Literature DB >> 12890258

Gorlin's syndrome: diffuse appendicular skeletal involvement with scintigraphic correlation.

Justin Q Ly1, Douglas P Beall.   

Abstract

Gorlin's syndrome (also known as basal cell nevus syndrome, Gorlin-Goltz syndrome, and nevoid basal cell carcinoma syndrome) is a rare, inherited disorder characterized by multiple basal-cell epitheliomas, intracranial calcification, keratocysts of the mandible, and unusual and striking skeletal abnormalities. We present the interesting case of a 45-year-old woman who was informed that she had fibrous dysplasia of the extremity at another institution before extensive radiological work-up showed a diffuse skeletal process. The skeletal abnormalities, in conjunction with the patient's history of multiple basal cell carcinomas, is consistent with the diagnosis of Gorlin's syndrome. We describe this unusual case of striking radiological and scintigraphic findings in a patient with Gorlin's syndrome.

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Year:  2003        PMID: 12890258     DOI: 10.1046/j.1440-1673.2003.01186.x

Source DB:  PubMed          Journal:  Australas Radiol        ISSN: 0004-8461


  2 in total

1.  [Calcification of the falx cerebri. A pathognomonic symptom of Gorlin-Goltz syndrome].

Authors:  J T Lambrecht; S Stübinger; B Siewert; F Härle
Journal:  HNO       Date:  2005-08       Impact factor: 1.284

2.  Gorlin-Goltz syndrome with situs oppositus.

Authors:  Yadavalli Guruprasad; Prashanth R Prabhu
Journal:  Natl J Maxillofac Surg       Date:  2010-01
  2 in total

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