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FPCPD<br />

83358<br />

PLHBB<br />

9096<br />

Plasma Cell Proliferative Disorder (PCPD), FISH<br />

Clinical Information: Multiple myeloma is a hematologic neoplasm that generally originates in the<br />

bone marrow and develops from malignant plasma cells. There are 4 main categories of plasma cell<br />

proliferative disorders (PCPDs): asymptomatic myeloma, smoldering myeloma, indolent myeloma, and<br />

multiple myeloma. Asymptomatic myeloma patients have nonspecific symptoms that may be attributed to<br />

other diseases. Generalized bone pain, anemia, numbness or limb weakness, symptoms of hypercalcemia,<br />

and recurrent infections are all symptoms that may indicate myeloma. In smoldering myeloma there is a<br />

monoclonal protein spike, but it is stable. Indolent myeloma is a slowly progressing myeloma. As<br />

myeloma progresses, the malignant plasma cells interfere with normal blood product formation in the<br />

bone marrow resulting in anemia and leukopenia. Myeloma also causes an overstimulation of osteoclasts,<br />

causing excessive breakdown of bone tissue without the normal corresponding bone formation. These<br />

bone lesions are seen in approximately 66% of myeloma patients. In advanced disease, bone loss may<br />

reach a degree where the patient suffers fractures easily.<br />

Useful For: Aiding in the diagnosis of new cases of multiple myeloma or other plasma cell<br />

proliferative disorders Identifying prognostic markers based on the anomalies found<br />

Interpretation: A neoplastic clone is detected when the percent of cells with an abnormality exceeds<br />

the normal reference range for any given probe.<br />

Reference Values:<br />

An interpretive report will be provided.<br />

Clinical References: 1. Fonseca R, Blood E, Rue M, et al: Clinical and biologic implications of<br />

recurrent genomic aberrations in myeloma. Blood 2003 Jun 1;101(11):4569-4575 2. Fonseca R, Blood<br />

EA, Oken MM, et al: Myeloma and the t(11;14)(q13;q32); evidence for a biologically defined unique<br />

subset of patients. Blood 2002 May 15;99(10):3735-3741 3. Shaughnessy J, Tian E, Sawyer J, et al: High<br />

incidence of chromosome 13 deletion in multiple myeloma detected by multiprobe interphase FISH.<br />

Blood 2000 Aug 15;96(4):1505-1511<br />

Plasma Hemoglobin, Plasma<br />

Clinical Information: Plasma normally contains no free hemoglobin ie, no hemoglobin that is not<br />

contained in erythrocytes. Significant amounts of hemoglobin occur in plasma following hemolysis such<br />

as might result from a transfusion reaction or mechanical fragmentation of red blood cells during cardiac<br />

surgery.<br />

Useful For: Determining whether hemolysis is occurring such as from: -Transfusion reaction<br />

-Mechanical fragmentation of red blood cells<br />

Interpretation: Total hemoglobin: > or =12 months: 0.0-15.2 mg/dL Reference values have not been<br />

established for patients who are less than 12 months of age. Oxyhemoglobin: > or =12 months: 0.0-12.4<br />

mg/dL Reference values have not been established for patients who are less than 12 months of age.<br />

Reference Values:<br />

TOTAL HEMOGLOBIN<br />

> or =12 months: 0.0-15.2 mg/dL<br />

Reference values have not been established for patients who are less than 12 months of age.<br />

OXYHEMOGLOBIN<br />

> or =12 months: 0.0-12.4 mg/dL<br />

Reference values have not been established for patients who are less than 12 months of age.<br />

Clinical References: Fairbanks VF, Ziesmer SC, O'Brien PC: Methods for measuring plasma<br />

hemoglobin in micromolar concentration compared. Clin Chem 1992;38:132-140<br />

Current as of January 4, 2013 7:15 pm CST 800-533-1710 or 507-266-5700 or <strong>Mayo</strong><strong>Medical</strong><strong>Laboratories</strong>.com Page 1428

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