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VIPoma natural history, complications and prognosis

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Associate Editor(s)-in-Chief: Madhu Sigdel M.B.B.S.[2]Parminder Dhingra, M.D. [3] Homa Najafi, M.D.[4]

Overview

Overview

If left untreated, patients with VIPoma may progress to develop watery diarrhea, abdominal pain, bloating, nausea, vomiting, skin rash, backache, flushing, and lethargy. Common complications of VIPoma include metastasis, cardiac arrest from low blood potassium level, and dehydration. The presence of metastasis is associated with a particularly poor prognosis among patients with VIPoma, with a 5 year survival rate of 60%.

Natural History

Natural History

Complications

Complications

Common complications of VIPoma include:[2][3]

Prognosis

Prognosis

References

References

  1. Natanzi, Naveed; Amini, Mazyar; Yamini, David; Nielsen, Shawn; Ram, Ramin (2009). “Vasoactive Intestinal Peptide Tumor”. Scholarly Research Exchange. 2009: 1–7. doi:10.3814/2009/938325. ISSN 1687-8299.
  2. J. V. VERNER & A. B. MORRISON (1958). “Islet cell tumor and a syndrome of refractory watery diarrhea and hypokalemia”. The American journal of medicine. 25 (3): 374–380. doi:10.1016/0002-9343(58)90075-5. PMID 13571250. Unknown parameter |month= ignored (help)
  3. A. Ayub, M. Zafar, A. Abdulkareem, M. A. Ali, T. Lingawi & A. Harbi (1993). “Primary hepatic vipoma”. The American journal of gastroenterology. 88 (6): 958–961. PMID 8389095. Unknown parameter |month= ignored (help)
  4. Nilubol N, Freedman EM, Quezado MM, Patel D, Kebebew E (2016). “Pancreatic Neuroendocrine Tumor Secreting Vasoactive Intestinal Peptide and Dopamine With Pulmonary Emboli: A Case Report”. J Clin Endocrinol Metab. 101 (10): 3564–3567. doi:10.1210/jc.2016-2051. PMC 5052354. PMID 27583474.


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