Pheochromocytoma and Paraganglioma Pheochromocytoma and paraganglioma are
related tumors that differ mainly in location; pheochromocytomas are adrenal, and …

This is a consensus statement from an international group, mostly of clinical
endocrinologists. MEN1 and MEN2 are hereditary cancer syndromes. The commonest …

Objective: The aim was to formulate clinical practice guidelines for pheochromocytoma and
paraganglioma (PPGL). Participants: The Task Force included a chair selected by the …

This is an update of the guideline that was published in April 2011 [1] and whose scope
included literature through December 2010. A new systematic literature search using …

Nearly 600 cases of laparoscopic adrenalectomy have been described in the world
literature, documenting the safety and effectiveness of the procedure. Comparative studies …

Pheochromocytoma is a rare but important tumor of chromaffin cells that is frequently
considered in the evaluation of hypertension, arrhythmias, or panic disorder and in the …

Guidelines for diagnosis, treatment, and use of laparoscopy for surgical problems during
pregnancy | SpringerLink Skip to main content Advertisement SpringerLink Log in Menu Find …

Background Laparoscopic adrenalectomy (LA) has become the procedure of choice for
small benign lesions. Compared with open adrenalectomy (OA), it appears to achieve …

Laparoscopic adrenalectomy (LA) was first described in the literature in 1992, and has
become the preferred method for the removal of benign functioning and non-functioning …

SAGES guidelines for minimally invasive treatment of adrenal pathology | SpringerLink Skip
to main content Advertisement SpringerLink Log in Menu Find a journal Publish with us …