| Literature DB >> 25057422 |
Alexandre Simões Garcia1, Diego Maurício Bravo-Calderón1, Mariana Pisinato Ferreira1, Denise Tostes Oliveira1.
Abstract
Inverted Schneiderian papilloma is an uncommon benign tumor that presents tendency to recur and propensity to be associated with malignancy in approximately 10% of the cases. Some of these lesions are isolated in the maxillary sinus, and predominantly affect white males with mean age of 50 years. We report a case of squamous cell carcinoma arising from inverted Schneiderian papilloma in the maxillary sinus extending to the mouth. The patient was submitted to extraction of a maxillary molar tooth four months before the exacerbation of the symptoms of nasal airway obstruction and facial enlargement. Computed tomography scan revealed a sinonasal mass causing opacification of the right maxillary sinus with destruction of the lateral nasal wall and maxillary sinus floor. The patient was referred to an oncology center for treatment and died from tumor progression one year after the cancer was diagnosed. The intention of this report is to alert dentists to include the inverted Schneiderian papilloma, either associated with squamous cell carcinoma, or not, in the differential diagnosis of maxillary sinus tumors with aggressive behavior, which may extend to the oral cavity or involve roots of teeth.Entities:
Year: 2014 PMID: 25057422 PMCID: PMC4095724 DOI: 10.1155/2014/478092
Source DB: PubMed Journal: Case Rep Otolaryngol ISSN: 2090-6773
Figure 1Cone beam computed tomography scan showing a sinonasal mass causing opacification of the right maxillary sinus with erosion of the orbital floor, lateral nasal wall, and maxillary sinus floor.
Figure 2Typical histopathological features of the inverted Schneiderian papilloma showing endophytic growth of pseudostratified ciliated epithelium forming cystic spaces (H.E—25x).
Figure 3Pseudostratified ciliated epithelium of the Schneiderian mucosa with dysplastic areas (H.E—200x).
Figure 4Invasive squamous cell carcinoma showing intense pleomorphism, atypical mitosis, and focal necrosis (H.E—100x).