ABSTRACT
Multiple hepatic adenoma is a rare entity in which characterized by the presence of numerous adenomas within an otherwise normal liver. Although the disease is rare, its important lies in its tendency to produce symptoms such as abdominal pain and its potential for abdominal hemorrhages. However, the prognosis and the evolution of this entity is generally uncertain. We report a case multiple hepatic adenomas, which was proved by pathology, in 24 years old man who has been prescribed long-term oral steroid due to rheumatoid arthritis. He underwent incisional biopsy and mass enucleation of hepatic tumors with 95% alcohol injection. In the case, dissection of the liver showed many other diffuse and smaller nodules. Histologically, tumor was liver cell adenoma without pleomorphism, or mitosis. During the follow-up period of two years, new nodules were found by ultrasonography and magnetic resonance image without developed of serious complications.
Subject(s)
Humans , Young Adult , Abdominal Pain , Adenoma , Adenoma, Liver Cell , Arthritis, Rheumatoid , Biopsy , Follow-Up Studies , Hemorrhage , Liver , Mitosis , Pathology , Prognosis , UltrasonographyABSTRACT
Agenesis of the right lobe of the liver is a rare anomaly which may be associated with stone diseases, portal hypertension, and other congenital anomalies. The radiological differential diagnosis includes lobar atrophy due to cirrhosis or hilar cholangiocarcinoma. We present a case of agenesis of the right lobe of the liver with characteristic clinical and radiological findings.
Subject(s)
Atrophy , Diagnosis, Differential , Fibrosis , Hypertension, Portal , Klatskin Tumor , LiverABSTRACT
Agenesis of the right lobe of the liver is a rare anomaly which may be associated with stone diseases, portal hypertension, and other congenital anomalies. The radiological differential diagnosis includes lobar atrophy due to cirrhosis or hilar cholangiocarcinoma. We present a case of agenesis of the right lobe of the liver with characteristic clinical and radiological findings.
Subject(s)
Atrophy , Diagnosis, Differential , Fibrosis , Hypertension, Portal , Klatskin Tumor , LiverABSTRACT
Twenty patients with symptomatic congenital cysts in the liver, kidney, thyroid, and lower neck underwent, ultrasound guided percutaneous aspiration through a drainage catheter with temporary instillation of 95% ethanol into the cyst. Our procedure was based on the method as described by Bean and Rodan(16) in 1985. Additionaly, two othe steps were odded to prevent the dilutional effect of residual cyst fluid. One was the preliminary washing of the cyst with alcohol. The other was to treat with 30% replacement of alcohol every 10 minutes during the treatment secession. Minot complications of transient temperature elevation and hziness occurred, butj no major complications were encountered. After the alcohol treatment follow up examinations were performed with computed tomography or ultrasonography at 6 weeks. 6 months. 9 months and 15 months. Although there was diminished size, recurrence was noted in 6 of twenty patients(30%) at 6 weeks and one of twenty patients(5%) at 6 months. There was no recurrence at 9 months and 15 months. The results indicated that percutaneous aspiration and alcohol sclerotherapy are safe and effective therapy for symptomatic congenital cysts.