Results 41 to 50 of about 12,005 (203)

Desmoplastic fibroma of the lower jaw in a 2-year-old patient; report of a rare case

Dental Research Journal, 2020
Desmoplastic fibroma (DF) is a rare benign but aggressive fibrous lesion with an unknown etiology. It has an affinity for the mandible. DF has a high rate of recurrence after surgical resection.
Farnoosh Mohammadi, Gholamreza Shirani, Samira Derakhshan, Taraneh Faghihi   +3 more
doaj   +1 more source

Multiple Odontogenic Keratocysts as the Initial Manifestation of Gorlin Syndrome in a Child: A Case Report With Conservative Management and Diagnostic Considerations

Case Reports in Dentistry, Volume 2026, Issue 1, 2026.
Multiple odontogenic keratocysts are one of the major diagnostic criteria of Gorlin syndrome and may represent an early manifestation of the disorder in pediatric patients. This report describes the diagnostic process and management of an 11‐year‐old boy who presented with multiple mandibular cystic lesions associated with displacement of developing ...
V. Anguera-Ortega, P. Cahuana-Bartra, L. Brunet-Llobet, Y. González-Chópite, E. I. Mashala, J. Miranda-Rius, Priya Gusain   +6 more
wiley   +1 more source

Massive Desmoplastic Fibroma of the Proximal Tibia: Case Report [PDF]

Desmoplastic fibroma; Orthopedic; TibiaFibroma desmoplásico; Ortopedia; TibiaFibroma desmoplàstic; Ortopèdia; TíbiaDesmoplastic fibroma of bone is a very uncommon, benign but locally aggressive fibrogenic tumor.
Romagosa, Cleofé, Garzón Arana, Alejandro, Pujol, Oriol, García-Carrasco, María, Castellanos Alonso, Sara, Vélez, Roberto   +5 more
core   +1 more source

[Desmoplastic fibroma].

Revue de stomatologie et de chirurgie maxillo-faciale, 2010
Desmoplastic fibroma is a rare benign intraosseous neoplasms. They can affect the jaw. Posterior mandibular bone involvement is the most frequent localization. They are locally aggressive and recurrence is frequent. Radioclinical signs are not specific and the histological diagnosis may be difficult.
L, Ben Slama, A, Zaghbani, A, Zoghbani, S, Hidaya, B, Ruhin   +4 more
openaire   +3 more sources

A case report of desmoplastic fibroma in a three-year-old black African girl

Babcock University Medical Journal
Background: Desmoplastic fibroma is a very rare bone tumour that is commonly recognised by its striking resemblance to desmoid fibromatosis, commonly seen in soft tissues.
Olaejirinde Olaofe, Chigozie Okongwu, Godwin Umerah, Oluwatosin Omoyiola, Omolade Betiku   +4 more
doaj   +1 more source

Pathomorphology of Ameloblastomas

Хірургія дитячого віку, 2022
Objective. To study the pathomorphological structure of ameloblastomas and work out their classification. Materials and methods. Histological analysis of the material obtained after the removal of ameloblastomas of the jaws in 67 patients was carried ...
O. Tymofieiev, N. Ushko
doaj   +1 more source

The Rare Occurrence of a Solitary Collagenous Fibroma in the Gingiva of a 2‐Year‐Old Child: A Case Report

Case Reports in Dentistry, Volume 2026, Issue 1, 2026.
Background Desmoplastic fibroblastoma (DF), or collagenous fibroma (CF), is a distinct and rare benign soft tissue tumor, clinically presenting as a slow‐growing firm mass originating from fibroblastic and myofibroblast cells. The exact cause of CF remains unknown, and it is considered a sporadic lesion without any known genetic or environmental risk ...
Anagha Chonat, Aruna Sharma, A. Santha Devi, R. Narayane, A. Sanguida, Ramya Raja, Hannah Wesley   +6 more
wiley   +1 more source

Odontogenic Fibroma of Maxilla: A Rare Clinical Entity

Biomedical Research Journal, 2018
The odontogenic fibroma (OF) is a rare benign tumour of mesodermal origin characterized by varying amounts of inactive looking odontogenic epithelium embedded in a mature, fibrous stroma.
Shashikant A Pol, Arjun Dass, Nitin Gupta   +2 more
doaj   +1 more source

Secondary desmoplastic fibroma-like tissue changes in mandibular fibrous dysplasia: clinicopathological and molecular study of a case

, 2020
Fibrous dysplasia may show locally aggressive behaviour reflecting secondary intralesional changes, extension to soft tissue, or malignant transformation.
Fadda M. T., Riminucci M., Corsi A., Valentini V., Terenzi V.   +4 more
core   +1 more source

SUFU Loss‐of‐Function Heterozygous Variants Cause a Distinct Neurodevelopmental Delay With Simultaneous Effects on Brain Size

Human Mutation, Volume 2026, Issue 1, 2026.
Heterozygous loss‐of‐function variants in SUFU are associated with Gorlin syndrome (MIM:620343) and tumor predisposition, while biallelic missense variants underlie recessive Joubert syndrome (JS; MIM:617757). Interestingly, emerging evidence suggests that SUFU haploinsufficiency also contributes to neurodevelopmental disorders (NDDs).
Ludovico Graziani, Chiara Minotti, Miriam Lucia Carriero, Lorena Travaglini, Mathilde Nizon, Hilde Van Esch, Julie Vogt, Nick Drinkall, Joanna Jarvis, Emanuele Agolini, Mario Bengala, Alessandro Mussa, Antonio Novelli, Giuseppe Novelli, Stuart Scott   +14 more
wiley   +1 more source