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Turcot Syndrome, Report of a Case J. Kamiya 1 1The First Department of Surgery, Faculty of Medicine, University of Tokyo pp.913-917
Published Date 1982/8/25
DOI https://doi.org/10.11477/mf.1403108860

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  • Abstract
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 A 11-year-old girl was admitted to our hospital with complaint of anal bleeding. She had had transanal polypectomy for rectal polyp one year previously. Histology of the polyp was adenoma. After the polypectomy rectal bleeding persisted. Her parents and sister were in good health, but her aunt had been operated on for sigmoid colon cancer six years ago when she was aged 21.

 Barium enema examination disclosed seven colonic polyps, scattered in the transverse, descending and sigmoid colon, being 1 to 4 cm in size. There were café-au-lait spots on the chest, shoulder and extremities. Hemangioma was also present on the face.

 Total colonoscopy was performed under general anesthesia. Eight polyps were removed by cautery snare and two small polyps were treated by hotbiopsy. Histological study disclosed a sessile invasive cancer, 15 mm in diameter, of the sigmoid colon, and four focal cancers. The other polyps were adenomas. Because of the presence of invasive cancer further surgical intervention was attempted. At laparotomy advanced cancer of the cecum was found, the tumor was not well demonstrated on the barium enema examination. She had undergone right hemicolectomy. Postoperative course was uneventful. Soon after discharge from our hospital she complained of headache, nausea, vomitting and left hemiplegia.

 Computer tomography of the head disclosed a large tumor of right frontal lobe. Craniotomy was per-formed but the tumor was not resectable.

 Histological study of the brain tumor showed astrocytoma.

 At this stage she was diagnosed to have Turcot syndrome for the first time. She died two months after craniotomy.

 Autopsy revealed that she died of malignant astrocytoma and nine adenomas were still present in the remaining colon.

 In her family pedigree study her grandmothers were half sister and recessive inheritance of her disease was suggested.


Copyright © 1982, Igaku-Shoin Ltd. All rights reserved.

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電子版ISSN 1882-1219 印刷版ISSN 0536-2180 医学書院

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