小球性貧血
WordNet
- a deficiency of red blood cells (同)anaemia
- a lack of vitality (同)anaemia
- genus of terrestrial or lithophytic ferns having pinnatifid fronds; chiefly of tropical America (同)genus Anemia
Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2013/02/22 13:38:07」(JST)
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Microcytic anemia |
Classification and external resources |
ICD-10 |
D50.8 |
Microcytic anemia (BrE: anaemia) is a generic term for any type of anemia characterized by small red blood cells. The normal mean corpuscular volume (abbreviated to MCV on full blood count results) is 76-100 fL, with smaller cells (<76 fL) described as microcytic and larger cells (>100 fL) as macrocytic.
In microcytic anemia, the red blood cells (erythrocytes) are usually also hypochromic, meaning that the red blood cells are paler than usual. This can be quantified as the mean corpuscular hemoglobin or mean cell hemoglobin (MCH), the amount of hemoglobin per cell; the normal value is 27-32 picograms (pg). Similar is the mean corpuscular hemoglobin concentration (MCHC), giving the amount of hemoglobin per volume of erythrocytes (normally about 320-360 g/L or 32-36 g/dL). Typically, therefore, anemia of this category is described as "microcytic, hypochromic anemia".
Contents
- 1 Causes
- 2 See also
- 3 References
- 4 External links
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Causes
Typical causes of microcytic anemia include:
- childhood
- iron deficiency anemia,[1] by far the most common cause of anemia in general and of microcytic anemia in particular
- thalassemia
- adulthood
- blood loss
- iron deficiency anemia
- sideroblastic anemia, congenital or acquired
- anemia of chronic disease,[2] although this more typically causes normochromic, normocytic anemia. Microcytic anemia has been discussed by Weng et al.[2]
- lead poisoning
- pyridoxine deficiency
Other causes that are "typically" thought of as causing normocytic anemia or macrocytic anemia must also be considered, and the presence of two or more causes of anemia can distort the "typical" picture.
See also
References
- ^ Iolascon A, De Falco L, Beaumont C (January 2009). "Molecular basis of inherited microcytic anemia due to defects in iron acquisition or heme synthesis". Haematologica 94 (3): 395–408. doi:10.3324/haematol.13619. PMC 2649346. PMID 19181781. http://www.haematologica.org/cgi/pmidlookup?view=long&pmid=19181781.
- ^ a b Weng, CH; Chen JB, Wang J, Wu CC, Yu Y, Lin TH (2011). "Surgically Curable Non-Iron Deficiency Microcytic Anemia: Castleman's Disease.". Onkologie 34 (8-9): 456–8. doi:10.1159/000331283. PMID 21934347. http://content.karger.com/produktedb/produkte.asp?DOI=000331283&typ=pdf.
External links
- Emedicine on chronic anemia
Pathology: hematology, hematologic diseases of RBCs and megakaryocytes / MEP (D50-69,74, 280-287)
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Red
blood cells |
↑ |
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↓ |
Anemia |
Nutritional |
- Micro-: Iron deficiency anemia
- Macro-: Megaloblastic anemia
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Hemolytic
(mostly Normo-) |
Hereditary |
- enzymopathy: G6PD
- glycolysis
- hemoglobinopathy: Thalassemia
- Sickle-cell disease/trait
- HPFH
- membrane: Hereditary spherocytosis
- Minkowski-Chauffard syndrome
- Hereditary elliptocytosis
- Southeast Asian ovalocytosis
- Hereditary stomatocytosis
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Acquired |
- Drug-induced autoimmune
- Drug-induced nonautoimmune
- Hemolytic disease of the newborn
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Aplastic
(mostly Normo-) |
- Hereditary: Fanconi anemia
- Diamond–Blackfan anemia
- Acquired: PRCA
- Sideroblastic anemia
- Myelophthisic
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Blood tests |
- MCV
- Normocytic
- Microcytic
- Macrocytic
- MCHC
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Other |
- Methemoglobinemia
- Sulfhemoglobinemia
- Reticulocytopenia
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Coagulation/
coagulopathy |
↑ |
Hyper-
coagulability |
- primary: Antithrombin III deficiency
- Protein C deficiency/Activated protein C resistance/Protein S deficiency/Factor V Leiden
- Prothrombin G20210A
- acquired:Thrombocytosis
- DIC
- Congenital afibrinogenemia
- Purpura fulminans
- autoimmune
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↓ |
Hypo-
coagulability |
Thrombocytopenia |
- Thrombocytopenic purpura: ITP
- TM
- Heparin-induced thrombocytopenia
- May-Hegglin anomaly
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Platelet function |
- adhesion
- aggregation
- Glanzmann's thrombasthenia
- platelet storage pool deficiency
- Hermansky–Pudlak syndrome
- Gray platelet syndrome
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Clotting factor |
- Hemophilia
- von Willebrand disease
- Hypoprothrombinemia/II
- XIII
- Dysfibrinogenemia
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cell/phys (coag, heme, immu, gran), csfs
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rbmg/mogr/tumr/hist, sysi/epon, btst
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drug (B1/2/3+5+6), btst, trns
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UpToDate Contents
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English Journal
- Characterization of deletional and non-deletional alpha globin variants in a large cohort from Spain between 2009 and 2014.
- de la Fuente-Gonzalo F, Nieto JM, Villegas A, González FA, Martínez R, Ropero P.
- Annals of hematology. 2019 Jul;98(7)1537-1545.
- The hemoglobinopathies are a group of disorders passed down through families (inherited) in which there is abnormal production or structure of the hemoglobin molecule. They are among the most common inherited diseases around the world. Those that produce abnormal hemoglobin are called structural hem
- PMID 31025160
- Quantitative data on red cell measures of iron status and their relation to the magnitude of the systemic inflammatory response and survival in patients with colorectal cancer.
- McSorley ST, Tham A, Steele CW, Dolan RD, Roxburgh CS, Horgan PG, McMillan DC.
- European journal of surgical oncology : the journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology. 2019 Jul;45(7)1205-1211.
- Inflammation is recognised to be associated with perturbation of serum measures of iron status. However, the impact of colorectal cancer associated host inflammation on red cell measures of iron status has not been previously quantified. Patients undergoing elective surgery with curative intent, for
- PMID 30850153
- Iron Refractory Iron Deficiency Anemia Due to 374 Base Pairs Deletion in the TMPRSS6 Gene.
- Çakmakli S, Acipayam C, Yenmiş İnan MN, Doğan H.
- Journal of pediatric hematology/oncology. 2019 Jul;41(5)e333-e335.
- Iron refractory iron deficiency anemia is an autosomal recessive disorder arising from defects in iron metabolism that cause microcytic anemia to grow resistant to treatment. The patients usually do not respond to orally administered iron treatment and partially respond to intravenous iron administr
- PMID 30130276
Japanese Journal
- 症例報告 経過中に小球性貧血をきたした低亜鉛母乳による亜鉛欠乏症の1例
- 臨床皮膚科 = Japanese journal of clinical dermatology 69(10), 742-745, 2015-09
- NAID 40020566119
- Relationships Among Red Cell Distribution Width, Anemia, and Interleukin-6 in Adult Congenital Heart Disease
Related Links
- Microcytic anemia is characterized by smaller-than-normal red cells due to decreased production of hemoglobin. This review discusses diagnosis and treatment of thalassemia, anemia of inflammation, and iron-deficiency ...
- Microcytic anemia is one of the most common problems faced in the primary care physician’s office, and for many patients is synonymous with iron deficiency anemia. In fact the most common cause of microcytic anemia is iron ...
★リンクテーブル★
[★]
- 英
- microcytic anemia
- ラ
- anaemia microcytica
- 関
- 貧血、小球性低色素性貧血、低色素性貧血
概念
治療反応性による鑑別
HbA1cとの関連
- 赤血球産生が低下するために、代償的に赤血球寿命が延長し、その結果HbA1cが高値となる。しかし、血糖値高値を反映していないために、偽陽性となる。