scholarly journals A Rare Case of a Combination of Tessier Cleft 0 and 3 in a 4-Year-Old Child—A Case Report

2019 ◽  
Vol 52 (02) ◽  
pp. 250-251
Author(s):  
Bibhuti Bhusan Nayak ◽  
M. Lopamudra
Keyword(s):  
Rare Case ◽  
Upper Lip ◽  
Successful Management ◽  
Transposition Flap ◽  
Satisfactory Outcome ◽  
Straight Line ◽  
Median Cleft ◽  
Median Cleft Face Syndrome ◽  
Midline Cleft ◽  
Rule Out

AbstractDescription and successful management of a patient with Tessier no. 0 and 3 facial cleft is being presented. Appropriate evaluation was done to rule out the presence of median cleft face syndrome. Lip cleft was repaired by straight line technique with staggering at the vermilion border. Nasal cleft was reconstructed by a transposition flap and the flap taken from the upper lip after correction of the midline cleft. Satisfactory outcome was achieved for this singular deformity by conforming to the basic tenets of plastic surgery.

Median Cleft of the Upper Lip: A Rare Case

2010 ◽  
Vol 47 (6) ◽  
pp. 642-644 ◽  
Author(s):  
Nima P. Patel ◽  
M. Devi Prasad Tantri
Keyword(s):  
Rare Case ◽  
Upper Lip ◽  
Median Cleft

scholarly journals Frontonasal dysplasia (Median cleft face syndrome)

2012 ◽  
Vol 03 (01) ◽  
pp. 65-67 ◽  
Author(s):  
Seema Sharma ◽  
Vipin Sharma ◽  
Meenakshi Bothra
Keyword(s):  
Developing Countries ◽  
Birth Weight ◽  
Social Services ◽  
Rare Case ◽  
Maxillofacial Surgery ◽  
Associated Anomalies ◽  
Frontonasal Dysplasia ◽  
Median Cleft ◽  
History Of ◽  
Median Cleft Face Syndrome

ABSTRACTThis is a report of a rare case of frontonasal dysplasia (FND) in a full-term girl with birth weight of 2.750 kg. The baby had the classical features of FND. There were no other associated anomalies. There was no history of consanguinity and no family history of similar conditions. So inheritance of this case could be considered sporadic. Maxillofacial surgery should be considered for all patients for whom improvement is possible. However, in developing countries where there are considerable limitations in provision of social services, with economic and educational constraints, correction of such major defects remains a challenging task.

A RARE CASE OF MEDIAN CLEFT OF THE UPPER LIP ASSOCIATED WITH ENLARGED FRENULUM AND PALATAL MASSES

2002 ◽  
Vol 109 (4) ◽  
pp. 1465-1466 ◽  
Author(s):  
Koichi Asada ◽  
Katsunori Ishibashi ◽  
Hiroyuki Usui ◽  
Youhachirou Hirano
Keyword(s):  
Rare Case ◽  
Upper Lip ◽  
Median Cleft

scholarly journals Median cleft lip: an uncommon and unique anomaly

2019 ◽  
Vol 6 (8) ◽  
pp. 3035
Author(s):  
Vivek Parameswara Sarma
Keyword(s):  
Central Nervous System ◽  
Nasal Septum ◽  
Cleft Lip ◽  
Relevant Literature ◽  
Upper Lip ◽  
Craniofacial Malformations ◽  
Median Cleft ◽  
The Central Nervous System ◽  
Associated Abnormalities ◽  
Midline Cleft

Median or midline cleft lip [MCL] is an uncommon anomaly characterized by a midline vertical cleft through the upper lip and are either isolated or part of multiple anomalies. It can involve the pre-maxilla, the nasal septum, and the central nervous system. MCL includes Complete (42%), Incomplete (49%), and Minor forms (9%). The three main groups distinguished were: 1. Isolated MCL; 2. MCL with craniofacial malformations; and 3. MCL with extra-facial malformations. To analyze two operated cases of median cleft lip and review the relevant literature. The details of two cases of median cleft lip that were operated in 2017 were analysed. Both cases underwent wedge excision with the classical inverted V incision and muscle reconstruction with satisfactory result. Both the patients had no syndromic association or associated anomaly. All cases of MCL require evaluation for associated abnormalities. Isolated MCL can be repaired surgically with a good outcome. 

Median cleft of the upper lip associated with a mass: A rare case

2014 ◽  
Vol 42 (8) ◽  
pp. 1557-1561 ◽  
Author(s):  
Xin-chun Jian ◽  
Lian Zheng ◽  
Pu Xu ◽  
De-yu Liu
Keyword(s):  
Rare Case ◽  
Upper Lip ◽  
Median Cleft

Duplication of the pituitary gland in a newborn with median cleft face syndrome and nasal teratoma

1998 ◽  
Vol 28 (5) ◽  
pp. 290-292 ◽  
Author(s):  
Michèle Hamon-Kérautret ◽  
Gustavo Soto Ares ◽  
Xavier Demondion ◽  
Véronique Rouland ◽  
Jean-Paul Francke ◽  
...  
Keyword(s):  
Pituitary Gland ◽  
Median Cleft ◽  
Median Cleft Face Syndrome

ANGIOLEIOMYOMA OF UPPER LIP: A RARE CASE REPORT

2017 ◽  
Vol 124 (2) ◽  
pp. e80
Author(s):  
LUIZ ARTHUR BARBOSA DA SILVA ◽  
EDUARDO ALONSO CRUZ MONROY ◽  
HUGO COSTA NETO ◽  
ANA MIRYAM COSTA DE MEDEIROS ◽  
PATRÍCIA TEIXEIRA DE OLIVEIRA ◽  
...  
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Upper Lip ◽  
Rare Case Report

scholarly journals A rare clinical case: schwannoma of tongue

2019 ◽  
Vol 5 (3) ◽  
pp. 789
Author(s):  
Chandra Veer Singh ◽  
Sheetal Radia ◽  
Saalim Sheikh ◽  
Vijay Haribhakti
Keyword(s):  
Head And Neck ◽  
Rare Case ◽  
Neck Region ◽  
Surgical Excision ◽  
Imaging Studies ◽  
Head And Neck Tumours ◽  
Head And Neck Region ◽  
Complete Surgical Excision ◽  
Slow Growing ◽  
Rule Out

<p class="abstract">Schwannoma are slow growing tumours, which can arise from any peripheral nerve. 10% of schwannomas that occur in the head and neck region mostly originate from the vagus or sympathetic nervous system. Extracranial schwannomas in the head and neck region are rare neoplasm. Intraoral schwannoma are only 1% of the all head and neck tumours. Diagnosis is established by imaging studies such as magnetic resonance imaging or computed tomography, while FNAC is used to rule out other conditions. We report a rare case of lingual schwannomas generally present as a painless lump schwannoma of the tongue in a 27-year-old male complaining of asymptomatic swelling over a posterolateral surface of the tongue, treated by complete surgical excision. The diagnosis was established on the basis of clinical, histopathological, and immunohistochemical examination. We report a rare case of schwannoma over the posterolateral surface of tongue. Prognosis is good for the patient when this condition is correctly diagnosed as the condition rarely recurs after complete resection.</p>

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