Pernicious anemia associated with autoimmune hemolytic anemia.
نویسندگان
چکیده
منابع مشابه
Immunotherapy-associated autoimmune hemolytic anemia
BACKGROUND Immunotherapy has been widely used in the treatment of several solid and hematologic malignancies. Checkpoint inhibitors have been the forefront of cancer immunotherapy in recent years. Cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) and programmed cell death 1 (PD-1) pathway are the prototypic checkpoint targets for immunotherapy. When combined, CTLA-4 and PD-1 checkpoint inhib...
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A rare case of multiple myeloma associated with severe Coombs-positive hemolytic anemia is described. A 60-year-old woman was hospitalized for acute hemolysis due to an IgG warm autoantibody with pan-agglutinin specificity. Serum and urine electrophoresis revealed the presence of a monoclonal IgGk protein and a BJk protein, respectively. Bone marrow aspirates showed diffuse infiltration with pl...
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Unlike other autoimmune polyneuropathies, the linkage between chronic inflammatory demyelinating polyneuropathy (CIDP) and other immune mediated disorders is weak. We report a patient who developed monophasic and parallel courses of autoimmune hemolytic anemia (AIHA) and chronic demyelinating polyneuropathy. Both resolved in tandem with corticosteroid therapy. Distinct from Guillain-Barre Syndr...
متن کاملPernicious Anemia with Autoimmune Hemolytic Anemia: A Case Report and Literature Review
Pernicious anemia is a common cause of vitamin B12 deficiency. Here, we discuss a case of a young woman who presented with severe anemia along with a history of iron deficiency anemia. After a review of her clinical presentation and laboratory data, we identified an autoimmune hemolytic anemia and a concomitant pernicious anemia. The concurrence of both these hematological diagnoses in a patien...
متن کاملThymoma with Autoimmune Hemolytic Anemia
A 38-year-old Japanese male was referred to our hospital with abnormal chest X-ray results and severe Coombs-positive hemolytic anemia. He was diagnosed with a stage IV, WHO type A thymoma and was treated with oral prednisolone (1 mg/kg/day) and subsequent chemotherapy. After chemotherapy, the patient underwent surgical resection of the thymoma. Hemolysis rapidly disappeared and did not return ...
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ژورنال
عنوان ژورنال: Journal of the Japan Society of Blood Transfusion
سال: 1992
ISSN: 1883-8383,0546-1448
DOI: 10.3925/jjtc1958.38.573