Department of Pathology, The First Affiliated Hospital, Sun Yat-sen University, 58, Zhongshan Road II, Guangzhou 510080, China.
Diagn Pathol. 2014 Jan 29;9:24. doi: 10.1186/1746-1596-9-24.
As rare condition, mucoepidermoid carcinoma may occur in liver although its etiology and pathogenesis is still unclear. We report here a case of intrahepatic mucoepidermoid carcinoma misdiagnosed as cholangiocarcinoma and squamous cell carcinoma by preoperative radiologic and intraoperative histological examinations, respectively. A 60-year-old woman presented with a 1-month history of progressive jaundice, epigastric discomfort, and weight loss with slightly increased carbohydrate antigen 19-9 (CA19-9). Computed tomography (CT) showed a large tumor, 8.0 cm in diameter, in the left lobe of the liver. A preliminary diagnosis of a cholangiocarcinoma of the liver was made. In the intraoperative histological examination, a diagnosis of squamous cell carcinoma was made based on predominantly invasive epidermoid cells with abundant keratinization and absence of mucin-producing cell component. However, postoperative histological diagnosis of the lesion was mucoepidermiod carcinoma of liver by thoroughly microscopical inspection and the presence of mucin-producing cells confirmed by Alcian blue staining. Despite surgical excision and chemotherapy, the tumor showed very aggressive malignancy with tumor recurrence. The patient died shortly afterward, surviving 6 months after surgery. Due to its rarity and distinct morphological features, mucoepidermoid carcinoma might be erroneously interpreted as squamous cell carcinoma by those who were not familiar with this condition in unusual locations. Therefore, removal of sufficient tissue from different portions of the lesion is essential for the surgeons and pathologists to make a precise diagnosis in the intraoperative histological examination.
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尽管黏液表皮样癌在肝脏中较为罕见,但病因和发病机制尚不清楚。我们在此报告一例经术前影像学和术中组织学检查分别误诊为胆管细胞癌和鳞状细胞癌的肝内黏液表皮样癌。一名 60 岁女性因进行性黄疸、上腹部不适和体重减轻(略伴有癌抗原 19-9 升高)就诊,病程 1 个月。计算机断层扫描(CT)显示肝脏左叶有一直径 8.0cm 的大肿瘤。初步诊断为胆管细胞癌。术中组织学检查根据主要侵袭性表皮样细胞、丰富的角化和缺乏黏液产生细胞成分做出鳞状细胞癌的诊断。然而,术后组织学检查发现病变为肝黏液表皮样癌,通过彻底的显微镜检查和粘蛋白产生细胞的存在(通过阿辛蓝染色证实)做出该诊断。尽管进行了手术切除和化疗,但肿瘤仍表现出极强的恶性,发生肿瘤复发。此后患者不久后死亡,术后存活 6 个月。由于其罕见性和独特的形态特征,对于不熟悉这种罕见部位的黏液表皮样癌的人来说,可能会错误地将其解释为鳞状细胞癌。因此,外科医生和病理学家需要从病变的不同部位切除足够的组织,以便在术中组织学检查中做出准确诊断。
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