56 Benign Neck Disease • Pathophysiology • Types • Locations • Clinical features – 60% birth – 75% by 1 year – 90% by 2 years • Management • Characteristic features • Epidermoid cyst • True dermoid cyst • Teratoid cyst • Embryology • Presentation • Investigation • Treatment • 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 • Pathology – Dorsal—runs medial to conchal cartilage extending posteriorly to retroauricular scalp – Ventral—presents as sinus/cleft/fistula inferior to cartilaginous EAM • Clinical features – Middle/lower neck – Parotid – Pharynx – Posterior triangle
56.1 Congenital Neck Masses
56.1.1 Lymphangiomas
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
Simple—thin-walled capillary sized (40%)
Cavernous—dilated spaces (35%)
Cystic hygroma—various sizes (25%)
Oral 35%
Cervical 50 to 75%
Axillary 15%
Equal sex distribution
No preponderance to one side
Age at presentation:
Stridor with tracheal displacement
Brachial plexus compression with pain and hyperesthesia
Sudden increase in size due to haemorrhage may be fatal
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
56.1.2 Midline Dermoids
Always midline in neck
Equal sex distribution
Most common
No adnexal structures
Contains cheesy keratinous material
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
Rare
May be lined by respiratory epithelium
Contains elements from ectoderm, endoderm, and mesoderm
56.1.3 Thyroglossal Cysts
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
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
TFTs
Suprahyoid cysts—technetium scan ± MRI
USS
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
56.1.4 Thyroglossal Duct Carcinoma
56.1.5 Branchial Cysts (Fig. 56.1)
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%
Stratified squamous epithelium
80% have lymphoid tissue in wall
2 types of 1st-arch anomalies:
3 male:2 female
Peak age 3rd decade (range 1–70 years)
⅔ on left
⅔ anterior to upper ⅓ SCM
Other sites (⅓):
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