血小板非減少性紫斑病
- 関
- allergic purpura、anaphylactoid purpura、Henoch purpura、purpura fulminans、Schoenlein-Henoch purpura
WordNet
- any of several blood diseases causing subcutaneous bleeding (同)peliosis
Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2012/10/28 08:58:15」(JST)
[Wiki en表示]
Nonthrombocytopenic purpura |
Classification and external resources |
ICD-9 |
287.2 |
Nonthrombocytopenic purpura is a type of purpura (red or purple skin discoloration) not associated with thrombocytopenia.[1]
Examples/causes include:
- Henoch-Schönlein purpura.[2]
- Hereditary hemorrhagic telangiectasia[3]
- Congenital cytomegalovirus[1]
References
- ^ a b "MedlinePlus Medical Encyclopedia: Purpura". http://www.nlm.nih.gov/medlineplus/ency/article/003232.htm. Retrieved 2009-01-06.
- ^ "Evaluating the Child with Purpura - August, 2001 - American Family Physician". http://www.aafp.org/afp/20010801/419.html. Retrieved 2009-01-06.
- ^ Cotran, Ramzi S.; Kumar, Vinay; Fausto, Nelson; Nelso Fausto; Robbins, Stanley L.; Abbas, Abul K. (2005). Robbins and Cotran pathologic basis of disease. St. Louis, Mo: Elsevier Saunders. pp. 650. ISBN 0-7216-0187-1.
Further reading
- HORLER AR, TRUELOVE SC (March 1955). "Chronic leg ulcers in non-thrombocytopenic purpura". Br Med J 1 (4914): 635–6. doi:10.1136/bmj.1.4914.635. PMC 2061391. PMID 13230576. //www.ncbi.nlm.nih.gov/pmc/articles/PMC2061391/.
- MULDOON JP, BERG AM, KINNAIRD DW (November 1955). "Surgical implications of non-thrombocytopenic purpura". Ann. Surg. 142 (5): 817–23. doi:10.1097/00000658-195511000-00007. PMC 1465031. PMID 13269032. //www.ncbi.nlm.nih.gov/pmc/articles/PMC1465031/.
Pathology: hematology, hematologic diseases of RBCs and megakaryocytes / MEP (D50-69,74, 280-287)
|
|
Red
blood cells |
↑ |
|
|
↓ |
Anemia |
Nutritional |
- Micro-: Iron deficiency anemia
- Macro-: Megaloblastic anemia
|
|
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
|
|
Acquired |
- Drug-induced autoimmune
- Drug-induced nonautoimmune
- Hemolytic disease of the newborn
|
|
|
Aplastic
(mostly Normo-) |
- Hereditary: Fanconi anemia
- Diamond–Blackfan anemia
- Acquired: PRCA
- Sideroblastic anemia
- Myelophthisic
|
|
Blood tests |
- MCV
- Normocytic
- Microcytic
- Macrocytic
- MCHC
|
|
|
Other |
- Methemoglobinemia
- Sulfhemoglobinemia
- Reticulocytopenia
|
|
|
|
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
|
|
|
↓ |
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
|
|
Clotting factor |
- Hemophilia
- von Willebrand disease
- Hypoprothrombinemia/II
- XIII
- Dysfibrinogenemia
|
|
|
|
|
|
cell/phys (coag, heme, immu, gran), csfs
|
rbmg/mogr/tumr/hist, sysi/epon, btst
|
drug (B1/2/3+5+6), btst, trns
|
|
|
|
Pathology: hemodynamics
|
|
Decreases |
Thrombus/thrombosis
|
Renal vein thrombosis
|
|
Ischemia
|
Brain ischemia · Ischaemic heart disease · Ischemic colitis/Mesenteric ischemia
|
|
Infarction
|
general: Anemic infarct · Hemorrhagic infarct
regional: Myocardial infarction · Cerebral infarction · Splenic infarction · Limb infarction
|
|
|
Increases |
Hemorrhage
|
general Bruise/Hematoma: Petechia · Purpura · Ecchymosis
regional: head (Epistaxis, Hemoptysis, Intracranial hemorrhage, Hyphema, Subconjunctival hemorrhage) · torso (Hemothorax, Hemopericardium, Pulmonary hematoma) · abdomen (Gastrointestinal bleeding, Haemobilia, Hemoperitoneum, Hematocele, Hematosalpinx ) · joint (Hemarthrosis)
|
|
Edema
|
general: Anasarca · Angioedema/Lymphedema · Exudate/Transudate
regional: Cerebral edema · Pulmonary edema · Hydrothorax · Ascites/hydroperitoneum · Hydrosalpinx
|
|
Other
|
Hyperemia
|
|
|
UpToDate Contents
全文を閲覧するには購読必要です。 To read the full text you will need to subscribe.
English Journal
- [Glycosylation of autoantibodies in autoimmunes diseases].
- Goulabchand R, Batteux F, Guilpain P.SourceMédecine interne et maladies multi-organiques de l'adulte, centre de compétence pour « maladie auto-immunes rares », université Montpellier I, CHRU Saint-Éloi, 80, avenue Augustin-Fliche, 34295 Montpellier cedex 5, France.
- La Revue de médecine interne / fondée ... par la Société nationale francaise de médecine interne.Rev Med Interne.2013 Dec;34(12):746-53. doi: 10.1016/j.revmed.2013.09.005. Epub 2013 Oct 16.
- Protein glycosylation is one of the most common post-translational modifications, involved in the well described protein biosynthesis process. Protein glycosylation seems to play a major role in the pathogenesis of auto-immune diseases. Herein are described the main alterations of autoantibody glyco
- PMID 24139501
- Immune-mediated dermatoses.
- Rosenkrantz W.SourceAnimal Dermatology Clinic, 2965 Edinger Avenue, Tustin, CA 92780, USA. Electronic address: infotustin@adcmg.com.
- The Veterinary clinics of North America. Equine practice.Vet Clin North Am Equine Pract.2013 Dec;29(3):607-13. doi: 10.1016/j.cveq.2013.08.001.
- Pemphigus foliaceus is the most common autoimmune skin disease in horses and is associated with the production of autoantibodies directed against surface proteins of the keratinocyte. Pemphigus vulgaris is a rare autoimmune skin disease in horses. Systemic lupus erythematosus and cutaneous lupus ery
- PMID 24267678
- Images in clinical medicine. Cutaneous and gastrointestinal purpura.
- Naruse G, Shimada K.SourceTokyo Metropolitan Tama Medical Center, Tokyo, Japan kouta_shimada@tmhp.jp.
- The New England journal of medicine.N Engl J Med.2013 Nov 7;369(19):1843. doi: 10.1056/NEJMicm1302936.
- PMID 24195551
Related Links
- purpura [per´pu-rah] a hemorrhagic disease characterized by extravasation of blood into the tissues, under the skin, and through the mucous membranes, and producing spontaneous bruises, ecchymoses, and petechiae (small ...
- Nonthrombocytopenic purpura information including symptoms, causes, diseases, symptoms, treatments, and other medical and health issues. ... Introduction: Nonthrombocytopenic purpura Description of Nonthrombocytopenic ...
★リンクテーブル★
[★]
- 英
- nonthrombocytopenic purpura
- 関
- アレルギー性紫斑病、劇症紫斑病、アナフィラキシー様紫斑病、シェーンライン・ヘノッホ紫斑病、ヘノッホ紫斑病
[★]
シェーンライン・ヘノッホ紫斑病、Schoenlein-Henoch紫斑病
- 関
- allergic purpura、anaphylactoid purpura、Henoch purpura、nonthrombocytopenic purpura、purpura fulminans
[★]