Interactive Transcript
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As we saw with that graphic from Jatin Shah's Head and
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Neck Surgery textbook, overlapping sites is a very
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common location for malignancies of the sinonasal cavity.
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Here, for example, we have a mass, which is growing
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bilaterally into the ethmoid sinuses, but also
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into the nasal cavity, so an overlapping site and
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potentially even into the maxillary antrum in this case.
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Once again, the lesion is dark on the T2-weighted
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scan and shows some element of contrast enhancement.
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You notice that the left maxillary sinus is
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not showing solid enhancement and has brighter
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signal intensity on the T2-weighted scan.
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This helps us in defining the margins of
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the tumor because obstructed secretions,
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unless they're very hyperproteinaceous,
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by and large, are going to be bright on the T2-weighted scan
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until they get out to the 30% protein concentration,
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if you recall that graphic from Peter Som.
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So in this case, we can pretty much determine that this
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is the cancer, this is the obstructed maxillary sinus.
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This would be much more difficult to define on
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CT scanning because the tumor and the hyperdense
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secretions may look exactly alike.
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For that reason, MRI is the main driver and the workhorse
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for the evaluation of neoplasms of the sinonasal cavity.
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Nonetheless, with few exceptions, the signal
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intensity of the different histologies of
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malignancy of the sinonasal cavity will be similar.
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I cannot tell you whether this
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is a squamous cell carcinoma.
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Or an adenocarcinoma.
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I can't tell you whether this could be a lymphoma.
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They're all gonna be dark on T2.
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They're all gonna show enhancement on T1.
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Sometimes we will get lucky with some of the lesions
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that may have a chondromatrix, where we would
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call it a chondrosarcoma, or what we will see
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with olfactory neuroblastomas where you may have
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intracranial cysts associated with the neoplasm.
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This patient, we would not be able to say whether
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this was an inverted papilloma with secondary
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squamous cell carcinoma on the histology.
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So again, a bit nonspecific.
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More importantly, is there
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involvement of the orbital contents?
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Because a tumor that grows into the orbital
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where you have to have an orbital exenteration
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is a lot more disfiguring and worse prognosis
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than one where the periosteum of the
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orbit is intact.
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Similarly, we look for the intracranial extension
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to see whether there's any dural or parenchymal or
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pial enhancement that would suggest intracranial
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extension, which would lead to a craniofacial
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resection, and again, a worse prognosis.
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Then we also look for periorbital spread, which we mentioned
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with adenoid cystic carcinoma in the previous case
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where there may be intracranial spread along the
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cranial nerves, usually the fifth cranial nerve.
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Here's another example of where the tumor is
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identified very nicely on the T2 MRI scan as
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darkened signal intensity with obstructed secretions
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in the left maxillary antrum here on the CT scan.
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You probably would assume that this was obstructed
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secretions, but that differentiation between the
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tumor versus the obstructed secretions is much
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better visualized on the MRI scan, particularly
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T2-weighted scanning and post-gadolinium
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hand scanning than it is on the CT scan.
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As I mentioned, squamous cell carcinoma is the most
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common cancer to be identified in the maxillary sinus.
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In the nasal cavity.
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It sort of competes with melanoma, which is
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another of the common nasal cavity malignancies.
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It's less common in the ethmoid
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sinus where adenocarcinomas.
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Predominate when we have squamous cell carcinoma,
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like with adenoid cystic carcinoma, a minor
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salivary gland tumor, we look for perineural spread.
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Fortunately, nodal metastases in sinonasal
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malignancies are pretty uncommon.
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This is the T staging of maxillary sinus cancer.
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You see T1 limited to the sinus, T2 bone erosion,
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potentially even extending into the hard palate.
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Or into the nasal cavity, T3 involvement
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of the posterior wall of the maxillary
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sinus where we'll go into the perianal fat.
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The subcutaneous tissues as we saw with the example
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from the MRI that we saw involvement of the floor
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or medial wall of the orbit, or the pterygopalatine fossa,
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T4A invasion into the anterior orbital contents.
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By this we mean the anterior globe structures, the skin.
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The OID plates, the infratemporal fossa,
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which is analogous to the masticator space.
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The cribriform plate, where we
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potentially are talking about intracranial
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extension, sphenoid or frontal sinuses.
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And T4B, which is generally unresectable
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disease, is disease that extends into the
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orbital apex where it may affect the optic
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nerve, the dura, the brain, the middle cranial
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fossa, the cranial nerves, nasopharynx, orbits.
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So these are generally treated
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with chemoradiation therapy.
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