- 関
- peliosis、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)』「2015/11/16 19:14:20」(JST)
[Wiki en表示]
For other uses of "Purpura", see Purpura (disambiguation).
Purpura |
Petechiae and purpura on the lower limb due to medication induced vasculitis
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Classification and external resources |
Specialty |
Dermatology, hematology |
ICD-10 |
D69 |
ICD-9-CM |
287 |
DiseasesDB |
25619 |
MedlinePlus |
003232 |
MeSH |
D011693 |
Purpura is a condition of red or purple discolored spots on the skin that do not blanch on applying pressure. The spots are caused by bleeding underneath the skin usually secondary to vasculitis or dietary deficiency of vitamin C (scurvy).[1] They measure 0.3–1 cm (3–10 mm), whereas petechiae measure less than 3 mm, and ecchymoses greater than 1 cm.[2]
Pupura is common with typhus and can be present with meningitis caused by meningococci or septicaemia. In particular, meningococcus (Neisseria meningitidis), a Gram-negative diplococcus organism, releases endotoxin when it lyses. Endotoxin activates the Hageman factor (clotting factor XII), which causes disseminated intravascular coagulation (DIC). The DIC is what appears as a rash on the affected individual.
Contents
- 1 Classification
- 2 Etymology and pronunciation
- 3 See also
- 4 References
- 5 External links
Classification
Purpura are a common and nonspecific medical sign; however, the underlying mechanism commonly involves one of:
- Platelet disorders (thrombocytopenic purpura)
- Primary thrombocytopenic purpura
- Secondary thrombocytopenic purpura
- Post-transfusion purpura
- Vascular disorders (nonthrombocytopenic purpura)
- Microvascular injury, as seen in senile (old age) purpura, when blood vessels are more easily damaged
- Hypertensive states
- Deficient vascular support
- Vasculitis, as in the case of Henoch-Schönlein purpura
- Coagulation disorders
- Disseminated intravascular coagulation (DIC)
- Scurvy (vitamin C deficiency) - defect in collagen synthesis due to lack of hydroxylation of procollagen results in weakened capillary walls and cells
- Meningococcemia
- Cocaine use with concomitant use of the one-time chemotherapy drug and now veterinary deworming agent levamisole can cause purpura of the ears, face, trunk, or extremities, sometimes needing reconstructive surgery.[3] Levamisole is purportedly a common cutting agent.
- Decomposition of blood vessels including purpura is a symptom of acute radiation poisoning in excess of 2 Grays of radiation exposure. This is an uncommon cause in general, but is commonly seen in victims of nuclear disaster.
Cases of psychogenic purpura are also described in the medical literature,[4] some claimed to be due to "autoerythrocyte sensitization". Other studies[5] suggest the local (cutaneous) activity of tissue plasminogen activator can be increased in psychogenic purpura, leading to substantial amounts of localized plasmin activity, rapid degradation of fibrin clots, and resultant bleeding. Petechial rash is also characteristic of a rickettsial infection.
Etymology and pronunciation
The word purpura () comes from Latin purpura, "purple". It is a mass noun naming the condition or state, not the name of an individual spot (thus there is no *pupurum, *purpura or *purpura, *purpurae count declension).
See also
- Bruise, which is a hematoma caused by trauma
- Petechia, which is a small type of hematoma (<3mm)
- Ecchymosis, which is a large type of hematoma (>1 cm)
- Purpura secondary to clotting disorders
- Purpura haemorrhagica in horses
- Pigmented purpuric dermatosis
- Schamberg disease (progressive pigmentary purpura)
References
- ^ "UCSF Purpura Module" (PDF).
- ^ Mitchell RS; Kumar V; Robbins SL; Abbas AK; Fausto N (2007). Robbins basic pathology (8th ed.). Saunders/Elsevier. pp. 10–11. ISBN 1-4160-2973-7.
- ^ "Toxic Effects of Levamisole in a Cocaine User". New England Journal of Medicine.
- ^ Anderson JE, DeGoff W, McNamara M (1999). "Autoerythrocyte sensitization (psychogenic purpura): a case report and review of the literature". Pediatric emergency care 15 (1): 47–8. doi:10.1097/00006565-199902000-00014. PMID 10069314.
- ^ Lotti T, Benci M, Sarti MG, Teofoli P, Senesi C, Bonan P, et al. (1993). "Psychogenic purpura with abnormally increased tPA dependent cutaneous fibrinolytic activity". Int J Dermatol 32 (7): 521–3. doi:10.1111/j.1365-4362.1993.tb02840.x. PMID 8340191.
External links
- Evaluating the Child with Purpura from American Academy of Family Physicians
Diseases of red blood cells and clotting (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
- 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
- Congenital afibrinogenemia
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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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Disorders of hemodynamics
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Decreases |
Thrombus/thrombosis
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Renal vein thrombosis
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Ischemia
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- Brain ischemia
- Ischaemic heart disease
- large intestine: Ischemic colitis
- small intestine: Mesenteric ischemia
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Infarction
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- Anemic infarct
- Hemorrhagic infarct
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- Myocardial infarction
- Cerebral infarction
- Splenic infarction
- Limb infarction
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Increases |
Hemorrhage
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- Bruise/Hematoma
- Petechia
- Purpura
- Ecchymosis
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- head
- Epistaxis
- Hemoptysis
- Intracranial hemorrhage
- Hyphema
- Subconjunctival hemorrhage
- torso
- Hemothorax
- Hemopericardium
- Pulmonary hematoma
- abdomen
- Gastrointestinal bleeding
- Haemobilia
- Hemoperitoneum
- Hematocele
- Hematosalpinx
- joint
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Edema
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- Anasarca
- Angioedema/Lymphedema
- Exudate/Transudate
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- Cerebral edema
- Pulmonary edema
- Hydrothorax
- Ascites/hydroperitoneum
- Hydrosalpinx
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Other
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UpToDate Contents
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English Journal
- [Papular-purpuric gloves and socks syndrome and thrombocytopenia related to parvovirus B19 infection.]
- Elena-González A, Lozano-Durán C, Cuadros-Tito P, Gete-García L.SourceServicio de Medicina Interna, Hospital Príncipe de Asturias, Alcalá de Henares, Madrid, España. Electronic address: aelena83@hotmail.com.
- Enfermedades infecciosas y microbiologia clinica.Enferm Infecc Microbiol Clin.2013 Jul 8. pii: S0213-005X(13)00161-4. doi: 10.1016/j.eimc.2013.05.003. [Epub ahead of print]
- PMID 23845252
- [Henoch-Schönlein Purpura Resulting in an Obstructive Bladder Mass.]
- Comploj E, Cassar W, Trenti E, Palermo S, Reinstadler P, Ladurner C, Dechet C, Pycha A.SourceAbteilung für Urologie, Zentralkrankenhaus Bozen, Bozen, Italien.
- Aktuelle Urologie.Aktuelle Urol.2013 Jul 3. [Epub ahead of print]
- Henoch-Schönlein purpura (HSP) is the most common form of an immunological systemic vasculitis of childhood. The classic clinical symptoms include purpuric rash, abdominal pain, arthralgias, and haematuria, but the spectrum of HSP may vary to very rare forms. This arti-cle reports on an 8-year-old
- PMID 23824929
- The 2011 dengue haemorrhagic Fever outbreak in lahore - an account of clinical parameters and pattern of haemorrhagic complications.
- Ahmed S, Mohammad WW, Hamid F, Akhter A, Afzal RK, Mahmood A.SourceDepartment of Medicine, Combined Military Hospital, Lahore Cantt.
- Journal of the College of Physicians and Surgeons--Pakistan : JCPSP.J Coll Physicians Surg Pak.2013 Jul;23(7):463-7. doi: 07.2013/JCPSP.463467.
- Objective: To describe the frequency and outcome of dengue haemorrhagic fever (DHF) cases and determine the association of clinical and laboratory parameters with haemorrhagic complications. Study Design: A descriptive study. Place and Duration of Study: Combined Military Hospital, Lahore, from Augu
- PMID 23823947
Japanese Journal
- 症例 サイトメガロウイルス感染に伴って生じたPapular-purpuric Gloves and Socks Syndromeの1例
- 平野 亜由子,福本 隆也,藤井 秀孝 [他]
- 西日本皮膚科 = The Nishinihon journal of dermatology : 日本皮膚科学会西部支部機関誌 75(5), 444-447, 2013-10
- NAID 40019823351
- 白血球除去療法が有効であった下部消化管出血を伴った成人Henoch-Schönlein紫斑病(HSP)の2例
- 小林 園実,田端 秀日朗,安藤 明利 [他],西村 英樹,佐中 孜,新田 孝作,内藤 隆
- 日本透析医学会雑誌 46(7), 671-680, 2013
- 症例1は57歳,男性.感冒様症状が出現後,腹痛や関節痛および両下肢浮腫・紫斑が出現した.ネフローゼ症候群をきたし,皮膚生検および腎生検の病理結果よりHenoch-Schönlein紫斑病(HSP)と診断した.Prednisolone(PSL)投与にて両下肢の紫斑および関節痛は軽快傾向であったが,腹痛および下血は改善せず,白血球除去療法(leukocytapheresis:LCAP)を計7回施行し …
- NAID 130003372798
Related Links
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- ウィキペディアの英語版でPurpuricという用語が挙げてありますが、そこでは、以下の意味で使われています。Purpura (from Latin: purpura, meaning "purple") is the appearance of red or purple discolorations on the skin that do not blanch ...
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- 関
- purpura、purpuric