Alveolar soft-part sarcoma of the masseter and mandibular ramus: Report of a case and review of the literature.

Alveolar soft-part sarcomas are clinically and morphologically distinct soft-tissue sarcomas, with an unknown histogenesis. When the tumors affect the region of the head and neck, they are often located in the orbit and tongue. We report a case of an alveolar soft-part sarcoma in the left masseter of a 28-year-old female. The patient had chronic pain and paresthesia of her left lower lip. Panoramic radiography and computed tomography showed a well-delimited radiolucent mass in the left ramus. An incisional biopsy was performed, and the sample submitted for histopathological study. The tumor showed positive periodic acid-Schiff diastase-resistant granules. Immunohistochemically, the tumor cells were diffusely positive for myoglobin, and focally positive for actin and desmin.

Prevalence of oral mucosal lesions in an elderly population in the city of Valparaiso, Chile.

OBJECTIVE: Chilean population is ageing, which means an increase in the prevalence of multiple pathologies, including those located in the oral cavity. AIM: To measure the prevalence and distribution of oral mucosal lesions and to identify associated risk factors in elderly patients in the city of Valparaiso. MATERIAL AND METHODS: This study includes 126 patients over 60 years. The sample was calculated with a sampling error of 3.7% from a population size of 6000 file cards. Frequency and contingency tables were made together with odds ratios, with a confidence interval of 95%. Finally, we built a predictive model based on a binary logistic regression. RESULTS: From the whole sample, 85 patients (67.5%) had some oral mucosal lesion. The most frequent lesions were denture-induced stomatitis (37.1%). It was noted that there is a statistically significant association between the use of denture and the presence of oral candidiasis. The consumption of drugs and the use of denture increase the likelihood of having oral mucosal lesions. CONCLUSION: There is a high prevalence of oral lesions in the elderly patients of Valparaiso. The use of drugs and /or denture increases significantly the likelihood that a person over 60 years presents lesions in the oral mucosa.

Solitary intraosseous neurofibroma of the mandible. Apropos of a case

Neurofibroma is a benign neoplasm derived from peripheral nerves. Most of these are associated with Neurofibromatosisbut may also occur as solitary lesions. When found on the head and neck they are generally located inthe soft tissue. Intraosseous location is very rare.The following report describes a case of an intraosseous neurofibroma located in the left mandibular ramus of a14-year-old child. The patient did not had clinical evidence of the lesion and it was found on a routine radiographicexamination. Surgical excision of the lesion was scheduled and the sample was submitted to histopathologicalstudy. Representative sample cuts were studied using conventional techniques of hematoxylin-eosin and immunohistochemistryusing primary antibodies anti S-100 protein, vimentin, and neuroespecific enolase.A review of clinical, radiographic, histologic and immunohistochemical features of other cases of intraosseuosneurofibromas located in the jaws together with the possible differential diagnosis of the lesion are discussed.Our case corresponds to a intraosseous neurofibroma of controveltial diagnosis because even though it presentstypical neurofibroma histomorphological features it has immunophenotype different from usual (AU)

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Solitary intraosseous neurofibroma of the mandible. Apropos of a case.

Neurofibroma is a benign neoplasm derived from peripheral nerves. Most of these are associated with Neurofibromatosis but may also occur as solitary lesions. When found on the head and neck they are generally located in the soft tissue. Intraosseous location is very rare. The following report describes a case of an intraosseous neurofibroma located in the left mandibular ramus of a 14-year-old child. The patient did not had clinical evidence of the lesion and it was found on a routine radiographic examination. Surgical excision of the lesion was scheduled and the sample was submitted to histopathological study. Representative sample cuts were studied using conventional techniques of hematoxylin-eosin and immunohistochemistry using primary antibodies anti S-100 protein, vimentin, and neuroespecific enolase. A review of clinical, radiographic, histologic and immunohistochemical features of other cases of intraosseuos neurofibromas located in the jaws together with the possible differential diagnosis of the lesion are discussed. Our case corresponds to a intraosseous neurofibroma of controveltial diagnosis because even though it presents typical neurofibroma histomorphological features it has immunophenotype different from usual.