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1.
Ear Nose Throat J ; 100(10): NP432-NP437, 2021 Dec.
Article in English | MEDLINE | ID: mdl-32453644

ABSTRACT

OBJECTIVES: The aim of this study was to analyze the risk of malignancy in salivary gland tumors on the basis of the Milan System for Reporting Salivary Gland Cytopathology. METHODS: A retrospective review was performed of the charts of patients with salivary gland tumors in whom the final diagnosis was confirmed by surgical excision. Preoperative fine needle aspiration results were categorized according to the Milan System for Reporting Salivary Gland Cytopathology: non-diagnostic (category I), nonneoplastic (category II), atypia of undetermined significance (category III), neoplasm (category IV), suspicious for malignancy (category V), and malignant (category VI). Fine needle aspiration and final diagnosis were compared, and the risk of malignancy and operative/oncological outcomes were analyzed. RESULTS: A total of 288 patients were enrolled in this study. Postoperative histopathologic salivary gland malignancies were found in 30 (10.4%) patients. Risk of malignancy was 7.1%, 0%, 48.0%, 4.8%, 88.7%, and 100% in categories I, II, III, IV, V, and VI, respectively. The most common malignant tumor in category III was salivary duct carcinoma (37.5%), followed by acinic cell carcinoma (25.0%), mucoepidermoid carcinoma (25.0%), and squamous cell carcinoma (12.5%). The 5-year survival rate of patients with malignant tumors showed no statistical difference between category III and category V/VI (P = .140). Risk of malignancy was 88.9% and 100% in category V and VI, respectively. CONCLUSIONS: A half of atypia of undetermined significance (category III) cases were malignant. Once diagnosed, the prognosis of malignant tumor in category III was similar with that in category V/VI.


Subject(s)
Carcinoma/pathology , Salivary Gland Diseases/pathology , Salivary Gland Neoplasms/pathology , Salivary Glands/pathology , Adult , Aged , Biopsy, Fine-Needle , Carcinoma/epidemiology , Diagnosis, Differential , Female , Humans , Incidence , Male , Middle Aged , Retrospective Studies , Risk , Salivary Gland Diseases/mortality , Salivary Gland Diseases/surgery , Salivary Gland Neoplasms/mortality , Salivary Gland Neoplasms/surgery , Survival Rate
2.
Otolaryngol Clin North Am ; 48(1): 153-73, 2015 Feb.
Article in English | MEDLINE | ID: mdl-25439553

ABSTRACT

Salivary gland neoplasms are rare in children. In infants most tumors are benign hemangiomas, with some notable exceptions, such as sialoblastomas. An asymptomatic swelling in the periauricular region is the most common presenting complaint in older children. Approximately 50% of these lesions are malignant, which dictates a thorough diagnostic evaluation by a head and neck surgeon. Surgical excision is the primary treatment modality. Prognosis is primarily determined by histopathologic findings. This review discusses neoplastic lesions of the salivary glands in children, and malignant epithelial tumors in particular.


Subject(s)
Diagnostic Imaging/methods , Head and Neck Neoplasms/pathology , Head and Neck Neoplasms/surgery , Salivary Gland Neoplasms/pathology , Salivary Gland Neoplasms/surgery , Biopsy, Needle , Child , Child, Preschool , Female , Follow-Up Studies , Head and Neck Neoplasms/mortality , Hemangioma/mortality , Hemangioma/pathology , Hemangioma/surgery , Humans , Immunohistochemistry , Infant , Magnetic Resonance Imaging/methods , Male , Otorhinolaryngologic Surgical Procedures/methods , Parotid Neoplasms/mortality , Parotid Neoplasms/pathology , Parotid Neoplasms/surgery , Rare Diseases , Risk Assessment , Salivary Gland Diseases/mortality , Salivary Gland Diseases/pathology , Salivary Gland Diseases/surgery , Salivary Gland Neoplasms/mortality , Survival Rate , Tomography, X-Ray Computed/methods , Treatment Outcome , Ultrasonography, Doppler/methods
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