Tarditti Franco D, Torres Manuel B, Yazigi Nada A, Rumbo Carolina, Zandieh Arash R, Gondolesi Gabriel E
Medstar Georgetown Transplantation Institute, MedStar Georgetown University Hospital, Washington, D.C., USA.
Division of Pediatric Surgery, MedStar Georgetown University Hospital, Washington, D.C., USA.
Cureus. 2025 Jul 17;17(7):e88182. doi: 10.7759/cureus.88182. eCollection 2025 Jul.
Accessory liver lobes (ALLs) are rare anatomical variations characterized by supernumerary lobes of normal hepatic parenchyma in continuity with the liver. They are typically asymptomatic and most often discovered incidentally during imaging or surgical procedures. We report a unique case of a three-month-old premature infant with a history of gastroschisis and bladder herniation, who developed clinical and biochemical signs of progressive cholestasis. Imaging studies raised suspicion for an ALL, which was confirmed intraoperatively as a pedunculated ALL in continuity with the gallbladder. The lobe was resected en bloc. ALLs are infrequently diagnosed and often present with nonspecific symptoms. While imaging may suggest the diagnosis, definitive identification is commonly made during surgery, as ALLs can mimic masses and raise concern for neoplastic disease. To our knowledge, this is the first documented case of a symptomatic ALL presenting with signs of biliary obstruction. This rare case highlights the importance of including ALL in the differential diagnosis of cholestasis, as delayed recognition may lead to secondary biliary cirrhosis, potentially necessitating liver transplantation.
副肝叶(ALLs)是一种罕见的解剖变异,其特征为正常肝实质的额外叶与肝脏相连。它们通常无症状,最常在影像学检查或手术过程中偶然发现。我们报告了一例独特的病例,一名三个月大的早产儿,有腹裂和膀胱疝病史,出现了进行性胆汁淤积的临床和生化体征。影像学检查怀疑为副肝叶,术中证实为与胆囊相连的带蒂副肝叶。该叶被整块切除。副肝叶很少被诊断出来,且常表现为非特异性症状。虽然影像学检查可能提示诊断,但明确诊断通常在手术中进行,因为副肝叶可能类似肿块,并引发对肿瘤性疾病的担忧。据我们所知,这是第一例有症状的副肝叶表现为胆道梗阻体征的记录病例。这个罕见病例凸显了在胆汁淤积的鉴别诊断中纳入副肝叶的重要性,因为延迟识别可能导致继发性胆汁性肝硬化,可能需要进行肝移植。