Background Image
Table of Contents Table of Contents
Previous Page  376 / 492 Next Page
Information
Show Menu
Previous Page 376 / 492 Next Page
Page Background

VR-15

(VS)

RECURRENCE AFTER PARTIAL ADRENALECTOMY IN A CHILD WITH

METACHRONIC BILATERAL PHEOCHROMOCYTOMA - LAPAROSCOPIC APPROACH

Francisco DENES

1

, Lorena OLIVEIRA

1

, Roberto LOPES

1

, Alessandro TAVARES

1

, Marcos MACHADO

1

, Maria Helena

SIRCILI

2

and Berenice MENDONCA

2

1) Hospital das Clinicas - University of Sao Paulo, Urology, Sao Paulo, BRAZIL - 2) Hospital das Clinicas - University of

Sao Paulo, Endocrinology, Sao Paulo, BRAZIL

PURPOSE

To present a case of laparoscopic resection of a recurrent tumor after partial adrenalectomy in a child with metachronic

bilateral pheochromocytoma associated with von HippelLindau's disease.

MATERIAL AND METHODS

The patient, whose father had been diagnosed with von HippelLindau's disease and treated of an unilateral adrenal

pheochromocytoma, presented at age 7 symptoms of night sweating and palpitation, and had the diagnosis of a 2.7cm

right adrenal pheochromocytoma. He was then submitted to a successful total right laparoscopic adrenalectomy, with

complete remission of the symptoms. At age 12, the symptoms recurred, and a left 2.6cm adrenal tumor was

diagnosed. Prospective preoperative US showed that besides the tumor there was a non-affected postero-lateral

segment of the gland that could be preserved. He was submitted to a transperitonial laparoscopic procedure, that

included section of the main adrenal vein and complete resection of the tumor, leaving the well vascularized remnant

adrenal in situ. Cortisone replacement was initiated but interrupted after two weeks, since laboratory controls showed

that the remnant adrenal was functioning, with physiologic corticosteroid levels. After 21 months of follow up, a 2.3cm

recurrent left adrenal tumor was diagnosed. The patient underwent laparoscopic surgery with total resection of the

residual left adrenal.

RESULTS

Pathological examination of the specimen showed a benign pheochromocytoma with free margins. The patient had a

pancreatic fistula managed conservatively and was discharged from the hospital after 6 days. The child has a follow-up

of 23 months without any symptoms, currently receiving cortisone replacement.

CONCLUSIONS

Laparoscopic resection of a recurrent adrenal tumor after partial adrenalectomy is a feasible technique in children with

bilateral benign adrenal lesions.