Midgut neuroendocrine tumor presenting with acute intestinal ischemia
- PMID: 29259385
- PMCID: PMC5725304
- DOI: 10.3748/wjg.v23.i45.8090
Midgut neuroendocrine tumor presenting with acute intestinal ischemia
Abstract
Neuroendocrine tumors represent a heterogeneous group of neoplasms that arise from neuroendocrine cells and secrete various peptides and bioamines. While gastrointestinal neuroendocrine tumors, commonly called carcinoids, account for about 2/3 of all neuroendocrine tumors, they are relatively rare. Small intestine neuroendocrine tumors originate from intestinal enterochromaffin cells and represent about 1/4 of small intestine neoplasms. They can be asymptomatic or cause nonspecific symptoms, which usually leads to a delayed diagnosis. Imaging modalities can aid diagnosis and surgery remains the mainstay of treatment. We present a case of a jejunal neuroendocrine tumor that caused nonspecific symptoms for about 1 year before manifesting with acute mesenteric ischemia. Abdominal X-rays revealed pneumatosis intestinalis and an abdominal ultrasound and computed tomography confirmed the diagnosis. The patient was submitted to segmental enterectomy. Histopathological study demonstrated a neuroendocrine tumor with perineural and arterial infiltration and lymph node metastasis. The postoperative course was uneventful and the patient denied any adjuvant treatment.
Keywords: Carcinoid; Enterectomy; Enterochromaffin cells; Jejunum; Pneumatosis intestinalis; Small intestine.
Conflict of interest statement
Conflict-of-interest statement: No conflict of interest.
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