ヘモグロビン血症、血色素血症
WordNet
- presence of excessive hemoglobin in the blood plasma (同)haemoglobinemia
Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2013/09/04 15:23:16」(JST)
[Wiki en表示]
Hemoglobinemia (British Haemoglobinaemia) is a medical condition in which there is an excess of hemoglobin in the blood plasma. This is an effect of intravascular hemolysis, in which hemoglobin separates from red blood cells, a form of anemia. Hemoglobinemia can be caused by intrinisic or extrinsic factors. When hemoglobinemia is internally caused, it is a result of recessive genetic defects that cause the red blood cells to lyse, letting the hemoglobin spill out of the cell into the blood plasma. In externally caused hemoglobinemia, an outside attacker acts as an antibody against the red blood cells. This can cause the cells to be destroyed and their hemoglobin released.
References[edit source | edit]
- "Hemoglobinemia". WrongDiagnosis.com. Retrieved 2009-05-01.
- "Hemolytic Anemia". University of Virginia Health System. Retrieved 2009-05-01.
See also[edit source | edit]
- Coagulation
- Blood diseases
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
- Sticky platelet syndrome
- 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
- Aurin tricarboxylic acid self-protects by inhibiting aberrant complement activation at the C3 convertase and C9 binding stages.
- Lee M, Guo JP, McGeer EG, McGeer PL.SourceKinsmen Laboratory of Neurological Research, University of British Columbia, Vancouver, British Columbia, Canada.
- Neurobiology of aging.Neurobiol Aging.2013 May;34(5):1451-61. doi: 10.1016/j.neurobiolaging.2012.10.023. Epub 2012 Nov 20.
- Aberrant complement activation is known to exacerbate the pathology in a spectrum of degenerative diseases of aging. We previously reported that aurin tricarboxylic acid (ATA) is an orally effective agent which prevents formation of the membrane attack complex of complement. It inhibits C9 attachmen
- PMID 23177218
- A perspective on the role of extracellular hemoglobin on the innate immune system.
- Lee SK, Ding JL.SourceDepartment of Biological Sciences, National University of Singapore, Singapore, Singapore.
- DNA and cell biology.DNA Cell Biol.2013 Feb;32(2):36-40. doi: 10.1089/dna.2012.1897. Epub 2012 Dec 18.
- Host cell-derived danger-associated molecular patterns (DAMPs), such as the hemoglobin (Hb) can interact with the innate immune system either directly or through binding to pathogen-associated molecular patterns (PAMPs). Hemolysis occurs under various pathological conditions, leading to hemoglobinem
- PMID 23249270
- Use of preoperative visceral echo-color-Doppler in patients candidates to colonic surgery: preliminary report.
- Del Rio P, Bertocchi E, Sommaruga L, Iapichino G, Montana C, Dell'abate P, Sianesi M.SourceUnit of General Surgery and Organ Transplantation, Department of Surgical Science, University Hospital of Parma, Parma, Italy - paolo.delrio@unipr.it.
- Minerva chirurgica.Minerva Chir.2012 Dec;67(6):481-8.
- AIM: Postsurgical paralytic ileus is by definition an ileal paralysis longer than three days (72 hours) after a surgery on the gastrointestinal tract. At colorectal surgery we have performed on all candidates a visceral echo-color-Doppler to find a potential correlation with cardiovascular risk fact
- PMID 23334111
Japanese Journal
- 症例 不安定ヘモグロビン症Hb Buenos Aires, Bryn Mawr:18年の経過観察
- 安藤 智恵,森山 耕成,中島 與志行 [他],Ohyama Akira,Yoshikuni Hirofumi,Moriuchi Hiroyuki,Tsuji Yoshiro,Ohba Yuzo,Hattori Yukio,Kamitamari Akira,安藤 智恵,森山 耕成,中島 與志行,大宮 朗,吉國 裕文,森内 浩幸,辻 芳郎,大庭 雄三,服部 幸夫,上玉 利彰,アンドウ チエ,モリヤマ コウセイ,ナカシマ ヨシユキ,オオミヤ アキラ,ヨシクニ ヒロフミ,モリウチ ヒロユキ,ツジ ヨシロウ,オオバ ユウゾウ,ハットリ ユキオ,カミタマリ アキラ
- 福岡医学雑誌 95(11), 297-304, 2004-11-25
- … A 20-year-old man has been under observation for 18 years because of unstable hemoglobinemia, Hb Buenos Aires, Bryn Mawr (fl-globin, Phe85Ser). …
- NAID 120002834529
- グリコヘモグロビンA_1c異常パターンから検出されたヘモグロビン異常症4例の解析
- 中原 睦子,栗原 正子,木下 幸子
- 医学検査 : 日本臨床衛生検査技師会誌 = The Japanese journal of medical technology 51(10), 1396-1401, 2002-10-25
- NAID 10016218452
Related Links
- Hemoglobinemia (British Haemoglobinaemia) is a medical condition in which there is an excess of hemoglobin in the blood plasma. This is an effect of intravascular hemolysis, in which hemoglobin separates from red blood cells, a form of ...
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