Naito Zen, Noji Takehiro, Tanaka Kimitaka, Nakanishi Yoshitsugu, Nakajima Masahito, Mitsuhashi Tomoko, Hirano Satoshi
Department of Gastroenterological Surgery II, Faculty of Medicine, Hokkaido University, Sapporo, Hokkaido, Japan.
Hokkaido Nursing Division, Faculty of Health Sciences, Hokkaido University, Sapporo, Hokkaido, Japan.
Surg Case Rep. 2025;11(1). doi: 10.70352/scrj.cr.24-0160. Epub 2025 May 8.
Gallbladder carcinosarcoma is extremely rare, with fewer than 100 cases reported from its first description in 1907 until 2022. Collision carcinoma is a type of synchronous carcinoma in which 2 independently arising tumors come into contact or partially invade each other.
A man in his 80s was referred to our hospital with the primary complaints of weight loss and decreased appetite. Contrast-enhanced computed tomography revealed a large lobular tumor with heterogeneous enhancement, measuring 66 mm in maximum diameter, located in the fundus of the gallbladder. The mass showed clear signs of liver invasion, raising immediate concerns of malignancy. Magnetic resonance imaging provided additional crucial details. The lesion exhibited low signal intensity on T1-weighted images and high signal intensity on T2-weighted images. Notably, diffusion-weighted imaging demonstrated restricted diffusion, a characteristic often associated with malignant processes. These findings strongly suggested gallbladder cancer with liver invasion. The patient underwent cholecystectomy and hepatectomy involving segments 4, 5, and 8 of the liver. A subsequent pathological examination revealed a complex and unusual tumor composition. The hepatic lesion showed nests of varying sizes with a medullary growth pattern, which is characteristic of intrahepatic cholangiocarcinoma. In contrast, the gallbladder lesion displayed features of adenosquamous carcinoma with a partial sarcomatoid morphology, indicative of gallbladder carcinosarcoma. Intriguingly, the interface between these 2 distinct tumor types exhibited unique characteristics. In some areas, normal hepatocytes were interspersed between the 2 types of tumor cells. Other regions demonstrated an invasive tendency of tumor cells towards each other. This unusual pattern led to the diagnosis of a collision tumor, a rare occurrence in which 2 independent primary malignancies coexist in the same organ or site.
This was an extremely rare case of collision carcinoma involving both intrahepatic cholangiocarcinoma and gallbladder carcinosarcoma. The unique pathological findings and rarity of this tumor combination make this case particularly noteworthy. We present this case to contribute to the limited literature on such rare tumors, aiming to facilitate a better understanding and management of similar cases in the future.
胆囊癌肉瘤极为罕见,从1907年首次描述至2022年,报告的病例不足100例。碰撞癌是一种同步癌,其中两个独立发生的肿瘤相互接触或部分相互侵犯。
一名80多岁的男性因体重减轻和食欲减退的主要症状转诊至我院。增强计算机断层扫描显示胆囊底部有一个大的分叶状肿瘤,最大直径66毫米,强化不均匀。该肿块显示出明显的肝侵犯迹象,立即引起了对恶性肿瘤的担忧。磁共振成像提供了更多关键细节。病变在T1加权图像上呈低信号强度,在T2加权图像上呈高信号强度。值得注意的是,扩散加权成像显示扩散受限,这一特征通常与恶性病变相关。这些发现强烈提示胆囊癌伴肝侵犯。患者接受了胆囊切除术和包括肝第4、5和8段的肝切除术。随后的病理检查显示肿瘤成分复杂且不寻常。肝病变显示大小不一的巢状结构,呈髓样生长模式,这是肝内胆管癌的特征。相比之下,胆囊病变表现为腺鳞癌特征,部分呈肉瘤样形态,提示胆囊癌肉瘤。有趣的是,这两种不同肿瘤类型之间的界面表现出独特的特征。在一些区域,正常肝细胞散布在两种肿瘤细胞之间。其他区域显示肿瘤细胞相互侵入的趋势。这种不寻常的模式导致诊断为碰撞瘤,即两种独立的原发性恶性肿瘤在同一器官或部位共存的罕见情况。
这是一例极为罕见的涉及肝内胆管癌和胆囊癌肉瘤的碰撞癌。这种肿瘤组合独特的病理发现和罕见性使得该病例尤为值得关注。我们呈现此病例以丰富关于此类罕见肿瘤的有限文献,旨在促进未来对类似病例的更好理解和管理。