-80 岁)和 1:1.5。1 例 NSLAD 患者有考登综合征的种系易感性。对空气干燥的 Diff-Quik(DQ)、酒精染色巴氏涂片(Pap)和细胞块的玻璃载玻片和全玻片图像进行了关键细胞形态学特征的回顾。
SLAD 和 NSLAD 的 FNA 显示在淋巴背景中存在有空泡和基底样上皮簇。来自 SLAD 的空泡细胞显示出具有微泡细胞质的皮脂腺细胞,中央核缩进。来自 NSLAD 的空泡细胞呈柱状,偏心核,对应于腔面腺细胞。SLAD 按照米兰唾液腺细胞病理学报告系统进行分类,包括无诊断意义(11.1%)、非肿瘤性(44.4%)、不确定意义的非典型性(AUS)(22.2%)和唾液腺肿瘤恶性潜能不确定(SUMP)(22.2%)。NSLAD 被分类为 AUS(40%)、SUMP(40%)和良性肿瘤(20%)。
尽管罕见,但了解唾液腺 LAD 的细胞学特征对于避免诊断陷阱很重要。空泡细胞在 SLAD 和 NSLAD 抽吸物中都可能很明显。由于对所有肿瘤成分的采样不足,导致 LAD 的诊断分类存在明显差异,从而导致诊断问题。