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Int J Hematol ; 84(1): 70-3, 2006 Jul.
Article in English | MEDLINE | ID: mdl-16867906

ABSTRACT

Hepatic amyloidosis complicated with Castleman's disease is quite rare. A 48-year-old woman was referred to our hospital with general fatigue, low-grade fever, anemia, thrombocythemia, and liver dysfunction. Physical examination revealed anemia and hepatomegaly and abdominal computed tomography showed marked hepatomegaly and right upper abdominal masses. Technetium-99m pyrophosphate (99mTc-PYP) scintigraphy revealed the diffuse abnormal uptake of the enlarged liver, suggesting amyloid deposition. Liver biopsy showed destruction of the liver structure and the massive deposition of AA type amyloid protein. Surgical resection was performed on the abdominal masses. Histological examination of the masses showed Castleman's disease (plasma cell type). After resection, her fever resolved and the liver size gradually decreased to within the normal range. This case shows that surgical resection of the main lesion is effective for hepatomegaly due to AA type amyloidosis associated with Castleman's disease.


Subject(s)
Amyloidosis/complications , Amyloidosis/pathology , Castleman Disease/complications , Castleman Disease/pathology , Liver/pathology , Amyloidosis/metabolism , Castleman Disease/metabolism , Female , Hepatomegaly/complications , Hepatomegaly/metabolism , Hepatomegaly/pathology , Humans , Liver/metabolism , Middle Aged , Plasma Cells/metabolism , Plasma Cells/pathology , Serum Amyloid A Protein/metabolism
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