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Eosinophilic Granulomatosis with Polyangiitis Initially Diagnosed as Eosinophilic Gastroenteritis.
Itawaki, Ayako; Okada, Mayumi; Kawashima, Kousaku; Okimoto, Eiko; Sonoyama, Hiroki; Mishima, Yoshiyuki; Oshima, Naoki; Ishimura, Norihisa; Moriyama, Mayuko; Murakawa, Yohko; Araki, Asuka; Ishikawa, Noriyoshi; Maruyama, Riruke; Ishihara, Shunji; Kinoshita, Yoshikazu.
Afiliação
  • Itawaki A; Department of Internal Medicine II, Shimane University Faculty of Medicine, Japan.
  • Okada M; Department of Internal Medicine II, Shimane University Faculty of Medicine, Japan.
  • Kawashima K; Department of Internal Medicine II, Shimane University Faculty of Medicine, Japan.
  • Okimoto E; Department of Internal Medicine II, Shimane University Faculty of Medicine, Japan.
  • Sonoyama H; Department of Internal Medicine II, Shimane University Faculty of Medicine, Japan.
  • Mishima Y; Department of Internal Medicine II, Shimane University Faculty of Medicine, Japan.
  • Oshima N; Department of Internal Medicine II, Shimane University Faculty of Medicine, Japan.
  • Ishimura N; Department of Internal Medicine II, Shimane University Faculty of Medicine, Japan.
  • Moriyama M; Department of Rheumatology, Shimane University Faculty of Medicine, Japan.
  • Murakawa Y; Department of Rheumatology, Shimane University Faculty of Medicine, Japan.
  • Araki A; Department of Pathology, Shimane University Faculty of Medicine, Japan.
  • Ishikawa N; Department of Pathology, Shimane University Faculty of Medicine, Japan.
  • Maruyama R; Department of Pathology, Shimane University Faculty of Medicine, Japan.
  • Ishihara S; Department of Internal Medicine II, Shimane University Faculty of Medicine, Japan.
  • Kinoshita Y; Department of Internal Medicine II, Shimane University Faculty of Medicine, Japan.
Intern Med ; 59(8): 1029-1033, 2020 Apr 15.
Article em En | MEDLINE | ID: mdl-31875634
We herein report two cases of eosinophilic granulomatosis with polyangiitis (EGPA) initially diagnosed as eosinophilic gastroenteritis (EGE) based solely on endoscopic biopsy results. One year after the EGE diagnosis, one patient presented with multiple purpura, and skin biopsy findings resulted in a change of the diagnosis to EGPA. In another patient, multiple skin and colonic ulcerations emerged eight years after the diagnosis of EGE, at which time histological examinations of endoscopic biopsy specimens revealed vasculitis, and the diagnosis was changed to EGPA. Physicians should be aware of the possible existence of EGPA in cases diagnosed as EGE.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Granulomatose com Poliangiite / Eosinofilia Tipo de estudo: Diagnostic_studies Limite: Adult / Female / Humans / Middle aged Idioma: En Revista: Intern Med Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Granulomatose com Poliangiite / Eosinofilia Tipo de estudo: Diagnostic_studies Limite: Adult / Female / Humans / Middle aged Idioma: En Revista: Intern Med Ano de publicação: 2020 Tipo de documento: Article