結節性血管炎
WordNet
- relating to or characterized by or having nodules; "Nodular vaginitis"
- having nodules or occurring in the form of nodules; "nodular ores" (同)nodulated, noduled
- inflammation of a blood vessel
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- 節(ふし)の[ような]
Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2017/09/02 14:35:09」(JST)
[Wiki en表示]
Nodular vasculitis |
Classification and external resources |
Specialty |
dermatology |
ICD-10 |
L95.8 (ILDS L95.850) |
eMedicine |
article/1083213 |
[edit on Wikidata]
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Nodular vasculitis is a skin condition characterized by crops of small, tender, erythematous nodules on the legs, mostly on the calves and shins. Miroscopically there are epithelioid granulomas and vasculitis in the subcutaneous tissue, making it a form of panicullitis. Most of these cases are now thought to be manifestation of tuberculosis and indeed they respond well to anti-tuberculous treatment.[citation needed]
See also
- Panniculitis
- List of cutaneous conditions
References
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
- IgA vasculitis
- 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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Disorders of subcutaneous fat (M79.3, 729.3)
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Panniculitis |
Lobular |
- without vasculitis
- Cold
- Cytophagic histiocytic
- Factitial
- Gouty
- Pancreatic
- Traumatic
- needle-shaped clefts
- Subcutaneous fat necrosis of the newborn
- Sclerema neonatorum
- Post-steroid panniculitis
- Lipodermatosclerosis
- Weber–Christian disease
- Lupus erythematosus panniculitis
- Sclerosing lipogranuloma
- with vasculitis: Nodular vasculitis/Erythema induratum
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Septal |
- without vasculitis: Alpha-1 antitrypsin deficiency panniculitis
- Erythema nodosum
- with vasculitis: Superficial thrombophlebitis
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Lipodystrophy |
Acquired |
- generalized: Acquired generalized lipodystrophy
- partial: Acquired partial lipodystrophy
- Centrifugal abdominal lipodystrophy
- HIV-associated lipodystrophy
- Lipoatrophia annularis
- localized: Localized lipodystrophy
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Congenital |
- Congenital generalized lipodystrophy
- Familial partial lipodystrophy
- Marfanoid–progeroid–lipodystrophy syndrome
- Poland syndrome
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UpToDate Contents
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English Journal
- Sudden unexpected death due to severe pulmonary and cardiac sarcoidosis.
- Ginelliová A1, Farkaš D2, Farkašová Iannaccone S3, Vyhnálková V2.
- Forensic science, medicine, and pathology.Forensic Sci Med Pathol.2016 Jul 5. [Epub ahead of print]
- In this paper we report the autopsy findings of a 57 year old woman who died unexpectedly at home. She had been complaining of shortness of breath, episodes of dry coughing, and nausea. Her past medical and social history was unremarkable. She had no previous history of any viral or bacterial disea
- PMID 27379608
- Varicella zoster virus triggers the immunopathology of giant cell arteritis.
- Gilden D1, Nagel MA.
- Current opinion in rheumatology.Curr Opin Rheumatol.2016 Jul;28(4):376-82. doi: 10.1097/BOR.0000000000000292.
- PURPOSE OF REVIEW: Giant cell arteritis (GCA) is a severe form of vasculitis in the elderly. The recent discovery of varicella zoster virus (VZV) in the temporal arteries and adjacent skeletal muscle of patients with GCA, and the rationale and strategy for antiviral and corticosteroid treatment for
- PMID 27224742
- Difference in relapse-rate and clinical phenotype by autoantibody-subtype in Japanese patients with anti-neutrophil cytoplasmic antibody-associated vasculitis.
- Murosaki T1, Sato T1, Akiyama Y1, Nagatani K1, Minota S1.
- Modern rheumatology / the Japan Rheumatism Association.Mod Rheumatol.2016 Jun 20:1-7. [Epub ahead of print]
- OBJECTIVE: To correlate the serotype specificity to myeloperoxidase (MPO) and proteinase-3 (PR3) with clinical characteristics in anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV).METHODS: Clinical characteristics and outcomes of patients with AAV in our division from 2005 to 2
- PMID 27320904
Japanese Journal
- 両側聾が改善したANCA関連血管炎による難治性中耳炎
- 内田 真哉,上田 雅代
- Otology Japan 23(2), 92-97, 2013
- 患者は66歳女性で、両側の進行性難聴と耳漏を認め、鼓膜の白色病変から真珠腫を疑われて紹介された。初診時、CRP陽性、MPO-ANCA陽性、両側肺尖部の結節性病変、両側聾などの所見を認め、ANCA関連血管炎である肉芽腫性多発血管炎 (GPA) を疑われた。肺・鼻腔からの生検では病理組織学的診断がつかずGPA疑いと判定されたが、臨床的にはGPAと考えられた。耳鼻咽喉科的にはANCA関連血管炎による中耳 …
- NAID 130005065177
- 再燃を繰り返すANCA関連血管炎における肺結節陰影の鑑別
- 平山 浩一,長井 美穂,小林 正貴 [他],仙波 征太郎,澁谷 誠,河口 幸江,菊嶋 昭一,古川 欣也,大石 毅
- 東京醫科大學雜誌 70(4), 465-484, 2012-10-30
- NAID 10031143030
- 出雲 令子,豊口 光子,島川 眞知子 [他],篠崎 和美,高村 悦子,堀 貞夫
- 東京女子医科大学雑誌 82(E1), E173-E177, 2012-01-31
- 【目的】東京女子医大眼科における強膜炎の臨床像および全身疾患について調査した。,【方法】2009年4月から2010年3月までに当院眼科を受診した強膜炎42例を対象とし、Watson分類に従い強膜炎のタイプを分類し、臨床像、全身疾患、治療について検討した。,【結果】発症時の平均年齢は52.9±15.8歳、男性13例、女性29例であった。上強膜炎10例、強膜炎のうち前部30例(びまん性16例、結節性7 …
- NAID 110008767970
Related Links
- vasculitis [vas″ku-li´tis] inflammation of a blood or lymph vessel; see arteritis, lymphangitis, and phlebitis. Called also angiitis. Churg-Strauss vasculitis churg-strauss syndrome. hypersensitivity vasculitis a group of systemic ...
- vas·cu·li·tis (văs′kyə-lī′tĭs) n. Inflammation of a vessel of the body. vasculitis (ˌvæskjʊˈlaɪtɪs) n 1. (Pathology) inflammation of the blood vessels Thesaurus Antonyms Related Words Synonyms Legend: Noun 1. vasculitis - inflammation of a blood vessel
Related Pictures
★リンクテーブル★
[★]
- ラ
- erythema induratum Bazin
- 同
- 結節性血管炎 nodular vasculitis、硬結性皮膚結核 tuberculosis cutis indurativa、バザン病 Bazin disease
- 関
- 硬結性紅斑
[★]
- 英
- nodular vasculitis
- 関
- バザン硬結性紅斑
[★]
- 関
- nodal、nodosity、nodule、tophaceous、tubercular、varicose