scholarly journals Mental Nerve Paraesthesia: A Report of Two Cases Associated with Endodontic Etiology

2021 ◽  
Vol 2021 ◽  
pp. 1-8
Author(s):  
Neeta Patel ◽  
Akshayraj Langaliya ◽  
Shikha Kanodia ◽  
Aravind Kumbhar ◽  
Aastha Buch ◽  
...  

Paraesthesia of the mental nerve can occur due to various etiological factors. Rarely, dental infections can cause paraesthesia. However, this article discusses two cases of endodontic etiology in the mental nerve region as a causative factor for paraesthesia. In the first case, the patient had severe pain localized to his right mandible, with numbness of his lower lip. Endodontic treatment led to quick regression and resolution of paraesthesia. In the second case, a patient who was referred for retreatment of a mandibular second premolar infection developed profound paraesthesia in the region of the mental nerve distribution following prior therapy. Possible mechanisms responsible for periapical infection-related paraesthesia are discussed here. CBCT imaging may be useful in the diagnosis and management of such conditions.

Author(s):  
Showkat Ahmad Dar ◽  
Shaheen Shahdad ◽  
Javed Ahmad Khan ◽  
Gousia Nisa ◽  
Neelofar Jan ◽  
...  

Background: Marginal Mandibular nerve, a branch of facial nerve, emerges at the lower part of the anterior border of parotid gland. It supplies risorius, muscles of lower lip and chin and joins mental nerve. This nerve has an important relationship with the lower border of mandible and is likely to be damaged during procedures in or around the submandibular area and can lead to certain morbid conditions like deviation of angle of mouth, drooling of saliva and difficulty in phonation.Methods: Sixty formalin preserved specimens of head and neck were used for studying the branching pattern of marginal mandibular nerve. The present study was conducted in the department of Anatomy Govt Medical College Srinagar over a period of two and a half years from 2015 to 2017. Cadaveric dissection was also used in the study during the routine teaching of undergraduate MBBS and BDS students in the department. The photographs of the variations seen during the study were taken.Results: In Forty-seven specimens (78.33%) there was a single branch of marginal mandibular nerve, in 10 specimens (16.6%) there were two branches of marginal mandibular nerve and in three specimens (5.0%) the marginal mandibular nerve was having three branches.Conclusions: From the above study it was concluded that marginal mandibular nerve can have two or three branches. Therefore, it is advisable to take due care during surgical procedures in the lower part of face and upper part of neck to preserve marginal mandibular nerve and to ensure cosmesis and prevent morbidity.


2021 ◽  
Vol 2021 ◽  
pp. 1-5
Author(s):  
Jasmine Hattab ◽  
Abigail Rose Trachtman ◽  
Pietro Giorgio Tiscar ◽  
Marco Di Domenico ◽  
Jessica Maria Abbate ◽  
...  

A 3-week-old suckling piglet spontaneously died after septicemic colibacillosis. At postmortem examination, bulging and ulcerated lesions were seen, affecting the oral mucosa on the inner surface of the lower lip. After histopathological investigation, the diagnosis of congenital oral squamous cell carcinoma was made. To the best of our knowledge, this is the first case of congenital oral squamous cell carcinoma ever described. A relationship has been shown or suggested between papillomavirus infection and oral squamous cell carcinoma in humans and animals. However, next-generation sequencing study did not demonstrate any papillomavirus sequences in the case reported herein.


2018 ◽  
Vol 10 (3) ◽  
Author(s):  
Nicola Townell ◽  
Thomas Locke ◽  
Margaret Gibbons ◽  
Dan Murphy ◽  
Joshua Francis ◽  
...  

Mycetoma is a neglected tropical disease with an unknown global burden. Although considered endemic to South-east Asia, it has not previously been reported from Timor-Lest. We describe two cases in Timor-Leste, highlighting the challenges surrounding microbiological diagnosis and management shared by many low to middle-income countries. As characteristically described, both patients lived rurally and presented late with marked soft tissue involvement and multiple draining sinuses following a prolonged period of high morbidity. Nocardia brasiliensis, a beadedbranched, modified acid-fast, gram-positive bacilli, was isolated and confirmed by molecular testing in the first case. The causative organism in the second case could not be confirmed due to limited microbiological capabilities. Due to limited local laboratory capabilities, Nocardia spp. infection cannot be routinely confirmed in Timor- Leste. However, the microbiology laboratory is essential for the successful diagnosis and management of Mycetoma. In both cases, medical therapy alone resulted in cure and favorable outcomes, although supply of antibiotic remains an ongoing resource issue.


1985 ◽  
Vol 13 (4) ◽  
pp. 407-409 ◽  
Author(s):  
J. S. Smith ◽  
B. E. Dwyer ◽  
D. L. Rigg
Keyword(s):  

Brain Injury ◽  
2020 ◽  
Vol 34 (11) ◽  
pp. 1541-1547
Author(s):  
Eduardo E. Espinosa-Rodríguez ◽  
María López-Gutiérrez ◽  
Gloria Tresserras-Giné ◽  
Nuria Pesa-Vendrell ◽  
Melcior Martínez-Pérez

2017 ◽  
Vol 2017 ◽  
pp. 1-4 ◽  
Author(s):  
Ana Isabel Sánchez ◽  
Jorge Armando Rojas

Nicolaides-Baraitser syndrome (NCBRS) is a rare and well-recognized entity that was first described in 1993, with a prevalence that is currently not known. It is recognized as a distinctive entity, with some variability in its signs and symptoms. The most important characteristics include intellectual disability, peculiar facial features including sparse scalp hair, coarse facial features, low frontal hairline, and microcephaly, and seizures. Additional features may include epicanthic folds, thin upper lip vermilion with thick lower lip vermilion, skeletal abnormalities, and severe language impairment. The disorder is inherited in an autosomal dominant manner caused by de novo mutations in the SMARCA2 gene, with most being missense mutations. We report a young adult patient with NCBRS and, to our knowledge, the first case report of the syndrome in Latin America with a confirmed molecular diagnosis and a mild-to-moderate phenotype.


Author(s):  
Mahmoud Karimizadeh Esfahani ◽  
Alireza Eslampoor ◽  
Somayeh Dolatabadi ◽  
Mohammad J. Najafzadeh ◽  
Jos Houbraken

Background and Purpose: Herein, we report the first case of fungal keratitis due to Aspergillus minisclerotigenes in a 68-year-old rural woman admitted to the Ophthalmology Center of Khatam-Al-Anbia Hospital in Mashhad, northeast of Iran. Case report: The patient presented with severe pain, burning, foreign body sensation, and reduced vision in her right eye. She had long-term uncontrolled diabetes and was not able to close her eye due to an anatomical problem with the eyelid. The cornea smear sample was cultured, and the fungus was initially identified as Aspergillus flavus. The isolated strain was further identified by sequencing a part of the calmodulin gene as A. minisclerotigenes. The patient did not respond to any antifungal treatments (e.g., amphotericin B and voriconazole drops, and fluconazole 300 mg/day); therefore, she was eventually subjected to corneal transplantation surgery. Conclusion: Fungal keratitis can be caused by the less common species. The reliable identification of the causative agents can be accomplished by the implementation of molecular methods.


2015 ◽  
Vol 8 (4) ◽  
pp. 363-369 ◽  
Author(s):  
Anantheswar Y. N. Rao

Midline cleft of the lower lip and mandible is an extremely rare condition. Since 1819, when the first case was reported by Couronne, fewer than 80 cases have been described in the world literature so far. The cleft has also been described as facial cleft no. 30 by Paul Tessier. The condition varies in severity from a mild variety in which there is a submucous cleft and notching in the lower lip to a severe variety, involving the tongue, floor of the mouth, mandible, absent hyoid, atrophic neck muscles, and sternum. In this case report, a female child having complete midline cleft of the lower lip and mandible, with bifid tongue stuck to the floor of the mouth, absent hyoid bone and flexion contracture band extending from the confluence of the tip of the tongue, floor of the mouth, cleft mandible to the manubrium sterni is described, with special emphasis on surgical planning and management.


CJEM ◽  
2003 ◽  
Vol 5 (04) ◽  
pp. 259-262 ◽  
Author(s):  
Amy Turner-Iannacci ◽  
Eisa Mozaffari ◽  
Eric T. Stoopler

ABSTRACT Mental nerve neuropathy (MNN) or “numb chin syndrome” is a rare neurologic symptom most often associated with malignancy. Patients typically develop paresthesia or numbness localized to the chin and lower lip and will often seek care at their local emergency department. Pain and expansion of the lower jaw may also be present. We report a case of MNN associated with a metastatic lesion in the mandible. The purpose of this article is to highlight the importance of recognizing MNN, a potentially life-threatening symptom of metastatic carcinoma, and enable clinicians to properly diagnose MNN, which may mimic other conditions that affect the mandible.


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