Pheochromocytomas (PCs) are neuroendocrine tumors arising from the chromaffin cells of the adrenal gland, and paragangliomas (PGLs) are their extra-adrenal counterparts arising from ganglia along the sympathetic/parasympathetic chain. Surgery is the cornerstone of treatment. A sporatic or inherited germline mutation is commonly associated.
Pheochromocytomas and paragangliomas in children. Data from the Italian Cooperative Study (TREP) / Virgone, Calogero; Andreetta, Marina; Avanzini, Stefano; Chiaravalli, Stefano; De Pasquale, Deborah; Crocoli, Alessandro; Inserra, Alessandro; D'Angelo, Paolo; Alaggio, Rita; Opocher, Giuseppe; Cecchetto, Giovanni; Ferrari, Andrea; Bisogno, Gianni; Dall'Igna, Patrizia. - In: PEDIATRIC BLOOD & CANCER. - ISSN 1545-5009. - 67:8(2020). [10.1002/pbc.28332]
Pheochromocytomas and paragangliomas in children. Data from the Italian Cooperative Study (TREP)
Alaggio, Rita;
2020
Abstract
Pheochromocytomas (PCs) are neuroendocrine tumors arising from the chromaffin cells of the adrenal gland, and paragangliomas (PGLs) are their extra-adrenal counterparts arising from ganglia along the sympathetic/parasympathetic chain. Surgery is the cornerstone of treatment. A sporatic or inherited germline mutation is commonly associated.| File | Dimensione | Formato | |
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