Pathology Department of Instituto Português de Oncologia de Lisboa Francisco Gentil (D.D., A.F., J.F.); NOVA Medical School (D.D., D.V., F.S., A.F., J.F.); and Molecular Biopathology Research Unit of Instituto Português de Oncologia de Lisboa Francisco Gentil (C.M.); and Lisboa, Portugal.
Int J Gynecol Pathol. 2024 Nov 1;43(6):637-645. doi: 10.1097/PGP.0000000000001016. Epub 2024 Jan 22.
Adenoid cystic carcinoma (ACC) is a rare neoplasm most frequently observed in the salivary glands, that can occur in other organs, including the vulva and vagina. Oncogenic mechanisms involving MYB, NFIB , and MYB-NFIB rearrangements have been described, but evidence in the vulva and vagina remains scarce. Our aim is to report the clinicopathologic features, immunohistochemical, and molecular findings in a series of vulvar and vaginal ACCs. Five cases were included. Medical records and slides were reviewed. Formalin-fixed paraffin-embedded material was available in 4 cases, where additional immunohistochemical and molecular studies were carried out. Fluorescence in situ hybridization using MYB, MYBL1 , and NFIB bacterial artificial chromosome-clones break-apart and MYB::NFIB BAC-clones fusion probes was performed. The patients' mean age at diagnosis was 52 years. Tumor size ranged from 0.5 to 5 cm. Microscopic examination revealed tubular, cribriform, and solid patterns. Perineural invasion was seen in 4 cases. Patients were treated with surgery, some with adjuvant radiation therapy. During follow-up (mean: 11 yr), 4 patients developed local recurrences. Recently, one of these patients developed pulmonary disease. Cam 5.2, CK5/6, CD117, and DOG-1 were positive in all 4 cases and S100 and calponin were positive in 3 cases. MYB rearrangement was present in 3 cases, including one with concurrent MYB amplification. There were no MYBL1 or NFIB rearrangements and no MYB :: NFIB fusions. Our findings corroborate that the histologic, immunohistochemical, and oncogenic background is similar between ACCs of the lower female genital tract and ACCs elsewhere, although the canonical MYB::NFIB fusion seems to be a less common finding in this location.
腺样囊性癌(ACC)是一种罕见的肿瘤,最常发生于唾液腺,也可发生于其他器官,包括外阴和阴道。已描述了涉及 MYB、NFIB 和 MYB-NFIB 重排的致癌机制,但外阴和阴道的证据仍然很少。我们的目的是报告一系列外阴和阴道 ACC 的临床病理特征、免疫组织化学和分子发现。纳入了 5 例病例。复习了病历和切片。4 例有福尔马林固定石蜡包埋材料,进行了额外的免疫组织化学和分子研究。使用 MYB、MYBL1 和 NFIB 细菌人工染色体-克隆断裂分离和 MYB::NFIB BAC-克隆融合探针进行荧光原位杂交。患者诊断时的平均年龄为 52 岁。肿瘤大小从 0.5 厘米到 5 厘米不等。显微镜检查显示管状、筛状和实性模式。4 例有神经周围侵犯。患者接受了手术治疗,一些患者接受了辅助放疗。在随访期间(平均 11 年),4 例患者出现局部复发。最近,其中一名患者出现肺部疾病。Cam5.2、CK5/6、CD117 和 DOG-1 在所有 4 例中均为阳性,S100 和钙调蛋白在 3 例中为阳性。3 例存在 MYB 重排,包括 1 例伴有 MYB 扩增。没有 MYBL1 或 NFIB 重排,也没有 MYB::NFIB 融合。我们的发现证实,下女性生殖道的 ACC 和其他部位的 ACC 在组织学、免疫组织化学和致癌背景方面是相似的,尽管在这个位置,典型的 MYB::NFIB 融合似乎是一种不太常见的发现。