Journal of Current Surgery, ISSN 1927-1298 print, 1927-1301 online, Open Access
Article copyright, the authors; Journal compilation copyright, J Curr Surg and Elmer Press Inc
Journal website http://www.currentsurgery.org

Original Article

Volume 3, Number 2, October 2013, pages 66-72


Surgical Management of Pheochromocytoma in a Contemporary Setting

Tables

Table 1. Histology Findings of 85 Adrenalectomies
 
Histological diagnosisNumber of cases (n)Percentage of total (%)
Pheochromocytoma2428.24%
Adrenocortical carcinoma33.52%
  Cushing syndrome 2
  Incidentaloma 1
Benign cortical adenoma3743.52%
  Cushing syndrome 3
  Conn’s syndrome 13
  Incidentaloma 21
Adrenal Cortical hyperplasia55.88%
  Cushing’s syndrome 4
  Conn’s syndrome 1
Primary pigmented nodular adrenocortical disease22.35%
Lipoma11.18%
Schwannoma/ganglioneuroma44.71%
Adrenal cyst33.52%
Metastasis67.06%
  Melanoma 2
  Lung 3
  Renal cell carcinoma 1
Total85100%

 

Table 2. Clinical Presentations of Patients With Pheochromocytomas
 
Clinical presentationsTotal (n = 24)Percentage (%)
Investigation for hypertension1354%
  Asymptomatic 5
  Palpitation 2
  Headache 3
  Panic 1
  Flushing, palpitation, anxiety 2
Incidentalomas937.5%
  Abdominal pain or discomfort 4
  Non specific aches and pains 1
  Trauma 1
  Investigation for cardiac thrombus 1
  Asymptomatic 1
  SCC forehead, Staging CT 1
Screening for familial syndromes28.33%
  Von Recklinghausen’s disease 1
  MEN 2A syndrome 1

 

Table 3. Urinary Catecholamines Levels in Patients With Pheochromocytomas
 
Upper limit of normalNumber of patients (n = 24)
> 10 fold3
> 5 fold6
> 3 fold4
> 2 fold6
> 1.5 fold2
Unknown2
Elevated but exact figure unknown1

 

Table 4. Operative Approach
 
Laparoscopic AdrenalectomyLap converted to open adrenalectomyOpen resectionTotal
Adrenal pheochormocytoma153422
Extra-adrenal pheochromocytoma22
Total153624