後天性溶血性貧血
- 関
- hemolytic anemia、hemolytic jaundice、microangiopathic anemia
WordNet
- locate (a moving entity) by means of a tracking system such as radar
- win something through ones efforts; "I acquired a passing knowledge of Chinese"; "Gain an understanding of international finance" (同)win, gain
- relating to or involving or causing hemolysis; "hemolytic anemia" (同)haemolytic
- a deficiency of red blood cells (同)anaemia
- a lack of vitality (同)anaemia
- gotten through environmental forces; "acquired characteristics (such as a suntan or a broken nose) cannot be passed on"
- genus of terrestrial or lithophytic ferns having pinnatifid fronds; chiefly of tropical America (同)genus Anemia
PrepTutorEJDIC
- (不断の努力・習慣などで)…'を'『習得する』,身につける / 〈財産・権利など〉'を'手に入れる,取得する
Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2014/01/13 17:55:31」(JST)
[Wiki en表示]
Acquired hemolytic anemia |
Classification and external resources |
ICD-10 |
D59 |
ICD-9 |
283 |
Acquired hemolytic anemia can be divided into immune and non-immune mediated forms of hemolytic anemia.
Contents
- 1 Immune
- 2 Non-immune
- 3 Drug induced hemolysis
- 4 References
Immune[edit]
Immune mediated hemolytic anemia (direct Coombs test is positive)
- Autoimmune hemolytic anemia
- Warm antibody autoimmune hemolytic anemia
- Idiopathic
- Systemic lupus erythematosus (SLE)
- Evans' syndrome (antiplatelet antibodies and hemolytic antibodies)
- Cold antibody autoimmune hemolytic anemia
- Idiopathic cold hemagglutinin syndrome
- Infectious mononucleosis and mycoplasma (atypical) pneumonia
- Paroxysmal cold hemoglobinuria (rare)
- Alloimmune hemolytic anemia
- Hemolytic disease of the newborn (HDN)
- Rh disease (Rh D)
- ABO hemolytic disease of the newborn
- Anti-Kell hemolytic disease of the newborn
- Rhesus c hemolytic disease of the newborn
- Rhesus E hemolytic disease of the newborn
- Other blood group incompatibility (RhC, Rhe, Kidd, Duffy, MN, P and others)
- Alloimmune hemolytic blood transfusion reactions (i.e. from a non-compatible blood type)
- Drug induced immune mediated hemolytic anemia
- Penicillin (high dose)
- Methyldopa
Non-immune[edit]
Non-immune mediated hemolytic anemia (direct Coombs test is negative)
- Drugs (i.e., some drugs and other ingested substances lead to hemolysis by direct action on RBCs, e.g. ribavirin )
- Toxins (e.g., snake venom; plant poisons such as aesculin)
- Trauma
- Mechanical (from heart valves, extensive vascular surgery, microvascular disease, repeated mechanical vascular trauma)
- Microangiopathic hemolytic anemia (a specific subtype with causes such as TTP, HUS, DIC and HELLP syndrome)
- Infections (Note: Direct Coombs test is sometimes positive in hemolytic anemia due to infection)
- Malaria
- Babesiosis
- Septicemia
- Membrane disorders
- Paroxysmal nocturnal hemoglobinuria (rare acquired clonal disorder of red blood cell surface proteins)
- Liver disease
Drug induced hemolysis[edit]
Drug induced hemolysis has large clinical relevance. It occurs when drugs actively provoke red blood cell destruction. It can be divided in the following manner:
- Drug-induced autoimmune hemolytic anemia
- Drug-induced nonautoimmune hemolytic anemia
A total of four mechanisms are usually described, but there is some evidence that these mechanisms may overlap.[1]
References[edit]
- ^ Wright MS (1999). "Drug-induced hemolytic anemias: increasing complications to therapeutic interventions". Clin Lab Sci 12 (2): 115–8. PMID 10387489.
Pathology: hematology, hematologic diseases of RBCs and megakaryocytes / MEP (D50-69,74, 280-287)
|
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Red
blood cells |
↑ |
|
|
↓ |
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
|
|
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
- Sticky platelet syndrome
- acquired:Thrombocytosis
- DIC
- Congenital afibrinogenemia
- Purpura fulminans
- autoimmune
|
|
|
↓ |
Hypo-
coagulability |
Thrombocytopenia |
- Thrombocytopenic purpura: ITP
- TM
- Heparin-induced thrombocytopenia
- May-Hegglin anomaly
|
|
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
- [Hereditary Spherocytosis: Review. Part II. Symptomatology, outcome, complications, and treatment].
- Comité Nacional de Hematología.
- Archivos argentinos de pediatría.Arch Argent Pediatr.2015 Apr 1;113(2):168-76. doi: 10.1590/S0325-00752015000200025.
- Hereditary spherocytosis must always be suspected in children with anemia, hyperbilirubinemia, splenomegaly or cholelithiasis, in the asymptomatic individual with an affected relative, and in the neonate with hyperbilirubinemia with no blood group incompatibility; its early detection is key to avoid
- PMID 25727830
- Efficacy and safety of rituximab in auto-immune hemolytic anemia: A meta-analysis of 21 studies.
- Reynaud Q1, Durieu I2, Dutertre M1, Ledochowski S3, Durupt S1, Michallet AS4, Vital-Durand D1, Lega JC2.
- Autoimmunity reviews.Autoimmun Rev.2015 Apr;14(4):304-313. doi: 10.1016/j.autrev.2014.11.014. Epub 2014 Dec 9.
- OBJECTIVE: This study aims to evaluate the response to rituximab (RTX) treatment in auto-immune hemolytic anemia (AIHA) patients.METHODS: Studies were selected from MEDLINE up to March 2014. Two investigators independently extracted data on study design, patient characteristics, clinical features (A
- PMID 25497766
- Oxaliplatin-induced immune-mediated cytopenias: A case report and literature review.
- Forcello NP1, Khubchandani S2, Patel SJ3, Brahaj D2.
- Journal of oncology pharmacy practice : official publication of the International Society of Oncology Pharmacy Practitioners.J Oncol Pharm Pract.2015 Apr;21(2):148-56. doi: 10.1177/1078155213520262. Epub 2014 Feb 5.
- Oxaliplatin is a third-generation platinum antineoplastic agent that commonly causes diarrhea, nausea, vomiting, myelosuppression, and peripheral neuropathy. Less common adverse effects that are increasingly being reported include acute immune-mediated thrombocytopenia, hemolytic anemia, and pancyto
- PMID 24500808
Japanese Journal
- Rituximabが著効した後天性血友病Aと血栓性血小板減少性紫斑病の併発例
Related Links
- Hemolytic anemia (HEE-moh-lit-ick uh-NEE-me-uh) is a condition in which red blood cells are destroyed and removed from the bloodstream before their normal lifespan is over. Red blood cells are disc-shaped and look ...
- Important It is possible that the main title of the report Anemia, Hemolytic, Acquired Autoimmune is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s ...
Related Pictures
★リンクテーブル★
[★]
- 英
- acquired hemolytic anemia AHA
- 関
- 先天性溶血性貧血、自己免疫性溶血性貧血 AIHA。
[★]
[★]
微小血管症性貧血
- 関
- acquired hemolytic anemia、hemolytic anemia、hemolytic jaundice
[★]
溶血性黄疸
- 関
- acquired hemolytic anemia、hemolytic anemia、microangiopathic anemia
[★]
- 関
- acquisition、gain、get、obtain、procure、procurement、yield
[★]
- 関
- haemolysis、haemolytic、hemolysis、hemolyze