Nasal Cavity: Paranasal Sinuses
Diagnosis | Findings | Comments |
Congenital absence | Absence of frontal sinuses in 5% of population. | |
Cretinism | Delayed/decreased pneumatisation of sinuses. | |
Down syndrome | Absent frontal sinuses in 90%. | |
Kartegener syndrome | Absent frontal sinuses. | |
Fibrous dysplasia | Due to overgrowth of bony wall. | |
Hemolytic anemia Fig. 4.139, p. 382 | Overgrowth of bony wall. | |
Postsurgery | Post Caldwell Luc operation. |
Diagnosis | Findings | Comments |
Sinusitis—acute and chronic | Radiograph/CT/MRI: homogeneous opacification, mucosal swelling or air-fluid levels. May see bony sclerosis or destruction if chronic. | CT important to assess for anatomic variations prior to functional endoscopic sinus surgery. Use low-dose coronal scans. Also useful to look for complications. |
Trauma | Radiograph: soft-tissue swelling, maxillary sinus opacification, ± air-fluid level. CT: axial and coronal planes to visualize fracture. | |
Polyp/retention cyst | Radiograph: Opacification of single maxillary antrum. Soft-tissue mass in anterior nasopharyx on lateral view. CT: homogeneous soft-tissue masses with smooth margins, outlined by air (e.g., mucocoele). | Sequelae of sinonasal inflammation. |
Tooth bud | Radiograph: usually caused by projection and overlap. CT: shows true ectopic tooth bud within maxillary sinus. | |
Osteoma | Radiograph/CT: well-defined bony density. Mainly in frontal sinuses; rarely ethmoid and maxillary. | Assess for Gardner syndrome. |
Mucocoele | CT/MRI: appearance varies with water and mucoid content. Shows peripheral enhancement, distinguishing it from neoplasm. Exhibits mass effect on adjacent structures and often expands into orbit. | Due to obstruction of sinus ostium. Most commonly frontal and ethmoid sinuses. |
Primary malignancy | CT/MRI: MRI preferred due to superior soft-tissue contrast and to show intracranial extension. Need pre- and postcontrast studies. | Lymphoma, rhabdomyosarcoma, nasopharyngeal carcinoma, malignant histiocytoma. |
Metastases | CT: usually neuroblastoma and is associated with soft-tissue mass. | |
Juvenile angiofibroma | CT: isointense or low-density mass with widening of pterygopalatine fossa and bowing of posterolateral maxillary sinus. Marked CE. MRI: T1 hypointense, T2 hyperintense with flow voids and avid enhancement. Can show cysts, cavitation, and hemorrhage. | Benign, most common in adolescent boys. |
Osteomyelitis | Radiograph/CT: sclerosis and destruction of sinus wall in setting of infection. | Usually frontal sinus. |
Fibrous dysplasia | CT: depends on fibrous vs. osseous component. Varies from radiolucent to ground-glass. Unilocular/multilocular lesion, well-defined margin. MRI: sharply demarcated mass, variable signal intensity, diffuse CE. | |
Ossifying fibroma Fig. 4.114, p. 369 Fig. 4.138, p. 381 | CT/MRI: expansile lesion with prominent areas of nonossified fibrous tissue. Can be lytic, expansile containing calcification, and show cortical erosion. |