Answers are grounded in this paper and cite their sources.
Brief Reports1 August 1989Alpha-Interferon for Severe Cold Agglutinin DiseaseBrian M. O'Connor, MD, Jacqueline S. Clifford, BS, William D. Lawrence, MD, Gerald L. Logue, MDBrian M. O'Connor, MD, Jacqueline S. Clifford, BS, William D. Lawrence, MD, Gerald L. Logue, MDAuthor, Article, and Disclosure Informationhttps://doi.org/10.7326/0003-4819-111-3-255 SectionsAboutPDF ToolsAdd to favoritesDownload CitationsTrack CitationsPermissions ShareFacebookTwitterLinkedInRedditEmail ExcerptCold agglutinin disease may be classified as primary or secondary. Monoclonal IgM (occasionally IgG or IgA) proteins with the ability to bind to erythrocytes below body core temperature are found in the sera of patients with the primary (idiopathic) and secondary forms associated with lymphoproliferative disorders (1). In these disorders mild to moderate hemolytic anemia results from the deposition of complement as the cold agglutinin binds to the erythrocyte in the acral circulation. On exposure to cold, episodes of hemoglobinuria related to marked intravascular hemolysis may occur. Exposure to cold may also produce painful acrocyanosis caused by sludging and deoxygenation...References1. CrispPruznaski DW. B-cell neoplasms with homogeneous cold-reacting antibodies (cold agglutinins). Am J Med. 1982;72:915-22. CrossrefMedlineGoogle Scholar2. HippeJensenOlesenLindThomsen EKHKP. Chlorambucil treatment of patients with cold agglutinin syndrome. Blood. 1970;35:68-72. CrossrefMedlineGoogle Scholar3. DacieWorlledge JS. Autoimmune hemolytic anemias. In: Brown EB, Moore CV, eds. Progress in Hematology. v 6. New York: Grune and Stratton; 1969:82-120. Google Scholar4. Schubothe H. The cold hemagglutinin disease. Semin Hematol. 1966;3:27-47. MedlineGoogle Scholar5. TaftProppSullivan ERS. Plasma exchange for cold agglutinin hemolytic anemia. Transfusion. 1977;17:173-6. CrossrefMedlineGoogle Scholar6. SilbersteinRobertsonHarrisMoreauBesaNowell LGALEP. Etiologic aspects of cold agglutinin disease: evidence for cytogenetically defined clones of lymphoid cells and the demonstration that an anti-Pr cold autoantibody is derived from a chromosomally aberrant B cell clone. Blood. 1986;67:1705-9. CrossrefMedlineGoogle Scholar7. QuesadaGuttermanHersh JJE. Treatment of hairy cell leukemia with alpha interferons. Cancer. 1986;57:1678-80. CrossrefMedlineGoogle Scholar8. QuesadaAlexanianHawkins JRM. Treatment of multiple myeloma with recombinant alpha-interferon. Blood. 1986;67:275-8. CrossrefMedlineGoogle Scholar9. BonomoCasatoAfeltraCaccavo LMAD. Treatment of idiopathic mixed cryoglobulinemia with alpha interferon. Am J Med. 1987;83:726-30. CrossrefMedlineGoogle Scholar10. GoldsteinLaszlo DJ. Interferon therapy of cancer: from imaginon to interferon. Cancer Res. 1986;46:4315-29. MedlineGoogle Scholar This content is PDF only. To continue reading please click on the PDF icon. Author, Article, and Disclosure InformationAuthors: Brian M. O'Connor, MD; Jacqueline S. Clifford, BS; William D. Lawrence, MD; Gerald L. Logue, MDAffiliations: From the Buffalo Veterans Administration Medical Center and the State University of New York at Buffalo, Buffalo, New York. For current author addresses, see end of text. PreviousarticleNextarticle Advertisement FiguresReferencesRelatedDetails Metrics Cited byNew Insights in the Pathogenesis and Therapy of Cold Agglutinin-Mediated Autoimmune Hemolytic AnemiaHow I manage patients with cold agglutinin diseaseCold Agglutinin-Mediated Autoimmune Hemolytic AnemiaRed Cell Antibodies Against Self-Antigens, Bound Antigens and Induced AntigensPeripheral Gangrene Affecting a FamilyDiagnosis and treatment of cold agglutinin mediated autoimmune hemolytic anemiaHow I manage cold agglutinin diseaseCold Agglutinin Induced Hemolysis in a Newly Diagnosed Systemic Lupus ErythematosusCatastrophic multiple organ ischemia due to an anti-Pr cold agglutinin developing in a patient with mixed cryoglobulinemia after treatment with rituximabAnémies hémolytiques auto-immunesAutoimmune hemolytic anemia: classification and therapeutic approachesDiagnosis and treatment of autoimmune haemolytic anaemias in adults: a clinical reviewPrimary chronic cold agglutinin disease: An update on pathogenesis, clinical features and therapyHemolytic AnemiaRituximab in chronic cold agglutinin disease: a prospective study of 20 patientsA Last Resort Modality Using Cryofiltration Apheresis for the Treatment of Cold Hemagglutinin Disease in a Veterans Administration HospitalManagement of Autoimmune Hemolytic AnemiasAutoimmune hemolytic anemiaFavourable response to therapy with the anti-CD20 monoclonal antibody rituximab in primary chronic cold agglutinin diseaseRemission of severe cold agglutinin disease Rituximab therapyCold haemagglutinin disease: clinical significance of serum haemolysinsDual X-Ray Absorptiometry for the Measurement of Soft Tissue Composition and Skeletal MassAutoimmune hemolytic anemiaInterferon-α: Its Current Clinical Utility and Future PerspectivesChronic cold agglutinin disease of the "idiopathic" type is a premalignant or low-grade malignant lymphoproliferative diseaseFailure of interferon-α-2b therapy in chronic cold agglutinin diseaseSuccessful response to alpha-interferon 2b in a refractory IgM autoagglutinin-mediated hemolytic anemiaCryoglobulinemia in chronic liver diseases: Role of hepatitis C virus and liver damageLow-dose interferon-alpha in stage-I multiple myeloma and in IgM monoclonal gammopathyMixed cryoglobulinemia responsive to interferon-αA fatal case of low titer anti-PR cold agglutinin disease 1 August 1989Volume 111, Issue 3Page: 255-256KeywordsAgglutininsHemoglobinHemolytic anemiaLymphoproliferative disorderProteinsTemperature ePublished: 1 December 2008 Issue Published: 1 August 1989 PDF downloadLoading ...
No takes yet. Share an insight, caveat, or question.
Brian M. OʼConnor (1989) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: