Oncocytoma of Salivary Gland Origen

  •  Oncocytomas typically occur in older persons and are relatively rare:
    • Its a benign tumor composed of oncocytes:
      • It is also called oxyphilic adenoma
    • Represents 0.1% to 2% of salivary gland neoplasms:
      • They are more frequent than oncocytosis and oncocytic carcinoma:
        • They are classified according to the World Health Organization (WHO) classification, and histologically there are three distinct types:  oncocytosis, oncocytoma and oncocytic carcinoma

           

    • These tumors are characterized by a high mitochondrial content:
      • Which accounts for fluorodeoxyglucose avidity on positron emission tomography scans, similar to Warthin’s tumors. 
  • Clinical Features of Oncocytomas:
    • Usually there are identified in the parotid gland (78% to 84% cases), but the submandibular gland or minor salivary glands can be involved.
      • This tumor might be seen in other organs such as:
        • The nasal and thoracic cavities, ovaries, breast, kidney, thyroid, parathyroid, pituitary, larynx and pancreas
  • They often present as solitary slow growing painless masses:
    • Which are firm, multilobulated and mobile entities upon clinical examination.

 

  • They are diagnosed between the sixth through the eighth decades of life with a slightly higher incidence in women:
    • Mean age at presentation is 60 years.
    • 20% associated with radiation therapy or radiation exposure.
    • Rarely bilateral.
    • May be multiple.
    • Rarely synchronous with Warthin tumor or carcinoma ex pleomorphic adenoma
    • May occur in trisomy 7 or in BHD syndrome
  • Radiology Description:
    • Computed tomography (CT) and magnetic resonance imaging (MRI) are the image modalities of choice,

      • Specific MRI features:
        • T1 hypointense
        • Isointense to normal gland on fat saturated T2 and postcontrast T1
      • CT features:
        • Enhancing tumor and nonenhancing cystic component

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  • Pathology:
    • Well circumscribed with fibrous capsule, solid, tan-red-brown, lobulated, often small, may have cystic spaces
    • Microscopic description:
      • Eosinophilic or clear cell (glycogen) with sheets, trabeculae, acini or follicular patterns of monotonous large polygonal cells with well defined cell borders, deeply eosinophilic, granular cytoplasm, small round nuclei:
        • Oncocytic cells are thought to originate from the transformation of epithelial cells of salivary gland ducts or acini

      • Vascular stroma, may have clear cell change, background of oncocytic nodular hyperplasia, psammoma bodies, tyrosine rich crystals
      • No mitotic figures, no elastosis

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  • Complete surgical excision with a superficial parotidectomy is the treatments of choice.

Rodrigo Arrangoiz MS, MD, FACS a head and neck surgeon / surgical oncologist and is a member of Sociedad Quirúrgica S.C at the America British CowdrayMedical Center in Mexico City:

  • He is an expert in the management of salivary gland neoplasms:

    • If you have any questions about salivary gland neoplasms  please fill free to ask Dr. Arrangoiz

 

Training:

• General surgery:

• Michigan State University:

• 2005 al 2010

• Surgical Oncology / Head and Neck Surgery / Endocrine Surgery:

• Fox Chase Cancer Center (Filadelfia):

• 2010 al 2012

• Masters in Science (Clinical research for health professionals):

• Drexel University (Filadelfia):

• 2010 al 2012

• Surgical Oncology / Head and Neck Surgery / Endocrine Surgery:

• IFHNOS / Memorial Sloan Kettering Cancer Center:

• 2014 al 2016

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http://www.sociedadquirurgica.com

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