A case of Gardner's syndrome.
نویسندگان
چکیده
Further questioning revealed that the patient was delivered by Caesarean section in the 36th week of pregnancy because her mother had developed intestinal obstruction. Laparotomy performed at the same time showed the presence of multiple peritoneal secondary deposits. The patient's grandmother, two of her uncles and one aunt had died of bowel cancer. This family history together with the presence of skin tumours suggested a diagnosis of Gardner's syndrome and further investigation along these lines was carried out. At the time of her first admission to hospital in 1972 no sign of polyposis was seen at sigmoidoscopy but there was suspicion of multiple polypi on the barium enema examination and on barium meal and follow-through a few small lucent areas were noted in the small bowel suggestive of polypi.
منابع مشابه
A Case Report of Gardner's Syndrome and a Review of Literature
Gardner's syndrome is an autosomal dominant inherited disorder. Familial polyposis of the colon, osteomas, hypertrophy of the retinal-pigmented layer and a multitude of soft tissue tumors are characteristic features. The syndrome may be presented with colonic or extracolonic symptoms. A 75-year-old male patient presented to Al-zahra Clinic with diffuse abdominal pain. An abdominal surgery wa...
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BACKGROUND Gardner's syndrome can occasionally be complicated with intra-abdominal desmoid tumor. These tumors usually remain asymptomatic but can exhibit symptoms due to intestinal, vascular and ureteral compression and obstruction. CASE PRESENTATION A rare case of a 41-year-old male patient with Gardner's syndrome complicated with intra-abdominal desmoid tumor, which first presented as acut...
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Desmoid tumors are uncommon benign neoplasm of the fibroblasts. They occur rarely in the general population, but they are comparatively common in patients with familial polyposis coli with or without other elements of Gardner's syndrome. Herein, we report a 16-year-old woman with Gardner's syndrome complicated by desmoid tumors on the right subscapular area.
متن کاملOral and maxillofacial manifestations of familial adenomatous polyposis (Gardner's syndrome): a report of two cases.
AIM The aim of this case report is to emphasize the importance of an early diagnosis of Gardner's syndrome through the detection of lesions appearing in the oral and maxillofacial area as well as to present two cases of the disease. BACKGROUND Gardner's syndrome is an autosomal dominant disease characterized by gastrointestinal polyps that develop in the colon as well as in the stomach and up...
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We present a case of a 25-year-old female with diagnosed familial adenomatous polyposis and elevated carcinoembryonic antigen with negative family history. The suspicion of Gardner's syndrome was raised because extirpation of an osteoma of the left temporo-occipital region was made 10 years ago. Restorative procto-colectomy and ileal pouch anal anastomosis was made but histology delineated aden...
متن کاملMesenteric desmoid tumours in Gardner's syndrome--review of medical treatments.
Gardner's syndrome comprises a triad of polyposis coli, osteomata and soft tissue tumours including desmoid tumours which can often present difficult problems in management. We report a patient with Gardner's syndrome treated with tamoxifen and medroxyprogesterone acetate. The literature on this rare syndrome and its management is reviewed.
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ورودعنوان ژورنال:
- The Ulster Medical Journal
دوره 49 شماره
صفحات -
تاریخ انتشار 1980