Keywords
Paraganglioma
Biochemical Diagnosis
Gene Therapy
Surgical Treatment
Precision Medicine
Targeted Therapies
How to Cite
Abstract
Pheochromocytoma is a rare neuroendocrine tumor, originating in the chromaffin cells of the adrenal medulla, frequently associated with excessive production of catecholamines, resulting in severe hypertensive crises and cardiovascular complications. In recent years, significant advances have been observed in the management of this tumor, both in diagnosis and treatment, influenced by technological innovations and a greater understanding of molecular biology. This article reviews contemporary approaches, with an emphasis on new diagnostic and treatment strategies, and discusses clinical implications and future research directions. The review included a systematic analysis of the literature in the PubMed and Google Scholar databases, focusing on studies published between 2013 and 2023. Keywords: pheochromocytoma, paraganglioma, biochemical diagnosis, gene therapy, surgical treatment, precision medicine, targeted therapies.
References
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Copyright (c) 2024 Silas da Silva Santos, Bruna Luiza da Silva Costa, Ana Paula Bodanese , Rodrigo dos Santos Carneiro Andrade, Carticlei de Jesus Caetano , Janaína Pereira de Souza Florentino, Yago Feitosa dias Gomes Loiola, Jacks Daienne Galvão Pereira Júnior, Giovanna Louise Araujo Almeida Galvão, Anndryk César Portela Cunha, Marília Ursulino Barbosa