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Paranasal Sinus Cancer

(Sinus Cancer)


Bradley A. Schiff

, MD, Montefiore Medical Center, The University Hospital of Albert Einstein College of Medicine

Reviewed/Revised Dec 2022
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Paranasal sinus cancer is rare. It usually is squamous cell carcinoma but can also be adenocarcinoma, and it occurs most often in the maxillary and ethmoid sinuses. In most cases its cause is not known, symptoms develop late, and survival is generally poor.

Although rare in the US, paranasal sinus cancer is more common in Japan and among the Bantu people of South Africa. Men over 40 years are affected most often.

  • Regular inhalation of certain types of wood, leather, and metal dust

  • Smoking tobacco

Symptoms and Signs of Paranasal Sinus Cancer

Because the sinuses provide room for the cancer to grow, symptoms usually do not develop until the cancer is well advanced. The following symptoms result from local pressure of the cancer on adjacent structures:

  • Pain

  • Nasal obstruction and discharge

  • Epistaxis

  • Diplopia

  • Ear pain or fullness

  • Facial paresthesias

  • Loose maxillary teeth below the affected sinus

Tumor is sometimes visible in the oral or nasal cavities.

Diagnosis of Paranasal Sinus Cancer

  • Endoscopy, with biopsy

  • CT and MRI

Endoscopy, CT, and MRI are most often used to locate and help stage the tumor. Biopsy confirms the cell type. Staging, which includes assessing tumor spread to the brain, face, neck, lungs, and lymph nodes, helps determine treatment.

Prognosis for Paranasal Sinus Cancer

The earlier paranasal sinus cancer is treated, the better the prognosis. Prognosis also depends on histology. Survival is improving but remains generally poor. Overall, about 40% of people will have recurrent disease, and 5-year survival is about 60%.

Treatment of Paranasal Sinus Cancer

  • Surgery

  • Often radiation

  • Sometimes chemotherapy

Treatment for most early-stage paranasal sinus cancers is complete surgical excision. Recent advances in surgical techniques, particularly endoscopic techniques, can sometimes achieve complete tumor excisions, spare surrounding tissues, and achieve reconstruction.

If risk of recurrence is high, radiation therapy is given postoperatively. If surgical excision is not realistic or would cause excessive morbidity, radiotherapy plus chemotherapy may be used.

In some cases, chemotherapy is given to shrink the tumor; if the tumor responds well to the chemotherapy, it is resected surgically. If not, the tumor can be treated with radiation.

More Information

The following English-language resource may be useful. Please note that THE MANUAL is not responsible for the content of this resource.

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NOTE: This is the Professional Version. CONSUMERS: View Consumer Version
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