皮膚白血球破砕性血管炎
WordNet
- relating to or existing on or affecting the skin; "cutaneous nerves"; "a cutaneous infection" (同)cutaneal, dermal
- inflammation of a blood vessel
PrepTutorEJDIC
- 皮膚の,皮膚を冒す
Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2013/06/07 23:31:33」(JST)
[Wiki en表示]
Cutaneous small-vessel vasculitis (also known as "Cutaneous leukocytoclastic angiitis,"[1] "Cutaneous leukocytoclastic vasculitis,"[1] "Cutaneous necrotizing venulitis,"[1] and "Hypersensitivity angiitis"[1]) is inflammation of small blood vessels (usually post-capillary venules in the dermis), characterized by palpable purpura.[2]:831[3] It is the most common vasculitis seen in clinical practice. Leukocytoclasis refers to the damage caused by nuclear debris from infiltrating neutrophils in and around the vessels.[4]
Subtypes of small-vessel vasculitis include:[2]:833-6
-
- Henoch-Schönlein purpura
- Acute hemorrhagic edema of infancy
- Urticarial vasculitis
- Cryoglobulinemic vasculitis
- Erythema elevatum diutinum
- Granuloma faciale
Leukocytoclastic vasculitis[edit]
See also[edit]
- Skin lesion
- List of cutaneous conditions
References[edit]
- ^ a b c d Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. ISBN 1-4160-2999-0.
- ^ a b James, William D.; Berger, Timothy G.; et al. (2006). Andrews' Diseases of the Skin: clinical Dermatology. Saunders Elsevier. ISBN 0-7216-2921-0.
- ^ Lotti T, Ghersetich I, Comacchi C, Jorizzo JL (November 1998). "Cutaneous small-vessel vasculitis". J. Am. Acad. Dermatol. 39 (5 Pt 1): 667–87; quiz 688–90. doi:10.1016/S0190-9622(98)70039-8. PMID 9810883.
- ^ Harrison's Principles of Internal Medicine. 18th edition. Page 2798.
|
Cutaneous vasculitis and other vascular-related cutaneous conditions (L95, 709.1)
|
|
Cutaneous
vasculitis |
- Erythema elevatum diutinum
- Capillaritis
- Urticarial vasculitis
- Nodular vasculitis
|
|
| Microvascular occlusion |
- Calciphylaxis
- Cryoglobulinemic purpura/Cryoglobulinemic vasculitis
- vascular coagulopathy: Livedoid vasculitis
- Livedoid dermatitis
- Perinatal gangrene of the buttock
- Malignant atrophic papulosis
- Sneddon's syndrome
|
|
| Purpura |
- Nonthrombocytopenic purpura: Cryofibrinogenemic purpura
- Drug-induced purpura
- Food-induced purpura
- Henoch–Schönlein purpura
- Obstructive purpura
- Orthostatic purpura
- Purpura fulminans
- Purpura secondary to clotting disorders
- Purpuric agave dermatitis
- Pigmentary purpuric eruptions
- Solar purpura
- Traumatic purpura
- Waldenström hyperglobulinemic purpura
- Painful bruising syndrome
- ungrouped: Paroxysmal hand hematoma
- Postcardiotomy syndrome
- Deep venous thrombosis
- Superficial thrombophlebitis
- Mondor's disease
- Blueberry muffin baby
- Fibrinolysis syndrome
|
|
| Systemic vasculitis |
- see Template:Systemic vasculitis
|
|
| Vascular malformations |
- Arteriovenous malformation
- Bonnet–Dechaume–Blanc syndrome
- Cobb syndrome
- Parkes Weber syndrome
- Sinusoidal hemangioma
- lymphatic malformation
- Hennekam syndrome
- Aagenaes syndrome
- telangiectasia: Generalized essential telangiectasia
- Hereditary hemorrhagic telangiectasia
- Unilateral nevoid telangiectasia
|
|
| Ulcer |
- Venous insufficiency ulceration
- Arterial insufficiency ulcer
- Hematopoietic ulcer
- Neuropathic ulcer
- Acroangiodermatitis
|
|
| Lymphedema |
- see Template:Lymphatic disease
|
|
Ungrouped
vascular-related
cutaneous
conditions |
- Raynaud phenomenon
- Raynaud's disease
- Thromboangiitis obliterans
- Erythromelalgia
- Septic thrombophlebitis
- Arteriosclerosis obliterans
- Bier spots/Marshall–White syndrome
- Cholesterol embolus
- Reactive angioendotheliomatosis
- Trousseau's syndrome
|
|
|
|
|
noco (i/b/d/q/u/r/p/m/k/v/f)/cong/tumr (n/e/d), sysi/epon
|
proc, drug (D2/3/4/5/8/11)
|
|
|
|
|
Vasculitis/arteritis: systemic vasculitis (M30–M31, 446)
|
|
| Large vessel |
Takayasu's arteritis · Giant-cell arteritis
|
|
| Medium vessel |
Type III hypersensitivity (Polyarteritis nodosa) · Kawasaki disease
|
|
| Small vessel |
|
Pauci-immune
|
c-ANCA (Granulomatosis with polyangiitis (Wegener's)) · p-ANCA (Churg-Strauss syndrome, Microscopic polyangiitis)
|
|
|
Type III hypersensitivity
|
Hypersensitivity vasculitis/Henoch–Schönlein purpura
|
|
|
Ungrouped
|
Acute hemorrhagic edema of infancy · Cryoglobulinemic vasculitis · Bullous small vessel vasculitis · Cutaneous small-vessel vasculitis
|
|
|
| Other |
Goodpasture's syndrome · Sneddon's syndrome
|
|
|
|
anat (a:h/u/t/a/l,v:h/u/t/a/l)/phys/devp/cell/prot
|
noco/syva/cong/lyvd/tumr, sysi/epon, injr
|
proc, drug (C2s+n/3/4/5/7/8/9)
|
|
|
|
|
Immune disorders: hypersensitivity and autoimmune diseases (279.5–6)
|
|
Type I/allergy/atopy
(IgE) |
|
Foreign
|
Atopic dermatitis · Allergic urticaria · Hay fever · Allergic asthma · Anaphylaxis · Food allergy (Milk, Egg, Peanut, Tree nut, Seafood, Soy, Wheat), Penicillin allergy
|
|
|
Autoimmune
|
none
|
|
|
Type II/ADCC
(IgM, IgG) |
|
Foreign
|
Pernicious anemia · Hemolytic disease of the newborn
|
|
|
Autoimmune
|
|
Cytotoxic
|
Autoimmune hemolytic anemia · Idiopathic thrombocytopenic purpura · Bullous pemphigoid · Pemphigus vulgaris · Rheumatic fever · Goodpasture's syndrome
|
|
|
"Type 5"/receptor
|
Graves' disease · Myasthenia gravis
|
|
|
|
Type III
(Immune complex) |
|
Foreign
|
Henoch–Schönlein purpura · Hypersensitivity vasculitis · Reactive arthritis · Farmer's lung · Post-streptococcal glomerulonephritis · Serum sickness · Arthus reaction
|
|
|
Autoimmune
|
Systemic lupus erythematosus · Subacute bacterial endocarditis · Rheumatoid arthritis
|
|
|
Type IV/cell-mediated
(T-cells) |
|
Foreign
|
Allergic contact dermatitis · Mantoux test
|
|
|
Autoimmune
|
Diabetes mellitus type 1 · Hashimoto's thyroiditis · Guillain–Barré syndrome · Multiple sclerosis · Coeliac disease · Giant-cell arteritis
|
|
|
GVHD
|
Transfusion-associated graft versus host disease
|
|
|
Unknown/
multiple |
|
Foreign
|
Hypersensitivity pneumonitis (Allergic bronchopulmonary aspergillosis) · Transplant rejection · Latex allergy (I+IV)
|
|
|
Autoimmune
|
Sjögren's syndrome · Autoimmune hepatitis · Autoimmune polyendocrine syndrome (APS1, APS2) · Autoimmune adrenalitis · Systemic autoimmune disease
|
|
|
|
|
cell/phys/auag/auab/comp, igrc
|
|
|
|
|
|
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
- Epidemiology of Vasculitides in Khorasan Province, Iran.
- Jokar M1, Mirfeizi Z1.
- Iranian journal of medical sciences.Iran J Med Sci.2015 Jul;40(4):362-6.
- Vasculitides are a heterogeneous group of more than 20 diseases defined by inflammation and destruction of blood vessels. We aimed to study the demographic characteristics of the primary vasculitides in the North East of Iran. We retrospectively studied the medical records of patients diagnosed with
- PMID 26170524
- Capecitabine-induced leukocytoclastic vasculitis under neoadjuvant chemotherapy for locally advanced colorectal cancer.
- Al-Shamsi HO1, Kee BK1, Tetzlaff MT1, Wolff RA1.
- Journal of gastrointestinal oncology.J Gastrointest Oncol.2015 Jun;6(3):E40-3. doi: 10.3978/j.issn.2078-6891.2015.003.
- We describe a case of capecitabine-induced leukocytoclastic vasculitis in a patient with locally advanced rectal cancer under curative neoadjuvant concurrent chemoradiation using capecitabine. After 5 days of the initiation of capecitabine the patient developed a pruritic maculopapular rash in her e
- PMID 26029464
- Severe Henoch-Schönlein purpura with infliximab for ulcerative colitis.
- Song Y1, Shi YH1, He C1, Liu CQ1, Wang JS1, Zhao YJ1, Guo YM1, Wu RJ1, Feng XY1, Liu ZJ1.
- World journal of gastroenterology : WJG.World J Gastroenterol.2015 May 21;21(19):6082-7. doi: 10.3748/wjg.v21.i19.6082.
- Infliximab (IFX) is an anti-tumor necrosis factor chimeric antibody that is effective for treatment of autoimmune disorders such as Crohn's disease and ulcerative colitis (UC). IFX is well tolerated with a low incidence of adverse effects such as infections, skin reactions, autoimmunity, and maligna
- PMID 26019477
Japanese Journal
- Generalized Alopecia with Vasculitis-Like Changes in a Dog with Babesiosis
- TASAKI Yumi,MIURA Naoki,IYORI Keita [他],NISHIFUJI Koji,ENDO Yasuyuki,MOMOI Yasuyuki
- Journal of Veterinary Medical Science 75(10), 1367-1369, 2013
- … The cutaneous lesions had not responded to treatment with systemic antibiotics and prednisolone. … Histopathological examination of skin biopsies revealed findings suggestive of early leukocytoclastic vasculitis or ischemic vasculopathy. …
- NAID 130003362212
- 症例 全身の広範囲に浸潤を伴う紫斑を呈し好中球減少症を伴ったヒトパルボウイルスB19感染症による皮膚白血球核破砕性血管炎の1例
- Cutaneous vasculitis induced by TNF inhibitors : a report of three cases
- FUJIKAWA Keita,KAWAKAMI Atsushi,HAYASHI Tomayoshi,IWAMOTO Naoki,KAWASHIRI Shin-ya,ARAMAKI Toshiyuki,ICHINOSE Kunihiro,TAMAI Mami,ARIMA Kazuhiko,KAMACHI Makoto,YAMASAKI Satoshi,NAKAMURA Hideki,IDA Hiroaki,ORIGUCHI Tomoki,EGUCHI Katsumi
- Modern rheumatology 20(1), 86-89, 2010-02-01
- NAID 10027168537
Related Links
- Tai YJ, Chong AH, Williams RA, Cumming S, Kelly RI. Retrospective analysis of adult patients with cutaneous leukocytoclastic vasculitis. Australas J Dermatol. May 2006;47(2):92-6. [Medline]. Jennette JC, Falk RJ. Small-vessel. ...
- Cutaneous Leukocytoclastic Vasculitis from vasculitispictures.com. Causes Characteristics Symptoms Treatment Cutaneous Leukocytoclastic Vasculitis Vasculitis Sle Vasculitis Sle ...
Related Pictures
★リンクテーブル★
[★]
- 英
- cutaneous leukocytoclastic vasculitis
[★]
- 関
- cutaneously、cutis、dermal、skin