ABSTRACT
Idiopathic hypertrohpic cranial pachymeningitis is rare, and is essentially a diagnosis of exclusion. A 53-year-old man presented with headache and visual loss in the right eye, first experienced a month earlier. MR images depicted a mass in the right cavernous sinus. At T1-weighted imaging, both the mass and the thickened dura mater present in both fromted lobes were isointense, while at while T2-weighted imaging, the signal intensity of both the mass and the dura mater was low. After the injection of contrast medium, pachymeningeal enhancement was observed. We report the radiologic findings in a case of idiopathic hypertrophic cranial pachymeningitis, confirmed surgically and pathologically.
Subject(s)
Humans , Middle Aged , Cavernous Sinus , Diagnosis , Dura Mater , Headache , MeningitisABSTRACT
Inflammatory myofibroblastic tumor is a rare benign condition of unknown etiology, and may simulate malignancy. Histologically, it is composed of myofibroblasts, plasma cells and histiocytes, and is found in the lung, liver, orbit, skin, mesentery, retroperitoneum and maxillary sinus. We report a case of postoperative recurrent inflammatory myofibroblastic tumor of the retroperitoneum, occurring in a 45-year old man who complained of a palpable abdominal mass.