Multiple Myeloma Lab Workup
- Serum and urine evaluation for monoclonal protein (Densitométrico follow-up and Nephelometric quantification, immunofixation for Affirmation)
- Serum-Free Light chain assay (in all patients with newly identified plasma cell dyscrasias)
- Aspiration and/or bone marrow biopsy
- Serum Beta-2 microglobulin, albumin, and lactate dehydrogenase dimension
- Standard cytogenetics in metaphase
- Fluorescent hybridization in situ
- Skeletal study
- Magnetic resonance Imaging
See also: M Protein Levels in Multiple Myeloma
Let us not forget the risk of renal failure, particularly in the injection of contrast medium for imaging research. Be careful to restrict the publicity of the sick and maintain hydration.
Multiple Myeloma Lab Workup
Blood Research: Perform a full number of blood count (CBC) to decide if the affected person has anemia, thrombocytopenia, or leukopenia. CBC and differential can also show Pancytopenia. The memory of the reticulocytes is typically low. Peripheral blood smears may also show the formation of Rouleau.The price of erythrocyte sedimentation (ESR) is typically elevated. Coagulation studies can also give strange results. Acquire a complete metabolic panel to evaluate the grades of the following:
- Total protein, albumin, and globulin
- Blood urea nitrogen (BUN) and creatinine
- Uric acid (may be extended if the affected person has an excessive moving rotation or is dehydrated)
Urine Collection: Achieve a 24-hour urine collection for quantification of the protein Bence Jones (i.e. lambda light chains), protein and creatinine clearance. The quantification of proteinuria is beneficial for the analysis of MM (> 1 g of protein in 24 h is the main criterion) and for the follow-up of the reaction to be remediated. creatinine clearance may be beneficial in delineating the severity of the patient’s renal deterioration.
Electrophoresis and Immunofixation: Serum protein electrophoresis (SPEP) is used to decide the type of donation of each protein and may involve a characteristic curve (i.e., where the beak is observed). Urine protein electrophoresis (UPEP) is used to become aware of the presence of the protein Bence Jones in the urine. Inmunofixación is used to discover the protein subtype (i.e., IgA Lambda).
The recommendations of the medical practice of the complete National Network of cancer (NCCN, 2015 also advise the use of serum free light chain and fluorescent in situ hybridization (FISH) tests for 13, 13, T (4;, 1q21 amplification as part of the initial diagnosis). 2]
Multiple Myeloma Workup
The chemical screening, consisting of calcium and creatinine SPEP, immunofixation and quantification of immunoglobulin, can also show Azotemia, Hypercalcemia, an accelerated degree of alkaline phosphatase and hypoalbuminemia. An excessive level of lactate dehydrogenase (LDH) is predictive of an aggressive route lymphomatous.
See also: Stem Cell Transplant for Multiple Myeloma Life Expectancy
SPEP is a beneficial screening test to detect M proteins. One thing M is usually detected by high resolution SPEP. The Kappa-lambda ratio has been defended as a detection tool for detecting abnormalities in the M-aspect. A M-Issue serum care of 30 g/L is a minimum diagnostic criterion for mm. In approximately 25% of patients, M protein cannot be detected with the help of SPEP.
Recurrent urine test will not indicate the presence of Bence Jones proteinuria. Therefore, a 24-hour urine test may be required using UPEP or immunophoresis. UPEP or immunophoresis may also be used to detect an M chain and kappa or lambda light chains. The most important form of detecting MM is the electrophoretic size of immunoglobulins in each serum and urine.
Multiple myeloma workup – The quantitative degrees of immunoglobulin (IgG, IgA, IgM): Suppression of non-myelomatosis immunoglobulin is a lower diagnostic criterion for MM. The level of protein mm (i.e., the level of protein M), as documented by the degree of immunoglobulin, may be useful as a marker to evaluate the response to treatment.