eMedicine Specialties > Oncology > Carcinomas of the Gastrointestinal Tract
Carcinoid Tumor, Intestinal: Differential Diagnoses & Workup
Updated: Jan 8, 2009
- Overview
- Differential Diagnoses & Workup
- Treatment & Medication
- Follow-up
- Multimedia
Differential Diagnoses
Irritable Bowel Syndrome
Malignant Neoplasms of the Small
Intestine
Mastocytosis, Systemic
Thyroid, Medullary Carcinoma
Workup
Laboratory Studies
- Unfortunately, as already mentioned, most patients with carcinoid tumors present with metastatic disease. Only approximately 20% of patients are diagnosed with potentially resectable disease.8
- Urinalysis
- In persons with carcinoid syndrome, levels of urinary 5-HIAA are usually greatly increased. This is because tryptophan metabolism is diverted from protein and nicotinic acid metabolism to serotonin, with consequent breakdown to 5-HIAA. A very high (usually >5 times normal values) level of urinary 5-HIAA in a 24-hour collection is diagnostic, provided that avocados, bananas, plums, walnuts, pineapples, tomatoes, eggplants (aubergines), and cough medicines are excluded from the diet for 24 hours before the collection is made.
- In very rare cases, usually in bronchial carcinoids or gastric tumors (derived from the foregut), the tumor cells lack the aromatic amino acid decarboxylase enzyme, and hence the secretion of 5-HTP is increased. If this is the situation, then 5-HIAA urinary excretion would be normal. The diagnosis is confirmed by measuring total 5-hydroxyindole excretion. Such measurement includes 5-HTP, serotonin, and 5-HIAA.
Imaging Studies
- Ultrasound
- Ultrasound has limited use, particularly in lesions smaller than 1 cm.
- Endoscopic ultrasound is useful for detecting gastric, duodenal, and pancreatic lesions; experience in this technique is mainly in detecting duodenal gastrinomas and is highly operator dependent.9 It is also used to detect anal lesions.
- CT scan
- Noncontrast CT scan is the investigation of choice for carcinoid tumors because metastatic carcinoid tumors are usually extremely vascular; consequently, they tend to become isodense in the presence of contrast.8
- CT scan can also detect mesenteric involvement with tumor in 50% of patients with metastatic disease.
- MRI
- In the past, availability and the speed of the procedure initially limited use of this investigation. Another dilemma was the difficulty in distinguishing between small (<2 cm) vascular intrahepatic lesions and benign hemangiomas.
- With technical improvements, MRIs are increasingly being used as the supplemental abdominal investigation of choice.
- Radionucleotide scans
- Radionucleotides injected into the blood stream can bind to the neuroendocrine tumor cells and thus help localize the site of the tumor.
- The scan used most commonly is the OctreoScan in which octreotide (an analogue of somatostatin) is labelled with a radioactive isotope and injected. Carcinoid tumors often have somatostatin receptors on their surface. The radio-labelled analogue (111 In-octreotide) therefore binds to the tumor cells. Radiography then allows the tumor to be visualized. This test is particularly useful when other routine modalities have failed to localize the site of the carcinoid. Another compound used less commonly is I131 MIBG.
- PET scan
- This modality utilizes the ability of certain tumors to take up radiolabeled tracers and thus be used to assess the function of different metabolic pathways specific to the tissue being scanned. It is useful in those instances in which scintigraphy with In111 octreotide has been inconclusive.
- FDG (F18 labelled deoxyglucose) is the tracer that is useful in detecting less differentiated neuroendocrine tumors, as they have a higher metabolic rate.
- Well-differentiated tumors have slower metabolic rates and therefore do not take up FDG as avidly. These tumors are better visualized on PET scans, which use the tracer C15 5-HTP.
Other Tests
Endoscopy: Gastric and anal carcinoid tumors can be evaluated by endoscopic techniques. Standard gastroscopy is of limited use except in patients with multiple gastric carcinoids.
Staging
There is no single system of classification and staging of carcinoid tumors. The various different ways of classifying these tumors are as follows:
- Based on site of origin
- Lung
- Gastrointestinal
- World Health Organization (WHO) classification of carcinoids: The WHO now classifies these growths on the basis of their malignant potential into the following categories:
- Neuroendocrine tumors (benign)
- Neuroendocrine cancers (malignant), which are further subclassified as follows:
- Well differentiated (less aggressive)
- Poorly differentiated (aggressive)
- Based on spread
- Localized - Limited to the organ of origin
- Regional spread - Limited infiltration into surrounding tissues
- Distant metastasis
More on Carcinoid Tumor, Intestinal |
| Overview: Carcinoid Tumor, Intestinal |
Differential Diagnoses & Workup: Carcinoid Tumor, Intestinal |
| Treatment & Medication: Carcinoid Tumor, Intestinal |
| Follow-up: Carcinoid Tumor, Intestinal |
| Multimedia: Carcinoid Tumor, Intestinal |
| References |
| « Previous Page | Next Page » |
References
Oberndorfer S. Karzinoide tumoren des du¨nndarms. Frankfurt Zietschrift fur Pathologie. 1907;1:426–429.
Marshall JB, Bodnarchuk G. Carcinoid tumors of the gut. Our experience over three decades and review of the literature. J Clin Gastroenterol. Mar 1993;16(2):123-9. [Medline].
Thorson A, Biorck G, Bjorkman G, Waldenstrom J. Malignant carcinoid of the small intestine with metastases to the liver, valvular disease of the right side of the heart (pulmonary stenosis and tricuspid regurgitation without septal defects), peripheral vasomotor symptoms, bronchoconstriction, and an unusual type of cyanosis; a clinical and pathologic syndrome. Am Heart J. Jun 1954;47(5):795-817. [Medline].
Pearse AG. The cytochemistry and ultrastructure of polypeptide hormone-producing cells of the APUD series and the embryologic, physiologic and pathologic implications of the concept. J Histochem Cytochem. May 1969;17(5):303-13. [Medline].
American Cancer Society. Statistics for 2008. [Full Text].
Surveillance, Epidemiology, and End Results (SEER) Program. Public-Use Data (1973-1998), National Cancer Institute, DCCPS, Surveillance Research Program, Cancer Statistics Branch, released April 2001, based on the November 2000 submission. Available at http://seer.cancer.gov/.
Deans GT, Spence RA. Neoplastic lesions of the appendix. Br J Surg. Mar 1995;82(3):299-306. [Medline].
Sugimoto E, Lorelius LE, Eriksson B, Oberg K. Midgut carcinoid tumours. CT appearance. Acta Radiol. Jul 1995;36(4):367-71. [Medline].
Ruszniewski P, Amouyal P, Amouyal G, Grange JD, Mignon M, Bouche O, et al. Localization of gastrinomas by endoscopic ultrasonography in patients with Zollinger-Ellison syndrome. Surgery. Jun 1995;117(6):629-35. [Medline].
Diaco DS, Hajarizadeh H, Mueller CR, Fletcher WS, Pommier RF, Woltering EA. Treatment of metastatic carcinoid tumors using multimodality therapy of octreotide acetate, intra-arterial chemotherapy, and hepatic arterial chemoembolization. Am J Surg. May 1995;169(5):523-8. [Medline].
Mani S, Modlin IM, Ballantyne G, Ahlman H, West B. Carcinoids of the rectum. J Am Coll Surg. Aug 1994;179(2):231-48. [Medline].
Carrasco CH, Charnsangavej C, Ajani J, Samaan NA, Richli W, Wallace S. The carcinoid syndrome: palliation by hepatic artery embolization. AJR Am J Roentgenol. Jul 1986;147(1):149-54. [Medline].
National Comprehensive Cancer Network. NCCN Clinical Practice Guidelines in Oncology. http://www.nccn.org/professionals/physician_gls/f_guidelines.asp.
Ahlman H, Wangberg B, Jansson S, Friman S, Olausson M, Tylen U, et al. Interventional treatment of gastrointestinal neuroendocrine tumours. Digestion. 2000;62 Suppl 1:59-68. [Medline].
Anthony L, Johnson D, Hande K, Shaff M, Winn S, Krozely M, et al. Somatostatin analogue phase I trials in neuroendocrine neoplasms. Acta Oncol. 1993;32(2):217-23. [Medline].
Boudreaux JP, Putty B, Frey DJ, Woltering E, Anthony L, Daly I, et al. Surgical treatment of advanced-stage carcinoid tumors: lessons learned. Ann Surg. Jun 2005;241(6):839-45; discussion 845-6. [Medline].
Chen F, O'Dorisio MS, Hermann G, Hayes J, Malarkey WB, O'Dorisio TM. Mechanisms of action of long-acting analogs of somatostatin. Regul Pept. Apr 8 1993;44(3):285-95. [Medline].
Eriksson B, Orlefors H, Sundin A, Skogseid B, Langstrom B, Bergstrom M, et al. Positron emission tomography in neuroendocrine tumours. Ital J Gastroenterol Hepatol. Oct 1999;31 Suppl 2:S167-71. [Medline].
Godwin JD 2nd. Carcinoid tumors. An analysis of 2,837 cases. Cancer. Aug 1975;36(2):560-9. [Medline].
Gorden P, Comi RJ, Maton PN, Go VL. NIH conference. Somatostatin and somatostatin analogue (SMS 201-995) in treatment of hormone-secreting tumors of the pituitary and gastrointestinal tract and non-neoplastic diseases of the gut. Ann Intern Med. Jan 1 1989;110(1):35-50. [Medline].
Hajarizadeh H, Ivancev K, Mueller CR, Fletcher WS, Woltering EA. Effective palliative treatment of metastatic carcinoid tumors with intra-arterial chemotherapy/chemoembolization combined with octreotide acetate. Am J Surg. May 1992;163(5):479-83. [Medline].
Hofland LJ, van Hagen PM, Lamberts SW. Functional role of somatostatin receptors in neuroendocrine and immune cells. Ann Med. Oct 1999;31 Suppl 2:23-7. [Medline].
Hou W, Schubert ML. Treatment of gastric carcinoids. Curr Treat Options Gastroenterol. Mar 2007;10(2):123-33. [Medline].
Krenning EP, de Jong M, Kooij PP, Breeman WA, Bakker WH, de Herder WW, et al. Radiolabelled somatostatin analogue(s) for peptide receptor scintigraphy and radionuclide therapy. Ann Oncol. 1999;10 Suppl 2:S23-9. [Medline].
Kulke MH, Mayer RJ. Carcinoid tumors. N Engl J Med. Mar 18 1999;340(11):858-68. [Medline].
Neuroendocrine Carcinoma. In: Kantarjian H, Wolff R, Koller C, eds. M D Anderson Manual of Medical Oncology. New York: McGraw-Hill; 2006:449-459.
Maroun J, Kocha W, Kvols L, Bjarnason G, Chen E, Germond C, et al. Guidelines for the diagnosis and management of carcinoid tumours. Part 1: The gastrointestinal tract. A statement from a Canadian National Carcinoid Expert Group. Curr Oncol. Apr 2006;13(2):67-76. [Medline].
McCarthy KE, Woltering EA, Espenan GD, Cronin M, Maloney TJ, Anthony LB. In situ radiotherapy with 111In-pentetreotide: initial observations and future directions. Cancer J Sci Am. Mar-Apr 1998;4(2):94-102. [Medline].
Modlin IM, Lye KD, Kidd M. A 5-decade analysis of 13,715 carcinoid tumors. Cancer. Feb 15 2003;97(4):934-59. [Medline].
Modlin IM, Sandor A. An analysis of 8305 cases of carcinoid tumors. Cancer. Feb 15 1997;79(4):813-29. [Medline].
Moertel CG, Johnson CM, McKusick MA, Martin JK Jr, Nagorney DM, Kvols LK, et al. The management of patients with advanced carcinoid tumors and islet cell carcinomas. Ann Intern Med. Feb 15 1994;120(4):302-9. [Medline].
Moertel CG, Kvols LK, O'Connell MJ, Rubin J. Treatment of neuroendocrine carcinomas with combined etoposide and cisplatin. Evidence of major therapeutic activity in the anaplastic variants of these neoplasms. Cancer. Jul 15 1991;68(2):227-32. [Medline].
Oberg K. Established clinical use of octreotide and lanreotide in oncology. Chemotherapy. 2001;47 Suppl 2:40-53. [Medline].
Oberg K. Interferon in the management of neuroendocrine GEP-tumors: a review. Digestion. 2000;62 Suppl 1:92-7. [Medline].
Oberg K, Stridsberg M. Chromogranins as diagnostic and prognostic markers in neuroendocrine tumours. Adv Exp Med Biol. 2000;482:329-37. [Medline].
Perry RR, Vinik AI. Endocrine tumors of the gastrointestinal tract. Annu Rev Med. 1996;47:57-68. [Medline].
Rubin J, Ajani J, Schirmer W, Venook AP, Bukowski R, Pommier R, et al. Octreotide acetate long-acting formulation versus open-label subcutaneous octreotide acetate in malignant carcinoid syndrome. J Clin Oncol. Feb 1999;17(2):600-6. [Medline].
Szilvas A, Szekely G, Szilvasi I, Sagi S, Jakab F. The importance of follow-up examinations in patients with carcinoid tumor. Hepatogastroenterology. Sep-Oct 2003;50(53):1452-3. [Medline].
Vikman S, Essand M, Cunningham JL, de la Torre M, Oberg K, Totterman TH, et al. Gene expression in midgut carcinoid tumors: potential targets for immunotherapy. Acta Oncol. 2005;44(1):32-40. [Medline].
Öberg K. Carcinoid Tumors: Current Concepts in Diagnosis and Treatment. Oncologist. 1998;3(5):339-345. [Medline].
Further Reading
Keywords
intestinal carcinoid tumor, intestinal carcinoid tumour, gastroenteropancreatic neoplasm, GEP, GEP neoplasm, well-differentiated gastrointestinal neuroendocrine cancer, GI neuroendocrine tumor, neuroendocrine tumor, neuroendocrine tumour, argentaffinoma, carcinoid syndrome, small bowel malignancy, irritable bowel syndrome, IBS, idiopathic flushing, intestinal tumor, intestinal tumour, GI tumor, GI tumour, gastrointestinal tumor, gastrointestinal tumour, intestinal malignancy, appendectomy, cancer of the appendix, carcinoid tumor of the appendix, carcinoid tumor of the small intestine, distal small bowel malignancy
Differential Diagnoses & Workup: Carcinoid Tumor, Intestinal