List of hematologic conditions: Difference between revisions

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→‎Lymphoma: + 14 lymphomas
→‎Lymphoma: +Follicular Lymphoma, Mucosa-Associated Lymphatic Tissue lymphoma, and B-cell chronic lymphocytic leukemia write-ups
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|colspan="6"| Hepatosplenic T-cell lymphoma is a systemic [[neoplasm]] comprising medium-sized cytotoxic [[T-cells]] that show a significant sinusoidal infiltration in the [[liver]], [[spleen]], and [[bone marrow]]. <ref>{{cite book |author=Elaine Sarkin Jaffe, Nancy Lee Harris, World Health Organization, International Agency for Research on Cancer, Harald Stein, J.W. Vardiman |title=Pathology and genetics of tumours of haematopoietic and lymphoid tissues |publisher=IARC Press |location=Lyon |year=2001 |series=World Health Organization Classification of Tumors |volume=3 |isbn=92-832-2411-6 |url=http://books.google.com/?id=XSKqcy7TUZUC}}</ref> It is a rare and generally incurable form of [[lymphoma]]. <ref>{{cite journal |author=Mackey AC, Green L, Liang LC, Dinndorf P, Avigan M |title=Hepatosplenic T cell lymphoma associated with infliximab use in young patients treated for inflammatory bowel disease |journal=J. Pediatr. Gastroenterol. Nutr. |volume=44 |issue=2 |pages=265–7 |year=2007 |month=February |pmid=17255842 |doi=10.1097/MPG.0b013e31802f6424 |url=http://meta.wkhealth.com/pt/pt-core/template-journal/lwwgateway/media/landingpage.htm?an=00005176-200702000-00019}}</ref>
|colspan="6"| Hepatosplenic T-cell lymphoma is a systemic [[neoplasm]] comprising medium-sized cytotoxic [[T-cells]] that show a significant sinusoidal infiltration in the [[liver]], [[spleen]], and [[bone marrow]]. <ref>{{cite book |author=Elaine Sarkin Jaffe, Nancy Lee Harris, World Health Organization, International Agency for Research on Cancer, Harald Stein, J.W. Vardiman |title=Pathology and genetics of tumours of haematopoietic and lymphoid tissues |publisher=IARC Press |location=Lyon |year=2001 |series=World Health Organization Classification of Tumors |volume=3 |isbn=92-832-2411-6 |url=http://books.google.com/?id=XSKqcy7TUZUC}}</ref> It is a rare and generally incurable form of [[lymphoma]]. <ref>{{cite journal |author=Mackey AC, Green L, Liang LC, Dinndorf P, Avigan M |title=Hepatosplenic T cell lymphoma associated with infliximab use in young patients treated for inflammatory bowel disease |journal=J. Pediatr. Gastroenterol. Nutr. |volume=44 |issue=2 |pages=265–7 |year=2007 |month=February |pmid=17255842 |doi=10.1097/MPG.0b013e31802f6424 |url=http://meta.wkhealth.com/pt/pt-core/template-journal/lwwgateway/media/landingpage.htm?an=00005176-200702000-00019}}</ref>
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|[[Follicular lymphoma]] || || ||
|[[Follicular lymphoma]] || {{ICD10|C|82||c|81}} || ||
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|colspan="6"| Follicular Lymphoma also known as (indolent follicular lymphoma) is a type of non-hodgkin's lymphoma that involves both large and small B-cell lymphocytes that spreads from the lymphatic system and into the blood, bone marrow, and internal organs. Approximately 20 to 30 percent of non-hodgkin's lymphomas are diagnosed as follicular lymphoma, with a majority of cases involving those 60 years of age or older. <ref>{{cite web|url=http://www.lymphoma.org/atf/cf/%7B0363cdd6-51b5-427b-be48-e6af871acec9%7D/INDOLENT%20FOLLICULAR.PDF|title=Getting The Facts: Indolent Follicular Lymphoma|last=O’Connor,|first=Owen A.|coauthors=Vose, Julie M.|date=March 2008|publisher=Lymphoma Research Foundation|accessdate=2 April 2011}}</ref>
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|[[Mucosa-Associated Lymphatic Tissue lymphoma]] || || ||
|[[Mucosa-Associated Lymphatic Tissue lymphoma]] || || 31339 ||
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|colspan="6"| Mucosa-Associated Lymphatic Tissue lymphoma (as known as MALT lymphoma and extra-nodal marginal zone lymphoma) is a condition in which lymphatic tissue abnormally presents outside the lymphatic system (extra-nodular) and instead within the [[mucosa]] of the [[gastrointestinal tract]], typically as a lesion in the stomach. <ref>{{cite web|url=http://jmedicalcasereports.com/content/3/1/6|title=Mucosa associated lymphoid tissue lymphoma presenting within a solitary anti-mesenteric dilated segment of ileum: a case report|last=Storey|first=Rowland|coauthors=Gatt, Marcell, Bradford, Ian|date=January 6, 2009|work=Journal of Medical Case Reports|publisher=BioMed Central|accessdate=2 April 2011|archiveurl=;}}</ref>
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|[[Small cell lymphocytic lymphoma]] || || ||
|[[B-cell chronic lymphocytic leukemia]] || {{ICD10|C|91|1|c|81}} || 2641 ||
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|colspan="6"| B-cell chronic lymphocytic leukemia (also known as small cell lymphocytic lymphoma) is a blood cancer that involves the B-cell lymphocytes; responsible for the creation of antibodies. Of the two general types of chronic lymphocytic leukemias (the other involving T-cells), B-cell chronic lymphocytic leukemia accounts for approximately 95 percent of the diagnoses. <ref>{{cite web|url=http://www.cancer.net/patient/Cancer+Types/Leukemia+-+Chronic+Lymphocytic+-+CLL|title=Leukemia - Chronic Lymphocytic - CLL|date=Last Updated: December 02, 2010|work=Cancer.Net|publisher=American Society of Clinical Oncology (ASCO)|accessdate=2 April 2011}}</ref>
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Revision as of 02:08, 2 April 2011

This is an incomplete list, which may never be able to satisfy certain standards for completion.

There are many conditions of or affecting the human Hematologic system — the Biological system that includes plasma, platelets, leukocytes, and erythrocytes, the major components of blood and the bone marrow. [1]

Anemias

An anemia is a decrease in number of red blood cells (RBCs) or less than the normal quantity of hemoglobin in the blood. [2] [3] Based on 2005-2006 estimates, the Centers for Disease Control and Prevention, has stated that approximately 5.5 million Americans a year are either admitted to a hospital or seen by a physician, with some form of anemia as their primary diagnosis. [4]

Nutritional anemias

A nutritional anemia refers to a type of anemia that can be directly attributed to either a nutritional disorder or a nutritional deficiency.

Condition name ICD-10 coding number Diseases Database coding number Medical Subject Headings
Iron deficiency anemia D50 6947
Iron deficiency anemia (or iron deficiency anaemia) is a common anemia that occurs when iron loss (often from intestinal bleeding or menses) occurs, and/or the dietary intake or absorption of iron is insufficient. In such a state, hemoglobin, which contains iron, cannot be formed.[5]
Plummer-Vinson syndrome D50.1 10134
Plummer-Vinson syndrome (PVS), also called Paterson-Brown-Kelly syndrome or sideropenic dysphagia presents as a triad of dysphagia (due to esophageal webs), glossitis, and iron deficiency anemia.[6] It most usually occurs in postmenopausal women.
Vitamin B12 deficiency anemia E53.8 13905
Vitamin B12 deficiency anemia occurs when a "lower-than-normal" amount of the vitamin B12 is available within the body, leading to a decreased production of healthy red blood cells. [7]
Vitamin B12 deficiency anemia due to intrinsic factor deficiency D51.0
vitamin B12 deficiency is caused by a lack of intrinsic factor, as seen in pernicious anemia, causes a vitamin B12 deficiency
Pernicious anemia D51.0 9870
Pernicious anemia (also known as Macrocytic achylic anemia, Congenital pernicious anemia, Juvenile pernicious anemia, and Vitamin B12 deficiency) is one of many types of the larger family of megaloblastic anemias. It is caused by loss of gastric parietal cells, and subsequent inability to absorb vitamin B12. Pernicious anemia is the result of inadequate production of the protein intrinsic factor needed by the body to absorb vitamin B 12, causing a reduction of new red blood cells. [8]
Vitamin B 12 deficiency anemia due to selective vitamin B 12 malabsorption with proteinuria
Vitamin B 12 deficiency anemia due to selective vitamin B 12 malabsorption with proteinuria (also known as Imerslund-Gräsbeck syndrome) is a rare autosomal recessive disorder which requires the indefinite administration of Vitamin B12 injections. [9]
Megaloblastic hereditary anemia D51.1, D52.0, D53.1 29507
Megaloblastic anemia (or megaloblastic anaemia) is an anemia (of macrocytic classification) that results from inhibition of DNA synthesis in red blood cell production.[10]
Transcobalamin II deficiency D51.2
Transcobalamin II deficiency (TCII) (also known as hereditary transcobalamin II deficiency) is a rare autosomal recessive disorder that results in neurological dysfunction. [11] Transcobalamin II are a type of carrier proteins which bind with plasma vitamin B12 (cobalamin) in the production of red blood cells. [12]
Folate-deficiency anemia D52 E53.8 4894
Folate-deficiency anemia (also known as dietary folate-deficiency anemia) is a condition that develops when the body does not have the adequate supply of folic acid available that is needed for the production of new healthy blood cells. [13]
Nutritional megaloblastic anemia D51.1, D52.0, D53.1 29507
Nutritional Megaloblastic anemia is an anemia (of macrocytic classification) that results from inhibition of DNA synthesis in red blood cell production. [10]
Drug-induced folate deficiency anemia D52.1
Protein deficiency anemia
Protein deficiency anemia is an anemia that results from an inadequate intake of dietary protein. [14]
Scurvy E54 13930
Scurvy is a disease resulting from a deficiency of vitamin C,[15] which is required for the synthesis of collagen in humans.

Haemolytic, Aplastic and other anemias

The pale hand of a woman with severe anemia (right) in comparison to the normal hand of her husband (left)
Condition name ICD-10 coding number Diseases Database coding number Medical Subject Headings
Acanthocytosis
Acanthocytosis (also known as Abetalipoproteinemia, Apolipoprotein B deficiency, and Bassen-Kornzweig syndrome) is a rare, genetically inherited, autosomal recessive condition that causes the inability to fully digest dietary fats in the intestines. The gene responsible for this condition is the microsomal triglyceride transfer protein gene. [16]
Acute posthemorrhagic anemia D62.0
Acute posthemorrhagic anemia (also known as acute blood loss anemia) is a condition in which a person quickly loses a large volume of circulating hemoglobin. Acute blood loss is usually associated with an incident of trauma or a severe injury resulting in a large loss of blood. It can also occur during or after a surgical procedure. [17]
Alpha-thalassemia D56.0 448, 33334, 33678
Alpha-thalassemia (α-thalassemia) is a form of thalassemia involving the genes HBA1 [18] and HBA2 [19]. It is condition that causes a reduction of hemoglobin production. There are two types of Alpha-thalassemia named hemoglobin Bart hydrops fetalis syndrome (also known as Hb Bart syndrome) and HbH disease. [20]
Anemia D50-D64 663
Anemia is condition that results in a decrease in the number of red blood cells (RBCs) or less than the normal quantity of hemoglobin in the blood. [2]
Anemia of chronic disease
Anemia of chronic disease (ACD) (also known as anemia of inflammatory response) is a condition where the body converts iron into unused ferrin, causing a drop in hemoglobin production, and as a result; decreased red blood cell production and count. This is caused by a natural defense mechanism initiated by an inflammatory response in response to the underlying chronic disease. [21]
Anemia in Kidney Disease and Dialysis
Anemia in Kidney Disease and Dialysis results from the diseased kidney's inability to produce enough of the hormone erythropoietin. Erythropoietin is used to stimulate an adequate production of red blood cells from the bone marrow. [22]
Anemia of prematurity P61.2
Anemia of prematurity refers to a form of anemia affecting preterm infants[23] with decreased hematocrit.[24]
Aplastic anemia D60-D61 866
Aplastic anemia is a condition where bone marrow does not produce sufficient new cells to replenish blood cells.[25]
Autoimmune hemolytic anemia D59.0-D59.1
Autoimmune hemolytic anemia (AIHA) is a type of hemolytic anemia where the body's immune system attacks its own red blood cells (RBCs), leading to their destruction (hemolysis).[26][27] Types of AIHA include Warm autoimmune hemolytic anemia, Cold agglutinin disease, and Paroxysmal cold hemoglobinuria.
Beta-thalassemia D56.1 3087
Beta-thalassemia (β-thalassemia) is an autosomal dominant blood condition that results in the reduction of hemoglobin production. The cause for the disorder is related to a genetic mutation of the HBB gene. This gene is responsible for providing the instructions to produce beta-globin; one of the major components of hemoglobin. The two classification types of beta thalassemia are thalassemia major (also known as Cooley's anemia) and thalassemia intermedia. [28]
Diamond-Blackfan anemia D61.0 29062
Diamond–Blackfan anemia (DBA), (also known as Blackfan–Diamond anemia and Inherited erythroblastopenia) [29] is a congenital erythroid aplasia that usually presents in infancy.[30]
Congenital dyserythropoietic anemia D|64|4|d|60}
Congenital dyserythropoietic anemia (CDA) is a generically inherited autosomal recessive (types I and II) or autosomal dominant (type III) blood disorder that effects the normal maturation process of red blood cell production. Mutations to the CDAN1 gene (type I), SEC23B gene (type II), and a currently unknown gene for type III causes a disruption in the normal formation of [[erythropoiesis], thereby causing a reduction of circulating healthy mature red blood cells. [31]
Drug-induced autoimmune hemolytic anemia D59.0
Drug-induced autoimmune hemolytic anemia is a type of hemolytic anemia in which a mediated immune response triggers IgG and IgM antibody production in regards to the presence of high doses of penicillin via the the hapten mechanism causing the reduction of red blood cells in the spleen. [32]
Drug-induced nonautoimmune hemolytic anemia
Glucose-6-phosphate dehydrogenase deficiency
Hemoglobinopathy D58.2 19674
Hemoglobinopathy is a kind of genetic defect that results in abnormal structure of one of the globin chains of the hemoglobin molecule.[33] Hemoglobinopathies are inherited single-gene disorders; in most cases, they are inherited as autosomal co-dominant traits. [34] Hemoglobinopathies imply structural abnormalities in the globin proteins themselves.[35] Hemoglobinopathy variants include sickle-cell disease. [36]
Hemolytic anemia D55-D59 5534
Hemolytic anemia (also known as haemolytic anaemia) is an anemia due to hemolysis, the abnormal breakdown of red blood cells. A number of different mediating factors can cause this condition; either from within the blood cell itself ((intrinsic factors) or outside of the cell (extrinsic factors). [37]
Congenital hemolytic anemia
Hereditary spherocytosis D58.0 5827
Hereditary spherocytosis is a genetically-transmitted (autosomal dominant) form of spherocytosis, an auto-hemolytic anemia characterized by the production of red blood cells that are sphere-shaped rather than bi-concave disk shaped (Donut-Shaped), and therefore more prone to hemolysis.[38]
Hereditary elliptocytosis D58.1 4172
Hereditary elliptocytosis (HE) (also known as ovalocytosis), is an inherited blood disorder in which an abnormally large number of circulating red blood cells are elliptical or cigar shaped rather than the typical biconcave disc shape. It is caused in part by mutations in the formation of specific Spectrin tetramers or proteins responsible for giving the red blood cell its shape and elasticity causing continued deformation as the cell matures. [39] Subtypes of this condition include southeast Asian ovalocytosis and spherocytic elliptocytosis.
Hereditary pyropoikilocytosis
Hereditary xerocytosis
Acquired hemolytic anemia
Cold hemagglutinin disease D59.1 2949
Cold hemagglutinin disease (also known as cold agglutinin disease and autoimmune anemia due to cold-reactive antibodies)is an autoimmune disease characterized by the presence of high concentrations of circulating antibodies, usually IgM, directed against red blood cells.[40] It is a form of autoimmune hemolytic anemia, specifically one in which antibodies only bind red blood cells at low body temperatures, typically 28-31°C.
Paroxysmal cold hemoglobinuria D59.6 9679
Paroxysmal cold hemoglobinuria (PCH) (also known as Donath-Landsteiner syndrome) is a rare condition characterized by the sudden presence of hemoglobin in the urine (called hemoglobinuria), typically after exposure to cold temperatures. [41]
Hemolytic-uremic syndrome D59.3 13052
Hemolytic-uremic syndrome (HUS) (also known as haemolytic-uraemic syndrome) is a disease characterized by hemolytic anemia, acute renal failure (uremia) and a low platelet count (thrombocytopenia). It predominantly but not exclusively affects children. Most cases are preceded by an episode of diarrhea caused by E. coli O157:H7, which is acquired as a foodborne illness. [42]
Hereditary persistence of fetal hemoglobin
Hereditary stomatocytosis
Hexokinase deficiency D55.2
Hexokinase deficiency (also known as h)uman erythrocyte hexokinase deficiency) is an anemia-causing condition associated with inadequate hexokinase. [43]
Hyperanaemia
Hypochromic anemia
Hypochromic anemia is a generic term for any type of anemia in which the red blood cells (erythrocytes) are paler than normal. [44] This is caused by a proportionally reduced amount of hemoglobin present in relation to the size of the red blood cell.
Ineffective erythropoiesis
Ineffective erythropoiesis is an anemia caused by the premature apoptosis of the body's mature red blood cells [45] and subsequent reduction in an adequate production and full maturation of new healthy red blood cells. [46]
Inherited erythroblastopenia
Macrocytic anemia
Megaloblastic anemia D51.1, D52.0, D53.1 29507
Megaloblastic anemia (or megaloblastic anaemia) is an anemia of macrocytic classification that results from inhibition of DNA synthesis in red blood cell production. [10]
Microangiopathic hemolytic anemia
Minkowski-Chauffard syndrome
Myelophthisic anemia D61.9
Myelophthisic anemia (also known as myelophthisis) is a severe kind of anemia found in some people with diseases that affect the bone marrow. Myelophythisis refers to the displacement of hemopoietic bone-marrow tissue into the peripheral blood, [47] either by fibrosis, tumors or granulomas.
Neuroacanthocytosis
Non sideropenic hypochromic anaemias
Normocytic anemia
Paroxysmal nocturnal hemoglobinuria
Pyruvate kinase deficiency D55.2 11090
Pyruvate kinase deficiency, also called erythrocyte pyruvate kinase deficiency, [48] is an inherited metabolic disorder of the enzyme pyruvate kinase which affects the survival of red blood cells and causes them to deform into echinocytes on peripheral blood smears.
Rh deficiency syndrome
Sickle-cell disease
Sideroblastic anemia D64.0-D64.3 12110
Sideroblastic anemia or sideroachrestic anemia is a disease in which the bone marrow produces ringed sideroblasts rather than healthy red blood cells (erythrocytes). [49] It may be caused either by a genetic disorder or indirectly as part of myelodysplastic syndrome. [50]
Southeast Asian ovalocytosis D58.1
Southeast Asian ovalocytosis is a form of hereditary elliptocytosis common in some communities in Malaysia and Papua New Guinea, as it confers some resistance to cerebral Falciparum Malaria. [51]
Spur cell hemolytic anemia
Thalassemia
Triosephosphate isomerase deficiency D55.2 30116
Triosephosphate isomerase (TPI) deficiency is a genetically inherited autosomal recessive condition "characterized bychronic hemolytic anemia,cardiomyopathy, susceptibility to infections, severe neurological dysfunction, and, in most cases, death in early childhood." [52]
Warm autoimmune hemolytic anemia D59.1 29723
Warm autoimmune hemolytic anemia is an autoimmune hemolytic anemia (AIHA) characterized by formation of antibodies that attack the body's own red blood cells in a destructive immune system response. [53]

Blood cancers

A blood cancer or hematological malignancy is a type of cancer that affects either the blood, bone marrow, or lymph nodes. [54]

Lymphoma

Condition name ICD-10 coding number Diseases Database coding number Medical Subject Headings
Hodgkin lymphoma C81 5973
Non-Hodgkin lymphoma C82-C85 9065
The non-Hodgkin lymphomas (NHLs) are a diverse group of blood cancers that include any kind of lymphoma except Hodgkin's lymphomas.[55]
Anaplastic large cell lymphoma
Angioimmunoblastic T-cell lymphoma C84.4
Angioimmunoblastic T-cell lymphoma (AILT) (also known as Angioimmunoblastic lymphadenopathy with dysproteinemia) [56]: 747 ) is a mature T-cell lymphoma with systemic characterized by a polymorphous lymph node infiltrate showing a marked increase in follicular dendritic cells (FDCs) and high endothelial venules (HEVs) and systemic involvement. [57] It is also known as immunoblastic lymphadenopathy (Lukes-Collins Classification) and AILD-type (lymphogranulomatosis X) T-cell lymphoma (Kiel Classification) [57]
Hepatosplenic T-cell lymphoma
Hepatosplenic T-cell lymphoma is a systemic neoplasm comprising medium-sized cytotoxic T-cells that show a significant sinusoidal infiltration in the liver, spleen, and bone marrow. [58] It is a rare and generally incurable form of lymphoma. [59]
B-cell lymphoma
reticuloendotheliosis
reticulosis
Microglioma
Diffuse large B-cell lymphoma
Follicular lymphoma C82
Follicular Lymphoma also known as (indolent follicular lymphoma) is a type of non-hodgkin's lymphoma that involves both large and small B-cell lymphocytes that spreads from the lymphatic system and into the blood, bone marrow, and internal organs. Approximately 20 to 30 percent of non-hodgkin's lymphomas are diagnosed as follicular lymphoma, with a majority of cases involving those 60 years of age or older. [60]
Mucosa-Associated Lymphatic Tissue lymphoma 31339
Mucosa-Associated Lymphatic Tissue lymphoma (as known as MALT lymphoma and extra-nodal marginal zone lymphoma) is a condition in which lymphatic tissue abnormally presents outside the lymphatic system (extra-nodular) and instead within the mucosa of the gastrointestinal tract, typically as a lesion in the stomach. [61]
B-cell chronic lymphocytic leukemia C91.1 2641
B-cell chronic lymphocytic leukemia (also known as small cell lymphocytic lymphoma) is a blood cancer that involves the B-cell lymphocytes; responsible for the creation of antibodies. Of the two general types of chronic lymphocytic leukemias (the other involving T-cells), B-cell chronic lymphocytic leukemia accounts for approximately 95 percent of the diagnoses. [62]
Mantle cell lymphoma
Burkitt lymphoma
Mediastinal large B cell lymphoma
Waldenström macroglobulinemia
Nodal marginal zone B cell lymphoma
Splenic marginal zone lymphoma
Intravascular large B-cell lymphoma
Primary effusion lymphoma
Lymphomatoid granulomatosis
Nodular lymphocyte predominant Hodgkin's lymphoma

Leukemia

Condition name ICD-10 coding number Diseases Database coding number Medical Subject Headings
plasma cell leukaemia
Acute erythraemia and erythroleukaemia
Acute erythraemic myelosis
Guglielmo's disease
Chronic erythraemia
Heilmeyer-Schöner disease
Acute megakaryoblastic leukaemia
megakaryoblastic (acute)
megakaryocytic (acute)
Mast cell leukaemia
Acute panmyelosis
Acute myelofibrosis
Lymphosarcoma cell leukaemia
Acute leukaemia of unspecified cell type
Blast cell leukaemia
Stem cell leukaemia
Chronic leukaemia of unspecified cell type
Subacute leukaemia of unspecified cell type
Accelerated phase chronic myelogenous leukemia
Acute myeloid leukemia C92.0 203
Acute myeloid leukemia (AML), also known as acute myelogenous leukemia, is a cancer of the myeloid line of blood cells, characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells. [63]
Acute promyelocytic leukemia
Acute basophilic leukemia
Acute eosinophilic leukemia
Acute lymphoblastic leukemia
Acute monocytic leukemia
Acute myeloblastic leukemia with maturation
Acute myeloid dendritic cell leukemia
Adult T-cell leukemia/lymphoma
Aggressive NK-cell leukemia
B-cell prolymphocytic leukemia
B-cell chronic lymphocytic leukemia
B-cell leukemia
Chronic myelogenous leukemia
Chronic myelomonocytic leukemia
Chronic neutrophilic leukemia
Hairy cell leukemia

Myeloma

Condition name ICD-10 coding number Diseases Database coding number Medical Subject Headings
Multiple myeloma
Kahler's disease
Myelomatosis
solitary myeloma
Plasma cell leukaemia
Plasmacytoma, extramedullary
Malignant plasma cell tumour NOS
Plasmacytoma NOS
Solitary myeloma

Malignant immunoproliferative diseases

Condition name ICD-10 coding number Diseases Database coding number Medical Subject Headings
Monoclonal gammopathy
Angiocentric immunoproliferative lesion
Lymphoid granulomatosis
Angioimmunoblastic lymphadenopathy
T-gamma lymphoproliferative disease
Waldenström's macroglobulinaemia
Alpha heavy chain disease
Gamma heavy chain disease
Franklin's disease
Immunoproliferative small intestinal disease
Mediterranean disease
Malignant immunoproliferative disease, unspecified
Immunoproliferative disease NOS

Coagulation, purpura, and other hemorrhagic conditions

Condition name ICD-10 coding number Diseases Database coding number Medical Subject Headings
Disseminated intravascular coagulation (DIC, Defibrination syndrome)
Protein C deficiency
Protein C deficiency is a rare genetic trait that predisposes to thrombotic disease. [64]

Infection-related

Hematological disorders may be caused by a number of infection-related conditions involving the introduction of microorganisms into the host, such as bacteria and protozoa. [65]

Bacterium-related

Condition name ICD-10 coding number Diseases Database coding number Medical Subject Headings
Clostridium infection
Cholera infection
E. coli 0157:H7 infection
Typhoid fever

Protozoan-related

Condition name ICD-10 coding number Diseases Database coding number Medical Subject Headings
Leishmania infection * [[]]
Malaria infection (Plasmodium infection)
toxoplasmosis

Immune system regulation-related

Immunodeficiency with predominantly antibody defects

Condition name ICD-10 coding number Diseases Database coding number Medical Subject Headings
Hereditary hypogammaglobulinemia
Nonfamilial hypogammaglobulinemia
Selective deficiency of immunoglobulin A [IgA]
Selective deficiency of immunoglobulin G [IgG] subclasses
Selective deficiency of immunoglobulin M [IgM]
Immunodeficiency with increased immunoglobulin M [IgM]
Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinemia
Transient hypogammaglobulinemia of infancy

References

  1. ^ Saladin, Kenneth S. (2004). "18". Anatomy & Physiology: The Unity of form and Function (3rd ed.). Mc Graw-Hill. p. 679. ISBN 0-07-242903-8. {{cite book}}: Unknown parameter |coauthors= ignored (|author= suggested) (help)
  2. ^ a b MedicineNet.com --> Definition of Anemia Last Editorial Review: 12/9/2000 Retrieved March 27, 2011 Cite error: The named reference "medterms" was defined multiple times with different content (see the help page).
  3. ^ merriam-webster dictionary --> anemia Retrieved on March 27, 2011
  4. ^ "Anemia or Iron Deficiency". Centers for Disease Control and Prevention. Last reviewed April 15, 2010. Retrieved 28 March 2011. {{cite web}}: Check date values in: |date= (help)
  5. ^ Brady PG (2007). "Iron deficiency anemia: a call for". South. Med. J. 100 (10): 966–7. doi:10.1097/SMJ.0b013e3181520699. PMID 17943034. {{cite journal}}: Unknown parameter |doi_brokendate= ignored (|doi-broken-date= suggested) (help)
  6. ^ Novacek G (2006). "Plummer-Vinson syndrome". Orphanet J Rare Dis. 1: 36. doi:10.1186/1750-1172-1-36. PMC 1586011. PMID 16978405.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  7. ^ Mayo Clinic staff (March 4, 2011). "Vitamin deficiency anemia". Mayo Foundation for Medical Education and Research. Mayo Clinic. Retrieved 5 March 2011.
  8. ^ "Pernicious anemia". National Center for Biotechnology Information (NCBI). U.S. National Library of Medicine. November 23, 2008. Retrieved 1 March 2011.
  9. ^ Gräsbeck, R. (May 19, 2006). "Imerslund-Gräsbeck syndrome (selective vitamin B(12) malabsorption with proteinuria)". Pub Med. National Center for Biotechnology Information, U.S. National Library of Medicine. Retrieved 5 March 2011.
  10. ^ a b c "Megaloblastic Anemia: Overview - eMedicine Hematology". Retrieved 2009-02-07.
  11. ^ Kaikov, Y. (1991). "Transcobalamin II deficiency: Case report and review of the literature". European Journal of Pediatrics. European Journal of Pediatrics. pp. Volume 150, Number 12, 841–843, DOI: 10.1007/BF01955004. Retrieved 2 March 2011. {{cite web}}: Unknown parameter |coauthors= ignored (|author= suggested) (help)
  12. ^ Hall, C. A. (November, 1975). "Transcobalamins I and II as natural transport proteins of vitamin B12". PubMed Central. The Journal of Clinical Investigation. pp. 56(5): 1125–1131. doi: 10.1172/JCI108187. Retrieved 2 March 2011. {{cite web}}: Check date values in: |date= (help)
  13. ^ "Folate-deficiency anemia". National Center for Biotechnology Information. U.S. National Library of Medicine. reviewed January 31, 2010. Retrieved 2 March 2011. {{cite web}}: Check date values in: |date= (help)
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