血液疾患
- 関
- blood disease、blood disorder、blood dyscrasia、hematologic disease、hematological disorder、hemopathy
WordNet
- bring disorder to (同)disarray
- a physical condition in which there is a disturbance of normal functioning; "the doctor prescribed some medicine for the disorder"; "everyone gets stomach upsets from time to time" (同)upset
- a disturbance of the peace or of public order
- not arranged in order (同)unordered
PrepTutorEJDIC
- 〈U〉『無秩序』,混乱,乱雑(confusion) / 《しばしば複数形で》(社会的・政治的な)粉争,騒動 / 〈C〉(肉体的・精神的な)不調,異常,障害 / …‘の'秩序を乱す / 〈心身〉‘に'異常を起こさせる
Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2017/05/06 09:06:17」(JST)
[Wiki en表示]
Hematologic disease |
Classification and external resources |
MeSH |
D006402 |
[edit on Wikidata]
|
Hematologic diseases are disorders which primarily affect the blood. Hematology includes the study of these disorders.
Contents
- 1 Myeloid
- 2 Hematological malignancies
- 3 Miscellaneous
- 4 Hematological changes secondary to non-hematological disorders
- 5 External links
Myeloid
- Hemoglobinopathies (congenital abnormality of the hemoglobin molecule or of the rate of hemoglobin synthesis)
- Sickle-cell disease
- Thalassemia
- Methemoglobinemia
- Anemias (lack of red blood cells or hemoglobin)
- Iron deficiency anemia
- Megaloblastic anemia
- Vitamin B12 deficiency
- Folate deficiency
- Hemolytic anemias (destruction of red blood cells)
- Genetic disorders of RBC membrane
- Hereditary spherocytosis
- Hereditary elliptocytosis
- Congenital dyserythropoietic anemia
- Genetic disorders of RBC metabolism
- Glucose-6-phosphate dehydrogenase deficiency (G6PD)
- Pyruvate kinase deficiency
- 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 autoimmune hemolytic anemia
- Cold agglutinin disease
- Paroxysmal cold hemoglobinuria (rare)
- Infectious mononucleosis
- 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, Kid, Duffy, MN, P and others)
- Drug induced immune mediated hemolytic anemia
- Penicillin (high dose)
- Methyldopa
- Hemoglobinopathies (where these is an unstable or crystalline hemoglobin)
- Paroxysmal nocturnal hemoglobinuria (rare acquired clonal disorder of red blood cell surface proteins)
- Direct physical damage to RBCs
- Microangiopathic hemolytic anemia
- Secondary to artificial heart valve(s)
- Aplastic anemia
- Fanconi anemia
- Diamond-Blackfan anemia (inherited pure red cell aplasia)
- Acquired pure red cell aplasia
- Decreased numbers of cells
- Myelodysplastic syndrome
- Myelofibrosis
- Neutropenia (decrease in the number of neutrophils)
- Agranulocytosis
- Glanzmann's thrombasthenia
- Thrombocytopenia (decrease in the number of platelets)
- Idiopathic thrombocytopenic purpura (ITP)
- Thrombotic thrombocytopenic purpura (TTP)
- Heparin-induced thrombocytopenia (HIT)
- Myeloproliferative disorders (Increased numbers of cells)
- Polycythemia vera (increase in the number of cells in general)
- Erythrocytosis (increase in the number of red blood cells)
- Leukocytosis (increase in the number of white blood cells)
- Thrombocytosis (increase in the number of platelets)
- Myeloproliferative disorder
- Coagulopathies (disorders of bleeding and coagulation)
- Thrombocytosis
- Recurrent thrombosis
- Disseminated intravascular coagulation
- Disorders of clotting proteins
- Hemophilia
- Hemophilia A
- Hemophilia B (also known as Christmas disease)
- Hemophilia C
- Von Willebrand disease
- Disseminated intravascular coagulation
- Protein S deficiency
- Antiphospholipid syndrome
- Disorders of platelets
- Thrombocytopenia
- Glanzmann's thrombasthenia
- Wiskott-Aldrich syndrome
Hematological malignancies
- Hematological malignancies
- Lymphomas
- Hodgkin's disease
- Non-Hodgkin's lymphoma {includes the next five entries}
- Burkitt's lymphoma
- Anaplastic large cell lymphoma
- Splenic marginal zone lymphoma
- Hepatosplenic T-cell lymphoma
- Angioimmunoblastic T-cell lymphoma (AILT)
- Myelomas
- Multiple myeloma
- Waldenström macroglobulinemia
- Plasmacytoma
- Leukemias increased WBC
- Acute lymphocytic leukemia (ALL)
- Chronic lymphocytic leukemia (CLL){now included in theCLL/SCLL type NHL}
- Acute myelogenous leukemia (AML)
- Chronic Idiopathic Myelofibrosis (MF)
- Chronic myelogenous leukemia (CML)
- T-cell prolymphocytic leukemia (T-PLL)
- B-cell prolymphocytic leukemia (B-PLL)
- Chronic neutrophilic leukemia (CNL)
- Hairy cell leukemia (HCL)
- T-cell large granular lymphocyte leukemia (T-LGL)
- Aggressive NK-cell leukemia
Miscellaneous
- Hemochromatosis
- Asplenia
- Hypersplenism
- Monoclonal gammopathy of undetermined significance
- Hemophagocytic lymphohistiocytosis
- Tempi syndrome
Hematological changes secondary to non-hematological disorders
- Anemia of chronic disease
- Infectious mononucleosis
- AIDS
- Malaria
- Leishmaniasis
External links
- http://www.hematologic.niddk.nih.gov/info/index.htm
- Myeloproliferative Disorders (MPD) Foundation and Research Alliance
- International Registry of Rare Bleeding Disorders
Diseases of red blood cells (D50–69,74, 280–287)
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↑ |
|
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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
|
|
Blood tests |
- MCV
- Normocytic
- Microcytic
- Macrocytic
- MCHC
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Other |
- Methemoglobinemia
- Sulfhemoglobinemia
- Reticulocytopenia
|
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Diseases of clotting (D50–69,74, 280–287)
|
|
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
- autoimmune
|
|
|
↓ |
Hypo-
coagulability |
Thrombocytopenia |
- Thrombocytopenic purpura: ITP
- TM
- TTP
- Upshaw Schulman syndrome
- Heparin-induced thrombocytopenia
- May–Hegglin anomaly
|
|
Platelet function |
- adhesion
- aggregation
- Glanzmann's thrombasthenia
- platelet storage pool deficiency
- Hermansky–Pudlak syndrome
- Gray platelet syndrome
|
|
Clotting factor |
- Hemophilia
- von Willebrand disease
- Hypoprothrombinemia/II
- Factor VII deficiency
- Factor X deficiency
- Factor XII deficiency
- Factor XIII deficiency
- Dysfibrinogenemia
- Congenital afibrinogenemia
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|
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Hematologic disease: Monocyte and granulocyte disease (CFU-GM/CFU-Baso/CFU-Eos), including immunodeficiency (D70-D71, 288)
|
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Monocytes/
macrophages |
↑ |
- Histiocytosis
- Chronic granulomatous disease
|
|
-cytosis: |
|
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↓ |
|
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Granulocytes |
↑ |
-cytosis: |
- granulocytosis
- Neutrophilia
- Eosinophilia/Hypereosinophilic syndrome
- Basophilia
- Bandemia
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|
|
↓ |
-penia: |
- Granulocytopenia/agranulocytosis (Neutropenia/Kostmann syndrome
- Eosinopenia
- Basopenia)
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|
|
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PBD |
chemotaxis/degranulation: |
- Leukocyte adhesion deficiency
- Chédiak–Higashi syndrome
- Neutrophil-specific granule deficiency
|
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respiratory burst: |
- Chronic granulomatous disease
- Neutrophil immunodeficiency syndrome
- Myeloperoxidase deficiency
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Certain conditions originating in the perinatal period / fetal disease (P, 760–779)
|
|
Maternal factors and
complications of pregnancy,
labour and delivery |
placenta: |
- Placenta praevia
- Placental insufficiency
- Twin-to-twin transfusion syndrome
|
|
chorion/amnion: |
|
|
umbilical cord: |
- Umbilical cord prolapse
- Nuchal cord
- Single umbilical artery
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|
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Length of gestation
and fetal growth |
- Small for gestational age/Large for gestational age
- Preterm birth/Postmature birth
- Intrauterine growth restriction
|
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Birth trauma |
- scalp
- Cephalhematoma
- Chignon
- Caput succedaneum
- Subgaleal hemorrhage
- Brachial plexus lesion
- Erb's palsy
- Klumpke paralysis
|
|
By system |
Respiratory |
- Intrauterine hypoxia
- Infant respiratory distress syndrome
- Transient tachypnea of the newborn
- Meconium aspiration syndrome
- pleural disease
- Pneumothorax
- Pneumomediastinum
- Wilson–Mikity syndrome
- Bronchopulmonary dysplasia
|
|
Cardiovascular |
- Pneumopericardium
- Persistent fetal circulation
|
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Haemorrhagic and
hematologic disease |
- Vitamin K deficiency
- Haemorrhagic disease of the newborn
- HDN
- ABO
- Anti-Kell
- Rh c
- Rh D
- Rh E
- Hydrops fetalis
- Hyperbilirubinemia
- Kernicterus
- Neonatal jaundice
- Velamentous cord insertion
- Intraventricular hemorrhage
- Germinal matrix hemorrhage
- Anemia of prematurity
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Digestive |
- Ileus
- Necrotizing enterocolitis
- Meconium peritonitis
|
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Integument and
thermoregulation |
- Erythema toxicum
- Sclerema neonatorum
|
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Nervous system |
- Periventricular leukomalacia
|
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Musculoskeletal |
- Gray baby syndrome
- muscle tone
- Congenital hypertonia
- Congenital hypotonia
|
|
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Infectious |
- Vertically transmitted infection
- Neonatal infection
- Congenital rubella syndrome
- Neonatal herpes simplex
- Mycoplasma hominis infection
- Ureaplasma urealyticum infection
- Omphalitis
- Neonatal sepsis
- Group B streptococcal infection
- Neonatal conjunctivitis
|
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Other |
- Miscarriage
- Perinatal mortality
- Stillbirth
- Infant mortality
- Neonatal withdrawal
|
UpToDate Contents
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English Journal
- Carboplatin AUC 10 for IGCCCG good prognosis metastatic seminoma.
- Tookman L, Rashid S, Matakidou A, Phillips M, Wilson P, Ansell W, Jamal-Hanjani M, Chowdhury S, Harland S, Sarwar N, Oliver T, Powles T, Shamash J.SourceDepartment of Medical Oncology, St Bartholomew's Hospital, West Smithfield , London , UK.
- Acta oncologica (Stockholm, Sweden).Acta Oncol.2013 Jun;52(5):987-93. doi: 10.3109/0284186X.2012.714078. Epub 2012 Sep 3.
- Abstract Objective. Metastatic seminoma is a highly curable disease. Standard treatment comprises of combination chemotherapy. The short- and long-term toxicities of this treatment are increasingly recognised and the possibility of over treatment in such a curable disease should be considered. We ha
- PMID 22943385
- Acute neutropenia associated with initiation of febuxostat therapy for hyperuricaemia in patients with chronic kidney disease.
- Kobayashi S, Ogura M, Hosoya T.SourceDivision of Nephrology and Hypertension, Department of Internal Medicine, The Jikei University School of Medicine, Tokyo, Japan.
- Journal of clinical pharmacy and therapeutics.J Clin Pharm Ther.2013 Jun;38(3):258-61. doi: 10.1111/jcpt.12057. Epub 2013 Mar 18.
- WHAT IS KNOWN AND OBJECTIVE: Febuxostat is a new non-purine selective inhibitor of xanthine oxidase for the treatment of hyperuricaemia in patients with gout. Febuxostat is recommended as the first-line pharmacologic urate-lowering therapy for gout in the American College of Rheumatology guidelines.
- PMID 23506426
- Oral etoposide as first-line therapy in the treatment of patients with advanced classic Kaposi's sarcoma (CKS): a single-arm trial (oral etoposide in CKS).
- Tas F, Sen F, Keskin S, Kilic L.SourceInstitute of Oncology, University of Istanbul, Istanbul, Turkey.
- Journal of the European Academy of Dermatology and Venereology : JEADV.J Eur Acad Dermatol Venereol.2013 Jun;27(6):789-92. doi: 10.1111/j.1468-3083.2011.04404.x. Epub 2011 Dec 20.
- Background Classic Kaposi's sarcoma (CKS) affects an elderly population; it is important to have effective treatment options with high activity and relatively low toxicity, and availability to be used for long periods. Objective We investigated the activity and safety of single-agent etoposide
- PMID 22188463
Japanese Journal
- 抗リン脂質抗体症候群が疑われ, 妊娠前よりprednisoloneとlow-dose aspirinの併用療法を行い生児を得られた1症例
- 日本臨床免疫学会会誌 = Japanese journal of clinical immunology 20(1), 67-72, 1997-02-28
- NAID 10007309708
- 骨髄線維症に対するPartial splenic embolization therapyの効果
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★リンクテーブル★
[★]
- 関
- blood disorder、blood dyscrasia、haematological disease、haematological disorder、hematologic disease、hematologic disorder、hematological disease、hematological disorder、hemopathy
[★]
- 関
- blood disease、blood dyscrasia、haematological disorder、hematologic disease、hematological disorder、hemopathy
[★]
血液疾患
- 関
- blood disease、blood disorder、blood dyscrasia、haematological disorder、hematologic disease、hematological disorder
[★]
血液疾患
- 関
- blood disease、blood disorder、blood dyscrasia、haematological disorder、hematologic disease、hemopathy
[★]
- 障害:個人的苦痛や機能の障害があるので「疾病」とは言えるものの、その背景にある臓器障害がもう一つはっきりしない場合に用いられる。(PSY.9)
- an untidy state; a lack of order or organization (⇔order)
- violent behaviour of large groups of people
- an illness that cause a part of the body to stop functioning correctly
- disease <> illness <> disorder
- 乱す、乱雑にする。(人)の(心身の)調子を狂わせる。
[★]
血液学的な
- 関
- haematological、haematologically、hematologic、hematological、hematologically
[★]
血液学的な
- 関
- haematologic、haematologically、hematologic、hematological、hematologically