*Institute of Pathology, University Hospital, Erlangen †Comprehensive Cancer Center Mainfranken, Institute of Pathology, University of Würzburg, Würzburg ‡Institute of Pathology, Klinikum Augsburg, Augsburg §Laboratory for Dermatohistology & Oral Pathology ∥Institute of Pathology, Ludwig Maximilian University, München, Germany.
Am J Surg Pathol. 2015 Sep;39(9):1206-12. doi: 10.1097/PAS.0000000000000440.
Most of the lymphoproliferative diseases involving the salivary glands represent indolent non-Hodgkin B-cell lymphoma (marginal zone lymphoma) related to chronic autoimmune sialadenitis (Sjögren disease). Other types of non-Hodgkin lymphomas involve the salivary glands less frequently. On rare occasions, classical Hodgkin lymphoma (CHL) and nodular lymphocyte-predominant Hodgkin lymphoma (NLPHL) present initially as a primary salivary gland mass. We analyzed a series of CHL (n=3) and NLPHL (n=6) presenting initially as parotid gland tumors concerning their pattern (parenchymal vs. intraparotid lymph node) and the presence of salivary inclusions and epithelial proliferations within the lymphoma infiltrate. The pattern of infiltration was determined on hematoxylin and eosin-stained slides assisted by immunostaining for pancytokeratin to highlight lobular salivary gland parenchyma. Patients included 6 male and 3 female individuals with a mean age of 62 years (range, 36 to 88 y). Lymphoma was localized within intraparotid lymph nodes in 8 cases and was limited to salivary parenchyma in 1 case. Parenchymal involvement in nodal-based cases was scored as absent (3) or minimal (5). Salivary inclusions (acini and ductules) within affected lymph nodes were noted in 6 cases (4/5 NLPHLs and 2/3 CHLs). In 3/6 NLPHL cases, salivary inclusions showed variable proliferative changes ranging from prominent lymphoepithelial lesions to cystic and oncocytic (Warthin-like) epithelial changes. Scanty small lymphoepithelial lesions were seen in 1 of the 3 CHL cases. One NLPHL in the intraparotid lymph node was accompanied by prominent lymphoepithelial sialadenitis in the absence of clinical signs of Sjögren disease. This study highlights that a majority of parotid gland Hodgkin lymphomas arise within intraparotid lymph nodes. Frequent entrapment and proliferation of salivary ducts and acini within the lymphoma infiltrate might mimic a variety of benign lymphoepithelial mass-forming lesions (nonsebaceous lymphadenoma, Warthin tumor, and autoimmune sialadenitis). Pancytokeratin stain is helpful for reliable assessment of the background architecture.
大多数累及唾液腺的淋巴组织增生性疾病表现为惰性非霍奇金 B 细胞淋巴瘤(边缘区淋巴瘤),与慢性自身免疫性唾液腺炎(干燥综合征)相关。其他类型的非霍奇金淋巴瘤较少累及唾液腺。在极少数情况下,经典霍奇金淋巴瘤(CHL)和结节性淋巴细胞为主型霍奇金淋巴瘤(NLPHL)最初表现为原发性唾液腺肿块。我们分析了一组最初表现为腮腺肿瘤的 CHL(n=3)和 NLPHL(n=6),涉及肿瘤模式(实质与腮腺内淋巴结)以及淋巴瘤浸润中是否存在唾液腺内含物和上皮增生。浸润模式通过苏木精和伊红染色切片确定,并通过免疫组化染色用于细胞角蛋白泛染来突出小叶唾液腺实质。患者包括 6 名男性和 3 名女性,平均年龄 62 岁(范围 36 至 88 岁)。淋巴瘤局限于腮腺内淋巴结 8 例,局限于唾液腺实质 1 例。淋巴结内病例的实质受累评分分为无(3)或轻微(5)。受影响淋巴结内的唾液腺内含物(腺泡和小管)在 6 例中可见(4/5 NLPHL 和 2/3 CHL)。在 3/6 NLPHL 病例中,唾液腺内含物显示出不同程度的增生性改变,从明显的淋巴上皮病变到囊性和嗜酸细胞性(Warthin 样)上皮改变。在 3 例 CHL 病例中,仅 1 例可见少量小淋巴上皮病变。1 例位于腮腺内淋巴结的 NLPHL 伴有明显的淋巴上皮性唾液腺炎,而无干燥综合征的临床征象。本研究强调,大多数腮腺霍奇金淋巴瘤起源于腮腺内淋巴结。淋巴瘤浸润中唾液导管和腺泡的频繁捕获和增生可能模仿各种良性淋巴上皮肿块形成病变(非皮脂性淋巴结瘤、Warthin 瘤和自身免疫性唾液腺炎)。细胞角蛋白泛染有助于可靠评估背景结构。