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Spontaneous rupture of non-parasitic or non-neoplastic multiple and giant liver cysts: report of a case

机译:非寄生虫或非肿瘤性多发性和巨大肝囊肿的自发破裂:一例报告

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摘要

Simple liver cysts occasionally cause pressure symptoms of the abdomen. We herein report an extremely rare case of spontaneous rupture of simple liver cysts. A 65-year-old woman suffered abdominal fullness and dyspnea. Laboratory examinations revealed general inflammation and mild hepatorenal dysfunction. Computed tomography revealed giant polycystic liver and ascites. Echinococcus antibody was not detected. Abdominal paracentesis provided dark brown transparent ascites in which any parasites or tumor cells were not observed. We diagnosed spontaneous rupture of isolated polycystic liver disease (PCLD) and continuously drained the ascites. After the symptoms and laboratory data were improved, resection of liver cysts and left lateral segmentectomy were performed. Histopathologically, simple columnar epithelia inside of cyst walls were observed. The patient remains well without recurrence of the symptoms 10 months after the surgery. We reviewed characteristics of PCLD and considered appropriate treatment for spontaneous rupture of simple liver cysts based on the previous case reports including the present case.
机译:简单的肝囊肿有时会引起腹部压力症状。我们在此报告了极少见的单纯性肝囊肿自发破裂的情况。一名65岁的妇女腹部饱胀和呼吸困难。实验室检查发现全身发炎和轻度肝肾功能不全。计算机断层扫描显示巨大的多囊性肝和腹水。未检测到棘球菌抗体。腹腔穿刺术提供深棕色透明腹水,其中未观察到任何寄生虫或肿瘤细胞。我们诊断为孤立性多囊性肝病(PCLD)自发性破裂,并不断排出腹水。在症状和实验室数据得到改善后,进行肝囊肿切除和左侧外侧节段切除术。在组织病理学上,观察到囊壁内的简单柱状上皮。手术后10个月,患者保持良好状态,无症状复发。我们回顾了PCLD的特征,并根据以前的病例报告(包括本例),考虑了对于单纯性肝囊肿自发破裂的适当治疗。

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