Aplastic anemia
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Aplastic anemia
Hematological system
Anemias
Iron deficiency anemia
Beta-thalassemia
Alpha-thalassemia
Sideroblastic anemia
Anemia of chronic disease
Lead poisoning
Hemolytic disease of the newborn
Glucose-6-phosphate dehydrogenase (G6PD) deficiency
Autoimmune hemolytic anemia
Pyruvate kinase deficiency
Paroxysmal nocturnal hemoglobinuria
Sickle cell disease (NORD)
Hereditary spherocytosis
Anemia of chronic disease
Aplastic anemia
Fanconi anemia
Megaloblastic anemia
Folate (Vitamin B9) deficiency
Vitamin B12 deficiency
Fanconi anemia
Diamond-Blackfan anemia
Heme synthesis disorders
Acute intermittent porphyria
Porphyria cutanea tarda
Lead poisoning
Coagulation disorders
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Vitamin K deficiency
Platelet disorders
Bernard-Soulier syndrome
Glanzmann's thrombasthenia
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Mixed platelet and coagulation disorders
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Leukemias
Chronic leukemia
Acute leukemia
Leukemoid reaction
Leukemoid reaction
Dysplastic and proliferative disorders
Myelodysplastic syndromes
Polycythemia vera (NORD)
Myelofibrosis (NORD)
Essential thrombocythemia (NORD)
Langerhans cell histiocytosis
Mastocytosis (NORD)
Plasma cell dyscrasias
Multiple myeloma
Monoclonal gammopathy of undetermined significance
Waldenstrom macroglobulinemia
Hematological system pathology review
Microcytic anemia: Pathology review
Non-hemolytic normocytic anemia: Pathology review
Intrinsic hemolytic normocytic anemia: Pathology review
Extrinsic hemolytic normocytic anemia: Pathology review
Macrocytic anemia: Pathology review
Heme synthesis disorders: Pathology review
Coagulation disorders: Pathology review
Platelet disorders: Pathology review
Mixed platelet and coagulation disorders: Pathology review
Thrombosis syndromes (hypercoagulability): Pathology review
Lymphomas: Pathology review
Leukemias: Pathology review
Plasma cell disorders: Pathology review
Myeloproliferative disorders: Pathology review
Assessments
Aplastic anemia
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Aplastic anemia
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Which of the following would most likely be seen on microscopic examination of this patient’s bone marrow?
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Aplastic anemia p. 429
in anemia taxonomy p. 425
chloramphenicol p. 189
as drug reaction p. 251
Fanconi anemia p. 718
neutropenia with p. 431
thionamides p. 362
Benzene
aplastic anemia p. 251, 429
Café-au-lait spots
aplastic anemia and p. 429
Carbamazepine
aplastic anemia p. 251
Chloramphenicol p. 189
aplastic anemia and p. 251, 429
Epstein-Barr virus (EBV) p. 162
aplastic anemia p. 429
Erythropoietin (EPO)
aplastic anemia p. 429
Hepatitis
aplastic anemia and p. 429
Hepatitis viruses p. 170
aplastic anemia p. 429
HIV (human immunodeficiency virus) p. 172
aplastic anemia in p. 429
Immunosuppressants
for aplastic anemia p. 429
Leukemias p. 440
aplastic anemia and p. 417
Methimazole p. 362
aplastic anemia p. 251
Nonsteroidal anti-inflammatory drugs (NSAIDs) p. 499
aplastic anemia p. 251
Pallor in aplastic anemia p. 429
Parvovirus B16
aplastic anemia p. 417
Petechiae
aplastic anemia as cause p. 429
Propylthiouracil
aplastic anemia p. 251
Purpura
aplastic anemia p. 429
Radiation exposure
aplastic anemia p. 431
Reticulocytes p. 415
in aplastic anemia p. 429
Stem cells
in aplastic anemia p. 429
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Transcript
Content Reviewers
Viviana Popa, MDAplastic anemia is a pancytopenia, meaning all blood cell lines are decreased - so the term aplastic anemia, which just refers to low red blood cell count, is actually a misnomer.
So with aplastic anemia, there’s actually anemia, as well as leukocytopenia, or low white blood cells, as well as thrombocytopenia, or low platelet levels.
This condition takes many forms, ranging from mild to severe depending on the cause.
Now, blood cells are produced in the bones of the body, mainly in the bones of the pelvis, ribs and sternum, through a process called hematopoiesis.
This process starts in the bone marrow, the innermost portion of bone, where the hematopoietic stem cells reside.
These serve as progenitor cells for all the different cell types found in the blood.
First, hematopoietic stem cells, also called hemocytoblasts, can become lymphoid progenitors or myeloid progenitors.
The lymphoid progenitors can develop into lymphoblasts, which can then differentiate into some white blood cells like T-lymphocytes, B-lymphocytes, or natural killer cells.
The myeloid progenitors can differentiate into erythrocytes, or red blood cells, megakaryocytes, which eventually give rise to platelets, or myeloblasts, which can then become other white blood cells like monocytes, neutrophils, basophils, and eosinophils.
The most common cause of aplastic anemia is autoimmune destruction of hematopoietic stem cells.
The details of this mechanism are not fully understood, but research shows that there are alterations in the immunologic appearance of hematopoietic stem cells because of genetic disorders, or after exposure to environmental agents, like radiation or toxins.
This means that the hematopoietic stem cells start expressing non-self antigens and the immune system subsequently targets them for destruction.
Summary
Aplastic anemia is a rare blood disorder caused by bone marrow failure to produce new blood cells. Even though it's referred to as aplastic anemia, it typically presents with pancytopenia, meaning that all three major blood cell lines - the red blood cells, white blood cells, and platelets are affected.
People with aplastic anemia may experience fatigue, shortness of breath, ecchymoses and mucosal bleeding, and frequent infections pallor Aplastic anemia can be caused by a variety of factors, including exposure to radiation or chemotherapy, viral infections, and autoimmune disorders.
Sources
- "Robbins Basic Pathology" Elsevier (2017)
- "Pathophysiology of Disease: An Introduction to Clinical Medicine 8E" McGraw-Hill Education / Medical (2018)
- "Current concepts in the pathophysiology and treatment of aplastic anemia" Hematology (2013)
- "Aplastic anaemia" Hematology (2013)
- "Aplastic Anemia" New England Journal of Medicine (2018)
- "Harrison's Principles of Internal Medicine" McGraw-Hill (2004)
- "The complex pathophysiology of acquired aplastic anaemia" Clinical & Experimental Immunology (2015)
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