Pancytopenia: Difference between revisions
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==Causes== | ==Causes== | ||
===Life Threatening Causes=== | |||
===Common Causes=== | ===Common Causes=== | ||
* [[Aplastic anemia]] | * [[Aplastic anemia]] | ||
* [[Myelodysplastic syndrome]] | * [[Myelodysplastic syndrome]] | ||
* [[Leukemia]] | * [[Leukemia]] | ||
* [[Leishmaniasis]] | * [[Leishmaniasis]] | ||
* [[Folate deficiency]] | |||
* | * [[Vitamin B12 deficiency]] | ||
* [[Paroxysmal nocturnal hemoglobinuria]] | |||
* [[Paroxysmal nocturnal hemoglobinuria]] | * [[Viral infection]]s e.g. ([[HIV]] most common) | ||
* | |||
===Causes by Organ System=== | ===Causes by Organ System=== | ||
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===Causes in Alphabetical Order=== | ===Causes in Alphabetical Order=== | ||
{{col-begin|width=84%}} | {{col-begin|width=84%}} | ||
{{col-break|width=33%}} | {{col-break|width=33%}} | ||
*Aclarubicin | *Aclarubicin | ||
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*[[Xeroderma pigmentosum]] | *[[Xeroderma pigmentosum]] | ||
{{col-end}} | |||
===Causes by Pathophysiology=== | |||
====Bone Marrow Failure==== | |||
* Insufficient production ([[aplastic anemia]]) | |||
* Inability of cells or mature ([[myelodysplasia]]) | |||
* Replacement of normal bone marrow with [[fibrosis]] ([[myelofibrosis]]) | |||
====Peripheral Sequestration/Destruction==== | |||
* [[Splenomegaly]] | |||
* [[Hypersplenism]] | |||
===Causes by Mode of Inheritance=== | |||
===Congenital=== | |||
*[[Cartilage hair hypoplasia]] | |||
*[[Diamond-Blackfan syndrome]] | |||
*[[Dubowitz syndrome]] | |||
*[[Dyskeratosis congenita]] | |||
*[[Familial aplastic anemia]] | |||
*[[Fanconi's anemia]] | |||
*[[Pearson syndrome]] | |||
*[[Schwachman-Diamond syndrome]] | |||
*[[TAR syndrome]] | |||
===Acquired=== | |||
*[[Albers-Schonberg disease]] | |||
*[[Banti's Syndrome]] | |||
*[[Bone marrow]] [[tumor]] | |||
*[[Cirrhosis]] | |||
*[[Drug]]s/[[Toxins]] | |||
*[[Felty's Syndrome]] | |||
*[[Gaucher's Disease]] | |||
*[[Graft-versus-host disease]] | |||
*[[Infection]]s | |||
*[[Kala-Azar]] | |||
*[[Leukemia]] | |||
*[[Lymphoma]] | |||
*[[Lymphoproliferative Disorders]] | |||
*[[Myelodysplastic syndrome]] | |||
*[[Myelofibrosis]] | |||
*[[Niemann-Pick Disease]] | |||
*[[Osteoporosis]] | |||
*[[Pernicious anemia]] | |||
*[[Reticulosis]] | |||
*[[Sarcoidosis]] | |||
*[[Thymoma]] | |||
*[[Tuberculosis]] | |||
==References== | ==References== |
Revision as of 15:10, 9 March 2015
Pancytopenia is not equivalent with bone marrow suppression. Pancytopenia is a lab finding that may related to either bone marrow suppression or peripheral sequestration/destruction. For details about bone marrow suppression click here.
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor-In-Chief: Cafer Zorkun, M.D., Ph.D. [2]
Overview
Pancytopenia is the reduction in numbers of all three bone marrow cell types (RBCs + WBCs + platelets). It is not a disease, but rather a lab finding that may related to 1) bone marrow suppression caused by either insufficient production (aplastic anemia), inability of cells or mature (myelodysplasia), or replacement of normal bone marrow with fibrosis (myelofibrosis) or 2) peripheral sequestration/destruction that is not related to the bone marrow (e.g. splenomegaly or hypersplenism). HIV (Human Immunodeficiency Virus) is itself a cause for pancytopenia. Chemotherapy is associated with pancytopenia. Pancytopenia usually requires a bone marrow biopsy in order to distinguish among different causes.
Causes
Life Threatening Causes
Common Causes
- Aplastic anemia
- Myelodysplastic syndrome
- Leukemia
- Leishmaniasis
- Folate deficiency
- Vitamin B12 deficiency
- Paroxysmal nocturnal hemoglobinuria
- Viral infections e.g. (HIV most common)
Causes by Organ System
Causes in Alphabetical Order
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|
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Causes by Pathophysiology
Bone Marrow Failure
- Insufficient production (aplastic anemia)
- Inability of cells or mature (myelodysplasia)
- Replacement of normal bone marrow with fibrosis (myelofibrosis)
Peripheral Sequestration/Destruction
Causes by Mode of Inheritance
Congenital
- Cartilage hair hypoplasia
- Diamond-Blackfan syndrome
- Dubowitz syndrome
- Dyskeratosis congenita
- Familial aplastic anemia
- Fanconi's anemia
- Pearson syndrome
- Schwachman-Diamond syndrome
- TAR syndrome
Acquired
- Albers-Schonberg disease
- Banti's Syndrome
- Bone marrow tumor
- Cirrhosis
- Drugs/Toxins
- Felty's Syndrome
- Gaucher's Disease
- Graft-versus-host disease
- Infections
- Kala-Azar
- Leukemia
- Lymphoma
- Lymphoproliferative Disorders
- Myelodysplastic syndrome
- Myelofibrosis
- Niemann-Pick Disease
- Osteoporosis
- Pernicious anemia
- Reticulosis
- Sarcoidosis
- Thymoma
- Tuberculosis
References