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Published on: April 11, 2025
Solitary hepatic lymphangioma: a one-case report
Qu Liu1, Cheng-Jun Sui2, Bao-Shan Li3
1Department of Special Treatment, Eastern Hepatobiliary Surgery Hospital, Second Military Medical University, Shanghai, 200438 China ; Department of Hepatobiliary Surgery, People's Republic of China No. 254 Hospital, Tianjin, 300142 China.
Abstract:
Hepatic lymphangiomas, malformations of the liver lymphatic system, are extremely rare conditions in adults. A 41-year-old man presented with right upper abdominal pain for 6 months was introduced in this report. Ultrasound (US) and computed tomography (CT) scan demonstrated a giant cystictumor with a pedunculatedextrahepatic growth pattern. Due to diagnostic uncertainty, a partial hepatectomy was performed and pathological results confirmed the diagnosis of solitary hepatic lymphangioma. In this article, we reviewed the clinical and pathology features, preoperative diagnostic challenges, and treatments of hepaticlymphangiomas.
