Comparison of simulated cone beam computed tomography to conventional helical computed tomography for imaging of rhinosinusitis

OBJECTIVES/HYPOTHESIS: Cone beam computed tomography (CBCT) has emerged as a low radiation dose alternative to traditional computed tomography (CT) to evaluate the paranasal sinuses. The purpose of our study was to determine how often clinically important findings would be missed if CBCT was used routinely for sinus imaging. STUDY DESIGN: Retrospective review. METHODS: We evaluated all maxillofacial CT scans performed for sinusitis over a 1-year period. The original multidetector CT (MDCT) images were reviewed retrospectively. A theoretical CBCT was then created from the original study utilizing only the bone algorithm images and separately reviewed. We calculated the proportion of abnormal findings that were identified on the MDCT but would have been missed by the theoretical CBCT, and reviewed the medical record to determine which potentially missed findings would have changed management. Radiation dose from the MDCT scanners was calculated and compared to published dose estimates for the paranasal sinuses on CBCT. RESULTS: Maxillofacial CTs from 361 consecutive patients were included, of which 12 (3.3%) demonstrated findings that would have been missed on the theoretical CBCT. Of those, four (1.1%) would have resulted in a change in management. Effective radiation dose for our scanners ranged from 0.67 mSv to 2.15 mSv, compared to a published estimated dose of 0.2 mSV for CBCT. CONCLUSIONS: In the majority of patients undergoing simulated CBCT for evaluation of sinusitis, incidental findings of soft-tissue disease were rare. With appropriate selection of patients, CBCT can offer substantial radiation dose reduction and may provide a viable alternative to standard MDCT sinus imaging protocols

Unusual case of recurrent SMART (stroke-like migraine attacks after radiation therapy) syndrome

Stroke-like migraine attacks after radiation therapy (SMART) syndrome is a rare delayed complication of cerebral radiation therapy. A 53-year-old female initially presented with headache, confusion and left homonymous hemianopia. Her medical history was notable for cerebellar hemangioblastoma, which was treated with radiation in 1987. Her initial brain MRI (magnetic resonance imaging) revealed cortical enhancement in the right temporo-parieto-occipital region. She improved spontaneously in 2 weeks and follow-up scan at 4 weeks revealed no residual enhancement or encephalomalacia. She presented 6 weeks later with aphasia. Her MRI brain revealed similar contrast-enhancing cortical lesion but on the left side. Repeat CSF studies was again negative other than elevated protein. She was treated conservatively and recovered completely within a week. Before diagnosing SMART syndrome, it is important to rule out tumor recurrence, encephalitis, posterior reversible encephalopathy syndrome (PRES) and stroke. Typically the condition is self-limiting, and gradually resolves

Congenital intestinal hypoganglionosis: A radiologic mimic of Hirschsprung's disease

Intestinal hypoganglionosis or isolated hypoganglionosis is a rare entity with a clinical and radiologic presentation that can mimic Hirschsprung's disease in the neonatal period. The diagnosis of this entity can be challenging with suction rectal biopsies that are standard for diagnosing Hirschsprung's disease. We present this case of congenital intestinal hypoganglionosis detailing the neonatal course, due to its rarity and the conundrums faced before an eventual diagnosis could be rendered. This case also illustrates the role of full thickness rectal biopsy in selected cases such as ours where the radiologic features are typical of Hirschsprung's, despite negative suction biopsies. Keywords: Intestinal hypoganglionosis, Hirschsprung's disease, Enteric neuropath