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Carcinoid tumors of the gastrointestinal tract. A review and the Duke University institutional overview.

Publication ,  Journal Article
Onaitis, M; White, R; Tyler, D
Published in: Minerva Chir
February 2003

Carcinoid tumors are relatively rare neoplasms arising from the amine precursor uptake and decarboxylation (APUD) cells of the gastrointestinal tract and bronchial tree. Presenting symptoms vary by site of origin, and various modalities may be used to diagnose them. Initial treatment is surgical, with procedure depending upon site of origin. Several experimental therapies may be used in treatment of metastatic carcinoid tumors.

Duke Scholars

Published In

Minerva Chir

ISSN

0026-4733

Publication Date

February 2003

Volume

58

Issue

1

Start / End Page

1 / 8

Location

Italy

Related Subject Headings

  • Surgery
  • Retrospective Studies
  • Prognosis
  • Octreotide
  • Liver Neoplasms
  • Interferon-alpha
  • Incidence
  • Humans
  • Gastrointestinal Neoplasms
  • Embolization, Therapeutic
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Onaitis, M., White, R., & Tyler, D. (2003). Carcinoid tumors of the gastrointestinal tract. A review and the Duke University institutional overview. Minerva Chir, 58(1), 1–8.
Onaitis, M., R. White, and D. Tyler. “Carcinoid tumors of the gastrointestinal tract. A review and the Duke University institutional overview.Minerva Chir 58, no. 1 (February 2003): 1–8.
Onaitis, M., et al. “Carcinoid tumors of the gastrointestinal tract. A review and the Duke University institutional overview.Minerva Chir, vol. 58, no. 1, Feb. 2003, pp. 1–8.

Published In

Minerva Chir

ISSN

0026-4733

Publication Date

February 2003

Volume

58

Issue

1

Start / End Page

1 / 8

Location

Italy

Related Subject Headings

  • Surgery
  • Retrospective Studies
  • Prognosis
  • Octreotide
  • Liver Neoplasms
  • Interferon-alpha
  • Incidence
  • Humans
  • Gastrointestinal Neoplasms
  • Embolization, Therapeutic