Song Ji Soo, Noh Sang Jae, Cho Baik Hwan, Moon Woo Sung
Department of Radiology, Research Institute of Clinical Medicine and Research Institute for Endocrine Sciences, Chonbuk National University Medical School, Jeonju, Korea.
Korean J Pathol. 2013 Jun;47(3):275-8. doi: 10.4132/KoreanJPathol.2013.47.3.275. Epub 2013 Jun 25.
Multicystic biliary hamartoma (MCBH) is a very rare hamartomatous cystic nodule of the liver, which has recently been described as a new entity of a hepatic nodular lesion. We report a unique case of MCBH with a review of the literatures. A hepatic multicystic mass of segment 3 was detected in a 52-year-old male by abdominal computed tomography, and resection of this lesion was performed. Macroscopic examination revealed a 2.7×2.0 cm nodular mass with a multicystic honeycomb cut surface. Histologically, this lesion consisted of multiple dilated cystic ducts lined by biliary type epithelial cells, periductal glands and connective tissue, which included small amounts of hepatic parenchyma and blood vessels. Recognition of this unusual lesion is essential to avoid confusion with other cystic tumors of the liver, and to learn more about its natural history and response to treatment.
多囊性胆管错构瘤(MCBH)是一种非常罕见的肝脏错构瘤性囊性结节,最近被描述为肝结节性病变的一种新实体。我们报告一例独特的MCBH病例并复习相关文献。一名52岁男性经腹部计算机断层扫描发现肝3段有一个多囊性肿块,并对该病变进行了切除。大体检查显示一个2.7×2.0 cm的结节状肿块,切面呈多囊性蜂窝状。组织学上,该病变由多个内衬胆管型上皮细胞的扩张囊性导管、导管周围腺体和结缔组织组成,其中包括少量肝实质和血管。认识这种不寻常的病变对于避免与肝脏其他囊性肿瘤混淆以及更多地了解其自然病史和对治疗的反应至关重要。