Results 151 to 160 of about 41,102 (196)

Case Report: Endoscopic Sistrunk and thyroidectomy via the areola approach in patients with thyroglossal duct cysts and thyroid cancer. [PDF]

open access: yesFront Oncol
Hu J   +12 more
europepmc   +1 more source

Infected Thyroglossal Duct Cyst with an Emergent Airway Threat. [PDF]

open access: yesTurk Arch Otorhinolaryngol
Lee TH   +3 more
europepmc   +1 more source
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Congenital Trilobe Tongue Associated with Cleft Palate: A Rare Anomaly

The Cleft Palate Craniofacial Journal, 2014
Cleft of the palate and congenital anomaly of the tongue is a rare occurrence. A child with the tongue in three segments is being presented for the first time in the literature. This child also had partial cleft palate. The cleft palate was repaired at 7 months of age, and the tongue was reconstructed at 15 months.
Karoon, Agrawal   +3 more
openaire   +4 more sources

Incomplete Cleft Palate, Bifid Tongue, and Oral Hamartomas: A Rare Congenital Anomaly

Journal of Craniofacial Surgery, 2020
Abstract Congenital bifid tongue is a rare malformation, which is usually present in association with other oral findings such as cleft palate and tongue mass. The authors present a rare case of congenital bifid tongue together with cleft palate, labial-buccal frenulum deformity, absence of lingual frenulum, and 3 hamartomas in
Shilu, Yin, Zhenmin, Zhao
openaire   +4 more sources

Klippel-Feil Anomaly, Cleft Palate, and Bifid Tongue

Annals of Plastic Surgery, 1990
The Klippel-Feil anomaly is a condition characterized by congenital vertebral fusion, which may be associated with a short neck and a low posterior hairline. In the patient presented here, there was congenital cervical fusion, cleft palate, and bifid tongue.
openaire   +4 more sources

Lower lip cleft, bifid tongue and fibrolipoma: a case report of rare congenital anomaly

British Journal of Oral and Maxillofacial Surgery, 2014
A non-syndromic bifid tongue with fibrolipoma, ankyloglossia, and clefts of the lower lip and alveolus is rare. We describe a case in which a bifid anterior tongue was separated by a fibrolipomatous mass. We excised the mass and repaired the lip and the tongue with satisfactory results.
Jin, Shi   +3 more
openaire   +4 more sources

Bilobed tongue base associated with multiple branchial anomalies

BMJ Case Reports, 2021
A bilobed tongue base was identified in an infant with multiple other head, neck and cardiac congenital anomalies. This anatomical variation of the posterior tongue is rare, with only two other cases identified in the literature. We report a case of a 5-month-old boy with a bilobed posterior tongue incidentally identified during workup for cardiac ...
Sevasti Konstantinidou   +3 more
openaire   +2 more sources

Presentation of a Rare Lobulated Tongue Anomaly

The Cleft Palate Craniofacial Journal, 2018
The presence of a bilobed tongue is a rare congenital malformation. There are multiple reports of a bifid anterior lobe; however, a case with complete separation of isolated anterior and posterior lobes has not been previously described. We report the case of a 2-year-old male, who presented with a V-shaped mandible and glossoptosis in the setting of ...
Kelly P, Schultz   +2 more
openaire   +2 more sources

Intralesional photocoagulation of vascular anomalies of the tongue

British Journal of Plastic Surgery, 1999
Vascular anomalies remain a challenge for patients and reconstructive surgeons. Recently, promising results have been reported using intralesional photocoagulation (ILP) to treat large, deep vascular lesions. We report our experience in treating 12 patients with vascular anomalies of the tongue (10 venous malformations and two haemangiomas) using ...
C J, Chang, D M, Fisher, Y R, Chen
openaire   +2 more sources

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