好酸球性筋膜炎
WordNet
- a pattern of symptoms indicative of some disease
- a complex of concurrent things; "every word has a syndrome of meanings"
PrepTutorEJDIC
- (疾患の徴候となる一群の)症徴候,症候群 / (事件・社会的状態などのパターンを示す)徴候形態
UpToDate Contents
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English Journal
- [Eosinophilic fasciitis, morphea and vitiligo in a single patient].
- Lakjiri S1, Meziane M2, Benani A3, Harmouch T3, Amarti A3, Mernissi FZ2.
- Annales de dermatologie et de vénéréologie.Ann Dermatol Venereol.2014 Oct;141(10):598-602. doi: 10.1016/j.annder.2014.06.019. Epub 2014 Aug 7.
- BACKGROUND: Fasciitis with eosinophilia (FE), or Shulman syndrome, is a rare disease of unknown origin for which the nosological profile has not been clearly defined. It is clinically characterised by oedema and induration of the limbs with hypereosinophilia. It may be associated with morphea, in wh
- PMID 25288063
- Thrombotic thrombocytopenic purpura: 2012 American Society for Apheresis (ASFA) consensus conference on classification, diagnosis, management, and future research.
- Sarode R1, Bandarenko N, Brecher ME, Kiss JE, Marques MB, Szczepiorkowski ZM, Winters JL.
- Journal of clinical apheresis.J Clin Apher.2014 Jun;29(3):148-67. doi: 10.1002/jca.21302. Epub 2013 Oct 17.
- The American Society for Apheresis (ASFA) conducted a 1 day consensus conference on Thrombotic Thrombocytopenic Purpura (TTP) during its annual meeting in Atlanta, GA, on April 10, 2012. The authors of this article, a subcommittee of ASFA's Clinical Applications Committee, developed several question
- PMID 24136342
- Linear depressions and progressive tightening of the extremities.
- Mitchum M, Spillane E1, Meyerle J, Galeckas K.
- Cutis.Cutis.2013 Dec;92(6):E11-3.
- PMID 24416750
Japanese Journal
- Successful treatment of severe Shulman's syndrome by allogeneic bone marrow transplantation
- Diffuse fasciitisの炎症病態に関する免疫組織化学的検討
Related Links
- M725 好酸球性筋膜炎 Eosinophilic Fasciitis, Shulman syndrome EF (検索用語句: Shulman症候群 ) 激しい運動や外傷を契機として急速に、皮膚の硬化と関節の運動制限 をきたす疾患で、病変部の好酸球浸潤又は末梢血好酸球増 ...
- Shulman's syndrome symptoms, causes, diagnosis, and treatment information for Shulman's syndrome (Eosinophilic fasciitis) with alternative diagnoses, full-text book chapters, misdiagnosis, research treatments, prevention, and ...
★リンクテーブル★
[★]
- 英
- eosinophilic fasciitis
- 同
- シャルマン症候群 Shulman syndrome Shulman's syndrome
- 好酸球性びまん性筋膜炎 好酸球増加を伴うびまん性筋膜炎 diffuse fasciitis with eosinophilia、
- 関
- 全身性強皮症
概念
- 強皮症類似疾患
- 激しい運動、労作の後に数日以内に急激に発症
- 四肢に対称性有痛性腫脹 → 硬化(orange peel sign)
- 近位関節の運動制限と拘縮。
- 顔面に皮膚硬化が及ぶことはまれ
- レイノー現象を伴わない
病理
- 四肢の強皮症様の皮膚硬化
- 末梢血好酸球の増加
- 筋膜の著明な肥厚
検査
- 末梢血好酸球増加、高γグロブリン血症
- 自己抗体陰性
診断
- 血算、皮膚生検(筋膜、筋を含めた生検。筋膜肥厚、好酸球浸潤)
治療
[★]
- 英
- posttransfusion purpura, post-transfusion purpura
- 同
- シュルマン症候群 Shulman syndrome
- 関
- 輸血後合併症
- Sabiston Textbook of Surgery, 18th ed.
- Table 6-4 -- Categories and Management of Adverse Transfusion Reactions
Delayed (>24 Hours) Transfusion Reactions?Immunologic
|
TYPE
|
INCIDENCE
|
ETIOLOGY
|
MANIFESTATION
|
DIAGNOSTIC TESTING
|
THERAPEUTIC/PROPHYLACTIC APPROACH
|
Post-transfusion purpura
|
Rare
|
Recipient platelet antibodies (apparent alloantibody, usually anti? HPA-1) destroy autologous platelets
|
Thrombocytopenic purpura, bleeding 8-10 days after transfusion
|
Platelet antibody screen and identification
|
IGIV|HPA-1?negative platelets|Plasmapheresis
|
[★]
- 英
- Shulman syndrome
[★]