Thalassemia differential diagnosis

Thalassemia Microchapters
Home
Patient Information
Overview
Historical Perspective
Classification
Pathophysiology
Causes
Differentiating Thalassemia from other Diseases
Epidemiology and Demographics
Risk Factors
Screening
Natural History, Complications and Prognosis
Diagnosis
Diagnostic Study of Choice
History and Symptoms
Physical Examination
Laboratory Findings
Electrocardiogram
X Ray
Echocardiography and Ultrasound
CT
MRI
Other Imaging Findings
Other Diagnostic Studies
Treatment
Medical Therapy
Surgery
Primary Prevention
Secondary Prevention
Cost-Effectiveness of Therapy
Future or Investigational Therapies
Case Studies
Case #1
Thalassemia differential diagnosis On the Web
Most recent articles
Most cited articles
Review articles
CME Programs
Powerpoint slides
Images
American Roentgen Ray Society Images of Thalassemia differential diagnosis All Images X-rays Echo & Ultrasound CT Images MRI
Ongoing Trials at Clinical Trials.gov
US National Guidelines Clearinghouse
NICE Guidance
FDA on Thalassemia differential diagnosis
CDC on Thalassemia differential diagnosis
Thalassemia differential diagnosis in the news
Blogs on Thalassemia differential diagnosis
Directions to Hospitals Treating Thalassemia
Risk calculators and risk factors for Thalassemia differential diagnosis

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Shyam Patel [2] Please help WikiDoc by adding more content here. It's easy! Click here to learn about editing.

Differential Diagnosis

Characteristic/Parameter	Etiology	Mean corpuscular volume	Laboratory abnormalities	Physical examination	Treatment	Other associated abnormalities
Thalassemia	Genetic defect with alpha- or beta-globin production Absence of alpha or beta-globin chains	Microcytic (<80 femtoliter) in most cases	Abnormal hemoglobin electrophoresis Abnormal high performance liquid chromatography Elevated ferritin (due to frequent transfusions and iron overload) Microcytic hypochromic anemia	Irritability Growth retardation Jaundice Hepatomegaly Splenomegaly	Transfusion support Iron chelation Gene therapy if available Patient education and genetic counseling	Extramedullary hematopoiesis Mental retardation Myelodysplastic syndrome
Sickle cell anemia	Genetic defect resulting in sickled hemoglobin Point mutation in beta-globin chain, converting glutamic acid to valine	Microcytic (<80 femtoliter) or normocytic	Abnormal hemoglobin electrophoresis with elevated HbSS fraction Sickled [red blood cells]] on peripheral blood smear Elevated ferritin (due to frequent transfusions and iron overload) Elevated red blood cell mass	Vaso-occlusion in peripheral vascular beds Jaundice from hemolysis Hepatomegaly Splenomegaly	Folate supplemention Hydroxyurea (to increase fetal hemoglobin production Oxygen supplemention Transfusion support Iron chelation Gene therapy if available Crizanlizumab (P-selectin inhibitor) Patient education and genetic counseling	Extramedullary hematopoiesis Pain crises Acute chest syndrome
Iron deficiency anemia	Loss of iron from occult bleeding Gastrointestinal blood loss Menstrual blood loss Dietary iron deficiency	Microcytic (<80 femtoliter)	Low serum iron Elevated transferrin Low transferrin saturation Low ferritin	Pallor Weakness Positive occult blood testing (if GI bleeding)	Intravenous or oral iron supplementation Blood transfusions	Chronic blood loss
Hemolytic anemia	Medication-induced Autoimmunity Red blood cell membrane defect Red blood cell enzyme defect Shear stress from mechanical valves	Normocytic (80-100 femtoliter)	Indirect hyperbilirubinemia Reticulocytosis Low haptoglobin Elevated LDH	Pallor Jaundice	Removal of offending agent causing hemolysis Steroids Alternative immunosuppression	HELLP syndrome TTP CLL
Sideroblastic anemia	Alcoholism Lead poisoning Vitamin B6 deficiency Isoniazid Chloramphenicol	Microcytic (<80 femtoliter) Or Normocytic (80-100 femtoliter)	Ringed sideroblasts in bone marrow Low vitamin B6 level High lead level	Pallor Weakness	Removal of offending medication High-dose vitamin B6 (up to 200mg daily) Avoidance of splenectomy Symptomatic transfusion support with iron chelation as needed	Myelodysplastic syndrome Myeloproliferative neoplasm Iron overload
Anemia of chronic disease	Chronic kidney disease Rheumatologic disease Cancer HIV Chronic infection; excess release of IL-1 and IL-6	Normocytic (80-100 femtoliter)	Elevated ESR and CRP Elevated hepcidin Low serum iron Low transferrin Elevated ferritin	Pallor Weakness	Treatment of the underlying cause; erythropoiesis-stimulating agents Supportive red blood cell transfusions	Inflammatory bowel disease
Erythropoietin deficiency	Chronic kidney disease or other renal dysfunction	Normocytic (80-100 femtoliter)	Low erythropoietin level	Pallor Weakness Signs of chronic kidney disease	Epoetin alfa 50-100 units/kg 3 times weekly Darbepoietin 0.45 mcg/kg weekly or 0.75 mcg/kg every 2 weeks	Dialysis dependence Myelodysplastic syndrome
Vitamin B12 or folate deficiency	Pernicious anemia Diphyllobothrium latum infection Nutritional deficiency Crohn's disease of terminal ileum	Macrocytic (>100 femtoliter)	Low vitamin B12 or folate level Megaloblastic anemia with hypersegmented neutrophils	Numbness Weakness Tingling Paresthesias	Vitamin B12 1000mcg daily Folate 1mg daily	Neuropathy