Literature DB >> 9915410

Management of hereditary pheochromocytoma in von Hippel-Lindau kindreds with partial adrenalectomy.

M M Walther1, H R Keiser, P L Choyke, W Rayford, J C Lyne, W M Linehan.   

Abstract

PURPOSE: In patients with von Hippel-Lindau disease multiple bilateral adrenal pheochromocytoma can develop, which has traditionally been treated with adrenalectomy. Partial adrenalectomy can preserve normal adrenal function and avoid the morbidity associated with medical adrenal replacement. We demonstrate whether adrenal function could be preserved by partial adrenalectomy in patients with von Hippel-Lindau disease.
MATERIALS AND METHODS: From 1995 to 1998, 13 consecutive von Hippel-Lindau disease patients with pheochromocytoma underwent 14 partial and 6 complete unilateral adrenalectomies. Function of residual normal adrenal and recurrence of adrenal pheochromocytoma were determined at followup.
RESULTS: Of the patients 2 had undergone unilateral adrenalectomy and 1 had undergone complete and partial adrenalectomy previously. Following surgery residual normal adrenal tissue consisted of 1 partial adrenal in 3 patients, bilateral partial adrenal in 5, partial and complete adrenal gland in 1, 1 complete adrenal gland in 3 and no adrenal tissue in 1. Three patients with residual adrenal tissue were placed on medical adrenal replacement until adrenocorticotropic hormone stimulation testing demonstrated adrenocortical function. In 2 patients 1 adrenal and 2 extra-adrenal new pheochromocytomas developed 11 and 152 months, respectively, after partial adrenalectomy. No morbidity related to pheochromocytoma was observed during followup.
CONCLUSIONS: Partial adrenalectomy can preserve adrenal function in patients with a hereditary form of pheochromocytoma.

Entities:  

Mesh:

Year:  1999        PMID: 9915410

Source DB:  PubMed          Journal:  J Urol        ISSN: 0022-5347            Impact factor:   7.450


  23 in total

1.  Outcomes and timing for intervention of partial adrenalectomy in patients with a solitary adrenal remnant and history of bilateral phaeochromocytomas.

Authors:  Thomas H Sanford; Benjamin Barckley Storey; William Marston Linehan; Craig A Rogers; Peter A Pinto; Gennady Bratslavsky
Journal:  BJU Int       Date:  2010-08-19       Impact factor: 5.588

Review 2.  Minimal access adrenal surgery.

Authors:  L M Brunt
Journal:  Surg Endosc       Date:  2006-01-25       Impact factor: 4.584

Review 3.  Adrenal-preserving minimally invasive surgery: update on the current status of laparoscopic partial adrenalectomy.

Authors:  Grant I S Disick; Ravi Munver
Journal:  Curr Urol Rep       Date:  2008-01       Impact factor: 3.092

4.  Laparoscopic management of recurrent pheochromocytoma: A case report.

Authors:  Harshit Garg; Manpreet Uppal; Sreesanth Kelu Sreedharan; Sandeep Aggarwal
Journal:  J Minim Access Surg       Date:  2016 Jul-Sep       Impact factor: 1.407

5.  Partial adrenalectomy minimizes the need for long-term hormone replacement in pediatric patients with pheochromocytoma and von Hippel-Lindau syndrome.

Authors:  Dmitry Volkin; Nitin Yerram; Faisal Ahmed; Dawud Lankford; Angelo Baccala; Gopal N Gupta; Anthony Hoang; Jeffrey Nix; Adam R Metwalli; David M Lang; Gennady Bratslavsky; W Marston Linehan; Peter A Pinto
Journal:  J Pediatr Surg       Date:  2012-11       Impact factor: 2.545

6.  Robot-assisted laparoscopic partial adrenalectomy: initial experience.

Authors:  Ronald S Boris; Gopal Gupta; W Marston Linehan; Peter A Pinto; Gennady Bratslavsky
Journal:  Urology       Date:  2010-12-03       Impact factor: 2.649

7.  Adrenalectomy for familial pheochromocytoma in the laparoscopic era.

Authors:  L Michael Brunt; Terry C Lairmore; Gerard M Doherty; Mary A Quasebarth; Mary DeBenedetti; Jeffrey F Moley
Journal:  Ann Surg       Date:  2002-05       Impact factor: 12.969

Review 8.  [Recurrent operations on the adrenal glands].

Authors:  M Brauckhoff; H Dralle
Journal:  Chirurg       Date:  2005-03       Impact factor: 0.955

9.  Epidemiological study of a von Hippel-Lindau family in northwest China.

Authors:  Jingyao Zhang; Dapeng Wu; Hong Ai; Jigang Bai; Shunbin Dong; Qinling Yang; Kai Qu; Lei Zhou; Xinsen Xu; Chang Liu
Journal:  Front Med       Date:  2013-07-05       Impact factor: 4.592

Review 10.  A clinical overview of pheochromocytomas/paragangliomas and carcinoid tumors.

Authors:  Ioannis Ilias; Karel Pacak
Journal:  Nucl Med Biol       Date:  2008-08       Impact factor: 2.408

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