Mesenteric desmoid tumor in its cystic form: Case report of a very rare variant

Desmoid tumors, also known as deep fibromatosis or desmoid-type fibromatosis, represent a rare subset of deep fibromatoses. It is a locally aggressive tumor, with no specific symptoms, and no metastatic potential. We report a case of a 38-year-old male patient with an abdominal mass. Radiological fi...

Full description

Saved in:
Bibliographic Details
Main Authors: Nourrelhouda Bahlouli, Kaouthar Imrani, Esseti Sara, Fatima Chait, Faraj Chaimae, Moatassimbillah Nabil, Ittimad Nassar, Sassi Samia, Derqaoui Sabrine, Bernoussi Zakia, Babana Alaoui Amina, Touhami Ouazzani Youssef, Lahjomri Ismail, Hadj Omar El Malki, Ifrine Lahcen, Belkouchi Abdelkader, Belkouchi Omar
Format: Article
Language:English
Published: Elsevier 2025-02-01
Series:Radiology Case Reports
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S1930043324012081
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Desmoid tumors, also known as deep fibromatosis or desmoid-type fibromatosis, represent a rare subset of deep fibromatoses. It is a locally aggressive tumor, with no specific symptoms, and no metastatic potential. We report a case of a 38-year-old male patient with an abdominal mass. Radiological findings showed 2 tumors, the first was a solid inguinal mass of the left lateral iliac pedicle, and the second was a giant cystic mass in the abdominal cavity. An elective explorative laparotomy was performed to remove the 2 masses. Histopathological examination confirmed the desmoid tumor diagnosis of both lesions.
ISSN:1930-0433