[HTML][HTML] Surgical management of the adrenal gland tumors-single center experience
Objective. Our aim was to evaluate the surgical technique option in relation with clinical and
histopathologic features. Design. We performed a retrospective study that included patients …
histopathologic features. Design. We performed a retrospective study that included patients …
Bilateral pheochromocytomas: clinical presentation and morbidity rate related to surgery technique and genetic status
SML Burciulescu, ML Gheorghiu… - Endocrine …, 2024 - ec.bioscientifica.com
Background Pheochromocytomas (PHEOs) are rare catecholamine-secreting adrenal
tumors. Approximately 60–90% of bilateral PHEOs are hereditary. We retrospectively …
tumors. Approximately 60–90% of bilateral PHEOs are hereditary. We retrospectively …
[HTML][HTML] A 40-year follow-up of a patient with multiple paragangliomas and a SDHD mutation
A Elenkova, R Robeva… - Acta Endocrinologica …, 2019 - ncbi.nlm.nih.gov
Objective We present the case of a patient carrying a germline SDHD mutation responsible
for multiple PGLs, who was followed for 40 years. He was initially diagnosed with a left …
for multiple PGLs, who was followed for 40 years. He was initially diagnosed with a left …