World Journal of Oncology, ISSN 1920-4531 print, 1920-454X online, Open Access
Article copyright, the authors; Journal compilation copyright, World J Oncol and Elmer Press Inc
Journal website http://www.wjon.org

Review

Volume 2, Number 5, October 2011, pages 209-216


Primary Hepatic Neuroendocrine Tumor: What Do We Know Now?

Table

Table 1. Characteristics of 124 Cases of PHNETs
 
CharacteristicsN* (%)
*This is based on detail of the individual cases reviewed.
Age(years)
  Range8-89
  Mean51.9 ± 16.5
Gender
  Male61/124 (49.2%)
  Female63/124 (50.8%)
Presentation
  Symptomatic88/120 (73.3%)
    Abdominal Pain57/88 (65.0%)
    Abdominal Mass11/88 (12.5%)
    Jaundice4/88 (45.0%)
    Classic carcinoid syndrome6/88 (6.8%)
  Asymptomatic32/120 (26.7%)
Method of diagnosis
  Surgery94/124 (77.4%)
  Biopsy14/124 (11.3%)
  Autopsy14/124 (11.3%)
Tumor location
  Right lobe60/124 (48.4%)
  Left lobe41/124 (33.1%)
  Bi-lobar23/124 (18.5%)
Tumor Size
  Range (cm)1.5-27
  Mean (cm)9.4 (SD ± 5.8)
Tumor number
  Single90/118 (76.3%)
  Multiple28/118 (23.7%)
Management
  Liver resection98/116 (84.5%)
  Liver transplant3/116 (2.6%)
  Chemotherapy7/116 (6.0%)
  Transcatherer arterial embolization(TACE)5/116 (4.3%)
  Radiofrequency ablation1/116 (0.8%)
Immunohistochemical stains
  Chromogranin A90/95 (94.7%)
  Synaptophysin48/95 (50.5%)
  Cytokeratin13/95 (13.7%)
  Neuron specific enolase46/95 (48.4%)
Disease free interval (months)
  Minimum1
  Maximum180
  Mean33.6
Recurrence
  Recurrence23/116 (19.8%)
  No recurrence93/116 (80.2%)
Survival
  Death34/118 (28.8%)
  Alive84/118 (71.2%)
Follow up (months)
  Longest survival> 192
  Shortest survival< 1
  Mean survival41
Metastases
  Metastase21/113 (18.6%)
  No metastases92/113 (81.4%)
Survival
  1 year82.0% (CI 0.74-0.89)
  5 years75.0% (CI 0.66-0.83)
  10 years73.4% (CI 0.64-0.82)