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Thyroglossal cyst
Classification & external resources

ICD-10	Q89.2
ICD-9	759.2
OMIM	188455
DiseasesDB	13070
eMedicine	ent/283
MeSH	D013955

A thyroglossal cyst is a fibrous cyst that forms from a persistent thyroglossal duct.

Contents 1 Presentation 2 Embryology 3 Symptoms 4 Clinical features 5 Treatment 6 Bibliography

It usually presents as a midline neck lump, which is painful if infected. There may be difficulty breathing, dysphagia (difficulty swallowing), and/or dyspepsia (discomfort in the upper abdomen), especially if the lump becomes large.

The most common locations for a thyroglossal cyst is midline or slightly off midline, between the isthmus of the thyroid and the hyoid bone or just above the hyoid bone. A thyroglossal cyst can develop anywhere along a thyroglossal duct, though cysts within the tongue or in the floor of the mouth are rare.

A thyroglossal cyst will move upwards with protrusion of the tongue.

Thyroglossal cysts are associated with an increased incidence of ectopic thyroid tissue. Occasionally, a lingual thyroid can be seen as a flattened strawberry-like lump at the base of the tongue.

Very rarely, the persistent duct can become cancerous, called thyroglossal duct carcinoma. In the case of thyroglossal duct carcinoma, the cancerous cells are ectopic thyroid tissue that has been deposited along the thyroglossal duct and usually follows exposure to radiation.

The thyroglossal tract arises from the foramen caecum at the junction of the anterior two-thirds and posterior one-third of the tongue. Any part of the tract can persist causing a sinus, fistula or cyst. Most fistulae are acquired following rupture or incision of the infected thyroglossal cyst.

Thyroglossal duct cysts most often present with a palpable (able to be felt) asymptomatic midline neck mass below the level of the hyoid bone. The mass on the neck moves during swallowing. Some patients will have neck or throat pain, or dysphagia.

The persistent duct or sinus can promote oral secretions, which may cause cysts to become infected. Up to half of thyroglossal cysts are not diagnosed until adult life. The tract can lie dormant for years or even decades until some kind of stimulus leads to cystic dilation. Infection can sometimes cause the transient appearance of a mass or enlargement of the cyst, at times with periodic recurrences. Spontaneous drainage may also occur.

Clinical features can be found in the subhyoid portion of the tract and 75% present as midline swellings. The remainder can be found as far lateral as lateral tip of the hyoid bone.

Treatment for a thyroglossal cyst is surgical resection, often requiring concomitant removal of the midsection of the hyoid bone. Although generally benign the cyst will be removed if the patient exhibits difficulty in breathing or swallowing, or if the cyst is infected. Even if these symptoms are not present the cyst may be removed to eliminate the chance of infection or development of a carcinoma, or for cosmetic reasons if there is unsightly protrusion from the neck.

Surgical management requires excision not only of the cyst but also of the path's tract and branches. A removal of the central portion of the hyoid bone is indicated to ensure complete removal of the tract. It is unlikely that there will be a recurrence after such an operation. At times antibiotics can be indicated if there is sign of infection.

Thyroid scans and thyroid function studies are ordered preoperatively, this is important to demonstrate that normally functioning thyroid tissue is in its usual location.

• Brewis C, Mahadevan M, Bailey CM, Drake DP (2000). "Investigation and treatment of thyroglossal cysts in children". Journal of the Royal Society of Medicine 93 (1): 18-21. PMID 10700841. 

• http://www.doctoronline.nhs.uk/masterwebsite1Asp/targetpages/testandprocedures/surgery/thyroglo.asp

v • d • e Phakomatoses and other congenital malformations not elsewhere classified (Q85-Q89, 759)
Phakomatoses	Neurofibromatosis (type I, type II) - Tuberous sclerosis - Sturge-Weber syndrome - Von Hippel-Lindau disease - Incontinentia pigmenti - Ataxia telangiectasia
Due to known exogenous causes	Fetal alcohol syndrome - Phocomelia (via Thalidomide)
Affecting multiple systems	facial (Mobius syndrome, Goldenhar syndrome, Cyclopia, Apert syndrome) short stature (Aarskog-Scott syndrome, Cockayne syndrome, Cornelia de Lange Syndrome, Dubowitz syndrome, Noonan syndrome, Robinow syndrome, Silver-Russell dwarfism, Seckel syndrome, Smith-Lemli-Opitz syndrome) limbs (Holt-Oram syndrome, Klippel-Trenaunay-Weber syndrome, Nail-patella syndrome, Rubinstein-Taybi syndrome, Sirenomelia, VACTERL association) overgrowth (Beckwith-Wiedemann syndrome, Sotos syndrome, Weaver syndrome) Marfan syndrome - Alport syndrome - Bardet-Biedl syndrome - Zellweger syndrome
Other	Asplenia - Splenomegaly - Persistent thyroglossal duct - Thyroglossal cyst - Situs inversus - Conjoined twins - Cowden syndrome - Hamartoma - Peutz-Jeghers syndrome