دورية أكاديمية

Central Myoepithelioma of the Maxilla.

التفاصيل البيبلوغرافية
العنوان: Central Myoepithelioma of the Maxilla.
المؤلفون: Rodrigues-Fernandes CI; Oral Pathology Unit, Department of Clinic and Preventive Dentistry, Universidade Federal de Pernambuco, Recife, Pernambuco, 50740-600, Brazil. carla.rodrigues212@gmail.com., Farias DM; Oral Pathology Unit, Department of Clinic and Preventive Dentistry, Universidade Federal de Pernambuco, Recife, Pernambuco, 50740-600, Brazil., de Castro JFL; Oral Pathology Unit, Department of Clinic and Preventive Dentistry, Universidade Federal de Pernambuco, Recife, Pernambuco, 50740-600, Brazil., Dos Santos LP; Public Health Department, Belém, Pará, Brazil., de Almeida OP; Department of Oral Diagnosis, Semiology and Pathology Areas, Piracicaba Dental School, University of Campinas, Piracicaba, São Paulo, Brazil., da Cruz Perez DE; Oral Pathology Unit, Department of Clinic and Preventive Dentistry, Universidade Federal de Pernambuco, Recife, Pernambuco, 50740-600, Brazil.
المصدر: Head and neck pathology [Head Neck Pathol] 2024 Jun 28; Vol. 18 (1), pp. 61. Date of Electronic Publication: 2024 Jun 28.
نوع المنشور: Case Reports; Journal Article
اللغة: English
بيانات الدورية: Publisher: Country of Publication: United States NLM ID: 101304010 Publication Model: Electronic Cited Medium: Internet ISSN: 1936-0568 (Electronic) Linking ISSN: 1936055X NLM ISO Abbreviation: Head Neck Pathol Subsets: MEDLINE
أسماء مطبوعة: Publication: June 2011- : New York : Springer Science+ Business Media
Original Publication: Secaucus, NJ : Humana Press
مواضيع طبية MeSH: Myoepithelioma*/pathology , Maxillary Neoplasms*/pathology , Maxillary Neoplasms*/surgery, Humans ; Female ; Adolescent ; Biomarkers, Tumor/analysis
مستخلص: Myoepithelioma is a benign salivary gland tumor. Central myoepitheliomas are very rare. The aim of this report was to describe a case of maxillary myoepithelioma. A 14-year-old female patient presented with an multilocular lesion in the anterior maxilla, with nearly 8 months of duration. The lesion was asymptomatic, and the patient's dental history was unremarkable. The diagnostic hypothesis was an odontogenic tumor. Biopsy specimen consisted of nests of plasmacytoid cells in a myxoid stroma without duct formation. No cellular atypia or bone and cartilage formation were noted. The neoplastic cells were positive for Pan-cytokeratin, S100, CK7, and CK8. The final diagnosis was myoepithelioma. The patient was treated by surgical excision followed by bone curettage, and no signs of recurrence were found after 8 years of treatment.
(© 2024. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.)
References: Oral Surg Oral Med Oral Pathol Oral Radiol. 2012 Dec;114(6):e49-53. (PMID: 22951143)
J Oral Maxillofac Surg. 2003 Mar;61(3):379-86. (PMID: 12618980)
Ultrastruct Pathol. 2019;43(6):312-325. (PMID: 31766935)
Pathol Int. 2019 Jan;69(1):42-47. (PMID: 30605259)
Neuroophthalmology. 2014 Jan 28;38(1):14-20. (PMID: 27928268)
J Oral Maxillofac Surg. 2008 Apr;66(4):800-3. (PMID: 18355609)
Am J Surg Pathol. 2013 Jul;37(7):960-8. (PMID: 23681076)
Histopathology. 2014 Dec;65(6):917-22. (PMID: 25066216)
فهرسة مساهمة: Keywords: Bone; Jaw; Maxilla; Myoepithelioma
المشرفين على المادة: 0 (Biomarkers, Tumor)
تواريخ الأحداث: Date Created: 20240628 Date Completed: 20240628 Latest Revision: 20240701
رمز التحديث: 20240701
مُعرف محوري في PubMed: PMC11213834
DOI: 10.1007/s12105-024-01665-y
PMID: 38940938
قاعدة البيانات: MEDLINE
الوصف
تدمد:1936-0568
DOI:10.1007/s12105-024-01665-y