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A rare cause of calcified abdominopelvic masses

  • Hajar Hamri;
    • Imaging Department, Mohammed V University, Rabat, Morocco
  • Sanae Chaoui;
    • Imaging Department, Mohammed V University, Rabat, Morocco
  • Meriem Menany;
    • Imaging Department, Mohammed V University, Rabat, Morocco
  • Nabil Moatassim Billah;
    • Imaging Department, Mohammed V University, Rabat, Morocco
  • Ittimad Nassar
    • Imaging Department, Mohammed V University, Rabat, Morocco
  • Corresponding Author(s): Hajar Hamri

  • Imaging Department, Ibn Sina Hospital, Faculty of Medicine and Pharmacy, Mohammed V University, Rabat, Morocco

  • hamri.hajar@yahoo.fr

  • Hamri H (2019).

  • This Article is distributed under the terms of Creative Commons Attribution 4.0 International License

Received : Aug 12, 2019
Accepted : Sep 09, 2019
Published Online : Sep 11, 2019
Journal : Journal of Radiology and Medical Imaging
Publisher : MedDocs Publishers LLC
Online edition : http://meddocsonline.org

Cite this article: Hamri H, Chaoui S, Menany M, Billah NM, Nassar I. A rare cause of calcified abdominopelvic masses. J Radiol Med Imaging. 2019; 2(1): 1019.

Clinical Image

      A 78-year-old patient, treated 30 years ago for papillary carcinoma of the thyroid and who consults for constipation and weight loss. The physical examination found multiple abdominopelvic masses solid on palpation, non-movable and painless. The abdominopelvic CT showed multiple intraperitoneal abdominal and pelvic masses, partially calcified and associated with intraperitoneal effusion (Figure 1). The histological diagnosis retained following a CT scan was that of calcified peritoneal metastases of papillary carcinoma of the thyroid gland. Papillary carcinoma of the thyroid gland is a malignant epithelial tumor that is the most common form of thyroid tumors; it is a multicentric carcinoma with essentially lymphophile development. The distant metastases are mainly pulmonary and bone. However, some cases of unusual localization have been reported, often associated with lung and/or bone metastases. A few rare cases of the literature have reported the late discovery, years after tumor resection, of secondary axillary, uveal, and adrenal localizations of papillary carcinoma of the thyroid.

Figure 1: Pre-contrast (a) and post-contrast (b, c) axial CT showed multiple intraperitoneal abdominal and pelvic masses, partially calcified and associated with intraperitoneal effusion.

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