| Literature DB >> 15052458 |
Tsutomu Takashima1, Naoyoshi Onoda, Tetsuro Ishikawa, Tsuyoshi Koyama, Masaaki Inaba, Yoshiki Nishizawa, Tatsuya Nakatani, Kenichi Wakasa, Kosei Hirakawa.
Abstract
Idiopathic retroperitoneal fibrosis (IRF) is characterized by the progressive proliferation of connective tissue, but it rarely results in the formation of a mass. Herein, we report a rare case of tumor-forming IRF. A 76-year-old woman was referred to our hospital after a tumor in the right retroperitoneum was found by ultrasonography and computed tomography. Magnetic resonance imaging showed a 5 x 8 x 5-cm irregularly shaped tumor, lying adjacent to the right kidney, with a high-intensity T1-weighted image and a high-intensity T2-weighted image. Hormonal levels were within normal limits. Surgery was performed because of the possibility of an adrenal cancer. The tumor was firm, measured 7 x 8 x 4 cm, and weighed 115 g. The pathological diagnosis was retroperitoneal fibrosis. It is very difficult to distinguish tumor-forming IRF from malignancy. Several examinations, including needle aspiration cytology and biopsy, are necessary for the diagnosis and treatment of this disease.Entities:
Mesh:
Year: 2004 PMID: 15052458 DOI: 10.1007/s00595-003-2695-z
Source DB: PubMed Journal: Surg Today ISSN: 0941-1291 Impact factor: 2.549