Polycystic liver disease presenting with an exudative pleural effusion: A case report

被引:6
作者
Kerry Woolnough
Altav Palejwala
Simon Bramall
机构
[1] Department of Gastroenterology, Queen's Hospital, Burton-on-Trent, West Midlands
[2] University Hospital of Birmingham, West Midlands
关键词
Pleural Effusion; Pleural Fluid; Hydatid Disease; Hepatic Cyst; Asbestosis;
D O I
10.1186/1752-1947-6-107
中图分类号
学科分类号
摘要
Introduction. Polycystic liver disease is asymptomatic in 95% of patients. In the remaining 5% it causes symptoms due to the local mass effect of the polycystic liver. We describe the case of a patient who presented with symptoms of a pleural effusion and was also found to have polycystic liver disease. The effusion recurred despite repeated efforts at drainage and only resolved following surgical debridement of the cystic liver. Case presentation. A 50-year-old Caucasian woman presented with a two-week history of increasing dyspnoea. An examination revealed a large right pleural effusion and gross hepatomegaly. An ultrasound confirmed a large polycystic liver and diagnostic thoracocentesis revealed an exudate, which was sterile to culture. The pleural effusion proved refractory to drainage and our patient underwent surgery to deroof the main hepatic cysts in an attempt to reduce the pressure on her right diaphragm. The histology was compatible with that of polycystic liver disease. No evidence of malignancy was found. After surgery, our patient had no recurrence of her effusion and, to date, has remained asymptomatic from her polycystic liver disease. Conclusion: The case in this report illustrates that an exudative pleural effusion is a rare complication of polycystic liver disease. We feel that the mechanical effects of a large polycystic liver, and subsequent disruption of sub-diaphragmatic capillaries, resulted in a persistent exudative pleural effusion. Thus, surgical debulking of the hepatic cysts is required to manage these effusions. © 2012 Woolnough et al; licensee BioMed Central Ltd.
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