scholarly journals Peripheral Ameloblastoma of Upper Gingiva in a Patient with Port-Wine Stain

2020 ◽  
Vol 2020 ◽  
pp. 1-5
Author(s):  
Natheer H. Al-Rawi ◽  
Sahar Othman ◽  
Ab Rani Samsudin

The peripheral ameloblastoma (PA), also known as extraosseous ameloblastoma, is a rare soft tissue tumor of odontogenic origin, accounting for 1–5% of all ameloblastoma. In some cases, saucerization of underlying bone is the only radiological evidence of this lesion, and PA has identical histological characteristics of intraosseous ameloblastoma. However, it is slow growing, less aggressive, and less invasive in nature. The present report describes a rare case of PA in the maxillary labial gingiva of a 37-year-old man with port-wine vascular malformation. PA was clinically diagnosed as a pyogenic granuloma, and following the surgical treatment of the lesion, its histological features were of ameloblastoma. This case illustrates the importance of including peripheral ameloblastoma in the differential diagnosis of painless exophytic gingival swelling.

2001 ◽  
Vol 144 (3) ◽  
pp. 644-645 ◽  
Author(s):  
R. Katta ◽  
K. Bickle ◽  
L. Hwang

2019 ◽  
Vol 12 (1) ◽  
pp. e225640
Author(s):  
Aakash Pandita ◽  
Astha Panghal ◽  
Girish Gupta ◽  
Kirti M Naranje

We present here two-term neonates presenting with right lower limb hypertrophy, a port-wine stain, acral abnormalities and clubfeet. These neonates had overlapping features of Klippel Trenaunay syndrome and congenital lipomatous overgrowth, vascular malformation, epidermal nevi and scoliosis/skeletal abnormalities. Such overgrowth syndrome has not been previously described in the literature. Both the neonates are doing well and are under regular follow-up.


2015 ◽  
Vol 2015 ◽  
pp. 1-6
Author(s):  
Andrew Rockafellow ◽  
Whitney Florin ◽  
Elizabeth Philipone ◽  
David Koslovsky

Pyogenic granuloma is a type of inflammatory hyperplasia often seen in the oral cavity and occurs in response to stimuli such as local irritants and hormonal factors. Pyogenic granulomas associated with pregnancy are referred to as pregnancy tumors. This report describes the presentation and surgical management of a large pregnancy tumor occurring in a patient with an overlying isolated facial port-wine stain.


2010 ◽  
Vol 52 (4) ◽  
pp. e8-e10 ◽  
Author(s):  
Karl Rodins ◽  
Dallas Gramp ◽  
Daniel James ◽  
Sandeep Kumar

2021 ◽  
Vol 15 (10) ◽  
pp. 20-26
Author(s):  
Satyam Satyam ◽  
Alpana Manchanda ◽  
Ramya Kamraj ◽  
Anju Garg ◽  
Kaushik Majumdar

Alveolar soft part sarcoma is a rare soft tissue tumor with uncertain histogenesis. It is a slow growing tumor with a high rate of metastasis. The tumor is not easily identified as clinical symptoms are not pronounced. The retroperitoneum is a rare location of tumor, with a few cases published in literature. Surgical excision is the mainstay of treatment. Here we describe a rare case of a large retroperitoneal Alveolar soft part sarcoma in a young female with radiological and histopathological findings.


2014 ◽  
Vol 28 (6) ◽  
pp. 1564.e9-1564.e14 ◽  
Author(s):  
Girish D. Deore ◽  
Abhijit N. Gurav ◽  
Rahul Patil ◽  
Abhijeet R. Shete ◽  
Ritam S. NaikTari ◽  
...  

2018 ◽  
Vol 28 (4) ◽  
pp. 274
Author(s):  
Raiana Costa Silva ◽  
Bruna Milhomens de Sousa ◽  
Luisa Moura Fialho ◽  
Rodrigo Lorenzi Poluha

O granuloma piogênico (GP) é um processo proliferativo não neoplásico. Este termo entretanto, é equivocado, uma vez que não está relacionado a qualquer infecção, não contém pus e não é um verdadeiro granuloma. A ocorrência do GP recorrente associado a lesões vasculares na pele, tais como manchas de vinho do porto, tem sido descrita na literatura. Paciente do gênero masculino com 23 anos de idade foi atendido na Universidade Federal do Maranhão apresentando uma lesão com características de granuloma piogênico na vestibular do primeiro molar, associada à mancha vinho do porto. O diagnóstico foi confi rmado através de biopsia excisional e análise histopatológica. Devido à recorrência da lesão após a abordagem cirúrgica, injeções intralesionais de corticoides foram realizadas três vezes. Após dois anos de acompanhamento, não houve recorrência. Pode-se concluir que, apesar da alta prevalência de recorrência do granuloma piogênico, injeções intralesionais com corticoides podem ser uma alternativa ao tratamento cirúrgico convencional.


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