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[Gardner-syndrome: case report].

Eva Kertész¹, Jozsef Túri, Vilmos Gyenes

¹Magyar Honvédség Központi Honvéd Kórház, Fej-nyak Sebészeti Szájsebészet Osztály, Budapest.

Fogorvosi Szemle

|December 1, 2005

Summary

Gardner syndrome, a genetic disorder, presents with multiple osteomas, desmoid tumors, and colon polyps. Early diagnosis is crucial for managing potential malignant transformations.

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Area of Science:

Oncology
Genetics
Gastroenterology

Background:

Gardner syndrome is an inherited condition characterized by a specific triad of symptoms.
It is an autosomal dominant disorder, a variant of Familial Adenomatous Polyposis (FAP).

Observation:

The case presented exhibits the hallmark features of Gardner syndrome.
Key symptoms include multiple osteomas, desmoid tumors, and numerous colon polyps.

Findings:

The colon polyps associated with Gardner syndrome have a high propensity for malignant transformation.
The study details the clinical presentation and diagnostic considerations for this rare syndrome.

Implications:

Emphasizes the critical need for early and accurate diagnosis of Gardner syndrome.
Prompt identification allows for timely intervention and surveillance to mitigate cancer risk.

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