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Rev Hosp Clin Fac Med Sao Paulo ; 55(6): 219-24, 2000.
Artigo em Inglês | MEDLINE | ID: mdl-11313662

RESUMO

UNLABELLED: The Peutz-Jeghers syndrome is a hereditary disease that requires frequent endoscopic and surgical intervention, leading to secondary complications such as short bowel syndrome. CASE REPORT: This paper reports on a 15-year-old male patient with a family history of the disease, who underwent surgery for treatment of an intestinal occlusion due to a small intestine intussusception. DISCUSSION: An intra-operative fiberscopic procedure was included for the detection and treatment of numerous polyps distributed along the small intestine. Enterotomy was performed to treat only the larger polyps, therefore limiting the intestinal resection to smaller segments. The postoperative follow-up was uneventful. CONCLUSION: We point out the importance of conservative treatment for patients with this syndrome, especially those who will undergo repeated surgical interventions because of clinical manifestation while they are still young.


Assuntos
Endoscopia Gastrointestinal/métodos , Enterostomia/métodos , Obstrução Intestinal/cirurgia , Intestino Delgado/cirurgia , Síndrome de Peutz-Jeghers/cirurgia , Adolescente , Humanos , Obstrução Intestinal/etiologia , Intussuscepção/etiologia , Intussuscepção/cirurgia , Masculino , Síndrome de Peutz-Jeghers/complicações , Síndrome do Intestino Curto/complicações , Síndrome do Intestino Curto/etiologia , Síndrome do Intestino Curto/cirurgia
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