ASH Clinical News September 2015 | Page 56

You Make the Call Each month in “You Make the Call,” we’ll pick a challenging clinical question submitted through the Consult-a-Colleague program and post the expert’s response. But, what would YOU do? We’ll also pose a submitted question and ask you to send your responses. See how your answer matches up to the experts’ in the next print issue. This month, Robert A. Kyle, MD, answers a question about the “faint monoclonal band” of IgG kappa or IgG lambda in a dense polyclonal background. Clinical Dilemma: Consult a Colleague Through ASH Consult a Colleague is a service for ASH members that helps facilitate the exchange of information between hematologists and their peers. ASH members can seek consultation on clinical cases from qualified experts in 11 categories: • Anemias What is your approach to a patient who is referred for an immunofixation showing a “faint band” of monoclonal IgG kappa or IgG lambda in a dense polyclonal background with or without an increase of that involved heavy chain? • Hematopoietic cell transplantation • Hemoglobinopathies • Hemostasis/thrombosis • Lymphomas Experts Make the Call • Lymphoproliferative disorders Robert A. Kyle, MD Professor of Laboratory Medicine & Pathology Professor of Medicine Mayo Clinic Rochester, Minnesota • Multiple myeloma & Waldenström macroglobulinemia • Leukemias • Myeloproliferative Disorders • Myelodysplastic Syndromes • Thrombocytopenias In the case of the “faint band” of monoclonal IgG kappa or IgG lambda in a dense polyclonal background, the first thing to do is determine the size of the polyclonal gamma component. If it is increased, I would not be concerned about the faint band and simply follow with a repeat electrophoresis and immunofixation in six months. The small monoclonal protein may disappear or another small monoclonal protein may appear.  If it persists and is still stable, I would simply repeat the tests at annual intervals. Further evaluation such as bone marrow examination, skeletal x-rays, etc. are not necessary.  As you know, patients with a polyclonal increase in immunoglobulins have an inflammatory or reactive process. The most common causes for these processes in patients living in the United States today are connective tissue disorders or chronic liver disease, whereas in other parts of the world tuberculosis and other infectious diseases may be major causes.  DISCLAIMER: ASH does not recommend or endorse any specific tests, physicians, products, procedures, or opinions, and disclaims any representation, warranty, or guaranty as to the same. Reliance on any information provided in this article is solely at your own risk. Assigned volunteers (“colleagues”) will respond to inquiries within two business days (either by email or phone). Have a puzzling clinical dilemma? Submit a question, and read more about Consult-a-Colleague volunteers at hematology.org/Clinicians/Consult.aspx or scan the QR code. *If you have a request related to a hematologic disorder not listed here, please email your recommendation to ashconsult@ hematology.org so it can be considered for addition in the future. Next Month’s Clinical Dilemma: The patient is a 73-year-old man with blastic plasmacytoid dendritic cell neoplasm and a long history of anemia. A bone marrow biopsy three years ago showed only iron deficiency and a gastrointestinal evaluation was unremarkable. The patient received iron replacement 54 ASH Clinical News therapy, but his anemia never improved. He now presents with purple skin lesions. A biopsy showed blastic plasmacytoid dendritic cell neoplasm, and a bone marrow biopsy showed very cellular bone marrow with 60 to 70 percent blastic plasmacytoid dendritic cell neoplasm. Results from a cytogenetic analysis are pending. Meanwhile, he has been relatively asymptomatic. He is active and healthy and his blood count has been stable for the last three years (white blood cell count is 3.3 x 109/L, hemoglobin count is 10.3 g/dl, and platelet count is 135 x 109/L). He is worried about toxicities with acute lymphocytic leukemia–type treatment. How would you treat this patient? What result can you expect from treatment? How would you respond? Email us at [email protected]. September 2015