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Differential Diagnosis For Reticulocytosis
- Trauma Causes
Puerperal hemorrhage/tears/lacerations- Electromagnetic, Physics, trauma, Radiation Causes
Burns/severe/extensive- Surgical, Procedure Complication
Bleeding complications/Surgery- Infectious Disorders (Specific Agent)
Hepatitis, viral
Leptospirosis/severe (Weils) type
Hemolysis with viral infection
Leptospiral disease
Babesiosis
Chronic malaria
Malaria
Leptospirosis Ictohemorrhagica- Infected organ, Abscesses
Hemolytic anemia of infection/acute- Neoplastic Disorders
Colon polyp (adenoma, benign)
Hodgkin's disease
Metastatic bone marrow
Monocytic leukemia, acute
Carcinoma, bone marrow metastasis
Myelogenous leukemia, chronic
Polycythemia vera
Primary Myelofibrosis/Myeloid metaplasia
Atrial myxoma
Erythropoetin producing tumor- Allergic, Collagen, Auto-Immune Disorders
Hemolytic disease of newborn
Hemolytic anemia, autoimmune
HELLP syndrome of pregnancy
Anemia, cryopathic autoimmune
Cold autoimmune hemolytic anemia
Evan's syndrome (AHA/Immune TP)
Paroxysmal Cold Hemoglobinuria
Atypical Hemolytic Uremic Syndrome- Metabolic, Storage Disorders
Glucose 6 PD deficiency
Abetalipoproteinemia (Bassen Kornzweig)
Phosphoglycerate Kinase Deficiency/Systemic homozygous PGKD
Anemia due to glutathione metab def
Wilsons Disease
Gaucher's disease
Phosphofructokinase def/GSD VII (Tarui)- Deficiency Disorders
Vitamin E defic. in newborns
Vitamin E deficiency- Congenital, Developmental Disorders
Congenital disorders
Anemia, congenital hemolytic
Congenital cyanotic heart disease
Meckel diverticulum/Peptic ulcer
Congenital clubbing, digital
Congenital dyserythropoetic anemia- Hereditary, Familial, Genetic Disorders
Sickle cell crisis
Sickle cell/thalassemia disease
Thalassemia major
Thalassemia minor
Spherocytosis, crisis phase
Pyruvate kinase deficiency RBC's
Sickle cell anemia
Sickle cell-hemoglobin D disease
Spherocytosis, hereditary
Hemoglobin H disease
Elliptocytosis, hereditary
Hemoglobin S/C disease
Anemia, hereditary hemolytic,nonspher'c
Thalassemia-hemoglobin C disease- Anatomic, Foreign Body, Structural Disorders
Gastrointestinal bleeding
Uterus, hemorrhage, postpartum
Exsanguinating hemorrhage
Hemorrhage, acute
Internal bleeding/trauma
Lower GI bleeding
Peptic ulcer hemorrhage
Postpartum hemorrhage
Upper GI bleeding
Uterine hemorrhage
Peritoneal bleeding/hemorrhage
Massive intraperitonael hemorrhage- Vegetative, Autonomic, Endocrine Disorders
Erythropoetin, autonomous production- Reference to Organ System
Disseminated intravascular coagulopathy
Anemia, blood loss
Chronic blood loss
Cerebral thrombotic thrombocytopenia
Hemolysis acute
Myelophthisic anemia
Hemolysis process
Hemolysis/non-immune
Hemolytic-uremic syndrome
Paroxysmal Nocturnal Hemoglobinuria
Thrombotic thrombocytopenic purpura
Hypersplenism
Spherocytosis, acquired
Hemolytic Anemia- Pathophysiologic
Anemia, under therapy
Myeloid metaplasia pathophysiology- Drugs
Hydrazine Sulfate Administration/Toxicity
Drug induced Hemolysis- Poisoning (Specific Agent)
Fava-bean hemolysis (G6PD RBC defect)
Arsine gas (Hydrogen arsenide) poisoning
Copper salts exposure/Copper toxicity
Copper sulfate poisoning
Lead poisoning
Arsenic poisoning/Acute ingestion- Organ Poisoning (Intoxication)
Anemia, hemolytic, toxic
Anemia, hemolytic chemical, acquired- Definition
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Increase in reticulocyte percentage or absolute reticulocyte count in blood beyond normal for age; Reticulocytes are young red cells just after the nucleus is removed; high percent in red cell destruction disorders and low percent in bone marrow depression or deficiency diseases such as iron deficiency.
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- External Links Related to Reticulocytosis
- Wikipedia
- Merck
- Images
- PubMed (National Library of Medicine)
- NGC (National Guideline Clearinghouse)
- Medscape (eMedicine)
- Harrison's Online (accessmedicine)
- NEJM (The New England Journal of Medicine)