SÍNDROME DE PROTEUS: UMA REVISÃO BIBLIOGRÁFICA

Doi: 10.47094/978-65-81609-96-2/68-78

PALAVRAS CHAVE: Síndrome de proteus. Hamartoma. Lipoma. Síndrome de Cowden.

KEYWORDS: Proteus syndrome. Hamartoma. Lipoma. Cowden Syndrome.

ABSTRACT:
The proteus syndrome is a rare congenital disease, which presents itselfs as variety of clinical sings, like the asymmetric tumors of disproportionate growth, cranial anomalies, partial gigantism of hands and feet and dermatological modifications. Its pathophysiology is not yet well stated, although there are some evidence of being an outcome of a genetic mutation on the AKT1 gene. The research is to understand the syndrome, pitching in a better diagnosys of the disease. To achieve this goal will be made a literature review about the topic, founded in articles provided by well-stablished databases, where will be regarded the clínical presentation and the evolution of the patient medical history with the study developed about the syndrome and avaluate the threatments used.

Autores

• Aline Rosa Marosti

• Eduardo Henrique Wentz Ribeiro

• Giulia Miquelão Sala

• Rodrigo Corrêa Campos Ribeiro