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World J Surg Oncol ; 12: 129, 2014 Apr 28.
Article in English | MEDLINE | ID: mdl-24773769

ABSTRACT

BACKGROUND: Malignant mesothelioma is a rare neoplasm that generally develops in the pleural or peritoneal cavity. Distant metastases are common; it rarely metastatizes to the head and neck region. CASE PRESENTATION: A 54-year-old white man, a non-smoker, was treated with chemotherapy, surgery and radiation for a malignant pleural mesothelioma. Seven months after the last treatment, he developed a right submandibular enlargement: clinical examination, ultrasound and computerized tomography scans revealed a salivary gland hypertrophy. Anti-inflammatory and antibiotic treatment was then started, without improvement. An ultrasound (US)-guided fine-needle aspiration biopsy (FNAB) showed atypical mesothelial cells with nuclear enlargement and increased chromatin representation. Immunocytochemistry showed positivity for calretinin and WT-1.A diagnosis of right submandibular salivary gland involvement from mesothelioma was established, allowing an adequate treatment. CONCLUSION: We report a very rare site of metastasis from malignant pleural mesothelioma. We suggest that US-guided FNAB is a useful, quick, and cheap procedure for a definite diagnosis.


Subject(s)
Lung Neoplasms/pathology , Mesothelioma/pathology , Pleural Neoplasms/pathology , Submandibular Gland Neoplasms/secondary , Humans , Hypertrophy , Lung Neoplasms/therapy , Male , Mesothelioma/therapy , Mesothelioma, Malignant , Middle Aged , Pleural Neoplasms/therapy , Prognosis , Submandibular Gland Neoplasms/therapy
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