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Chronic intestinal pseudo-obstruction: a diagnosis to be considered
Muñoz-Yagüe, M. T; Solís-Muñoz, P; Salces, I; Ballestín, C; Colina, F; Ibarrola, C; López-Alonso, G; Carreira, P; Cruz Vigo, F; Solís Herruzo, J. A.
Afiliação
  • Muñoz-Yagüe, M. T; University Hospital 12 de Octubre. Madrid. Spain
  • Solís-Muñoz, P; University Hospital 12 de Octubre. Madrid. Spain
  • Salces, I; University Hospital 12 de Octubre. Madrid. Spain
  • Ballestín, C; University Hospital 12 de Octubre. Madrid. Spain
  • Colina, F; University Hospital 12 de Octubre. Madrid. Spain
  • Ibarrola, C; University Hospital 12 de Octubre. Madrid. Spain
  • López-Alonso, G; University Hospital 12 de Octubre. Madrid. Spain
  • Carreira, P; University Hospital 12 de Octubre. Madrid. Spain
  • Cruz Vigo, F; University Hospital 12 de Octubre. Madrid. Spain
  • Solís Herruzo, J. A; University Hospital 12 de Octubre. Madrid. Spain
Rev. esp. enferm. dig ; 101(5): 336-342, mayo 2009. tab
Artigo em Espanhol | IBECS | ID: ibc-74399
Biblioteca responsável: ES1.1
Localização: BNCS
ABSTRACT
Chronic intestinal pseudoobstruction (CIPO) is a rare entitycharacterized by recurrent clinical episodes of intestinal obstructionin which no mechanical cause is identified. There are multiplecauses for this syndrome but two main groups can be distinguisheda) secondary to a systemic non-gastrointestinal disease;and b) primary or idiopathic originated from alterations in thecomponents of the intestinal wall. The latter forms are the mostuncommon and their diagnosis is generally difficult. In the presentarticle, we describe nine patients with CIPO that were diagnosedin our center over the last six years. Four of them were diagnosedwith primary or idiopathic form of CIPO and another four wereclearly secondary to a systemic disease. The ninth case, whichwas initially diagnosed as secondary, is probably also a primaryform of the disease. The number of patients diagnosed in our center,even thought small, makes us to hypothesize that the prevalenceof CIPO is probably greater than is generally believed andthat the reasons of its rarity are the incomplete understanding ofits physiopathology and the difficulties to achieve a correct diagnosis(AU)
Assuntos
Texto completo: Disponível Coleções: Bases de dados nacionais / Espanha Base de dados: IBECS Assunto principal: Escleroderma Sistêmico / Pseudo-Obstrução Intestinal / Trânsito Gastrointestinal / Ileostomia / Músculo Liso / Doenças Neuromusculares Tipo de estudo: Estudo diagnóstico / Estudo de etiologia / Estudo prognóstico Limite: Adulto / Feminino / Humanos Idioma: Espanhol Revista: Rev. esp. enferm. dig Ano de publicação: 2009 Tipo de documento: Artigo Instituição/País de afiliação: University Hospital 12 de Octubre/Spain
Texto completo: Disponível Coleções: Bases de dados nacionais / Espanha Base de dados: IBECS Assunto principal: Escleroderma Sistêmico / Pseudo-Obstrução Intestinal / Trânsito Gastrointestinal / Ileostomia / Músculo Liso / Doenças Neuromusculares Tipo de estudo: Estudo diagnóstico / Estudo de etiologia / Estudo prognóstico Limite: Adulto / Feminino / Humanos Idioma: Espanhol Revista: Rev. esp. enferm. dig Ano de publicação: 2009 Tipo de documento: Artigo Instituição/País de afiliação: University Hospital 12 de Octubre/Spain
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