Turcot syndrome with colonic obstruction and small intestinal invagination: Report of a case View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

1999-08

AUTHORS

Chikashi Shibata, Iwao Sasaki, Hiroo Naito, Yuji Funayama, Kouhei Fukushima, Tsuyoshi Masuko, Ken-Ichi Takahashi, Hitoshi Ogawa, Shun Saio, Tatsuya Ueno, Akihiko Hashimoto, Seiki Matsuno, Yoshitaka Kinouchi, Nobuo Hiwatashi

ABSTRACT

We report herein the case of a 16-year-old boy diagnosed as having turcot syndrome, otherwise known as glioma-polyposis syndrome. The patient was transferred from the Department of Neurosurgery where he was undergoing investigation of a brain tumor, to the Department of Medicine for investigation of gastrointestinal symptoms. The patient was diagnosed as having Turcot syndrome, and was then transferred to the Department of Surgery for treatment of an obstruction in the sigmoid colon and small intestinal invagination. A subtotal colectomy with side-to-end ileoproctostomy and release of the invaginations was carried out. Multiple polyps were found in the colon, two of which, including a large polyp that obstructed the colonic lumen, were confirmed histologically to be adenocarcinoma. The remaining polyps were adenomas. A biopsy of the brain tumor confirmed a diagnosis of astrocytoma (WHO grade II). This case report describes the characteristic features of Turcot syndrome presented by this patient. More... »

PAGES

785-788

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/bf02482328

DOI

http://dx.doi.org/10.1007/bf02482328

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1035631558

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/10483758


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