AI Summary & Key Takeaways
AI InsightNo local recurrence could be found after a follow-up of more than two years.
📌 3 Key Takeaways
Abstract
Biliary cystadenocarcinoma is rare tumor that originates from the hepatobiliary epithelium, and its clinical diagnosis is difficult during the preoperative course. A 65-year-old woman with biliary cystadenocarcinoma was misdiagnosed as hepatic abscess and underwent ultrasonography-guided percutaneous catheter drainage. Ten months later, the patient was re-admitted to our department with a mucin-producing cauliflower-like mass measuring 10x10x5 cm3 at the site of puncture. Tumor seeding through the percutaneous catheter drainage tract was diagnosed. Complete resection of the primary and metastatic tumor with partial abdominal wall tissue was performed. No local recurrence could be found after a follow-up of more than two years.
Özet
Safra yolu kistadenokarsinomu hepatobiliyer epitelden köken alan nadir görülen bir tümördür ve preoperatif tanısı zordur. Karaci¤ er absesi tanısı yanlışlıkla konulmuş olan 65 yaşında kadın hastaya ultrason eşli¤inde perkütan drenaj uygulanmıştır. On ay sonra hasta klini¤imize ponksiyon yerinde gelişen 10x10x5 cm boyutlarında müsin üreten karnıbahar şeklinde kitle ile başvurmuştur. Perkütan girişim hattında tümör yayılımı tanısı konulmuştur. Primer tümör ile beraber metastazı bir miktar abdomen duvarı ile beraber rezeke edilmiştir ve 2 yıllık takibin sonunda lokal rekürrens tespit edilmemiştir.