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Malignant pleural mesothelioma metastatic to the submandibular salivary gland, simulating glandular hypertrophy, diagnosed by fine-needle aspiration biopsy: a case report and literature review.

AbstractBACKGROUND:
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.
AuthorsMassimo Ambroggi, Elena Orlandi, Raoul P Foroni, Luigi Cavanna
JournalWorld journal of surgical oncology (World J Surg Oncol) Vol. 12 Pg. 129 (Apr 28 2014) ISSN: 1477-7819 [Electronic] England
PMID24773769 (Publication Type: Case Reports, Journal Article, Review)
Topics
  • Humans
  • Hypertrophy
  • Lung Neoplasms (pathology, therapy)
  • Male
  • Mesothelioma (pathology, therapy)
  • Mesothelioma, Malignant
  • Middle Aged
  • Pleural Neoplasms (pathology, therapy)
  • Prognosis
  • Submandibular Gland Neoplasms (secondary, therapy)

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