scholarly journals Surgical Management of a Rare Case of Congenital DoubleUpper Lip

2011 ◽  
Vol 2011 ◽  
pp. 1-3 ◽  
Author(s):  
Adit Srivastava ◽  
Ajit Parihar ◽  
Romesh Soni ◽  
M. C. Shashikanth ◽  
T. P. Chaturvedi
Keyword(s):  
Surgical Management ◽  
Rare Case ◽  
Developmental Anomaly ◽  
Upper Lip ◽  
Facial Deformity ◽  
Cosmetic Reason

Congenital double lip is a rare developmental anomaly which usually involves the upper lip. It may occur in isolation or as a part of Ascher's syndrome. The occurrence of double lip may result in facial deformity especially when patient attempts to talk, smile, or even try to show the teeth. It affects esthetics and also interferes with speech and mastication. Although surgery may be undertaken to facilitate speech and mastication, majority of cases are operated for cosmetic reasons. A case of congenital double upper lip which was surgically treated for cosmetic reason is reported.

Non-syndromic double upper lip with triple frena: cosmetic cheiloplasty

2021 ◽  
Vol 14 (9) ◽  
pp. e243156
Author(s):  
Monika Gupta ◽  
Harshita Vig ◽  
Yajas Kumar ◽  
Aliza Rizvi
Keyword(s):  
Psychological Distress ◽  
Present Article ◽  
Surgical Management ◽  
Surgical Intervention ◽  
The Other ◽  
Upper Lip ◽  
Lower Lip ◽  
Facial Anomaly ◽  
The Aesthetic ◽  
Functional Problems

Double lip or macrocheilitis is a rare facial anomaly, mostly congenital in origin. It commonly involves the upper lip than the lower lip. It may occur in isolation or as part of the Ascher’s syndrome. It results due to deposition of excessive areolar tissue and non-inflammatory hyperplasia of labial mucosa gland of pars villosa. It may be acquired as a result of injury to the lips or lip-biting habit. The double lip becomes conspicuous when the lips are retracted during smiling resulting in the characteristic ‘cupid’s bow’ appearance. This disfigurement can pose aesthetic and functional problems and may result in psychological distress. A surgical intervention is must for restoration of functions and to address the aesthetic concerns. The present article reports a case of non-syndromic double upper lip with triple labial frena and its surgical management with laser on one side and with scalpel on the other side.

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 Pleomorphic xanthoastrocytoma at the pineal region: rare case report with successful surgical management

2021 ◽  
Vol 36 (1) ◽  
Author(s):  
Saraj Kumar Singh ◽  
Krishan Kumar Sharma ◽  
Tarun Kumar
Keyword(s):  
Surgical Management ◽  
Rare Case ◽  
Case Reports ◽  
Internal Capsule ◽  
Pleomorphic Xanthoastrocytoma ◽  
Pineal Region ◽  
Low Grade ◽  
Pineal Region Tumors ◽  
Pediatric Age Group ◽  
Rare Case Report

Abstract Background Pineal region tumors are commonly present in the pediatric age group. However, pleomorphic xanthoastrocytoma (PXA) is very rare at this region, and only few case reports have been reported till now in literature. Case presentation Here, we report a rare case of pineal region, juxta-thalamic, pleomorphic xanthoastrocytoma (PXA) in an 11-year-old male child. The child presented with severe headache after which MRI was done. It was suggestive of pineal region low-grade tumor. The patient was operated in Parkbench position with SCIT (supracerebellar approach) in a retractor-free manner. Gross total resection was done. However, the patient developed postoperative left-sided hemiparesis. It got improved in 1 month, and the patient became ambulatory. Histopathology came out as pleomorphic xanthoastrocytoma. Conclusion Surgical management should include careful resection near the internal capsule to avoid postoperative hemiparesis. Also, shunt should be delayed in the cystic cavity created by resection of tumor.

scholarly journals Rare Case of Double Intussusception in a Pup and Its Surgical Management

2018 ◽  
Vol 5 (3) ◽  
pp. 38-40
Author(s):  
Sandeep Saharan ◽  
◽  
Ram Niwas ◽  
Ribu Varghese Mathew ◽  
Divya Agnihotri
Keyword(s):  
Surgical Management ◽  
Rare Case

scholarly journals Surgical management of congenital foetal hydrocephalus in a crossbred cow

2021 ◽  
Vol 52 (2) ◽  
Author(s):  
P. Dangi ◽  
S. Ruhil ◽  
H. Singh ◽  
A. Samdhyan ◽  
S. Potliya
Keyword(s):  
Surgical Management ◽  
Surgical Approach ◽  
Rare Case ◽  
Ventral Midline ◽  
Crossbred Cow

A rare case of dystocia due to external congenital hydrocephalic foetus with ankylosis of forelimbs managed by ventral midline surgical approach in a crossbred cow is reported.

scholarly journals A rare case of Hamartoma of nose and upper lip

2001 ◽  
Vol 53 (4) ◽  
pp. 313-314
Author(s):  
S. K. Dutta ◽  
D. M. Munsi ◽  
S. N. Ghosh
Keyword(s):  
Rare Case ◽  
Upper Lip

scholarly journals Leiomyosarcoma of the inguinal canal

2014 ◽  
Vol 96 (6) ◽  
pp. e8-e9 ◽  
Author(s):  
R Patel ◽  
P Chana ◽  
J Armstrong ◽  
R Lawrence
Keyword(s):  
Inguinal Hernia ◽  
Surgical Management ◽  
Rare Case ◽  
Inguinal Canal ◽  
Histological Findings

We describe a rare case of a leiomyosarcoma in the inguinal canal in a patient presenting clinically with an inguinal hernia. The clinical details, histological findings and surgical management are reviewed.

scholarly journals Glomus Tumor of the Oral Cavity: Report of a Rare Case and Literature Review

2019 ◽  
Vol 30 (2) ◽  
pp. 185-190 ◽  
Author(s):  
Celeste Sánchez-Romero ◽  
Maria Eduarda Pérez de Oliveira ◽  
Jurema Freire Lisboa de Castro ◽  
Elaine Judite de Amorim Carvalho ◽  
Oslei Paes de Almeida ◽  
...  
Keyword(s):  
Literature Review ◽  
Oral Cavity ◽  
Rare Case ◽  
English Language ◽  
Glomus Tumor ◽  
Benign Neoplasm ◽  
Upper Lip ◽  
Middle Aged Adults ◽  
Glomus Body ◽  
Language Literature

Abstract Glomus tumor is a benign neoplasm composed of a perivascular proliferation of glomic cells that resembles the normal glomus body. Usually, it appears as a solitary, symptomatic small blue-red nodule, located in the deep dermis or subcutis of upper or lower extremities of young to middle-aged adults. Cases affecting the oral cavity are very rare, with only 23 well-documented cases reported in the English-language literature. Herein, we present a rare case of glomus tumor of the upper lip, and review the literature of cases involving the mouth.

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