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1.
Korean Journal of Pediatric Gastroenterology and Nutrition ; : 112-118, 2004.
Article in Korean | WPRIM | ID: wpr-74107

ABSTRACT

Cowden syndrome is very rare clinical condition with characteristic mucocutaneous lesions associated with abnormalities of the breast, thyroid, and gastrointestinal tract. Here, the case of a 16-year-old girl with diverse gastrointestinal polyposis with breast and thyroid lesions is reported as a definite case of Cowden syndrome. During follow up for 4 years, changes in the characteristic lesions were observed; Esophageal acanthosis and oropharyngeal polyps were newly developed. Gastric, duodenal, rectal and ileal polyps were noted at the first visit when she was 12 years of age and revealed histologically hyperplastic polyps. Mucocutaneous lesions, the pathognomonic finding of Cowden syndrome, were not noted at the first visit or during the follow up period. Breast and thyroid masses were noted at the first visit. Breast aspiration showed highly cellular ductal epithelial fragments and fibroblastic stromal cell fragments, and a thyroid biopsy shows proliferation of irregular sized follicles, with variable colloid contents. Macrocephaly was also noted at the first visit. The characteristic lesions of Cowden syndrome change with the patient's age, and the long-term follow up is recommended in cases suspected with this syndrome.


Subject(s)
Adolescent , Female , Humans , Biopsy , Breast , Colloids , Fibroblasts , Follow-Up Studies , Gastrointestinal Tract , Hamartoma Syndrome, Multiple , Megalencephaly , Polyps , Stromal Cells , Thyroid Gland
2.
Korean Journal of Gastrointestinal Endoscopy ; : 113-117, 2001.
Article in Korean | WPRIM | ID: wpr-19775

ABSTRACT

Cronkhite-Canada syndrome is characterized by generalized gastrointestinal polyposis, ectodermal changes, and the eventual development of diarrhea and weight loss. The pathogenesis of the disease is unknown, and there is no established therapy. The disease has a poor prognosis because of malnutrition resulting from altered absorption in the gastrointestinal tract. We experienced a case of a 56-year-old female with Cronkhite-Canada syndrome. After enteral nutrition and administration of prednisolone for 3 months, clinical improvement was noted with cessation of diarrhea, increased serum protein, disappearance of pigmentation, and regrowth of the scalp hair, finger-and toenails. Endoscopy showed resolution of the gastrointestinal polyposis. So we report here a case of diffuse gastrointestinal polyposis which has been in remission with steroid therapy.


Subject(s)
Female , Humans , Middle Aged , Absorption , Diarrhea , Ectoderm , Endoscopy , Enteral Nutrition , Gastrointestinal Tract , Hair , Intestinal Polyposis , Malnutrition , Nails , Pigmentation , Prednisolone , Prognosis , Scalp , Weight Loss
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