Sunitinib in the treatment of neuroendocrine tumors of the gastrointestinal tract – case study
MUDr. Dagmar Brančíková, Ph.D.
Interní hematologická a onkologická klinika LF MU a FN Brno
Pheochromocytomas are rare tumors. Bilateral adrenal medullary pheochromocytomas are components of MEN- Ila and MEN Ilb (multiple endocrine neoplasia). Patient 55 years old with inoperable pheochromocytoma, with liver and abdomen cavity metastases in the time of diagnosis had high levels of adrenalin, noradrenalin and dopamin. Patient was treated by TACE, lanreotide and target therapy. The patient lives 5 years after the diagnosis of disease dissemination and 18 years after the first manifestation, with very good effect and quality of life. The case demonstrates the good effect of hormonal and anti-cancer treatment.
pheochromocytoma, multiple endocrine neoplasia, TACE, lanreotide, target therapy
The full article is only available to subscribers
Become a regular subscriber to our Oncological Review...