Skip to main content
Top
Published in: European Journal of Pediatrics 12/2018

01-12-2018 | Original Article

Long-term outcomes in pediatric appendiceal carcinoids: Turkey experience

Authors: Fatih Akova, Emrah Aydin, Y. Nur Eray, Nurseli Toksoy, Senay Yalcin, Serdar Altinay, Umit Seza Tetikkurt

Published in: European Journal of Pediatrics | Issue 12/2018

Login to get access

Abstract

The tendency of non-operative management of appendicitis let us explore the natural history of appendiceal carcinoids, compare them with appendicitis patients, and determine the possibility of deciding the extent of the surgery and post-operative follow-up on behalf of the intraoperative findings. A retrospective review was performed of patients with appendicitis between 2009 and 2017. Of 2781 patients, 10 (0.36%) were diagnosed with appendiceal carcinoids. Sixty percent were female with an average age of 13.10 ± 1.73. The mean tumor size was 0.97 ± 0.34 cm with 70% located at the tip. Majority had an insular pattern (n = 9), six had subserosal fat tissue invasion, one had extension to mesoappendix, one had vascular invasion, and two had lymphatic invasion. The average mitotic index was 3.20 ± 1.40/50HPF, and Ki 67 activity was 3 ± 1.7%. The mean follow-up period was 66.40 ± 25.92 months. Patients were further evaluated with ultrasonography (n = 10), CT (n = 3), and MRI (n = 10). Serum markers including chromogranin (n = 9), NSE (n = 6), and 5-HIAA (n = 6) were normal. None required further treatment and had any symptoms of carcinoid syndromes or recurrences post-operatively.
Conclusion: Other than appendectomy, no additional surgery or follow-up is required in appendiceal carcinoids less than 1.5 cm in size, regardless of the lymphoid or vascular invasion.
What is Known:
• The treatment of patients with a 1–2-cm tumor is not clear in both the pediatric and adult populations, and additional resection is needed.
• Patients are monitored post-operatively with radiological and/or biochemical testing.
What is New:
• Appendectomy is curative for tumors less than 2 cm.
• No additional surgery or follow-up is required in appendiceal carcinoids less than 1.5 cm in size regardless of the lymphoid or vascular invasion.
Literature
2.
go back to reference Assadi M, Kubiak R, Kaiser G (2002) Appendiceal carcinoid tumors in children: does size matter? Med Pediatr Oncol 38:65–66CrossRef Assadi M, Kubiak R, Kaiser G (2002) Appendiceal carcinoid tumors in children: does size matter? Med Pediatr Oncol 38:65–66CrossRef
3.
go back to reference Bosman F, Carneiro F, Hruban R et al (eds) (2010) WHO classification of tumours of the digestive system. International Agency for Research on Cancer, Lyon, p 417 Bosman F, Carneiro F, Hruban R et al (eds) (2010) WHO classification of tumours of the digestive system. International Agency for Research on Cancer, Lyon, p 417
4.
go back to reference Boudreaux JP, Klimstra DS, Hassan MM, Woltering EA, Jensen RT, Goldsmith SJ, Nutting C, Bushnell DL, Caplin ME, Yao JC, North American Neuroendocrine Tumor Society (NANETS) (2010) The NANETS consensus guideline for the diagnosis and management of neuroendocrine tumors: well-differentiated neuroendocrine tumors of the jejunum, ileum, appendix, and cecum. Pancreas 39:753–766CrossRef Boudreaux JP, Klimstra DS, Hassan MM, Woltering EA, Jensen RT, Goldsmith SJ, Nutting C, Bushnell DL, Caplin ME, Yao JC, North American Neuroendocrine Tumor Society (NANETS) (2010) The NANETS consensus guideline for the diagnosis and management of neuroendocrine tumors: well-differentiated neuroendocrine tumors of the jejunum, ileum, appendix, and cecum. Pancreas 39:753–766CrossRef
6.
go back to reference Corpron CA, Black CT, Herzog CE et al (1995) A half century of experience with carcinoid tumors in children. Am J Surg 170:606–608CrossRef Corpron CA, Black CT, Herzog CE et al (1995) A half century of experience with carcinoid tumors in children. Am J Surg 170:606–608CrossRef
7.
go back to reference Fallon SC, Hicks MJ, Carpenter JL, Vasudevan SA, Nuchtern JG, Cass DL (2015) Management of appendiceal carcinoid tumors in children. J Surg Res 198:384–387CrossRef Fallon SC, Hicks MJ, Carpenter JL, Vasudevan SA, Nuchtern JG, Cass DL (2015) Management of appendiceal carcinoid tumors in children. J Surg Res 198:384–387CrossRef
8.
go back to reference Henderson L, Fehily C, Folaranmi S, Kelsey A, McPartland J, Jawaid WB, Craigie R, Losty PD (2014) Management and outcome of neuroendocrine tumours of the appendix—a two centre UK experience. J Ped Surg 49:1513–1517CrossRef Henderson L, Fehily C, Folaranmi S, Kelsey A, McPartland J, Jawaid WB, Craigie R, Losty PD (2014) Management and outcome of neuroendocrine tumours of the appendix—a two centre UK experience. J Ped Surg 49:1513–1517CrossRef
9.
go back to reference Oberg K, Akerstrom G, Rindi G et al (2010) Neuroendocrine gastroenteropancreatic tumours: ESMO clinical practice guidelines for diagnosis, treatment and follow-up. Ann Oncol 21:223–227CrossRef Oberg K, Akerstrom G, Rindi G et al (2010) Neuroendocrine gastroenteropancreatic tumours: ESMO clinical practice guidelines for diagnosis, treatment and follow-up. Ann Oncol 21:223–227CrossRef
Metadata
Title
Long-term outcomes in pediatric appendiceal carcinoids: Turkey experience
Authors
Fatih Akova
Emrah Aydin
Y. Nur Eray
Nurseli Toksoy
Senay Yalcin
Serdar Altinay
Umit Seza Tetikkurt
Publication date
01-12-2018
Publisher
Springer Berlin Heidelberg
Published in
European Journal of Pediatrics / Issue 12/2018
Print ISSN: 0340-6199
Electronic ISSN: 1432-1076
DOI
https://doi.org/10.1007/s00431-018-3258-z

Other articles of this Issue 12/2018

European Journal of Pediatrics 12/2018 Go to the issue