Gang Sujin, Choi YoungRok, Lee Sola, Hong Su Young, Suh Sanggyun, Han Eui Soo, Hong Suk Kyun, Yi Nam-Joon, Lee Kwang-Woong, Suh Kyung-Suk
Department of Surgery, Seoul National University Hospital, Seoul, Korea.
Department of Pediatric Surgery, Asan Medical Center, Seoul, Korea.
Ann Hepatobiliary Pancreat Surg. 2022 Nov 30;26(4):407-411. doi: 10.14701/ahbps.22-022. Epub 2022 Aug 23.
Mesenchymal hamartoma of the liver (MHL) is a rare benign tumor that often presents in early childhood, and it rarely occurs in adulthood. Aberrant development of the portal tract is a known cause of MHL. Although limited information is available on the natural course of MHL, malignant transformation has been reported in a few cases. Here, we report a case of a 26-year-old female with intrahepatic cholangiocarcinoma secondary to unresected MHL. The patient underwent resection of the hepatic mass, which was diagnosed as MHL at 2 years of age, due to an increase in mass size and a suspicion of malignant transformation during work-up. Histopathology confirmed intrahepatic adenosquamous carcinoma in the background of MHL, with a T2N0M0 pathological stage (stage II). The surgical margin was free from tumor cells. The patient fully recovered postoperatively and started receiving adjuvant chemotherapy. Previous case reports have only reported about the development of undifferentiated embryonal sarcoma or angiosarcoma as malignant transformation of MHL. Cases of other malignancies have not been published; however, it is difficult to rule out the occurrence of various malignancies related to the portal tract when considering the pathogenesis of the disease. To the best of our knowledge, this is the first case report of adenocarcinoma of bile duct origin secondary to MHL. This case report suggests that aggressive surgical management should be considered after the initial diagnosis of MHL.
肝间叶性错构瘤(MHL)是一种罕见的良性肿瘤,常于儿童早期出现,在成人中很少发生。已知门静脉分支发育异常是MHL的病因。尽管关于MHL自然病程的信息有限,但已有少数病例报告发生了恶性转化。在此,我们报告一例26岁女性,患有继发于未切除MHL的肝内胆管癌。该患者因肿块增大且在检查过程中怀疑发生恶性转化,接受了肝脏肿块切除术,该肿块在患者2岁时被诊断为MHL。组织病理学证实为MHL背景下的肝内腺鳞癌,病理分期为T2N0M0(II期)。手术切缘无肿瘤细胞。患者术后完全康复并开始接受辅助化疗。既往病例报告仅报道了MHL恶性转化为未分化胚胎性肉瘤或血管肉瘤。其他恶性肿瘤的病例尚未见报道;然而,考虑到该疾病的发病机制,很难排除与门静脉分支相关的各种恶性肿瘤的发生。据我们所知,这是首例关于继发于MHL的胆管源性腺癌的病例报告。本病例报告提示,在MHL初步诊断后应考虑积极的手术治疗。