Salivary Gland Pathology. Группа авторов

Salivary Gland Pathology - Группа авторов


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      a Depends on degree of fat deposition.

      b Depends on the hemoglobin concentration and hematocrit.

      c Depends on age and fat deposition.

      d Very limited evaluation secondary to partial volume effect.

      CSF = cerebrospinal fluid.

      Although the density of the salivary glands is variable, the parotid glands tend to be slightly lower in density relative to muscle, secondary to a higher fat content and become progressively more fat replaced over time. The CT density of parotid glands varies from −10 to +30 H. The submandibular glands are denser than parotid glands and are equivalent in density to muscle. The submandibular glands vary in density from +30 to +60 H.

Photo depicts CT angiogram (CTA) of the neck at the level of the parotid gland demonstrating the retromandibular vein and adjacent external carotid artery (large white arrow).

      Newer CT techniques including CT perfusion and dynamic contrast‐enhanced multi‐slice CT have been studied. Dynamic multi‐slice contrast‐enhanced CT is obtained while scanning over a region of interest and simultaneously administering IV contrast. The characteristics of tissues can then be studied as the contrast bolus arrives at the lesion and “washes in” to the tumor, reaches a peak presence within the mass, and then decreases over time, i.e. “washes out.” This technique has demonstrated differences in various histologic types of tumors, for example, with early enhancement in Warthin's tumor with a time to peak at 30 seconds and subsequent fast washout. The malignant tumors show a time to peak at 90 seconds. The pleomorphic adenomas demonstrate a continued rise in enhancement in all four phases (Yerli et al. 2007).

      CT perfusion attempts to study physiologic parameters of blood volume, blood flow, mean transit time, and capillary permeability surface product. Statistically significant differences between malignant and benign tumors have been demonstrated with the mean transit time measurement. A rapid mean transit time of less than 3.5 seconds is seen with most malignant tumors, but with benign tumors or normal tissue the mean transit time is significantly longer (Rumboldt et al. 2005).

      Magnetic resonance imaging (MRI) represents imaging technology with great promise in characterizing salivary gland pathology. The higher tissue contrast of MRI, when compared to CT, enables subtle differences in soft tissues to be demonstrated. Gadolinium contrast‐enhanced MRI further accentuates the soft‐tissue contrast. Subtle pathologic states such as perineural spread of disease are better delineated when compared with CT. This along with excellent resolution and exquisite details make MRI a very powerful technique in head and neck imaging, particularly at the skull base. This notwithstanding, its susceptibility to motion artifacts and long imaging time as well as contraindication due to claustrophobia, pacemakers, aneurysm clips, deep brain and vagal nerve stimulators limit its usefulness in the general population as a routine initial diagnostic and follow‐up imaging modality. Many of the safety considerations are well defined and detailed on the popular website, www.mrisafety.com.

      Although the physics and instrumentation of MRI are beyond the scope of this text, a fundamental understanding of the variety of different imaging sequences and techniques should be understood by clinicians to facilitate reciprocal communication of the clinical problem, and understanding of imaging reports.

      The impact of MRI is in the soft‐tissue contrast that can be obtained, noninvasively. The relaxation times of tissues can be manipulated to bring out soft‐tissue detail. The routine sequences used in clinical scanning are spin‐echo (SE), gradient echo (GRE), and echo‐planar (EPI). Typical pulse sequences for head and neck and brain imaging include spin‐echo T1, spin‐echo T2, proton density (PD), fluid attenuation inversion recovery (FLAIR), diffusion weighted images (DWI), post‐contrast T1 and STIR. A variant of the spin‐echo, the fast spin‐echo sequence (FSE) allows for a more rapid acquisition of spin‐echo images. Any one of these can be obtained in the three standard orientations of axial, coronal, and sagittal planes. Oblique planes may be obtained in special circumstances.


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