1.Ultrastructure of Chronic Liver Diseases ; Kupffer Cells of the Hepatic Sinusoids.
The Korean Journal of Hepatology 2002;8(4):505-514
No abstract available.
Human
;
Kupffer Cells/*ultrasonography
;
Liver Diseases/*pathology
2.Focal Nodular Hyperplasis in Liver.
Ki Ho SEONG ; Jae Ho CHO ; Jae Chun CHANG
Yeungnam University Journal of Medicine 1995;12(2):400-404
Focal nodular hyperplasia is a benign hepatic tumor mainly composed of nodules of hepatocytes and Kupffer cells separated by fibrous septa. In general, it is difficult to differentiate focal nodular hyperplasia and hepatocellular carcinoma on ultrasonography, conventional CT(computerized tomography), and angiography. But IV bolus CT is of particular value in the diagnosis of focal nodular hyperplasia because it can divide enhanced CT into early and late phase and can characterize tumor vascularity and analyze any intratumoral elements. In our case, it was seen as a hypoechoic mass lesion on ultrasonograpl'hy and hyperdense mass lesion on early-phase IV bolus CF and isodense mass, lesion on late-phase IV bolus CT. On angiography, hypertrophy of the feeding artery and tumor staining were well visualized. The patient underwent operation and the mass was pathologically confirmed to a focal nodular hyperplasia. We report the first case of focal nodular hyperplasia on IV bolus CT in Korea.
Angiography
;
Arteries
;
Carcinoma, Hepatocellular
;
Diagnosis
;
Focal Nodular Hyperplasia
;
Hepatocytes
;
Humans
;
Hypertrophy
;
Korea
;
Kupffer Cells
;
Liver*
;
Ultrasonography
3.A Case of Erythropoietic Protoporphyria with Severe Liver Dysfunction and Neurological Symptoms.
Bo Hyun KIM ; Young Nyun PARK ; Ki Sup CHUNG
Korean Journal of Pediatric Gastroenterology and Nutrition 2005;8(2):263-268
Erythropoietic protoporphyria is a genetic disorder due to a deficiency of ferrochelatase resulting in excessive accumulation and excretion of protoporphyrin. The predominant clinical feature is photosensitivity. Severe hepatic failure occurs in a small percentage of patients, and neurological symptoms are very rare. We report a case of erythropoietic protoporphyria associated with severe hepatic dysfunction and neurological symptoms. A 9-year-old girl presented with severe abdominal pain, nausea, weakness and pain of extremities, and urinary retention. Ultrasonogram and abdominal CT scanning revealed a diffuse infiltrated and enlarged liver. Liver biopsy showed deposition of dense dark brown pigment within the bile, hepatocytes and Kupffer cells. Plus, dense dark brown deposits gave a red birefringent under polarize light. Porphyrin studies demonstrated markedly elevated serum free erythrocyte protoporphyrin. This girl was diagnosed as erythropoietic protoporphyria with severe liver dysfunction and neurological symptoms.
Abdominal Pain
;
Bile
;
Biopsy
;
Child
;
Erythrocytes
;
Extremities
;
Female
;
Ferrochelatase
;
Hepatocytes
;
Hepatomegaly
;
Humans
;
Kupffer Cells
;
Liver Diseases*
;
Liver Failure
;
Liver*
;
Nausea
;
Protoporphyria, Erythropoietic*
;
Tomography, X-Ray Computed
;
Ultrasonography
;
Urinary Retention