Myelofibrosis Associated with IgG Myeloma
Author(s) -
Giuseppe Leone,
Flavia Scuderi,
Mauro Carlesimo,
Filippo Crivelli
Publication year - 1982
Publication title -
acta haematologica
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.574
H-Index - 56
eISSN - 1421-9662
pISSN - 0001-5792
DOI - 10.1159/000207042
Subject(s) - myelofibrosis , multiple myeloma , medicine , immunoglobulin g , immunology , myeloma protein , antibody , bone marrow
Dr. Giuseppe Leone, Flavia Scuderi, Mauro Carlesimo, Filippo Crivelli, Università Cattolica, Largo Gemelli 8, I-00168 Roma (Italy) Idiopathic myelofibrosis is considered a myelo-proliferative disease. Myelofibrosis is sometimes found in malignancies and is typically present in hairy cell leukemia [14]: yet in all instances myelofibrosis in considered a secondary reaction [3]. Myelofibrosis associated with myeloma has been reported in a few patients [2]. We would like to report on a further case. A 49-year-old woman was admitted suffering from easy fatigability, diffuse musculoskeletal pain and episodes of hemoptysis. Physical examination revealed a mild hepatomegaly. Chest Xray was normal. A complete skeletal survey indicated the presence of dense trabeculae in the vertebrae and in the pelvic bones, but no lytic lesions were observed in the bones examined. Laboratory studies revealed a hemoglobin level of 7.8 g/dl, a WBC count of 10.5 X 10VI, with 60% polymorphonu-clear leukocytes, 7% myelocytes, 2% > eosinophils, 23% lymphocytes and 9% monocytes, 8 normo-blasts per 100 WBC, platelet count 71 × 10V1, and ESR HOmm/h. Serum immunoelectrophoresis revealed an 1⁄8G//í + paraprotein. An open bone marrow biopsy of the iliac crest showed fibrosis of the marrow with nests of plasma cells. Normal hemopoietic cells were absent. The coexistence of myelomatosis and myelofibrosis in this patient is well established. The clinical and laboratory features are typical and the bone marrow biopsy, done before any therapy was given, confirms the diagnosis. The finding of myelofibrosis and myelomatosis in the same patient is a rare event. Though it is possible that these two unrelated disorders coexist merely by chance, it is tempting to presume that they are somehow associated. At present, myelofibrosis is generally considered a secondary reaction [3], yet the mechanism of production of fibrosis is not clear. Recently, an increased urinary hydroxyproline excretion has been signaled in myelofibrosis associated with metastasis but not in agnogenic myeloid metaplasFig. 1. Radiograph of dorsal and lumbar spine revealing omogenous osteocondensation. 140 Leone/Scuderi/Carlesimo/Crivelli
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