Ileal Neuroendocrine Tumor in a Patient with Sclerosing Mesenteritis: Which Came First?
Adult
Male
Panniculitis
Settore MED/18 - CHIRURGIA GENERALE
610
Articles
Fibrosis
Panniculitis, Peritoneal
3. Good health
Pancreatic Neoplasms
Neuroendocrine Tumors
03 medical and health sciences
0302 clinical medicine
Peritoneal
Intestinal Neoplasms
Humans
Mesentery
Gastrointestinal Neoplasms
DOI:
10.12659/ajcr.931372
Publication Date:
2021-05-07T14:13:39Z
AUTHORS (11)
ABSTRACT
BACKGROUND Jejunoileal neuroendocrine tumors (JI-NETs) are rare tumors that can be associated with mesenteric fibrosis. This case report is of an incidental finding of a JI-NET in a patient who was previously misdiagnosed with sclerosing mesenteritis. CASE REPORT A 42-year-old man was admitted to our institution with diffuse abdominal pain and clinical and radiographic signs of bowel obstruction. He had a previous diagnosis of sclerosing mesenteritis, which had been histologically diagnosed after an exploratory laparoscopy performed in 2009 for recurrent acute abdominal pain. He was also annually monitored through computed tomography scans for an incidentally discovered, gradually enlarging mesenteric mass for which a "wait and watch" management approach was adopted. After a period of fasting and observation, the patient underwent an urgent exploratory laparotomy because of his worsening condition. Intraoperatively, an ileocecal resection was performed, along with excision of the known mesenteric mass. The pathology report revealed an ileal NET with nodal metastases within the mesentery and mesenteric tumor deposits (pT3N1). CONCLUSIONS JI-NETs are rare entities, which are usually encountered as incidental findings or in patients with unspecific abdominal pain. Our case represents a probable delayed diagnosis of JI-NET in the context of sclerosing mesenteritis; therefore, a possible association between these 2 conditions should be investigated.
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