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A Neuroendocrine Tumor of Unknown Primary Origin: A Case Report and Review of the Literature.
Patresan, John; Patel, Harsh; Singh, Angelica.
Affiliation
  • Patresan J; Department of Internal Medicine, New York-Presbyterian Brooklyn Methodist Hospital, Brooklyn, USA.
  • Patel H; Department of Internal Medicine, New York-Presbyterian Brooklyn Methodist Hospital, Brooklyn, USA.
  • Singh A; Department of Hematology and Oncology, New York-Presbyterian Brooklyn Methodist Hospital, Brooklyn, USA.
Cureus ; 16(7): e65200, 2024 Jul.
Article in En | MEDLINE | ID: mdl-39176372
ABSTRACT
Neuroendocrine tumors (NETs) are uncommon malignancies that develop from neuroendocrine cells which most commonly occur in the GI tract, lung, and pancreas. Treatment courses for these tumors are largely dictated by the primary origin site, which can present diagnostic and therapeutic challenges in NETs of unknown primary origin. Herein, we present a case of an NET of unknown primary origin with significant liver metastases. Our aim is to highlight the key components of the workup of NETs of unknown primary origin and detail the biochemical, histopathological, and imaging modalities as recommended by current literature. We highlight the importance of a multidisciplinary approach to both diagnosis and treatment of these patients as well as touch upon therapeutic options.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Cureus Year: 2024 Document type: Article Affiliation country: United States Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Cureus Year: 2024 Document type: Article Affiliation country: United States Country of publication: United States