1991
DOI: 10.1016/0277-5379(91)90020-e
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Changing clinical presentation of multiple myeloma

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Cited by 107 publications
(54 citation statements)
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“…Follow-up At diagnosis a complete history was obtained and the general performance and objective clinical status of the patient were assessed, together with a number of routine haematological laboratory parameters (including erythrocyte sedimentation rate, haemoglobin level, white cell count and differential, platelets, serum creatinine, urea nitrogen, uric acid, calcium, protein electrophoresis, and normal immunoglobulin level, as assessed by serum radial immunodiffusion, immunoelectrophoresis or immunofixation), 24 h urine examination (for Bence Jones proteinuria, calciuria, hydroxyprolinuria), BM biopsy and aspiration (with myelogram, for the BMPC %), complete radiological bone survey and special evaluations (such as plasma viscosity, serum alkaline phosphatase isoenzymes, serum P2-microglobulin and thymidine kinase levels, bone marrow plasma cell labelling index, DNA flow cytometry and standard cytogenetics of bone and/or peripheral blood cells) (Riccardi et al, 1991).…”
Section: Methodsmentioning
confidence: 99%
“…Follow-up At diagnosis a complete history was obtained and the general performance and objective clinical status of the patient were assessed, together with a number of routine haematological laboratory parameters (including erythrocyte sedimentation rate, haemoglobin level, white cell count and differential, platelets, serum creatinine, urea nitrogen, uric acid, calcium, protein electrophoresis, and normal immunoglobulin level, as assessed by serum radial immunodiffusion, immunoelectrophoresis or immunofixation), 24 h urine examination (for Bence Jones proteinuria, calciuria, hydroxyprolinuria), BM biopsy and aspiration (with myelogram, for the BMPC %), complete radiological bone survey and special evaluations (such as plasma viscosity, serum alkaline phosphatase isoenzymes, serum P2-microglobulin and thymidine kinase levels, bone marrow plasma cell labelling index, DNA flow cytometry and standard cytogenetics of bone and/or peripheral blood cells) (Riccardi et al, 1991).…”
Section: Methodsmentioning
confidence: 99%
“…[6] Therefore, primary clinical presentation includes bone pain, and anemia. [7,8] Extramedullary plasmacytomas have been reported in 15-20% of patients at diagnosis and in an additional 15% during the course of PCM, and these patients are often associated with highrisk diseases like myelomatous pleural effusion (MPE). [9] Extramedullary existence of plasmacytoma is not common and the incidence of thoracic cases is low, especially in patients presenting with pulmonary plasmacytoma and malign pleural efusion to simulate a pleural mesothelioma or lung cancer.…”
Section: Discussionmentioning
confidence: 99%
“…The incidence of weight loss at presentation is 24%. 16,17 Some patients are asymptomatic at presentation, with incidental abnormalities found on laboratory testing (34%). 16,17 Some of the more common direct effects of multiple myeloma are listed in Table 1.…”
Section: Clinical Presentation Skeletal Complications On Presentationmentioning
confidence: 98%
“…11,15 In the setting of vertebral body compression fracture, weakness and paresthesias of the lower limbs may occur. 16,17 Other Presenting Complications Anorexia, nausea, somnolence, and polydipsia are symptoms associated with hypercalcemia, which is commonly seen in multiple myeloma. Carpal tunnel syndrome is the most common peripheral neuropathy.…”
Section: Clinical Presentation Skeletal Complications On Presentationmentioning
confidence: 98%