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Paragangliomas, also known as glomus tumors or chemodectomas, are tumors arising from chemoreceptor tissue (paraganglia), which are neural crest in origin and found in higher concentration along the glossopharyngeal and vagal cranial nerve. Three types of paragangliomas are related with the temporal bone: glomus tympanicum, glomus jugulare, and glomus vagale. The role of computed tomography (CT) and magnetic resonance imaging (MRI) in diagnosing these types of tumors is discussed, along with the importance of arteriography in aiding the diagnosis and treatment. This article discusses the choice between CT and MR based on clinical symptoms and tumor location, and illustrates the newest CT, MR, and angiography applications. A brief discussion on treatment options is given.

In a retrospective study of 14 cases of duodenal neoplasms evaluated by computed tomography (CT), there were four primary adenocarcinomas of the duodenum, one lymphoma, five metastatic carcinomas, two duodenal lipomas, one villous adenoma, and one leiomyoma. The CT findings were diagnostic in patients with duodenal lipomas. In 11 cases, a primary origin of the mass was clearly identifiable in the duodenum. Thickening of the bowel wall, tumor necrosis, ulceration, and intraluminal defects were common. The relationship of the masses to adjacent structures was clearly shown on CT scans. Extraluminal extent of the lesion was noted on CT scans in seven patients; however, at surgery only four of six were found to have extramural disease. The presence of adenopathy, liver metastases, and vascular and mesenteric invasion were also demonstrated on CT scans. Twelve patients underwent upper gastrointestinal tract series. A duodenal abnormality was seen in all 12 patients, but the extramural extent and distant metastatic involvement could not be seen on these examinations. CT scans allowed the accurate staging of eight of ten malignant lesions and thus helped in the management of duodenal tumors.

The authors present a variety of common and uncommon extraosseous cystic lesions encountered in the spine. Accurate localization of a detected lesion within the spinal canal, assessment of its imaging features, and understanding its relationship with surrounding structures will help differentiate many of the lesions and aid in the preoperative diagnosis. Congenital spinal and spinal cord malformations referred to as spinal dysraphisms will not be discussed in this article. This pictorial review discusses the imaging findings and distinguishing features of a variety of intramedullary and extramedullary intraspinal cystic lesions with the use of MR imaging, CT, myelography, and sonography.