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[How I do in front of an hemolytic anemia of unknown etiology?]
- Source :
-
Annales de biologie clinique [Ann Biol Clin (Paris)] 2018 Oct 01; Vol. 76 (5), pp. 493-503. - Publication Year :
- 2018
-
Abstract
- The most frequent causes of hemolytic anemias are immune or infectious diseases, drug induced hemolysis, thrombotic microangiopathies, hereditary spherocytosis, glucose-6-phosphate dehydrogenase or pyruvate kinase deficiencies, thalassemia's and sickle cell disease. Sometimes no cause is found because a rarer etiology is involved. The goal of this review is to remember some unfrequent constitutional or acquired causes and to point out difficulties to avoid wrong interpretations of analysis results.
- Subjects :
- Anemia, Hemolytic blood
Anemia, Hemolytic, Congenital Nonspherocytic blood
Anemia, Hemolytic, Congenital Nonspherocytic complications
Anemia, Hemolytic, Congenital Nonspherocytic diagnosis
Anemia, Sickle Cell blood
Anemia, Sickle Cell complications
Anemia, Sickle Cell diagnosis
Diagnosis, Differential
Glucosephosphate Dehydrogenase Deficiency blood
Glucosephosphate Dehydrogenase Deficiency complications
Glucosephosphate Dehydrogenase Deficiency diagnosis
Hematologic Tests methods
Hematologic Tests standards
Humans
Pyruvate Kinase blood
Pyruvate Kinase deficiency
Pyruvate Metabolism, Inborn Errors blood
Pyruvate Metabolism, Inborn Errors complications
Pyruvate Metabolism, Inborn Errors diagnosis
Spherocytosis, Hereditary blood
Spherocytosis, Hereditary complications
Spherocytosis, Hereditary diagnosis
Thrombotic Microangiopathies blood
Thrombotic Microangiopathies complications
Thrombotic Microangiopathies diagnosis
Anemia, Hemolytic diagnosis
Anemia, Hemolytic etiology
Subjects
Details
- Language :
- French
- ISSN :
- 1950-6112
- Volume :
- 76
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- Annales de biologie clinique
- Publication Type :
- Academic Journal
- Accession number :
- 30226192
- Full Text :
- https://doi.org/10.1684/abc.2018.1381