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Grade 3 Neuroendocrine Tumor (G3 NET) in a Background of Multiple Serotonin Cell Neoplasms of the Ileum Associated with Carcinoid Syndrome and Aggressive Behavior
Authors:Francesca Capuano  Oneda Grami  Luigi Pugliese  Marco Paulli  Andrea Pietrabissa  Enrico Solcia  Alessandro Vanoli
Affiliation:1.Anatomic Pathology Unit, Department of Molecular Medicine,University of Pavia and Fondazione IRCCS Policlinico San Matteo,Pavia,Italia;2.Unit of General Surgery 2, Department of Clinical-Surgical, Diagnostic and Pediatric Sciences,University of Pavia and Fondazione IRCCS Policlinico San Matteo,Pavia,Italy
Abstract:
Grade 3 well-differentiated neuroendocrine tumors (G3 NETs) have been characterized in the pancreas and stomach and distinguished from low-to-intermediate grade (G1–G2) NETs, as well as from highly malignant, poorly differentiated neuroendocrine carcinomas (NECs). Up to now, no G3 NET has been thoroughly described in the distal small intestine. We herein report a case of a 61-year-old man presenting with carcinoid syndrome. The surgical specimen showed, in a background of small G1 ileal NETs, a larger, grade 3 NET, which retained the nesting pattern and the expression of serotonin, chromogranin-A, and type 2A somatostatin receptors, typical of well-differentiated jejuno-ileal NETs. The patient had G3 NET metastasis to the liver and he died 14 months after surgery, due to deterioration in his clinical conditions.
Keywords:
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