Aplastic anemia history and symptoms

Jump to navigation Jump to search

Aplastic anemia Microchapters

Home

Patient Information

Overview

Historical Perspective

Classification

Pathophysiology

Causes

Differentiating Aplastic anemia 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

Chest X Ray

CT

MRI

Echocardiography or Ultrasound

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

Aplastic anemia history and symptoms On the Web

Most recent articles

cited articles

Review articles

CME Programs

Powerpoint slides

Images

American Roentgen Ray Society Images of Aplastic anemia history and symptoms

All Images
X-rays
Echo & Ultrasound
CT Images
MRI

Ongoing Trials at Clinical Trials.gov

US National Guidelines Clearinghouse

NICE Guidance

FDA on Aplastic anemia history and symptoms

CDC on Aplastic anemia history and symptoms

Aplastic anemia history and symptoms in the news

Blogs on Aplastic anemia history and symptoms

Directions to Hospitals Treating Aplastic anemia

Risk calculators and risk factors for Aplastic anemia history and symptoms

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Overview

Aplastic anemia is seen as a result of hypoplastic bone marrow causing pancytopenia (anemia, neutropenia, thrombocytopenia). The history and symptoms seen are secondary to these abnormalities.

Symptoms

Lower than normal numbers of red blood cells, white blood cells, and platelets cause most of the signs and symptoms of aplastic anemia.

Red Blood Cells

  • Fatigue (secondary to anemia)
  • Shortness of breath
  • Dizziness, especially when standing up
  • Headaches
  • Coldness in hands or feet
  • Pale skin
  • Chest pain.

If you don't have enough hemoglobin-carrying red blood cells, your heart has to work harder to move the reduced amount of oxygen in your blood. This can lead to arrhythmias (irregular heartbeats), a heart murmur, an enlarged heart, or even heart failure.

White Blood Cells White blood cells help fight infections. Signs and symptoms of a low white blood cell count include fevers, frequent infections that can be severe, and flu-like illnesses that linger.

Platelets Platelets stick together to seal small cuts or breaks on blood vessel walls and stop bleeding. People who have low platelet counts tend to bruise and bleed easily, and the bleeding may be hard to stop.

Common types of bleeding associated with a low platelet count include nosebleeds, bleeding gums, pinpoint red spots on the skin, and blood in the stool. Women also may have heavy menstrual bleeding.

Other Signs and Symptoms Aplastic anemia can cause signs and symptoms that aren't directly related to low blood cell counts. Examples include nausea (feeling sick to your stomach) and skin rashes.

Paroxysmal Nocturnal Hemoglobinuria Some people who have aplastic anemia have a red blood cell disorder called paroxysmal (par-ok-SIZ-mal) nocturnal hemoglobinuria (HE-mo-glo-bi-NOO-re-ah), or PNH. Most people who have PNH don't have any signs or symptoms.

If symptoms do occur, they may include:

•Shortness of breath •Swelling or pain in the abdomen or swelling in the legs caused by blood clots •Blood in the urine •Headaches •Jaundice (a yellowish color of the skin or whites of the eyes) In people who have aplastic anemia and PNH, either condition can develop first.

Symptoms

Diagnosis and management of aplastic anemia [1] (DONOT EDIT)

Diagnosis and Evaluation of aplastic anemia

  • Careful history and clinical examination
  • Detailed drug and occupational exposure history
  • Patients presenting with aplastic anaemia should be assessed to:
    • Confirm the diagnosis and exclude other possible causes of pancytopenia with hypocellular bone marrow
    • Classify the disease severity using standard blood and bone marrow criteria
    • Document the presence of associated paroxysmal nocturnal haemoglobinuria (PNH) and cytogenetic clones
    • Exclude a possible late onset inherited bone marrow failure disorder
  • Multidisciplinary approach
  • Referral to specialist if necessary

References

  1. Marsh JC, Ball SE, Cavenagh J, Darbyshire P, Dokal I, Gordon-Smith EC; et al. (2009). "Guidelines for the diagnosis and management of aplastic anaemia". Br J Haematol. 147 (1): 43–70. doi:10.1111/j.1365-2141.2009.07842.x. PMID 19673883.