Literature DB >> 1111674

The occult osteomatous changes in the mandible in patients with familial polyposis coli.

J Utsunomiya, T Nakamura.   

Abstract

Characteristic radio-opaque lesions were detected in the manibular bone, most clearly on the panoramic X-ray, in 27 or 93-2 per cent out of 29 cases in 15 families with familial polyposis coli, including 21 cases without Gardner's stigmata, 7 cases with the incomplete syndrome and 1 with the complete syndrome. Only 3 out of 19 members of these families who were free from polposis had radio-opaque jaw lesions. The cases with polyposis of other types also showed a negative result. The radiological diagnosis suggested that the lesions were of the character of endosteoma. Our observation is considered to be significant evidence in the understanding of the pathogenesis of Gardner's syndrome as well as a useful method of the early detection of carriers in the polyposis family.

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Year:  1975        PMID: 1111674     DOI: 10.1002/bjs.1800620111

Source DB:  PubMed          Journal:  Br J Surg        ISSN: 0007-1323            Impact factor:   6.939


  23 in total

Review 1.  Overview of screening and management of familial adenomatous polyposis.

Authors:  M Rhodes; D M Bradburn
Journal:  Gut       Date:  1992-01       Impact factor: 23.059

Review 2.  A Comprehensive Overview of Skeletal Phenotypes Associated with Alterations in Wnt/β-catenin Signaling in Humans and Mice.

Authors:  Kevin A Maupin; Casey J Droscha; Bart O Williams
Journal:  Bone Res       Date:  2013-03-29       Impact factor: 13.567

Review 3.  The history of familial adenomatous polyposis.

Authors:  Steffen Bülow; Terri Berk; Kay Neale
Journal:  Fam Cancer       Date:  2006       Impact factor: 2.375

Review 4.  Extracolonic manifestations associated with familial adenomatous polyposis.

Authors:  T G Parks
Journal:  Ann R Coll Surg Engl       Date:  1990-05       Impact factor: 1.891

5.  Diagnosis of familial adenomatous polyposis.

Authors:  S Bülow
Journal:  World J Surg       Date:  1991 Jan-Feb       Impact factor: 3.352

6.  Value of the congenital hypertrophy of the retinal pigment epithelium in the diagnosis of familial adenomatous polyposis.

Authors:  Rosario Touriño; Rogelio Conde-Freire; José M Cabezas-Agrícola; Teresa Rodríguez-Aves; Maria Jesús López-Valladares; José L Otero-Cepeda; Carmen Capeans
Journal:  Int Ophthalmol       Date:  2004-03       Impact factor: 2.031

7.  Gastrointestinal Polyposis: Syndromes and Genetic Mechanisms.

Authors:  E J Gardner; R W Burt; J W Freston
Journal:  West J Med       Date:  1980-06

8.  Value of combined phenotypic markers in identifying inheritance of familial adenomatous polyposis.

Authors:  F M Giardiello; G J Offerhaus; E I Traboulsi; J C Graybeal; I H Maumenee; A J Krush; L S Levin; S V Booker; S R Hamilton
Journal:  Gut       Date:  1991-10       Impact factor: 23.059

9.  The UK Northern region genetic register for familial adenomatous polyposis coli: use of age of onset, congenital hypertrophy of the retinal pigment epithelium, and DNA markers in risk calculations.

Authors:  J Burn; P Chapman; J Delhanty; C Wood; F Lalloo; M B Cachon-Gonzalez; K Tsioupra; W Church; M Rhodes; A Gunn
Journal:  J Med Genet       Date:  1991-05       Impact factor: 6.318

10.  Familial polyposis coli: the spectrum of ocular and other extracolonic manifestations.

Authors:  M H Heinemann; R H Baker; H H Miller; J J DeCosse
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  1991       Impact factor: 3.117

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