AlMheiri Mira, Mrayyan Hala B, Krishnamurthy Balaji, Dsouza Ajay P
Pediatric Gastroenterology, Al Jalila Children's Specialty Hospital, Dubai, ARE.
Gastroenterology and Hepatology, Dubai Medical College, Dubai, ARE.
Cureus. 2024 Feb 20;16(2):e54508. doi: 10.7759/cureus.54508. eCollection 2024 Feb.
Congenital portosystemic shunts (CPSS) or congenital extrahepatic portosystemic shunts (CEPS) is a rare malformation. This congenital anomaly presents with a diverse array of clinical manifestations, ranging from asymptomatic to severe complications such as cardiac failure, pronounced pulmonary hypertension, and widespread pulmonary arteriovenous malformations. CPSS increases the risk of developing benign or malignant liver tumors, including nodular regenerative hyperplasia, focal nodular hyperplasia, hepatic adenoma, hepatocellular carcinoma, and hepatoblastoma. We report a case of a 15-month-old boy, identified with Abernethy's malformation type Ib, who presented with an abdominal mass during a follow-up. A comprehensive assessment established a diagnosis of hepatoblastoma. The patient was transferred to a specialized liver transplant center for further treatment and management. This is a review of literature highlighting the complexity of Abernethy malformation and its associated risk of liver tumors.
先天性门体分流(CPSS)或先天性肝外门体分流(CEPS)是一种罕见的畸形。这种先天性异常表现出各种各样的临床表现,从无症状到严重并发症,如心力衰竭、明显的肺动脉高压和广泛的肺动静脉畸形。CPSS增加了发生良性或恶性肝脏肿瘤的风险,包括结节性再生性增生、局灶性结节性增生、肝腺瘤、肝细胞癌和肝母细胞瘤。我们报告一例15个月大的男孩,被诊断为I b型阿伯内西畸形,在随访期间出现腹部肿块。综合评估确诊为肝母细胞瘤。该患者被转至一家专门的肝移植中心进行进一步治疗和管理。本文是一篇文献综述,强调了阿伯内西畸形的复杂性及其相关的肝脏肿瘤风险。