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International Journal of Advances In Case Reports

Volume 11, Issue 1, 2024
Mcmed International
International Journal of Advances In Case Reports
Issn
XXX-XXXX (Print), 2349 - 8005 (Online)
Frequency
bi-annual
Email
editorijacr@mcmed.us
Journal Home page
http://mcmed.us/about/ijacr
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Abstract
Title
A VERY RARE TUMOR IN A RENAL TRANSPLANT DONOR CANDIDATE: PRIMARY MESENTERIC NEUROENDOCRINE TUMOR
Author
Ayse Sinangil*¹, Vedat Celik¹, Soykan Barlas², Fatmagul Kusku Cabuk3, Emin Baris Akin2, Tevfik Ecder1
Email
aysesinangil@gmail.com
keyword
Neuroendocrine tumors, Mesentery, Neoplasms.
Abstract
Neuroendocrine tumors arise from neuroendocrine system cells, and constitute a heterogeneous group of neoplasms. Usually these tumors cause no symptoms and are diagnosed during several screenings incidentally. In this case; a renal transplantation donor candidate, who had no complaints of any illnesses, was diagnosed with a rare primary mesenchymal neuroendocrine tumor based on the calcified mass found in the examinations. A computed abdominal tomography angiography was carried out in order to view the kidney arteries of the donor candidate. We determined a mass at the small curvature of the stomach, a large part of which had calcifications. The mass was found between the mesenteric fat planes and it caused a thrust in the small curvature of the stomach in cardioesophageal junction. The tumor was resected surgically. The pathological diagnosis was considered as a low-grade, secondary, degenerative neuroendocrine tumor. This case demonstrates the importance of rigorous screening of renal transplant donor candidates renal transplant donor candidates should be screened rigorously. In case report a very rare primary mesenteric neuroendocrine tumor, which was detected incidentally during the screenings, is presented in the light of existing literature.
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