Endoscopy 2025; 57(S 02): S359
DOI: 10.1055/s-0045-1805896
Abstracts | ESGE Days 2025
ePosters

Undescribed metastases within a pancreatic neuroendocrine tumour

Authors

  • E Moya-Valverde

    1   Francisco de Vitoria University, Madrid, Spain
    2   Hospital Universitario Príncipe de Asturias, Alcalá de Henares, Spain
  • J Núñez-Otero

    3   Hospital Universitario del Sureste, Arganda del Rey, Spain
    1   Francisco de Vitoria University, Madrid, Spain
  • M Martin-Matas

    3   Hospital Universitario del Sureste, Arganda del Rey, Spain
  • A Díaz-Sánchez

    3   Hospital Universitario del Sureste, Arganda del Rey, Spain
    1   Francisco de Vitoria University, Madrid, Spain
  • M Muñiz-Muñoz

    3   Hospital Universitario del Sureste, Arganda del Rey, Spain
    1   Francisco de Vitoria University, Madrid, Spain
  • L Diéguez-Montes

    3   Hospital Universitario del Sureste, Arganda del Rey, Spain
    1   Francisco de Vitoria University, Madrid, Spain
  • R Manzano-Fernández

    3   Hospital Universitario del Sureste, Arganda del Rey, Spain
    1   Francisco de Vitoria University, Madrid, Spain
  • A I González-Tallón

    3   Hospital Universitario del Sureste, Arganda del Rey, Spain
    1   Francisco de Vitoria University, Madrid, Spain
  • M Rivero-Fernández

    3   Hospital Universitario del Sureste, Arganda del Rey, Spain
    1   Francisco de Vitoria University, Madrid, Spain
    4   Rey Juan Carlos University Campus of Madrid, Madrid, Spain
 

63-year-old male hospitalised due to jaundice. CT scan showed a mass in the pancreatic body and tail with vascular damage and amputation of the common bile duct. Retroperitoneal lymph nodes of pathological appearance and a 20 mm subcutaneous nodule compatible with metastasis were also described. There were no liver metastases [1].

Ultrasound-guided core needle biopsy of the subcutaneous nodule and endoscopic ultrasonography-guided fine needle aspiration of the pancreatic mass showed a high-grade neuroendocrine tumour positive for synaptophysin, CD56, chromogranin and CK19 in both cases. The hormonal study was normal, so it was a nonfunctional neuroendocrine tumour.

The patient also reported odynophagia, identifying in the exploration a mass in the right palatine tonsil with a malignant appearance. The histological study revealed a high-grade neuroendocrine tumour with the same immunohistochemical characteristics as the other two samples (positive for synaptophysin, CD56, chromogranin and CK19). Therefore, it was a tonsillar metastasis of a non-functioning pancreatic neuroendocrine tumour.

We have not found any reports on a pancreatic neuroendocrine tumour with tonsillar metastasis (a previously undescribed location of metastasis), or primary neuroendocrine tumours of the tonsil making this an exceptional case.



Publikationsverlauf

Artikel online veröffentlicht:
27. März 2025

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