간염 양상으로 나타난 원발성 간림프종

We report here on a case of non-Hodgkin`s lymphoma in which liver involvement was the predominant clinical manifestation. A healthy 44-year-old man presented with upper abdominal pain, hepatosplenomegaly, thrombocytopenia, elevated AST, ALT and bilirubin, and marked elevation of lactate dehydrogenas...

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Veröffentlicht in:Clinical and molecular hepatology 2005-09, Vol.11 (3), p.284
Hauptverfasser: 강경미, Kyung Mi Kang, 정우철, Woo Chul Chung, 이강문, Kang Moon Lee, 허성은, Sung Eun Hur, 나종명, Jong Myoung Nah, 김지희, Gee Hee Kim, 백주열, Ju Yeal Back, 김성경, Sung Kyoung Kim, 양진모, Jin Mo Yang, 최현주, Hyun Joo Choi
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Zusammenfassung:We report here on a case of non-Hodgkin`s lymphoma in which liver involvement was the predominant clinical manifestation. A healthy 44-year-old man presented with upper abdominal pain, hepatosplenomegaly, thrombocytopenia, elevated AST, ALT and bilirubin, and marked elevation of lactate dehydrogenase and alkaline phosphatase. The abdominal CT scan showed only diffuse hepatosplenomegaly and uneven contrast enhancement of the spleen without any definite mass of the liver and spleen. US-guided aspiration biopsy of liver and the histologic examination confirmed a diagnosis of non-Hodgkin`s lymphoma, the diffuse large B cell type. Bone marrow biopsy showed the infiltration of malignant lymphoma cells. PET-CT showed an increased FDG uptake of the liver, spleen and long bones. The patient was treated with combination regimen of cyclophosphamide, doxorubicin, vincristine and prednisone chemotherapy. Even in the absence of a mass lesion or lymphadenopathy, primary hepatic or hepatosplenic lymphoma should be considered in differential diagnosis of hepatitis or liver cirrhosis, especially for patients with diffuse hepatosplenomegaly and markedly elevated LDH. (Korean J Hepatol 2005;11:284-288)
ISSN:2287-2728