正色素性貧血
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)』「2015/06/27 11:56:35」(JST)
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Normochromic is a form of anemia in which the concentration of hemoglobin in the red blood cells is within the standard range. However, there are insufficient numbers of red blood cells. This includes: aplastic, posthemorrhagic, and hemolytic anemias and anemia of chronic disease.
See also
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
- TTP
- Upshaw Schulman syndrome
- 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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Index of cells from bone marrow
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Description |
- Immune system
- Cells
- Physiology
- coagulation
- proteins
- granule contents
- colony-stimulating
- heme and porphyrin
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Disease |
- Red blood cell
- Monocyte and granulocyte
- Neoplasms and cancer
- Histiocytosis
- Symptoms and signs
- Blood tests
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Treatment |
- Transfusion
- Drugs
- thrombosis
- bleeding
- other
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UpToDate Contents
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English Journal
- A case of pure red cell aplasia during nivolumab therapy for cardiac metastatic melanoma.
- Yuki A1, Takenouchi T, Takatsuka S, Ishiguro T.
- Melanoma research.Melanoma Res.2017 Dec;27(6):635-637. doi: 10.1097/CMR.0000000000000392.
- PMID 28872489
- Altered expression of intestinal duodenal cytochrome b and divalent metal transporter 1 might be associated with cardio-renal anemia syndrome.
- Naito Y1, Sawada H2, Oboshi M2, Okuno K2, Yasumura S2, Okuhara Y2, Eguchi A2, Nishimura K2, Soyama Y2, Asakura M2, Ishihara M3, Tsujino T4, Masuyama T2.
- Heart and vessels.Heart Vessels.2017 Nov;32(11):1410-1414. doi: 10.1007/s00380-017-1013-4. Epub 2017 Jul 1.
- PMID 28669019
- Study of Glucose-6-Phosphate Dehydrogenase Deficiency: 5 Years Retrospective Egyptian study.
- Hagag AAE1, Badraia IM1, Elfarargy MS1, Abd Elmageed MM1, Abo-Ali EA2.
- Endocrine, metabolic & immune disorders drug targets.Endocr Metab Immune Disord Drug Targets.2017 Oct 3. doi: 10.2174/1871530317666171003160350. [Epub ahead of print]
- PMID 28982343
Japanese Journal
- 短腸症候群にて長期中心静脈栄養管理中に発症した亜鉛,銅欠乏性貧血の1例
- 久保 孝文,佃 和憲,万代 康弘,大橋 龍一郎
- 日本腹部救急医学会雑誌 33(4), 759-762, 2013
- 要旨:83歳,男性。急性上腸間膜動脈塞栓症による腸管壊死で,大量腸管切除施行後,在宅中心静脈栄養管理中であった。術後5年半後に著明な鉄剤不応性大球性正色素性貧血と,白血球,好中球の減少を認めた。上,下部消化管内視鏡検査と骨髄検査で異常所見は認められなかった。採血検査で著明な亜鉛,銅,アルカリフォスファターゼ,セルロプラスミン濃度の低下を認めたため,亜鉛,銅欠乏性貧血と診断した。 ポラプレジンクの内 …
- NAID 130004509166
- クームス陰性自己免疫性溶血性貧血を併発しリツキシマブが奏効した後天性無巨核球性血小板減少性紫斑病
- 橋本 亜香利,藤見 章仁,蟹沢 祐司,松野 鉄平,奥田 敏徳,南 伸弥,土居 忠,石川 和真,植村 尚貴,外丸 詩野
- 臨床血液 54(6), 568-573, 2013
- 後天性無巨核球性血小板減少性紫斑病(AATP)は,骨髄巨核球が選択的に消失または高度に減少する希少疾患である。症例は67歳,男性。2ヶ月前からの出血傾向を自覚し近医を受診。高度の血小板減少を認め,当科紹介となった。骨髄は巨核球のみが欠如し,顆粒球系,赤芽球系に異形成を認めないことからAATPと診断した。また,軽度の正球性正色素性貧血,ハプトグロビン測定感度以下,直接・間接coombs試験陰性および …
- NAID 130004501825
- 抗糸球体基底膜抗体陽性と血栓性微小血管障害症を合併した acute kidney injury の1例
- 大久保 愛子,清水 優佳,入福 泰介 [他],内藤 隆之,小川 貴彦,正木 崇生
- 日本透析医学会雑誌 = Journal of Japanese Society for Dialysis Therapy 45(10), 973-978, 2012-10-28
- … However, her condition did not improve, and laboratory data revealed normocytic-normochromic anemia and thrombocytopenia on the sixth day. …
- NAID 10031130505
Related Links
- drug-induced hemolytic anemia (drug-induced immune hemolytic anemia) a form of immune hemolytic anemia induced by the taking of drugs, involving one of four different mechanisms: Immune complex problems: Ingestion of any of a ...
- drug-induced hemolytic anemia (drug-induced immune hemolytic anemia) a form of immune hemolytic anemia induced by the taking of drugs, involving one of four different mechanisms: Immune complex problems: Ingestion of any of a ...
★リンクテーブル★
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- 英
- normochromic anemia
- ラ
- anaemia normochromica
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正球性正色素性貧血