Searchable abstracts of presentations at key conferences in endocrinology

ea0099p314 | Pituitary and Neuroendocrinology | ECE2024

A complex clinical scenario: chiari type ii malformation coexisting with suprasellar paraganglioma and associated succinate dehydrogenase subunit b (SDHB) genetic mutation

Testa Stefano , Grossrubatscher Erika , Dalino Ciaramella Paolo , Zampetti Benedetta , Favero Vittoria , Chiodini Iacopo

Introduction: Paragangliomas are rare neuroendocrine tumors, that manifest as painless, slow-growing masses, becoming evident only when symptoms of catecholamine overproduction or mass effects emerge. Paragangliomas exhibit a broad spectrum of characteristics, existing as solitary or multiple entities, and may be sporadic or hereditary. These tumors can be either benign or malignant and have origin in the sympathetic or parasympathetic tissues. Paragangliomas are commonly foun...