Radiology Case Reports (Feb 2025)

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

  • 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

Journal volume & issue
Vol. 20, no. 2
pp. 980 – 988

Abstract

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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.

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