학술논문

Coma, Hyperviscosity Syndrome, Hyperammonemia and Myelofibrosis in a Patient with IgG, λ Type Multiple Myeloma / 昏睡,過粘稠症候群,高アンモニア血症,骨髄線維症を伴った(IgG, λ型)多発性骨髄腫の1例
Document Type
Journal Article
Source
臨床血液 / Rinsho Ketsueki. 1989, 30(3):361
Subject
coma
hyperammonemia
multiple myeloma
myelofibrosis
Language
Japanese
ISSN
0485-1439
1882-0824
Abstract
A 63-year-old man was admitted to our hospital with tremor and somnolence, followed soon by coma. Anemia and retinal bleeding were observed. The blood smear exhibited rouleaux formation and leukoerythroblastosis. A bone marrow aspiration resulted in dry tap. The biopsy specimens revealed remarkable infiltration of myeloma cells with fibrosis. The M-component of IgG-λ type and hyperammonemia were detected in the serum. Liver and renal functions, however, were within normal range. His consciousness recovered after plasmapheresis. Two courses of VMCP (vincristine, melphalan, carboquone and prednisolone) did not affect the paraproteinemia. Five courses of VAD (vincristine, adriamycin and dexamethasone) could lower the level of IgG. He died of pneumonia. The plasma of some patients with multiple myeloma may contain unidentified factors which increase the plasma ammonia.