ウェーバー・クリスチャン病
WordNet
- an impairment of health or a condition of abnormal functioning
- German conductor and composer of romantic operas (1786-1826) (同)Carl Maria von Weber, Baron Karl Maria Friedrich Ernst von Weber
- German physiologist who studied sensory responses to stimuli and is considered the father of psychophysics (1795-1878) (同)E. H. Weber, Ernst Heinrich Weber
- German sociologist and pioneer of the analytic method in sociology (1864-1920) (同)Max Weber
- United States abstract painter (born in Russia) (1881-1961) (同)Max Weber
- German physicist and brother of E. H. Weber; noted for his studies of terrestrial magnetism (1804-1891) (同)Wilhelm Eduard Weber
- relating to or characteristic of Christianity; "Christian rites"
- a religious person who believes Jesus is the Christ and who is a member of a Christian denomination
- caused by or altered by or manifesting disease or pathology; "diseased tonsils"; "a morbid growth"; "pathologic tissue"; "pathological bodily processes" (同)morbid, pathologic, pathological
- following the teachings or manifesting the qualities or spirit of Jesus Christ
PrepTutorEJDIC
- (体の)『病気』,疾患 / (精神・道徳などの)病気,病弊
- 女性の話術芸人 =diseur
- 『キリスト者』(教徒) / 《話》りっぱな人 / 『キリストの』;『キリスト教の』,キリスト教徒の / キリスト(キリスト教)を信じる / キリスト教徒にふさわしい / 《話》りっぱな
- 病気にかかった / 病的な,不健全な(morbid)
Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2016/02/29 17:16:22」(JST)
[Wiki en表示]
Weber–Christian disease |
Classification and external resources |
Specialty |
rheumatology |
ICD-10 |
M35.6 |
ICD-9-CM |
729.30 |
DiseasesDB |
14055 |
eMedicine |
ped/2429 |
MeSH |
D010201 |
[edit on Wikidata]
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Weber–Christian disease (also known as "Idiopathic Relapsing febrile non-suppurative panniculitis") is a cutaneous condition characterized by recurrent subcutaneous nodules that heal with depression of the overlying skin.[1]
It is type of panniculitis.[2] It is a rare disease seen in females 30-60 years of age. It is a recurring inflammation of fatty layers of tissue present beneath the skin. Clinical course is characterised by exacerbations and remissions. Lesions are bilaterally symmetrical and are usually seen in the lower legs.
Eponym
It is named for Frederick Parkes Weber and Henry Asbury Christian.[3][4][5]
See also
- Alpha-1 antitrypsin deficiency panniculitis
- List of cutaneous conditions
References
- ^ Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. ISBN 1-4160-2999-0.
- ^ "Weber-Christian disease" at Dorland's Medical Dictionary
- ^ Weber–Christian disease at Who Named It?
- ^ F. P. Weber. A case of relapsing non-suppurative nodular panniculitis, showing phagocytosis of subcutaneous fat-cells by macrophages. British Journal of Dermatology and Syphilis, Oxford, 1925, 37: 301-311. doi:10.1111/j.1365-2133.1925.tb10003.x
- ^ H. A. Christian. Relapsing febrile nodular nonsuppurative panniculitis. Archives of Internal Medicine, Chicago, 1928, 42: 338-351. doi:10.1001/archinte.1928.00020020026004
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
- Poland syndrome
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UpToDate Contents
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English Journal
- A 38-year old woman with a dural based lesion.
- Husain S, Alkhalidi HM, Raddaoui E.AbstractIsolated intracranial xanthogranulomas arising from the dura mater are extremely rare.We present a case of a symptomatic large right frontoparietal dura based intracranial xanthogranuloma in a 38-year-old female. Xanthogranulomas are benign non-Langerhans cell histiocytic lesions. They are frequently described in the skin of infants and children. Extracutaneous manifestations especially in the central nervous system are highly uncommon. Dural xanthogranulomas usually arise in association with familial hypercholesterolemia, with Erdheim Chester disease (ECD), and with Weber-Christian disease. Our case however, had no such associations. In this report, the authors describe the clinical, radiological and microscopic presentation of this case and the differential diagnoses of intracranial xanthogranuloma.
- Brain pathology (Zurich, Switzerland).Brain Pathol.2012 May;22(3):433-7. doi: 10.1111/j.1750-3639.2012.00591.x.
- Isolated intracranial xanthogranulomas arising from the dura mater are extremely rare.We present a case of a symptomatic large right frontoparietal dura based intracranial xanthogranuloma in a 38-year-old female. Xanthogranulomas are benign non-Langerhans cell histiocytic lesions. They are frequentl
- PMID 22497617
- Tetraspanin15 regulates cellular trafficking and activity of the ectodomain sheddase ADAM10.
- Prox J, Willenbrock M, Weber S, Lehmann T, Schmidt-Arras D, Schwanbeck R, Saftig P, Schwake M.SourceInstitut für Biochemie, Christian-Albrechts-Universität zu Kiel, Olshausenstrasse 40, 24098, Kiel, Germany.
- Cellular and molecular life sciences : CMLS.Cell Mol Life Sci.2012 Mar 25. [Epub ahead of print]
- A disintegrin and metalloproteinase10 (ADAM10) has been implicated as a major sheddase responsible for the ectodomain shedding of a number of important surface molecules including the amyloid precursor protein and cadherins. Despite a well-documented role of ADAM10 in health and disease, little is k
- PMID 22446748
Japanese Journal
- 症例 Klinefelter症候群患者にみられたWeber-Christian病の1例
- A case of Weber-Christian disease with later development of rheumatoid arthritis
- NANKE Yuki,ISHIGURO Naoko,YAGO Toru,KOBASHIGAWA Tsuyoshi,KAWAKAMI Michiko,KAWASHIMA Makoto,KOTAKE Shigeru
- 日本臨床免疫学会会誌 34(1), 49-52, 2011
- … Weber-Christian disease (WCD) is a syndrome characterized by recurrent subcutaneous nodules, fever, occasional lipoatrophy, fatigue, arthralgia, and myalgia. …
- NAID 130000673834
- シクロスポリンAが奏功した乳児期発症 Weber-Christian 病の1例
- 大坪 善数,荒木 恵子,山下 文,上玉利 彰,中下 誠郎
- 日本小児科学会雑誌 114(8), 1215-1221, 2010-08-01
- NAID 10027477339
Related Links
- (Weber-Christian disease). 従来,発熱などの全身症状を伴い,小葉性脂肪織炎の 病理所見をとる皮下. 結節が四肢や体幹に生じるものを Weber-Christian 病と称してい た.現在. では疾患独立性はほぼ否定され,硬結性紅斑,深在性エリテマトーデス, ...
- 2010年12月1日 ... 今回はWeber-Christian病の説明です。 ☆[Weber-Christian病]Weber-Christian disease☆ 【概念】 皮下脂肪組織に結節性の炎症を生じ、これが壊死化する傾向を 呈する症候群を結節性皮下脂肪炎nodular panniculitisといい、種々の ...
Related Pictures
★リンクテーブル★
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- 英
- Weber-Christian disease WCD
- 同
- Weber-Christian病
- プファイファー-ウェーバー-クリスチャン病 Pfeifer-Weber-Christian disease、結節性非化膿性皮下脂肪織炎、再発性熱性結節性非化膿性脂肪織炎 relapsing febrile nodular nonsuppurative panniculitis
[show details]
概念
- 原因不明の非化膿性皮下脂肪織炎と多発性の皮下結節を示す疾患で極めて稀
- 発熱と有痛性の非化膿性皮下脂肪織炎が主症状
- 発熱と皮下硬結をくり返す全身性の脂肪組織炎。
疫学
病因
参考
http://www2p.biglobe.ne.jp/~shiino/kakomonn/show-g/ria-t.html
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結節性非化膿性皮下脂肪織炎
- 関
- Weber-Christian disease
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ウェーバー・クリスチャン病 Weber-Christian disease
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プファイファー-ウェーバー-クリスチャン病
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- 疾患:illnessより厳密な概念。「ある臓器に明確な障害が確認され、それによって症状が出ているとはっきり説明できる場合」 (PSY.9)
- 特定の原因、病態生理、症状、経過、予後、病理組織所見が全てそろった場合 (PSY.9)
- something that is very wrong with people's attitudes, way of life or with society.
- 関
- ail、ailment、disease entity、disorder、ill、illness、malady、sick、sickness
- disease ≠ illness ≠ disorder
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ウェーバー
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クリスチャン