56 Benign Neck Disease • Pathophysiology Normally 2 jugular sacs, 2 posterior sciatic sacs, and 1 retroperitoneal sac develop endothelial outbuddings and extend centrifugally to form lymphatic system Endothelial fibrillar membranes sprout from walls of sacs, penetrate surrounding tissue, canalize it, and produce more cysts Pressure of cysts forces tumour along lines of least resistance into planes or spaces between large muscles or vessels • Types Simple—thin-walled capillary sized (40%) Cavernous—dilated spaces (35%) Cystic hygroma—various sizes (25%) • Locations Oral 35% Cervical 50 to 75% Axillary 15% • Clinical features Equal sex distribution No preponderance to one side Age at presentation: – 60% birth – 75% by 1 year – 90% by 2 years Stridor with tracheal displacement Brachial plexus compression with pain and hyperesthesia Sudden increase in size due to haemorrhage may be fatal • Management Cryotherapy and sclerosant injection met with limited success Excision required Preop CT to exclude mediastinal involvement Use nerve stimulator to avoid CNs VII, XI, and XII Excise excess skin Multiple excisions may be needed External approach for intraoral lesions Recurrence rate is 10 to 15%; cavernous type most likely to recur • Characteristic features Always midline in neck Equal sex distribution • Epidermoid cyst Most common No adnexal structures Contains cheesy keratinous material • True dermoid cyst Contains skin appendages—hair follicles, etc. Can be acquired through implantation of epidermis in a puncture wound Most occur in the floor of mouth with ¼ involving neck Present as slow-growing lesions Management is surgical excision • Teratoid cyst Rare May be lined by respiratory epithelium Contains elements from ectoderm, endoderm, and mesoderm • Embryology Thyroid arises from floor of primitive pharynx between 1st and 2nd pouches Median thyroid anlage loses lumen at 5 weeks and breaks into fragments—lower end divides into 2 portions that become lobes Stalk should atrophy at 6 weeks; if not, it becomes a duct Cysts form when epithelial cells cease to remain inactive Duct runs through hyoid to foramen cecum Fistula results from inadequate treatment • Presentation Equal sex distribution Mean age 5 (range 4 months–70 years) Midline (90%), lateral (left) 10% 3× more common than branchial cysts 65% infrahyoid, 20% suprahyoid, 15% juxtahyoid Also described intralingual, suprasternal, and intralaryngeal 5% present with infection; 15% present with fistulas Rare familial variants Usually painless and mobile, characteristically move on swallowing and tongue protrusion due to them lying deep to investing layer of deep cervical fascia and relation to hyoid, respectively May present acutely with increasing pain, neck swelling, dysphagia, dysphonia, airway obstruction, fistula, and fever • Investigation TFTs Suprahyoid cysts—technetium scan ± MRI USS • Treatment Sistrunk procedure with removal of central core of hyoid; stay medial to lesser cornua to reduce risk of hypoglossal nerve damage 7 to 8% recur Consider removal of core of central tongue musculature in recurrent cases • Suspect if cyst hard or irregular • 4th decade in women, 6th decade in men • Local excision and thyroxine suppression • Adjuvant thyroidectomy and radioiodine may be needed • Embryology Remains of branchial clefts/pharyngeal pouches Cervical sinus theory—remains of cervical sinus of His persist Thymopharyngeal duct theory—remnants of original connection between thymus and 3rd branchial pouch Inclusion theory—epithelial inclusions in lymph nodes 1st arch 5 to 25% 2nd arch 40 to 90% 3rd/4th 2 to 8% • Pathology Stratified squamous epithelium 80% have lymphoid tissue in wall 2 types of 1st-arch anomalies: – Dorsal—runs medial to conchal cartilage extending posteriorly to retroauricular scalp – Ventral—presents as sinus/cleft/fistula inferior to cartilaginous EAM • Clinical features 3 male:2 female Peak age 3rd decade (range 1–70 years) ⅔ on left ⅔ anterior to upper ⅓ SCM Other sites (⅓): – Middle/lower neck – Parotid – Pharynx – Posterior triangle
56.1 Congenital Neck Masses
56.1.1 Lymphangiomas
56.1.2 Midline Dermoids
56.1.3 Thyroglossal Cysts
56.1.4 Thyroglossal Duct Carcinoma
56.1.5 Branchial Cysts (Fig. 56.1)
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Benign Neck Disease
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