Pisani Antonio, Riccio Eleonora, Imbriaco Massimo, Capuano Ivana, Rossano Roberta, Santangelo Michele
Universita' Federico II, Cattedra di Nefrologia, Napoli, Italy.
G Ital Nefrol. 2012 Nov-Dec;29(6):716-9.
We present the case of a 39-year-old woman with autosomal dominant polycystic kidney disease (ADPKD). She was admitted to our hospital with marked dyspnea and epigastric pain. A diagnosis of giant hepatic cyst compressing the surrounding organs was made on the basis of the clinical and radiological findings. The patient underwent percutaneous aspiration of the cyst. The symptoms and radiological abnormalities were normalized within a few days of the minimally invasive aspiration procedure.
我们报告一例39岁的常染色体显性遗传性多囊肾病（ADPKD）女性患者。她因明显的呼吸困难和上腹部疼痛入院。根据临床和影像学检查结果，诊断为巨大肝囊肿压迫周围器官。患者接受了经皮囊肿抽吸术。在微创抽吸术后几天内，症状和影像学异常均恢复正常。
