- 関
- cutaneous vasculitis, idiopathic
WordNet
- relating to or existing on or affecting the skin; "cutaneous nerves"; "a cutaneous infection" (同)cutaneal, dermal
- inflammation of a blood vessel or lymph duct
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）』「2015/06/05 20:17:53」(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
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- Henoch-Schönlein purpura
- Acute hemorrhagic edema of infancy
- Urticarial vasculitis
- Cryoglobulinemic vasculitis
- Erythema elevatum diutinum
- Granuloma faciale
Leukocytoclastic vasculitis
See also
- Skin lesion
- List of cutaneous conditions
References
- ^ 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.
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Cutaneous vasculitis and other vascular-related cutaneous conditions (L95, 709.1)
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| Cutaneous vasculitis |
- Erythema elevatum diutinum
- Capillaritis
- Urticarial vasculitis
- Nodular vasculitis
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| Microvascular occlusion |
- Calciphylaxis
- Cryoglobulinemic purpura/Cryoglobulinemic vasculitis
- vascular coagulopathy: Livedoid vasculitis
- Livedoid dermatitis
- Perinatal gangrene of the buttock
- Malignant atrophic papulosis
- Sneddon's syndrome
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| 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 vein thrombosis
- Superficial thrombophlebitis
- Mondor's disease
- Blueberry muffin baby
- Fibrinolysis syndrome
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| Systemic vasculitis |
- see Template:Systemic vasculitis
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| 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
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| Ulcer |
- Venous ulcer
- Arterial insufficiency ulcer
- Hematopoietic ulcer
- Neuropathic ulcer
- Acroangiodermatitis
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| Lymphedema |
- see Template:Lymphatic vessel disease
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Ungrouped
vascular-related
cutaneous conditions |
- Raynaud's phenomenon
- Thromboangiitis obliterans
- Erythromelalgia
- Septic thrombophlebitis
- Arteriosclerosis obliterans
- Bier spots/Marshall–White syndrome
- Cholesterol embolus
- Reactive angioendotheliomatosis
- Trousseau's syndrome
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Index of skin
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| Description |
- Anatomy
- Physiology
- Development
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| Disease |
- Infections
- Vesiculobullous
- Dermatitis and eczema
- Papulosquamous
- Urticaria and erythema
- Radiation-related
- Pigmentation
- Mucinoses
- Keratosis, ulcer, atrophy, and necrobiosis
- Vasculitis
- Fat
- Neutrophilic and eosinophilic
- Congenital
- Neoplasms and cancer
- nevi and melanomas
- epidermis
- dermis
- Symptoms and signs
- Terminology
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| Treatment |
- Procedures
- Drugs
- antibiotics
- disinfectants
- emollients and protectives
- itch
- psoriasis
- other
- Wound and ulcer
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Systemic vasculitis (M30–M31, 446)
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| Large vessel |
- Takayasu's arteritis
- Giant-cell arteritis
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| Medium vessel |
- Type III hypersensitivity
- Kawasaki disease
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| Small vessel |
| Pauci-immune |
- c-ANCA
- Granulomatosis with polyangiitis
- p-ANCA
- Churg-Strauss syndrome
- Microscopic polyangiitis
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| Type III hypersensitivity |
- Hypersensitivity vasculitis/Henoch–Schönlein purpura
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| Ungrouped |
- Acute hemorrhagic edema of infancy
- Cryoglobulinemic vasculitis
- Bullous small vessel vasculitis
- Cutaneous small-vessel vasculitis
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| Other |
- Goodpasture's syndrome
- Sneddon's syndrome
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Index of the circulatory system
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| Description |
- Anatomy
- Arteries
- head and neck
- arms
- chest
- abdomen
- legs
- Veins
- head and neck
- arms
- chest
- abdomen and pelvis
- legs
- Development
- Cells
- Physiology
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| Disease |
- Congenital
- Neoplasms and cancer
- Lymphatic vessels
- Injury
- Vasculitis
- Other
- Symptoms and signs
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| Treatment |
- Procedures
- Drugs
- beta blockers
- channel blockers
- diuretics
- nonsympatholytic vasodilatory antihypertensives
- peripheral vasodilators
- renin–angiotensin system
- sympatholytic antihypertensives
- vasoprotectives
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Hypersensitivity and autoimmune diseases (279.5–6)
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Type I/allergy/atopy
(IgE) |
| Foreign |
- Atopic eczema
- Allergic urticaria
- Allergic rhinitis (Hay fever)
- Allergic asthma
- Anaphylaxis
- Food allergy
- Milk
- Egg
- Peanut
- Tree nut
- Seafood
- Soy
- Wheat
- Penicillin allergy
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| Autoimmune |
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Type II/ADCC
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| Foreign |
- Hemolytic disease of the newborn
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| Autoimmune |
| Cytotoxic |
- Autoimmune hemolytic anemia
- Idiopathic thrombocytopenic purpura
- Bullous pemphigoid
- Pemphigus vulgaris
- Rheumatic fever
- Goodpasture's syndrome
- Guillain–Barré syndrome
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| "Type V"/receptor |
- Graves' disease
- Myasthenia gravis
- Pernicious anemia
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Type III
(Immune complex) |
| Foreign |
- Henoch–Schönlein purpura
- Hypersensitivity vasculitis
- Reactive arthritis
- Farmer's lung
- Post-streptococcal glomerulonephritis
- Serum sickness
- Arthus reaction
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| Autoimmune |
- Systemic lupus erythematosus
- Subacute bacterial endocarditis
- Rheumatoid arthritis
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Type IV/cell-mediated
(T cells) |
| Foreign |
- Allergic contact dermatitis
- Mantoux test
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| Autoimmune |
- Diabetes mellitus type 1
- Hashimoto's thyroiditis
- Multiple sclerosis
- Coeliac disease
- Giant-cell arteritis
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| GVHD |
- Transfusion-associated graft versus host disease
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Unknown/
multiple |
| Foreign |
- Hypersensitivity pneumonitis
- Allergic bronchopulmonary aspergillosis
- Transplant rejection
- Latex allergy (I+IV)
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| Autoimmune |
- Sjögren's syndrome
- Autoimmune hepatitis
- Autoimmune polyendocrine syndrome
- Autoimmune adrenalitis
- Systemic autoimmune disease
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Index of the immune system
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| Description |
- Physiology
- cells
- autoantigens
- autoantibodies
- complement
- surface antigens
- IG receptors
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| Disease |
- Allergies
- Immunodeficiency
- Immunoproliferative immunoglobulin disorders
- Hypersensitivity and autoimmune disorders
- Neoplasms and cancer
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| Treatment |
- Procedures
- Drugs
- antihistamines
- immunostimulants
- immunosuppressants
- monoclonal antibodies
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UpToDate Contents
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English Journal
- Annular leukocytoclastic vasculitis associated with anti-tuberculosis medications: a case report.
- Chanprapaph K, Roongpisuthipong W, Thadanipon K.AbstractABSTRACT: INTRODUCTION: Anti-tuberculosis drug-induced cutaneous leukocytoclastic vasculitis has been rarely reported. To the best of our knowledge, this is the first reported case of annular leukocytoclastic vasculitis associated with anti-tuberculosis drug administration.
- Journal of medical case reports.J Med Case Rep.2013 Jan 31;7(1):34. [Epub ahead of print]
- ABSTRACT: INTRODUCTION: Anti-tuberculosis drug-induced cutaneous leukocytoclastic vasculitis has been rarely reported. To the best of our knowledge, this is the first reported case of annular leukocytoclastic vasculitis associated with anti-tuberculosis drug administration.CASE PRESENTATION: We repo
- PMID 23369624
- Cutaneous changes: an initial manifestation of pulmonary Wegener's granulomatosis.
- Zycinska K, Wardyn K, Zielonka TM, Nitsch-Osuch A, Smolarczyk R.SourceDepartment of Family Medicine, Warsaw Medical University, Warsaw, Poland. kzycinska@poczta.fm
- Advances in experimental medicine and biology.Adv Exp Med Biol.2013;755:307-10.
- Cutaneous vasculitis can occur as an isolated dermatologic disorder or as manifestation of a potentially life-threatening systemic vasculitis such as Wegener's granulomatosis (WG). The aim of the study was to characterize cutaneous lesions in 66 WG patients (30 female, 36 male) and to assess the via
- PMID 22826081
- [Cutaneous manifestations revealing cryofibrinogenaemia associated with monoclonal gammopathy].
- Delyon J, Bezier M, Cordoliani F, Malphettes M, Szalat R, Bagot M, Rybojad M.SourceService de dermatologie, hôpital Saint-Louis, AP-HP, 1, avenue Claude-Vellefaux, 75010 Paris, France. Electronic address: delyon.julie@gmail.com.
- Annales de dermatologie et de vénéréologie.Ann Dermatol Venereol.2013 Jan;140(1):30-5. doi: 10.1016/j.annder.2012.10.599. Epub 2012 Dec 11.
- BACKGROUND: Cryofibrinogenaemia is an under-recognized cutaneous thrombotic vasculopathy that may be revealed by purpura or chronic necrotic ulcerations. We report two original cases characterized by their severity, their association with a monoclonal gammopathy and their excellent response to treat
- PMID 23328357
Japanese Journal
- 潰瘍性大腸炎との関連を思わせた皮膚白血球破砕性血管炎の1例 (特集 血管炎・血行障害)
- マイコプラズマ感染で誘発された皮膚白血球破砕性血管炎の1例 (特集 血管炎・血行障害)
- 抗RNP抗体高値のMCTDおよびSLE患者の顔面紅斑にみられたLeukocytoclastic Vasculitis
- 折原 俊夫,塚田 篤子,古谷 達孝
- 西日本皮膚科 47(2), 236-241, 1985
- … 抗RNP抗体高値のMCTD1例, SLE2例の計3例に, その顔面紅斑の組織所見で著明な核破壊を伴う好中球浸潤, 出血および血管壁変性, すなわちleukocytoclastic vasculitisの所見が認められた。 …
- NAID 130004473117
Related Pictures
★リンクテーブル★
[★]
- 英
- angiitis
- 関
- 脈管炎 vasculitis vasculitides、血管内膜炎、血管炎症候群
分類
- CHCC2012
参考
- 血管炎症候群 - 日本内科学会雑誌第103巻第10号
- http://www.j-circ.or.jp/guideline/pdf/JCS2008_ozaki_h.pdf
- 血管炎・血管障害診療ガイドライン 2016 年改訂版 - 日本皮膚科学会
- https://www.dermatol.or.jp/uploads/uploads/files/vasculitisGL.pdf
[★]
白血球破壊性血管炎
- 関
- hypersensitivity angiitis、hypersensitivity vasculitis、leukocytoclastic vasculitis
[★]
- 関
- cutaneously、cutis、dermal、skin