extracolonic manifestations in familial adenomatous polyposis
نویسندگان
چکیده
introduction: due to the whole network of polyposis registers worldwide and early prophylactic treatment, survival of familial adenomatosis (fap) patients is improved. extracolonic manifestations are remarkable feature of fap. two extracolonic manifestations (duodenal adenomatosis, leading duodenal cancer and desmoid tumours) play a very important role in the reasons of death in polyposis population. materials and methods: data from the lithuanian polyposis register, containing 90 fap cases from 38 unrelated families (as stated on 2004.01.01) was used. indirect ophthalmoscopy (fundoscopy) was performed on 19 fap patients, orthopantomography - on 22, upper gastrointestinal tract endospopy on 21, distal small bowel examined in 11. 42 patients were examined for desmoid tumours and epidermoid cysts. results: in 18 (94.7%) of 19 examined chrpe was detected, in 15 (68.2%) of 22 -mandibular osteomas. out of 21 examined, 3 (14.3%) had fundic gland polyposis and 14 (66.7%) duodenal adenomas. distal ileal polyposis was present in 8 (72.7%) of the 11 patients. out of 42 live fap patients, 4 (7.1%) had desmoid tumours and 8 (14.3%) had epidermoid cysts. conclusions: extracolonic manifestations are typical in fap. some of them have negative impact on morbidity and mortality of fap patients and demand special surveillance and treatment.
منابع مشابه
Extracolonic manifestations of familial adenomatous polyposis after proctocolectomy.
HYPOTHESIS Extracolonic manifestations have a major effect on the morbidity and mortality of patients with familial adenomatous polyposis following proctocolectomy. DESIGN Case review study. SETTING Colorectal unit, university-affiliated hospital. PATIENTS Fifty patients (25 males and 25 females) with familial adenomatous polyposis WHO underwent proctocolectomy between January 1988 and Oc...
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A detailed clinical study of 30 families with familial polyposis coli is presented. Seven 'isolated' cases are also described. It was found that some families did not exhibit any extracolonic manifestations, but the majority of families showed various numbers of members who had these manifestations of differing types and degrees. In view of the great variability within the members of a family, ...
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Familial adenomatous polyposis (FAP) is a genetic disease created by an abnormality of chromosome number five resulting in a generalized cellular growth disorder. The growth abnormality created by the genetic defect dictates the development of benign and malignant lesions in different organs of the body. Even the term familial adenomatous polyposis does not fully describe the defect because les...
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Familijarna adenomatozna polipoza (FAP) je autozomno dominantni polipozni sindrom, odgovoran za pojavu oko 1% svih kolorektalnih karcinoma (CRC) . Ovaj sindrom se ispoljava kod 1/5 000 do 1/17 000 živorođene dece 2, 3 sa stopom penetracije od preko 90% . Zahvata podjednako oba pola i sve geografske lokalitete . Obolele osobe razvijaju 100−5 000 adenoma (prosečan broj adenoma > 1 000) tubularne ...
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BACKGROUND Duodenal adenomas develop in patients with familial adenomatous polyposis, incurring a risk of carcinoma. When this risk is high, surgery is indicated. The choice of surgical treatment can be difficult as evidence-based data are lacking. METHODS This is a systematic review of the literature on the non-medical management of duodenal lesions arising in the setting of familial adenoma...
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عنوان ژورنال:
گوارشجلد ۸، شماره ۴، صفحات ۱۷۸-۰
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