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Published on: October 30, 2013
Management of goblet cell carcinoid
John C Byrn1, Ju-Lin Wang, Celia M Divino
1Department of Surgery, Mount Sinai School of Medicine, New York, New York 10029, USA.
Goblet cell carcinoid, a rare appendiceal neoplasm, presents variedly. Surgical approach for appendiceal goblet cell carcinoid should be individualized, not solely based on pathology.
Area of Science:
- Gastroenterology
- Surgical Oncology
- Pathology
Background:
- Goblet cell carcinoid is a rare appendiceal neoplasm with intermediate malignant potential.
- These tumors represent a significant minority of neoplasms affecting the appendix.
Purpose of the Study:
- To describe the presentation, treatment, and outcomes of 16 cases of goblet cell carcinoid.
- To evaluate the necessity of right hemicolectomy for appendiceal goblet cell carcinoid presenting as appendicitis.
Main Methods:
- Retrospective review of 16 cases diagnosed between 1995 and 2005 at a single institution.
- Patients were categorized into two groups: incidental findings during surgery and presentation with mass or metastatic disease.
Main Results:
- Presenting diagnoses varied, including appendicitis, abdominal/liver mass, uterine/ovarian mass, and Crohn's disease exacerbation.
- Mortality rate was 19% over a mean follow-up of 12 months.
- Appendectomy was the initial procedure for most incidental findings; advanced presentations included Krukenberg lesions and abdominal masses.
Conclusions:
- Goblet cell carcinoid is a rare, predominantly appendiceal malignant tumor.
- Right hemicolectomy is not routinely supported for appendiceal goblet cell carcinoid presenting as appendicitis.
- Treatment decisions for goblet cell carcinoid require individual patient customization.
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