Department of General Surgery, Nanchang University Affiliated Infectious Diseases Hospital, Nanchang, China.
J Int Med Res. 2024 Jan;52(1):3000605231221088. doi: 10.1177/03000605231221086.
Caroli disease is a rare congenital malformation that predisposes to segmental cystic dilatation of the intrahepatic bile ducts. Banti syndrome is characterized by persistent splenomegaly due to chronic congestion, resulting in a low hematocrit and ultimately leading to pancytopenia. In this report, we describe a 29-year-old woman who presented with a >20-year history of hepatitis B surface antigen positivity and a >1-year history of recurrent fatigue and malaise. On examination, the patient had abdominal distension with marked splenomegaly (7 cm below the ribs) and ascites with tenderness of the abdominal muscles to palpation. A complete blood count showed a low white blood cell count, red blood cell count, and hemoglobin concentration. During the course of treatment, the patient developed multiple symptoms of pancytopenia and concomitant splenomegaly, and she was discharged after total splenectomy with good recovery. The combination of Banti syndrome and Caroli disease results in severe symptoms of portal hypertension.
Caroli 病是一种罕见的先天性畸形,易导致肝内胆管节段性囊状扩张。Banti 综合征的特征为持续性脾肿大,由于慢性充血,导致血细胞比容降低,最终导致全血细胞减少。本报告描述了一位 29 岁女性,其乙肝表面抗原阳性超过 20 年,反复疲劳和不适超过 1 年。体格检查发现患者腹胀,脾肿大明显(肋下 7cm),有腹水,腹肌触诊有压痛。全血细胞计数显示白细胞计数、红细胞计数和血红蛋白浓度均降低。在治疗过程中,患者出现多种全血细胞减少症的症状,同时伴有脾肿大,行全脾切除术后出院,恢复良好。Banti 综合征和 Caroli 病的合并导致严重的门静脉高压症状。