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Pathology of the Head and Neck

Pathology of the Head and Neck

Pathology of the Head and Neck

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Major <strong>and</strong> Minor Salivary Gl<strong>and</strong>s Chapter 5 135only occasionally in <strong>the</strong> parotid (see Sect. 5.8.10). Thelesions are <strong>of</strong>ten multifocal <strong>and</strong> usually small, but canreach 30 mm in diameter.5.6.3 Multifocal NodularOncocytic HyperplasiaThis rare condition consists <strong>of</strong> nodules <strong>of</strong> varying size,composed <strong>of</strong> oncocytic cells, <strong>of</strong>ten with relatively clearcytoplasm. The nodules appear to engulf normal acinigiving a false impression <strong>of</strong> invasion, but <strong>the</strong>re is nostromal or o<strong>the</strong>r response by <strong>the</strong> acini. Multifocal nodularoncocytic hyperplasia (MNOH) can be mistaken fora clear cell neoplasm with satellite deposits when onenodule is much larger than <strong>the</strong> o<strong>the</strong>rs. MNOH can alsobe bilateral, <strong>and</strong> it has been reported to co-exist with apleomorphic adenoma, which itself showed oncocyticchange [20, 158].lobular architecture, <strong>and</strong> some lobules are affectedmore severely than o<strong>the</strong>rs. The cysts vary in size up toa few millimetres, <strong>and</strong> <strong>the</strong>y are irregular in shape <strong>and</strong><strong>of</strong>ten interconnect. The lining epi<strong>the</strong>lium is flat, cuboidalto low columnar, sometimes with an apocrinelikeappearance. The lumen contains secretion withspherical microliths. Remnants <strong>of</strong> salivary acini areseen between <strong>the</strong> cysts, <strong>and</strong> thick fibrous interlobularsepta are <strong>of</strong>ten prominent.5.7.2 MucocelesA mucocele is defined as <strong>the</strong> pooling <strong>of</strong> mucus in a cysticcavity [62]. Two types are recognised – extravasation<strong>and</strong> retention; extravasation mucocele is described inSect. 5.2.1. Retention cysts can occur at any age, <strong>and</strong> <strong>the</strong>mucus pool is within an epi<strong>the</strong>lium-lined cavity, likelyto be a dilated excretory duct.5.7 CystsNon-neoplastic cysts <strong>and</strong> pseudocysts accounted forabout 6% <strong>of</strong> all lesions <strong>of</strong> <strong>the</strong> salivary gl<strong>and</strong>s in <strong>the</strong> Hamburgregistry <strong>of</strong> salivary neoplasms <strong>and</strong> tumour-like lesions[172]. They can be classified as:1. Dysgenetic, e.g. polycystic dysgenetic disease;2. Acquired cysts lined with epi<strong>the</strong>lium, e.g. lymphoepi<strong>the</strong>lialcystic lesions, duct cysts;3. Pseudocysts without an epi<strong>the</strong>lial lining, e.g. extravasationmucocele, including ranula;4. Cystic change in neoplasms, e.g. Warthin, variants<strong>of</strong> mucoepidermoid <strong>and</strong> acinic cell carcinomas, lymphoepi<strong>the</strong>lialsialadenitis (LESA), lymphoma, <strong>and</strong>rarely, pleomorphic adenoma;5. Miscellaneous o<strong>the</strong>r cysts.The commonest are mucoceles, including ranula (80%),parotid duct cysts (11%), lymphoepi<strong>the</strong>lial cystic lesions(7%) <strong>and</strong> dysgenetic cysts <strong>and</strong> congenital sialectasia (toge<strong>the</strong>r2%).5.7.1 Salivary PolycysticDysgenetic DiseaseThis very rare condition resembles cystic anomalies <strong>of</strong>o<strong>the</strong>r organs, such as <strong>the</strong> kidney, liver <strong>and</strong> pancreas,although no association has been described [62, 172,177]. Some cases are familial [207], <strong>and</strong> almost allcases occurred in females. Most patients present inchildhood, but some have not been recognised untiladulthood. It only affects <strong>the</strong> parotid gl<strong>and</strong>s, usuallybilaterally. Microscopically, <strong>the</strong> gl<strong>and</strong>s maintain <strong>the</strong>ir5.7.3 Simple Salivary Duct CystsSalivary duct cysts are acquired, <strong>and</strong> are due to dilatation<strong>of</strong> a salivary duct following obstruction, sometimesby a tumour [62]. They can occur at any age, althoughusually in patients over 30 years old. Most (85%) arisein <strong>the</strong> parotid <strong>and</strong> are unilateral <strong>and</strong> painless. They arewell-circumscribed, unilocular <strong>and</strong> up to 100 mm in diameter(usually 10 to 30 mm). They contain fluid that iswatery to viscous brown, occasionally with mucus. Thewall comprises dense fibrous tissue, 1–3 mm thick, <strong>and</strong><strong>the</strong>re is <strong>of</strong>ten mild to moderate chronic inflammation,although not <strong>the</strong> dense lymphoid infiltrate <strong>of</strong> a lymphoepi<strong>the</strong>lialcyst. The epi<strong>the</strong>lium is stratified squamous, ora single layer <strong>of</strong> cuboidal or columnar cells, with occasionalgoblet cells <strong>and</strong> oncocytes.5.7.4 Lymphoepi<strong>the</strong>lial Cystic LesionsSeven types <strong>of</strong> salivary lesions can be characterised bysingle or multiple epi<strong>the</strong>lial-lined cysts surrounded bylymphoid tissue including germinal centres: benignlymphoepi<strong>the</strong>lial cyst <strong>and</strong> cystic lymphoid hyperplasia<strong>of</strong> AIDS, in addition to Warthin’s tumour, LESA<strong>and</strong> mucosa-associated lymphoid tissue (MALT lymphoma)each with cystically dilated ducts, low-gradecyst-forming mucoepidermoid carcinoma with a heavylymphocytic response, <strong>and</strong> cystic metastases in intraparotidlymph nodes, each <strong>of</strong> which is discussed inSect. 5.14.

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