Retroperitoneal mixed neuroendocrine non-neuroendocrine neoplasm: A case report and review of literature
- PMID: 38525086
- PMCID: PMC10958797
- DOI: 10.1177/20363613241242383
Retroperitoneal mixed neuroendocrine non-neuroendocrine neoplasm: A case report and review of literature
Abstract
The existence of both neuroendocrine and non-neuroendocrine histology in variable proportion in a lesion has been described by the World Health Organisation (WHO) as mixed neuroendocrine and non-neuroendocrine neoplasm (MiNEN). The pathogenesis of this tumour remains controversial but molecular studies point towards a common monoclonal origin. Tumours are classified as functioning and nonfunctioning based on substances secreted. The nonfunctioning tumours may be discovered due to its local effect. Presented is a 66-year-old male with an intra-abdominal mass, underwent laparotomy and excision biopsy with transient right lower limb lymphoedema. Histology confirmed retroperitoneal MiNEN with no evidence of tumour recurrence 12 months following surgery. MiNENs should be considered as a differential diagnosis in patients with intra-abdominal mass. Surgical resection is recommended as this may offer the best treatment option.
Keywords: WHO classifications; mixed adenoneuroendocrine carcinoma; mixed neuroendocrine non-neuroendocrine neoplasm; retroperitoneum.
© The Author(s) 2024.
Conflict of interest statement
The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.
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