scholarly journals Giant maxillary ameloblastic fibroma, a case report from university hospital of yalgado ouédraogo (burkina faso)

Author(s):  
Idani Motandi ◽  
Millogo Mathieu ◽  
Badini Soutongnoma Ahmed Patrick ◽  
Ili Bévianda Vincent ◽  
Zango Adama ◽  
...  
2016 ◽  
Vol 06 (03) ◽  
pp. 252-255
Author(s):  
Angèle Kalmogho ◽  
Abdoulaye Ouattara ◽  
Chantal Zoungrana ◽  
Caroline Yonaba ◽  
Flore Ouédraogo ◽  
...  

Author(s):  
M.I.L.L.O.G.O. Mathieu ◽  
O.U.E.D.R.A.O.G.O. Richard Wend-Lasida ◽  
I.D.A.N.I. Motandi ◽  
I.L.I. Bévianda Vincent ◽  
C.O.U.L.I.B.A.L.Y. Arsène ◽  
...  

1998 ◽  
Vol 56 (3) ◽  
pp. 368-372 ◽  
Author(s):  
Edward L Mosby ◽  
David Russell ◽  
Scott Noren ◽  
Bruce F Barker

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.


OALib ◽  
2018 ◽  
Vol 05 (01) ◽  
pp. 1-12
Author(s):  
Koudougou Jonas Kologo ◽  
Georges Rosario Christian Millogo ◽  
Anna Thiam Tall ◽  
Théodore Boro ◽  
Georges Kinda ◽  
...  

2020 ◽  
Vol 7 (07) ◽  
pp. 4871-4874
Author(s):  
Amal Hajri ◽  
Abdessamad El Azhary ◽  
Driss Erguibi ◽  
Rachid Boufettal ◽  
Saad Rifki El Jai ◽  
...  

Primary anorectal malignant melanoma is an extremely rare condition. It appears at the third highest frequency after melanomas of the skin and retina. Its prognosis is dreadful because of the early onset of metastases. The treatment remains essentially surgical. We report an observation of primitive anorectal melanoma, collected at the department of surgery for digestive cancers and liver transplantation of the Ibn Rochd University Hospital of Casablanca, with a review of the literature. In order to analyse the clinical, paraclinical and therapeutic characteristics of primary anorectal melanoma.


2020 ◽  
Vol 35 (1) ◽  
pp. 63-65
Author(s):  
Anna Claudine Lahoz ◽  
Precious Eunice Grullo ◽  
Ryner Jose Carrillo

ABSTRACT Objective: To report a case of thyroglossal duct carcinoma with concurrent papillary thyroid carcinoma Methods: Design: Case Report Setting: Tertiary National University Hospital Patient: One Results: A 46-year-old woman was diagnosed with thyroglossal duct carcinoma after undergoing a Sistrunk procedure. Due to presence of thyroid nodules, the patient underwent second stage thyroidectomy with central neck dissection which revealed papillary thyroid carcinoma. Conclusion: Thyroglossal duct carcinomas are rare entities and there is no current consensus regarding their management. Difficulties arise in the diagnosis of these tumors as they present similarly to benign thyroglossal duct cysts. Most cases are diagnosed postoperatively. Proper preoperative assessment including head and neck examination, biopsy, and radiologic imaging is necessary to recognize patients who could benefit from more aggressive management. Keywords: thyroglossal carcinoma; thyroglossal duct cyst; papillary thyroid carcinoma


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