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1. 好酸球性筋膜炎eosinophilic fasciitis [show details]
… Eosinophilic fasciitis (EF, also called Shulman syndrome) is an uncommon disorder of unknown etiology and poorly understood pathogenesis . EF is characterized in its early phase by limb or trunk erythema …
2. 好酸球の生物学および好酸球増多症の原因eosinophil biology and causes of eosinophilia [show details]
…cetirizine , radiotherapy , topical tacrolimus , and thalidomide . Eosinophilic fasciitis – Eosinophilic fasciitis, also known as Shulman syndrome, is characterized by symmetrical induration of the skin. The …
3. 学会が公開する診療ガイドラインのリンク：好酸球性筋膜炎society guideline links eosinophilic fasciitis [show details]
…Dermatology Society (PCDS): Clinical guidance on eosinophilic fasciitis (2015) Diagnostic criteria, severity classification and guidelines of eosinophilic fasciitis (2018)…
4. 成人における限局性強皮症の病因、臨床症状、および診断pathogenesis clinical manifestations and diagnosis of morphea localized scleroderma in adults [show details]
…represent the atrophic stage of plaque-type morphea, or may be a separate disorder. Eosinophilic fasciitis, or Shulman syndrome, is a disorder that is characterized by the rapid onset of symmetric, painful, …
5. 悪性腫瘍およびリウマチ性疾患malignancy and rheumatic disorders [show details]
…cancer, other testing such as further imaging or checking tumor markers may be performed. Eosinophilic fasciitis (EF) is an uncommon condition, typically characterized by woody induration, which most often …

English Journal

Eosinophilic fasciitis: From pathophysiology to treatment.

, I I, H H, H H, .
Allergology international : official journal of the Japanese Society of Allergology. 2019 Mar;().
Eosinophilic fasciitis is a disease originally proposed as "diffuse fasciitis with eosinophilia" by Shulman in 1974. The patients with this disease often have history of strenuous exercise or labor a few days to 1-2 weeks before the onset. The chief symptoms are symmetrical, full-circumference swell
PMID 30910631

Morphoea profunda and its relationship to eosinophilic fasciitis.

Wlodek C, Korendowych E, McHugh N, Lovell CR.
Clinical and experimental dermatology. 2018 Apr;43(3)306-310.
In this small case series, all eight patients were women in their fifth and sixth decades. This is similar to the female predominance in morphoea and less in keeping with eosinophilic fasciitis (EF). All cases had diffuse induration of their limbs with both proximal and distal patterns of distributi
PMID 29277925

FOSB is a Useful Diagnostic Marker for Pseudomyogenic Hemangioendothelioma.

Hung YP, Fletcher CD, Hornick JL.
The American journal of surgical pathology. 2017 May;41(5)596-606.
Pseudomyogenic (epithelioid sarcoma-like) hemangioendothelioma is a distinctive vascular neoplasm of intermediate biological potential with a predilection for young adults and frequent multifocal presentation. Pseudomyogenic hemangioendothelioma is characterized by loose fascicles of plump spindled
PMID 28009608

Japanese Journal

Fasciitis in Mixed Connective Tissue Disease Successfully Treated with High-dose Intravenous Immunoglobulin

MATSUDA Masayuki,MIKI Jun,OGUCHI Kenya,TABATA Kenichi,IKEDA Shu-ichi
Internal medicine 42(9), 910-911, 2003-09-01
NAID 130000766898

落屑性紅斑をみとめた好酸球性筋膜炎

坂尾佳久,浦野芳夫,滝脇弘嗣,内田尚之,荒瀬誠治,武田己広
西日本皮膚科 = The Nishinihon journal of dermatology 60(1), 6-10, 1998-02-01
65歳の男性。重い荷物の運搬後, 四肢に瀰漫性の皮膚硬化が生じ, 次第に躯幹にも拡大し, 硬化部にほぼ一致して紅斑, 鱗屑が出現した。四肢末梢には異常なく, レイノー現象, 内臓病変もなかった。末梢血好酸球増多, 赤沈亢進, 高<I>γ</I>グロブリン血症, 病理組織学的にリンパ球の浸潤をともなう筋膜の肥厚が認められた。以上の所見より好酸球性筋膜炎と診断した。 …
NAID 10019106157