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Eosinophilic Enterocolitis: An Exceedingly Rare Entity.
Lopes Azevedo, Richard José; Pinto, João; Ribeiro, Helena; Pereira, Flávio; Leitão, Cátia; Caldeira, Ana; Pereira, Eduardo; Duarte Banhudo, António José.
Afiliação
  • Lopes Azevedo RJ; Department of Gastroenterology, Amato Lusitano Hospital, Castelo Branco, Portugal.
  • Pinto J; Department of Gastroenterology, Amato Lusitano Hospital, Castelo Branco, Portugal.
  • Ribeiro H; Department of Gastroenterology, Amato Lusitano Hospital, Castelo Branco, Portugal.
  • Pereira F; Department of Gastroenterology, Amato Lusitano Hospital, Castelo Branco, Portugal.
  • Leitão C; Department of Gastroenterology, Amato Lusitano Hospital, Castelo Branco, Portugal.
  • Caldeira A; Department of Gastroenterology, Amato Lusitano Hospital, Castelo Branco, Portugal.
  • Pereira E; Department of Gastroenterology, Amato Lusitano Hospital, Castelo Branco, Portugal.
  • Duarte Banhudo AJ; Department of Gastroenterology, Amato Lusitano Hospital, Castelo Branco, Portugal.
GE Port J Gastroenterol ; 25(4): 184-188, 2018 Jun.
Article em En | MEDLINE | ID: mdl-29998164
ABSTRACT
Eosinophilic enterocolitis is an exceptionally rare condition with few described cases in the literature, representing the least frequent manifestation of the wide spectrum of eosinophilic gastrointestinal disorders. We describe a case of a young male patient presenting with a panmural form of the disease, manifested by abdominal pain, distention, and watery diarrhea with 4 days of evolution, bowel wall thickening, and ascites. Eosinophilic ascites is probably the most unusual presentation form of this entity. It poses a diagnostic challenge because of its nonspecific symptoms, associated with the absence of standardized histological criteria, hence requiring a high level of suspicion. There is also no consensus regarding treatment it should be individualized according to the patient's age and severity of symptoms.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: GE Port J Gastroenterol Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Portugal

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: GE Port J Gastroenterol Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Portugal