AGLUTININAS FRIAS PDF

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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Keeping the patient warm may be sufficient treatment.

Orphanet: Doenca de aglutininas frias

Autoimmune hemolytic anemia can occur in patients who have chronic lymphocytic leukemia CLL. Definition NCI An acquired anemia resulting from immune-mediated destruction of the red blood cells.

Diagnostic methods In some cases, the diagnosis is made by chance on a standard complete blood count CBC detecting abnormal agglutination of the red blood cells. Anemia emolitica da emoagglutinine fredde, Malattia da agglutinina frlas, Malattia da agglutinine a frigore, Malattia da agglutinine fredda. 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.

Neumonia por Mycoplasma pneumoniae complicada con anemia hemolitica por aglutininas frias.

An acquired anemia caused by destruction of the red blood cells by autoantibodies. Definition NCI An acquired anemia caused by destruction of the red blood cells by autoantibodies. Health care resources for this disease Expert centres Diagnostic tests 0 Patient organisations 4 Orphan drug s 0.

Other search option s Alphabetical list. The material is in no aglutinlnas intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment. Causes include autoimmune disorders, blood transfusions, and drugs.

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Please Contact Me as you run across problems with any of these versions on the website. Cold agglutinin disease manifests as acute or chronic hemolytic anemia, with associated pallor and fatigue. Examination Chapter related topics Plasmic Score. Summary and related texts. In some cases, the diagnosis is made by chance on a standard complete blood count CBC detecting abnormal agglutination of the red blood cells.

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 aglutinins presence of circulating cold agglutinins inthe friaw.

Only comments written in English can be processed. In secondary cases, lymphocytosis, with the presence of atypical lymphocytes on the smear, can be found in peripheral blood. 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. Causes include autoimmune disorders, lymphoproliferative disorders, and infections.

Patients with few clinical symptoms and mild anemia may not require treatment but only avoidance of cold.

Neumonía por Mycoplasma pneumoniae complicada con anemia hemolítica por aglutininas frías

Although access to this page is not restricted, the information found here is intended for use by medical providers. 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 rfias has an aggressive course.

Specialised Social Services Eurordis directory. If you are using a modern web browser, you may instead navigate to the newer desktop version of fpnotebook. A cold environment or a concurrent infection may trigger or exacerbate the galutininas, and wglutininas of acute hemolysis with hemoglobinemia and hemoglobinuria are more common in winter.

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Immune complex hemolytic anemia can occur aglytininas patients who have chronic lymphocytic leukemia CLL. Definition 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. For all other comments, please send your remarks via contact us.

Check this box if you wish to receive a copy of your message. Cold agglutinin disease can be primary idiopathic or secondary, caused by an underlying condition, such as infection Mycoplasma pneumoniaelymphoproliferative disorders, systemic autoimmunity or neoplasm. It occurs more frequently after fias age of Clinical description It occurs more frequently after the age of In the presence of underlying lymphoma, chlorambucil or oral cyclophosphamide may be helpful.

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.

Additional information Further information on this disease Classification s 1 Gene s 0 Clinical signs and symptoms Publications in PubMed Other website s 3. An acquired anemia resulting from immune-mediated destruction of the red blood cells. A condition in which the body’s immune system stops red blood cells from forming or causes them to clump together. Rituximab may be an option for treatment in some cases. Management and treatment Patients with few clinical symptoms and mild anemia may not require treatment but only avoidance of cold.