Wissler-Fanconi syndrome

特発性敗血症。ヴィスラー・ファンコーニ症候群

WordNet

1. a pattern of symptoms indicative of some disease
2. a complex of concurrent things; "every word has a syndrome of meanings"

PrepTutorEJDIC

1. (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

Wikipedia preview

出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2015/12/17 10:32:20」(JST)

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Wissler's syndrome
Classification and external resources
DiseasesDB	33708
MeSH	D014924

Wissler's syndrome (or Wissler's disease or Wissler-Fanconi syndrome) is a rheumatic disease that has a similar presentation to sepsis. It is sometimes considered closely related to Still's disease. It is named for Guido Fanconi and Hans Wissler It was first described by Wissler in 1944 and Fanconi in 1946. Single observations by E. Uhse in 1943 («Febris maculosa intermittens»), Fykow in 1929 and Nowak in 1942.

Signs and symptoms

A symptom complex characterised by the clinical features of a high intermittent fever of septic type, constantly recurring exanthema, transient arthralgia, carditis, pleurisy, neutrophil leukocytosis, and increased erythrocyte sedimentation rate.

Causes

Etiology uncertain. Wissler suggested an allergic reaction to bacteraemia as the pathogenic factor.

Epidemiology

Children and adolescents are most frequently affected; age in the reported cases varied from 5 to 17 years.

References

UpToDate Contents

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• 1. 小児および思春期における特発性の重症再生不良性貧血およびファンコニ貧血に対する造血細胞移植 hematopoietic cell transplantation for idiopathic severe aplastic anemia and fanconi anemia in children and adolescents
• 2. アシュケナージ系ユダヤ人集団における遺伝的疾患の出生前スクリーニング prenatal screening for genetic disease in the ashkenazi jewish population
• 3. 幼児および小児における尿細管性アシドーシスの病因および臨床症状 etiology and clinical manifestations of renal tubular acidosis in infants and children
• 4. 低リン血症の原因 causes of hypophosphatemia
• 5. 小児および思春期における遺伝性再生不良性貧血 inherited aplastic anemia in children and adolescents

English Journal

• [Subsepsis hyperergica: another way of discussing Wissler-Fanconi syndrome?].

• Lorcerie B, Bonnotte B, Rousset H.
• La Revue de médecine interne / fondée ... par la Société nationale francaise de médecine interne.Rev Med Interne.2002 Sep;23(9):801-2.
• PMID 12378838

• [Can we still speak of Wissler-Fanconi syndrome?].

• Pouchot J.
• La Revue de médecine interne / fondée ... par la Société nationale francaise de médecine interne.Rev Med Interne.2002 Mar;23(3):257-8.
• PMID 11928372

Japanese Journal

• 診断に難渋したアレルギー性亜肺血症の1例

• 整形外科と災害外科 45(1), 254-257, 1996-03-25
• NAID 10011352575

• Subsepsis allergica Syndrome von Wissler-Fanconi〔邦文〕

• 皮膚科の臨床 12(3), 192-198, 1970-03
• NAID 40018449690

Related Links

• Wissler-Fanconi syndrome - RightDiagnosis.com

6 Nov 2012 ... Wissler-Fanconi syndrome symptoms, causes, diagnosis, and treatment information for Wissler-Fanconi syndrome (Adult onset Still's disease) with alternative diagnoses, full-text book chapters, misdiagnosis, research ...

• Wissler's syndrome - Wikipedia, the free encyclopedia

Wissler's syndrome (or Wissler-Fanconi syndrome) is a rheumatic disease that has a similar presentation to sepsis. It is sometimes considered closely related to Still's disease. It is named for Hans Wissler.

Related Pictures

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★リンクテーブル★

リンク元	「特発性敗血症」
関連記事	「Fanconi」「syndrome」「Fanconi syndrome」

「特発性敗血症」

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英

idiopathic sepsis

同

ヴィスラー・ファンコーニ症候群 Wissler-Fanconi syndrome

「Fanconi」

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ファンコニー、ファンコニ、ファンコーニ

「syndrome」

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• n.

• 症候群

　 　 　

「Fanconi syndrome」

　　[★] ファンコーニ症候群