Mesenteric fibromatosis is currently a diagnostic and therapeutic challenge. We report a case of mesenteric fibromatosis in a 29-year-old man with a 2-month history of periumbilical fullness who was discovered to have an abdominal mass with hydronephrosis. To the best of our knowledge, we report the first case of hydronephrosis in a mesenteric fibromatosis with Gardner's syndrome, which was successfully treated with a cyclo-oxygenase 2 inhibitor without surgical removal of the mesenteric fibromatosis. The hydronephrosis and mesenteric fibromatosis improved modestly with long-term celecoxib (200 mg twice daily). Our case also highlights the importance of performing a detailed examination in patients with hydronephrosis.

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.urology.2007.07.025DOI Listing

Publication Analysis

Top Keywords

mesenteric fibromatosis
24
report case
8
hydronephrosis mesenteric
8
mesenteric
6
fibromatosis
6
resolution hydronephrosis
4
hydronephrosis massive
4
massive mesenteric
4
fibromatosis cyclo-oxygenase
4
cyclo-oxygenase inhibitors
4

Similar Publications

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

Radiol Case Rep

February 2025

Department of Surgery « A », Ibn Sina Hospital, Mohammed V University, Faculty of Medicine and Pharmacy, Rabat, Morocco.

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.

View Article and Find Full Text PDF

Desmoid tumors or aggressive fibromatosis are locally aggressive benign tumors. These arise anywhere in the body but are commonly seen in the anterior abdominal wall. The main treatment choices are continuous surveillance, adjuvant chemotherapy, surgery, and postoperative chemotherapy.

View Article and Find Full Text PDF

Purpose: Three prospective observational studies (Italy, the Netherlands, France) on active surveillance (AS) in patients with extra-abdominal desmoid-type fibromatosis (DTF) support AS as a frontline approach. Identifying prognostic factors for the failure of AS will help determine the strategy. The aim of this study was to investigate the prognostic impact of clinical and molecular variables in a larger series.

View Article and Find Full Text PDF

Enamel Renal Syndrome: A Case Report.

Cureus

October 2024

Oral and Maxillofacial Pathology, Microbiology and Forensic Odontology, Goa Dental College and Hospital, Panjim, IND.

Article Synopsis
  • - Amelogenesis imperfecta is a genetic disorder that affects the enamel of teeth, which can lead to problems in both baby and adult teeth, sometimes linked with other health issues.
  • - A rare condition called enamel renal syndrome occurs when amelogenesis imperfecta is found alongside kidney stones, which complicates diagnosis due to unclear criteria.
  • - The case of a 12-year-old boy with tooth discoloration and kidney stones highlights the importance of thorough medical evaluations to avoid serious complications from these conditions.
View Article and Find Full Text PDF

Desmoid fibromatosis (DF) is defined as a borderline tumor of the soft tissues with a low malignant potential. The most common tumor sites are the extremity, trunk, abdominal cavity, and head and neck. Surgical resection has been the standard treatment for DF.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!