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Erschienen in: World Journal of Surgery 6/2020

13.02.2020 | Surgery in Low and Middle Income Countries

Surgery for Pheochromocytoma: A Single-Center Review of 60 Cases from South Africa

verfasst von: D. Nel, E. Panieri, F. Malherbe, R. Steyn, L. Cairncross

Erschienen in: World Journal of Surgery | Ausgabe 6/2020

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Abstract

Background

There is a paucity of data on the presentation and surgical management of pheochromocytoma in developing nations, particularly in Africa.

Methods

This study was a retrospective review, which included all patients managed by the Groote Schuur Hospital/University of Cape Town Endocrine Surgery unit for pheochromocytoma and abdominal paragangliomas, from January 2002 to June 2019.

Results

Sixty patients were included in the study, of which 33% were male and 67% female. The mean age was 47 years (range 14–81). The median tumor size was 6 cm, with 45% larger than 6 cm. 92% were located in the adrenal gland (87% unilateral, 5% bilateral), and 8% were extra-adrenal. The conversion rate for laparoscopic cases was 20%, with 55% of cases overall completed laparoscopically. Eleven patients with tumors > 6 cm were initially attempted laparoscopically, of which 3 were converted to open, without any associated increased morbidity. A major adverse event was recorded for 5 cases (8%), including 1 mortality. Overall morbidity, blood loss, operating time and hospital stay were all significantly reduced in the laparoscopic group. There were 5 patients with malignant disease (8%).

Conclusion

This large series, from an established academic endocrine surgery unit in Africa, can serve as a benchmark for units with similar settings and resource limitations, to compare their surgical management and perioperative outcomes.
Literatur
1.
Zurück zum Zitat Conzo G, Pasquali D, Colantuoni V et al (2014) Current concepts of pheochromocytoma. Int J Surg 12:469–474CrossRef Conzo G, Pasquali D, Colantuoni V et al (2014) Current concepts of pheochromocytoma. Int J Surg 12:469–474CrossRef
2.
Zurück zum Zitat Hodin R, Lubitz C, Phitayakorn R et al (2014) Diagnosis and management of pheochromocytoma. Curr Probl Surg 51:151–187CrossRef Hodin R, Lubitz C, Phitayakorn R et al (2014) Diagnosis and management of pheochromocytoma. Curr Probl Surg 51:151–187CrossRef
3.
Zurück zum Zitat Lenders JW, Eisenhofer G, Mannelli M et al (2005) Phaeochromocytoma. Lancet 366:665–675CrossRef Lenders JW, Eisenhofer G, Mannelli M et al (2005) Phaeochromocytoma. Lancet 366:665–675CrossRef
4.
Zurück zum Zitat Lenders JW, Duh QY, Eisenhofer G et al (2014) Pheochromocytoma and paraganglioma: an endocrine society clinical practice guideline. J Clin Endocrinol Metab 99:1915–1942CrossRef Lenders JW, Duh QY, Eisenhofer G et al (2014) Pheochromocytoma and paraganglioma: an endocrine society clinical practice guideline. J Clin Endocrinol Metab 99:1915–1942CrossRef
5.
Zurück zum Zitat Plouin PF, Amar L, Dekkers OM et al (2016) European society of endocrinology clinical practice guideline for long-term follow-up of patients operated on for a phaeochromocytoma or a paraganglioma. Eur J Endocrinol 174:G1–G10CrossRef Plouin PF, Amar L, Dekkers OM et al (2016) European society of endocrinology clinical practice guideline for long-term follow-up of patients operated on for a phaeochromocytoma or a paraganglioma. Eur J Endocrinol 174:G1–G10CrossRef
6.
Zurück zum Zitat Kazaryan AM, Kuznetsov NS, Shulutko AM et al (2004) Evaluation of endoscopic and traditional open approaches to pheochromocytoma. Surg Endosc 18:937–941CrossRef Kazaryan AM, Kuznetsov NS, Shulutko AM et al (2004) Evaluation of endoscopic and traditional open approaches to pheochromocytoma. Surg Endosc 18:937–941CrossRef
7.
Zurück zum Zitat Thomson BN, Moulton CA, Davies M et al (2004) Laparoscopic adrenalectomy for phaeochromocytoma: with caution. ANZ J Surg 74:429–433CrossRef Thomson BN, Moulton CA, Davies M et al (2004) Laparoscopic adrenalectomy for phaeochromocytoma: with caution. ANZ J Surg 74:429–433CrossRef
8.
Zurück zum Zitat Solorzano CC, Lew JI, Wilhelm SM et al (2007) Outcomes of pheochromocytoma management in the laparoscopic era. Ann Surg Oncol 14:3004–3010CrossRef Solorzano CC, Lew JI, Wilhelm SM et al (2007) Outcomes of pheochromocytoma management in the laparoscopic era. Ann Surg Oncol 14:3004–3010CrossRef
9.
Zurück zum Zitat Wilhelm SM, Prinz RA, Barbu AM et al (2006) Analysis of large versus small pheochromocytomas: operative approaches and patient outcomes. Surgery 140:553–560CrossRef Wilhelm SM, Prinz RA, Barbu AM et al (2006) Analysis of large versus small pheochromocytomas: operative approaches and patient outcomes. Surgery 140:553–560CrossRef
10.
Zurück zum Zitat Humphrey R, Gray D, Pautler S et al (2008) Laparoscopic compared with open adrenalectomy for resection of pheochromocytoma: a review of 47 cases. Can J Surg 51:276–280PubMedPubMedCentral Humphrey R, Gray D, Pautler S et al (2008) Laparoscopic compared with open adrenalectomy for resection of pheochromocytoma: a review of 47 cases. Can J Surg 51:276–280PubMedPubMedCentral
11.
Zurück zum Zitat Cotesta D, Petramala L, Serra V et al (2009) Clinical experience with pheochromocytoma in a single centre over 16 years. High Blood Press Cardiovasc Prev 16:183–193CrossRef Cotesta D, Petramala L, Serra V et al (2009) Clinical experience with pheochromocytoma in a single centre over 16 years. High Blood Press Cardiovasc Prev 16:183–193CrossRef
12.
Zurück zum Zitat Kercher KW, Novitsky YW, Park A et al (2005) Laparoscopic curative resection of pheochromocytomas. Ann Surg 241:919–926CrossRef Kercher KW, Novitsky YW, Park A et al (2005) Laparoscopic curative resection of pheochromocytomas. Ann Surg 241:919–926CrossRef
14.
Zurück zum Zitat Huddle KR (2011) Phaeochromocytoma in black South Africans–a 30-year audit. S Afr Med J 101:184–188CrossRef Huddle KR (2011) Phaeochromocytoma in black South Africans–a 30-year audit. S Afr Med J 101:184–188CrossRef
15.
Zurück zum Zitat Zorgani AE, Pirie FJ, Motala AA (2018) Characteristics and outcome of patients with pheochromocytoma at a tertiary endocrinology clinic in Durban, South Africa over 14 years. J Endocrinol Metab Diabetes S Afr 23:52–58 Zorgani AE, Pirie FJ, Motala AA (2018) Characteristics and outcome of patients with pheochromocytoma at a tertiary endocrinology clinic in Durban, South Africa over 14 years. J Endocrinol Metab Diabetes S Afr 23:52–58
16.
Zurück zum Zitat Johnson O (2004) Phaeochromocytoma: experience with 12 cases in Tikur Anbessa, Addis Ababa, Ethiopia. East Cent Afr J Surg 9:71–75 Johnson O (2004) Phaeochromocytoma: experience with 12 cases in Tikur Anbessa, Addis Ababa, Ethiopia. East Cent Afr J Surg 9:71–75
17.
Zurück zum Zitat Leye A, Ndiaye N, Leye YM et al (2018) Management of Pheochromocytoma in Dakar: diagnostic and Therapeutic Advances throughout 16 Cases. Open J Endocr Metab Dis 8:19–28CrossRef Leye A, Ndiaye N, Leye YM et al (2018) Management of Pheochromocytoma in Dakar: diagnostic and Therapeutic Advances throughout 16 Cases. Open J Endocr Metab Dis 8:19–28CrossRef
18.
Zurück zum Zitat Agarwal G, Sadacharan D, Aggarwal V et al (2012) Surgical management of organ-contained unilateral pheochromocytoma: comparative outcomes of laparoscopic and conventional open surgical procedures in a large single-institution series. Langenbeck’s Arch Surg 397:1109–1116CrossRef Agarwal G, Sadacharan D, Aggarwal V et al (2012) Surgical management of organ-contained unilateral pheochromocytoma: comparative outcomes of laparoscopic and conventional open surgical procedures in a large single-institution series. Langenbeck’s Arch Surg 397:1109–1116CrossRef
19.
Zurück zum Zitat Kopetschke R, Slisko M, Kilisli A et al (2009) Frequent incidental discovery of phaeochromocytoma: data from a German cohort of 201 phaeochromocytoma. Eur J Endocrinol 161:355–361CrossRef Kopetschke R, Slisko M, Kilisli A et al (2009) Frequent incidental discovery of phaeochromocytoma: data from a German cohort of 201 phaeochromocytoma. Eur J Endocrinol 161:355–361CrossRef
20.
Zurück zum Zitat Baguet JP, Hammer L, Mazzuco TL et al (2004) Circumstances of discovery of phaeochromocytoma: a retrospective study of 41 consecutive patients. Eur J Endocrinol 150:681–686CrossRef Baguet JP, Hammer L, Mazzuco TL et al (2004) Circumstances of discovery of phaeochromocytoma: a retrospective study of 41 consecutive patients. Eur J Endocrinol 150:681–686CrossRef
21.
Zurück zum Zitat Shen WT, Grogan R, Vriens M et al (2010) One hundred two patients with pheochromocytoma treated at a single institution since the introduction of laparoscopic adrenalectomy. Arch Surg 145:893–897CrossRef Shen WT, Grogan R, Vriens M et al (2010) One hundred two patients with pheochromocytoma treated at a single institution since the introduction of laparoscopic adrenalectomy. Arch Surg 145:893–897CrossRef
23.
Zurück zum Zitat Lorenz K, Langer P, Niederle B et al (2019) Surgical therapy of adrenal tumors: guidelines from the German Association of Endocrine Surgeons. Langenbeck’s Arch Surg 404:385–401CrossRef Lorenz K, Langer P, Niederle B et al (2019) Surgical therapy of adrenal tumors: guidelines from the German Association of Endocrine Surgeons. Langenbeck’s Arch Surg 404:385–401CrossRef
24.
Zurück zum Zitat Li ML, Fitzgerald PA, Price DC et al (2001) Iatrogenic pheochromocytomatosis: a previously unreported result of laparoscopic adrenalectomy. Surgery 130:1072–1077CrossRef Li ML, Fitzgerald PA, Price DC et al (2001) Iatrogenic pheochromocytomatosis: a previously unreported result of laparoscopic adrenalectomy. Surgery 130:1072–1077CrossRef
Metadaten
Titel
Surgery for Pheochromocytoma: A Single-Center Review of 60 Cases from South Africa
verfasst von
D. Nel
E. Panieri
F. Malherbe
R. Steyn
L. Cairncross
Publikationsdatum
13.02.2020
Verlag
Springer International Publishing
Erschienen in
World Journal of Surgery / Ausgabe 6/2020
Print ISSN: 0364-2313
Elektronische ISSN: 1432-2323
DOI
https://doi.org/10.1007/s00268-020-05420-6

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