Request PDF on ResearchGate | Síndrome de aglutininas frías y púrpura trombocitopénica autoinmune: Un caso inusual de síndrome de. Abstract. ARANGO, Marcos; ARENAS, Mario and MARTINEZ, Octavio. Mycoplasma pneumoniae pneumonia complicated by cold agglutinin hemolytic anemia. QUINTANILLA-GALLO, Júvel; MARCHENA- PICADO, Margarita and GOURZONG- TAYLOR, Charles. Síndrome aglutininas frías. Acta méd. costarric [ online].
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Although access to this page is not restricted, the information found here is intended for use by medical providers. Examination Chapter related topics Aglutkninas Score.
You are currently viewing the original ‘fpnotebook. The disease has a chronic course and the outcome is usually benign, except in patients with aglutininnas episodes of severe anemia or in whom the underlying B-cell lymphoma has an aggressive course. The documents contained in this web site are presented for information purposes only.
An acquired anemia caused by destruction of the red blood aglutlninas by autoantibodies. An acquired anemia resulting from immune-mediated destruction of the red blood cells. Definition NCI An acquired anemia caused by destruction of the red blood cells by autoantibodies.
If you are using a modern web browser, you may instead navigate to the newer desktop version of fpnotebook. Etiology Cold agglutinin disease can be primary idiopathic or secondary, caused by an underlying condition, such as infection Mycoplasma pneumoniaelymphoproliferative disorders, systemic autoimmunity or neoplasm. In secondary aglutkninas, lymphocytosis, with the presence of atypical lymphocytes on the smear, can be found in peripheral blood.
aglutinina fría – English Translation – Word Magic Spanish-English Dictionary
Rituximab aglutijinas be an option for treatment in some cases. Differential diagnosis The differential agultininas for cold agglutinin disease is mixed AIHA see this term. Prognosis The disease has a chronic course and the outcome is usually benign, except in patients with recurrent episodes of severe anemia or in whom the underlying B-cell lymphoma has an aggressive course.
Keeping the patient warm may be sufficient treatment. Additional information Further information on this disease Classification s 1 Gene s 0 Clinical signs and symptoms Publications in PubMed Other website s 3.
Clinical description It occurs more frequently after the age of The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment. Anemia emolitica da emoagglutinine fredde, Malattia da agglutinina fredda, Malattia da agglutinine a frigore, Malattia da agglutinine fredda.
Specialised Social Services Eurordis directory. The disease may appear abruptly with anemia and hemoglobinuria, or onset may be more gradual and insidious.
Only comments seeking to improve the quality and accuracy of information on the Orphanet website are accepted. In the presence of underlying lymphoma, chlorambucil or oral cyclophosphamide may be helpful. Friss CSP due to acquired antierythrocyte autoantibodies causing premature erythrocyte clearance by the spleen; antibodies can be warm or cold active; usually slow developing and treatable.
In some cases, the diagnosis friaa made by chance on a standard complete blood count CBC detecting abnormal agglutination of the red blood cells.
It occurs more frequently after the age of Definition NCI An acquired anemia resulting from immune-mediated destruction of the red blood cells. The disease is usually refractory to corticosteroids. Other search option s Alphabetical list. Diagnosis is based on clinical or laboratory evidence of hemolytic anemia and the detection of autoantibodies, specifically IgM, with the direct anti-globulin test DAT, C3 positive pattern with the presence of circulating cold agglutinins inthe serum.
Idiopathic and lymphoma-associated cold AIHA tend to be chronic while infections tend to cause an acute disease. Causes include autoimmune disorders, blood transfusions, and drugs.
Immune complex hemolytic anemia can occur in patients who have chronic lymphocytic leukemia CLL.
Diagnostic methods In some cases, the diagnosis is made by chance on a standard complete blood count CBC friae abnormal agglutination of the red blood cells. Autoimmune hemolytic anemia can occur in patients who have chronic lymphocytic leukemia CLL. Cold agglutinin disease manifests as acute or chronic hemolytic anemia, with associated pallor and fatigue.