scholarly journals Management of a parotid sialocelein a young patient: case report and literature review

2010 ◽  
Vol 18 (4) ◽  
pp. 432-436 ◽  
Author(s):  
Melissa Rodrigues de Araujo ◽  
Bruna Stuchi Centurion ◽  
Danielle Frota de Albuquerque ◽  
Luiz Henrique Marchesano ◽  
José Humberto Damante
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Young Patient ◽  
Patient Case

Rare clear cell odontogenic carcinoma associated with impacted tooth in a young patient: case report and literature review

2021 ◽  
Author(s):  
Erasmo Bernardo Marinho ◽  
Ana Paula Negreiros Nunes Alves ◽  
Francisco Januário Farias Pereira-Filho ◽  
Antonio Ernando Carlos Ferreira-Junior ◽  
Mário Rogério Lima Mota ◽  
...  
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Young Patient ◽  
Clear Cell ◽  
Patient Case ◽  
Impacted Tooth ◽  
Clear Cell Odontogenic Carcinoma ◽  
Odontogenic Carcinoma

Ameloblastic fibro-odontoma in a child patient: case report and literature review

2021 ◽  
Vol 10 (2) ◽  
pp. e26610212430
Author(s):  
Gustavo Zanna Ferreira ◽  
Carolina Ferrairo Danieletto-Zanna ◽  
Liogi Iwaki Filho ◽  
Rômulo Maciel Lustosa ◽  
Willian Pecin Jacomacci ◽  
...  
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Bone Regeneration ◽  
Clinical Characteristics ◽  
Patient Case ◽  
Lesion Pattern ◽  
Local Bone ◽  
Ameloblastic Fibroma ◽  
Child Patient

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.

scholarly journals Successful treatment and FDG-PET/CT monitoring of HHV-6 encephalitis in a non-neutropenic patient: case report and literature review

2017 ◽  
Vol 23 (6) ◽  
pp. 908-912 ◽  
Author(s):  
Elda Righi ◽  
Alessia Carnelutti ◽  
Daniele Muser ◽  
Francesco Zaja ◽  
Elisa Lucchini ◽  
...  
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Successful Treatment ◽  
Fdg Pet ◽  
Neutropenic Patient ◽  
Patient Case ◽  
Pet Ct ◽  
Fdg Pet Ct

scholarly journals Ablepharon macrostomia syndrome in a Thai patient: case report and literature review

2020 ◽  
Vol 14 (2) ◽  
pp. 83-88
Author(s):  
Phawin Kor-anantakul ◽  
Kanya Suphapeetiporn ◽  
Somchit Jaruratanasirikul
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Exome Sequencing ◽  
Whole Exome Sequencing ◽  
Sequencing Analysis ◽  
Patient Case ◽  
Thai Patient ◽  
Labia Minora ◽  
Whole Exome ◽  
Rare Congenital Disorder

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.

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