Lyagoubi Manal, Mehdaoui Chourouq, Haloui Anass, Karish Nassira, Ismaili Zahi, Bennani Amal
Pathology, Faculty of Medicine and Pharmacy of Oujda, Mohammed 1st University, Oujda, MAR.
Pathology, Mohammed VI University Hospital, Faculty of Medicine, Mohammed 1st University, Oujda, MAR.
Cureus. 2024 Jul 4;16(7):e63803. doi: 10.7759/cureus.63803. eCollection 2024 Jul.
Primary squamous cell carcinoma (SCC) of the liver, a notably uncommon type of cancer, is frequently linked with diverse hepatic conditions including hepatic cysts, hepatolithiasis, and hepatic teratoma. Literature indicates that only approximately 30 cases of primary SCC of the liver have been documented. Herein, we report a 54-year-old previously healthy patient who was presented with cholangitis symptoms. Examinations revealed normal vitals. However, deranged liver function with transaminitis and hyperbilirubinemia were noticed. A CT scan showed a hepatic mass with bile duct dilation. Biopsy confirmed hepatic squamous cell carcinoma, leading to chemotherapy treatment. Despite treatment, the survival outcomes for this cancer remain limited, and the prognosis is generally unfavorable.
原发性肝鳞状细胞癌（SCC）是一种极为罕见的癌症类型，常与多种肝脏疾病相关，包括肝囊肿、肝内胆管结石和肝畸胎瘤。文献表明，仅有约30例原发性肝SCC的病例被记录在案。在此，我们报告一名54岁既往健康的患者，其出现了胆管炎症状。检查显示生命体征正常。然而，发现肝功能紊乱，伴有转氨酶升高和高胆红素血症。CT扫描显示肝脏有肿块伴胆管扩张。活检确诊为肝鳞状细胞癌，随后进行了化疗。尽管进行了治疗，这种癌症的生存结果仍然有限，预后通常不佳。
