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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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<strong>Neck</strong> Cysts, Metastasis, Dissection Chapter 9 267Fig. 9.3. First branchial cleft cyst, Type II. Squamous epi<strong>the</strong>liumlining <strong>the</strong> cystic cavity. Note <strong>the</strong> presence <strong>of</strong> skin appendage structures<strong>and</strong> cartilage in <strong>the</strong> stromaFig. 9.5. Branchogenic carcinoma. Inset: malignant squamous<strong>and</strong> respiratory epi<strong>the</strong>lium lining <strong>the</strong> cystic wallNei<strong>the</strong>r <strong>the</strong> fifth nor <strong>the</strong> sixth branchial arch formsclefts or pouches in humans [126]. Branchial cleft cystshave been reported infrequently in <strong>the</strong> parotid, thyroid<strong>and</strong> parathyroid gl<strong>and</strong>s, floor <strong>of</strong> <strong>the</strong> mouth, tonsil,pharynx <strong>and</strong> mediastinum [17]. Many <strong>of</strong> <strong>the</strong>se cystshave <strong>the</strong> microscopic features <strong>of</strong> lymphoepi<strong>the</strong>lial cysts(Fig. 9.4).9.3.2 Branchiogenic CarcinomaFig. 9.4. Lymphoepi<strong>the</strong>lial cyst. Note <strong>the</strong> absence <strong>of</strong> lymphoidhyperplasia<strong>the</strong> only effective treatment. In some cases, this may necessitatea superficial parotidectomy. First branchial cleftabnormalities must be differentiated pathologically fromepidermal cysts (especially type I), dermoids (especiallytype II), <strong>and</strong> cystic sebaceous lymphadenoma.Anomalies from <strong>the</strong> third <strong>and</strong> fourth branchial apparatusesare rare <strong>and</strong> toge<strong>the</strong>r account for fewer than 5% <strong>of</strong>all branchial cysts, sinuses <strong>and</strong> fistulae [80]. A fistula in<strong>the</strong> pyriform sinus is one <strong>of</strong> <strong>the</strong> more common manifestations<strong>of</strong> a third branchial anomaly [32]. Recurrent infections<strong>of</strong> <strong>the</strong> lower neck, including suppurative thyroiditis,<strong>and</strong> a fistulous tract into <strong>the</strong> pyriform sinus are <strong>the</strong> features<strong>of</strong> a fourth branchial cleft or pouch anomaly [80].Third <strong>and</strong> fourth branchial sinus anomalies can bedistinguished only by detailed surgical exploration. Athird branchial sinus always extends from <strong>the</strong> pyriformsinus through <strong>the</strong> thyroid membrane cranial to <strong>the</strong> superiorlaryngeal nerve. In contrast, a fourth branchialsinus extends from <strong>the</strong> pyriform sinus caudal to <strong>the</strong> superiorlaryngeal nerve <strong>and</strong> exits <strong>the</strong> larynx near <strong>the</strong> cricothyroidjoint [127].Branchiogenic carcinoma or primary cervical neoplasticcysts are <strong>of</strong> interest from an historical viewpoint [69,96]. Few <strong>of</strong> <strong>the</strong> purported examples <strong>of</strong> this entity fulfil<strong>the</strong> four criteria that Martin et al. considered necessaryto establish <strong>the</strong> diagnosis, which are as follows:1. The cervical tumour occurs along <strong>the</strong> line extendingfrom a point just anterior to <strong>the</strong> tragus, along <strong>the</strong>anterior border <strong>of</strong> <strong>the</strong> sternocleidomastoid muscle, to<strong>the</strong> clavicle;2. The histologic appearance must be consistent with anorigin from tissue known to be present in <strong>the</strong> branchialvestigial;3. No primary source <strong>of</strong> <strong>the</strong> carcinoma should be discoveredduring follow-up for at least 5 years;4. Cancer arising in <strong>the</strong> wall <strong>of</strong> an epi<strong>the</strong>lium-lined cystsituated in <strong>the</strong> lateral aspect <strong>of</strong> <strong>the</strong> neck can be demonstratedhistologically (Fig. 9.5) [69].The fulfilment <strong>of</strong> <strong>the</strong>se criteria is practically impossible,<strong>and</strong> <strong>the</strong> existence <strong>of</strong> “ branchiogenic carcinoma” mustremain entirely hypo<strong>the</strong>tical [69, 73, 96, 116]. The criteriahave been criticised on <strong>the</strong> grounds that <strong>the</strong>y aremuch too restrictive <strong>and</strong> nearly preclude a diagnosis <strong>of</strong>branchiogenic carcinoma [15, 86].Several authors have estimated that, even acceptingtentative examples <strong>of</strong> branchiogenic carcinoma, its incidencewould be minuscule (0.3% <strong>of</strong> all malignant su-

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