Vanoli Alessandro, Travaglino Erica, Minetto Marco, Gallotti Anna, Grillo Federica, Corallo Salvatore, Maestri Marcello, Peri Andrea, Fugazzola Paola, Antoci Francesca, Riboni Roberta, Di Sabatino Antonio, Ansaloni Luca, Pietrabissa Andrea, D'Ambrosio Gioacchino, Paulli Marco
Department of Molecular Medicine, University of Pavia, Via Carlo Forlanini 16, 27100, Pavia, Italy.
Unit of Anatomic Pathology, IRCCS San Matteo Hospital Foundation, Pavia, Italy.
Virchows Arch. 2025 Mar 21. doi: 10.1007/s00428-025-04077-7.
Adenomyoma/adenomyomatosis (AM) of the gallbladder is generally considered an incidental and innocuous finding; however, neoplastic lesions, including intracholecystic neoplasms (ICNs), flat-type dysplasia, and carcinomas, may arise within AM. AM-associated ICNs, composed of mural cystically dilated glands containing florid papillary proliferations lined by mucinous and/or overtly dysplastic epithelium, are very rare and poorly characterized. This study aimed at investigating the clinico-radiologic, phenotypic/immunophenotypic, and molecular features of a mono-institutional case series of four AM-ICNs (0.2% of cholecystectomies). Immunohistochemistry for CDX2, MUC2, MUC5AC, MUC6, MUC1, HER2, ß-catenin, and p53, as well as next-generation sequencing of 110 tumor-related genes (AmoyDx® Comprehensive Panel), were performed. Our study confirms the AM-ICN-associated clinico-demographic characteristics previously described, including the relatively low frequency of associated invasive carcinoma (one case, 25%), although high-grade dysplasia (HGD) was observed in three out of four cases. In two cases, imaging findings suspicious for neoplasm were seen. Segmental-type AM was seen in two cases. Predominantly cell phenotype was gastric foveolar in two AM-ICNs and pancreatobiliary in the other two cases (both with HGD), while the immunophenotype was hybrid/mixed in all cases. No case had nuclear ß-catenin expression nor Wnt pathway or KRAS gene alterations. One case showed both HER2 point mutation and HER2 amplification, while the AM-ICN associated with an invasive adenocarcinoma harbored TP53 mutation and p53 overexpression. In conclusion, our findings suggest the separation of AM-ICNs from other gallbladder dysplastic lesions.
胆囊腺肌瘤/腺肌瘤病(AM)通常被认为是一种偶然且无害的发现;然而,在AM内部可能会出现肿瘤性病变,包括胆囊内肿瘤(ICN)、扁平型发育异常和癌。由含有黏液性和/或明显发育异常上皮衬里的壁内囊状扩张腺体组成的AM相关ICN非常罕见,且特征描述不足。本研究旨在调查一个单中心病例系列中4例AM-ICN(占胆囊切除术的0.2%)的临床放射学、表型/免疫表型和分子特征。进行了CDX2、MUC2、MUC5AC、MUC6、MUC1、HER2、β-连环蛋白和p53的免疫组织化学检测,以及110个肿瘤相关基因的二代测序(AmoyDx®综合检测 panel)。我们的研究证实了先前描述的AM-ICN相关的临床人口统计学特征,包括相关浸润性癌的相对低发生率(1例,25%),尽管在4例中有3例观察到高级别发育异常(HGD)。在2例中,发现了可疑肿瘤的影像学表现。2例为节段型AM。在2例AM-ICN中主要细胞表型为胃小凹型,在另外2例(均有HGD)中为胰胆管型,而所有病例的免疫表型均为混合/杂合型。没有病例有核β-连环蛋白表达,也没有Wnt途径或KRAS基因改变。1例显示HER2点突变和HER2扩增,而与浸润性腺癌相关的AM-ICN存在TP53突变和p53过表达。总之,我们的研究结果表明AM-ICN应与其他胆囊发育异常病变区分开来。