Brannon R B, Sciubba J J, Giulani M
Oral and Maxillofacial Pathology Department, Louisiana State University School of Dentistry, LSU Health Sciences Center, New Orleans, LA 70119, USA.
Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2001 Jul;92(1):68-77. doi: 10.1067/moe.2001.115978.
The term ductal papilloma is used to identify a group of 3 rare benign papillary salivary gland tumors known as inverted ductal papilloma, sialadenoma papilliferum, and intraductal papilloma. They represent adenomas with unique papillary features and arise from the salivary gland duct system. We describe the clinical and microscopic features of 19 new cases of ductal papillomas and combine them with 116 cases previously published in the English-language medical literature. These 19 cases were composed of 13 inverted ductal papillomas, 3 sialadenoma papilliferums, and 3 intraductal papillomas. Collectively, these 19 ductal papillomas occurred most commonly in the sixth to eighth decade of life, with an average patient age of 54 years. Men predominated 1.37:1. The sialadenoma papilliferums presented as papillary lesions clinically with all 3 misinterpreted as squamous papillomas by the surgeons. The inverted ductal papillomas and intraductal papillomas appeared as submucosal nodules. The lip and the palate were the most common locations for inverted ductal papilloma and sialadenoma papilliferum, respectively. The sites for the 3 intraductal papillomas were the parotid papilla of the Stensen's duct, the upper lip, and the buccal mucosa. With light microscopy, inverted ductal papillomas appeared to arise from the excretory ducts near the mucosal surface, whereas intraductal papillomas appeared to arise from the excretory ducts at a deeper level. Sialadenoma papilliferum had a more complex histology, with a biphasic growth pattern of exophytic papillary and endophytic components. All 19 cases were treated by surgical excision. Follow-up information was available in only 2 cases, both inverted ductal papillomas. Neither case recurred during a 20-year period. Sialadenoma papilliferum, with a literature-derived recurrence rate of 10% to 15%, seems to assert a more significant biological behavior than inverted ductal papilloma and intraductal papilloma. Our findings justify the separation of these 3 entities based on clinical and histologic parameters. They are tumors of adulthood and, in addition, have in common their relationship to the excretory duct system, their anatomical distribution, and their general behavior.
导管乳头状瘤这一术语用于指代一组3种罕见的良性乳头状唾液腺肿瘤,即内翻性导管乳头状瘤、乳头状腺瘤和导管内乳头状瘤。它们是具有独特乳头状特征的腺瘤,起源于唾液腺导管系统。我们描述了19例新的导管乳头状瘤病例的临床和显微镜特征,并将其与先前发表在英文医学文献中的116例病例相结合。这19例病例包括13例内翻性导管乳头状瘤、3例乳头状腺瘤和3例导管内乳头状瘤。总体而言,这19例导管乳头状瘤最常见于60至80岁,患者平均年龄为54岁。男性占主导,男女比例为1.37:1。乳头状腺瘤临床上表现为乳头状病变,所有3例均被外科医生误诊为鳞状乳头状瘤。内翻性导管乳头状瘤和导管内乳头状瘤表现为黏膜下结节。内翻性导管乳头状瘤最常见的部位是唇部,乳头状腺瘤最常见的部位是腭部。3例导管内乳头状瘤的部位分别是腮腺导管乳头、上唇和颊黏膜。在光学显微镜下,内翻性导管乳头状瘤似乎起源于黏膜表面附近的排泄管,而导管内乳头状瘤似乎起源于更深层次的排泄管。乳头状腺瘤的组织学更为复杂,具有外生性乳头状和内生性成分的双相生长模式。所有19例病例均通过手术切除治疗。仅2例有随访信息,均为内翻性导管乳头状瘤。在20年期间,这2例均未复发。乳头状腺瘤的文献复发率为10%至15%,似乎比内翻性导管乳头状瘤和导管内乳头状瘤具有更显著的生物学行为。我们的研究结果证明,基于临床和组织学参数将这3种实体区分开来是合理的。它们是成人肿瘤,此外,它们在与排泄管系统的关系、解剖分布和一般行为方面具有共同之处。