Multiple Skull Base Meningiomata in a Transgender Patient: Case Report and Literature Review

Author(s):  
Andrew Alalade ◽  
Christopher Millward ◽  
Piyali Pal ◽  
Catherine Gilkes
Author(s):  
Jordina Rincon-Torroella ◽  
M Harrison Snyder ◽  
Deepa J. Galaiya ◽  
Meaghan Morris ◽  
Jon D. Weingart ◽  
...  

2021 ◽  
Vol 10 (2) ◽  
pp. e26610212430
Author(s):  
Gustavo Zanna Ferreira ◽  
Carolina Ferrairo Danieletto-Zanna ◽  
Liogi Iwaki Filho ◽  
Rômulo Maciel Lustosa ◽  
Willian Pecin Jacomacci ◽  
...  

The ameloblastic fibro-odontoma (AFO) is a mixed odontogenic tumor, with characteristics of ameloblastic fibroma, presenting enamel and dentin, which occurs more frequently in individuals aged 5 to 17 years. This paper reports na extensive case of ameloblastic fibro-odontoma in the mandible of a 3-year-old patient, discussed in comparison to cases selected from a brief literature review on the clinical characteristics, Evolution and therapeutic options for this lesion. In the last years, there was no consensus in the literature concerning its etiopathogenesis and classification, yet recently the AFO was classified as a developing odontoma. This case is in accordance with the 7 cases reported in the literature of AFO in the mandible of children aged 10 years or younger, especially concerning the lesion pattern and evolution and treatment adopted. The patient did not present relapse and exhibited local bone regeneration at the 3-year follow-up.


2017 ◽  
Vol 23 (6) ◽  
pp. 908-912 ◽  
Author(s):  
Elda Righi ◽  
Alessia Carnelutti ◽  
Daniele Muser ◽  
Francesco Zaja ◽  
Elisa Lucchini ◽  
...  

2017 ◽  
Vol 43 (1) ◽  
Author(s):  
Samvel Bardakhchyan ◽  
Leo Kager ◽  
Samvel Danielyan ◽  
Armen Avagyan ◽  
Nerses Karamyan ◽  
...  

2020 ◽  
Vol 14 (2) ◽  
pp. 83-88
Author(s):  
Phawin Kor-anantakul ◽  
Kanya Suphapeetiporn ◽  
Somchit Jaruratanasirikul

AbstractAblepharon macrostomia syndrome (AMS) is a rare congenital disorder. To our knowledge, only 20 cases have been reported to date, and all in patients from Western countries. We report a case of AMS in a Thai patient, who presented at age 3 months with severe ectropion of both upper and lower eyelids, alopecia totalis, no palpable clitoris, and hypoplasia of both labia minora and labia majora. Trio whole exome sequencing analysis was performed, which revealed a heterozygous missense c.223G>A (p.Glu75Lys) variation in TWIST2. To our knowledge, this is the first reported case of AMS in a patient from Thailand and the first reported case of AMS in Asia.


Cureus ◽  
2021 ◽  
Author(s):  
Farah Chohan ◽  
Angela Ishak ◽  
Tyler Alderette ◽  
Pedram Rad ◽  
George Michel

Sign in / Sign up

Export Citation Format

Share Document