Results 41 to 50 of about 1,403 (202)

Intraosseous Collagenous Fibroma (Desmoplastic Fibroblastoma) Involving Maxillary Bone [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2018
The collagenous fibroma (desmoplastic fibroblastoma) is a rare benign soft tissue tumour that can occur in the oral mucosa; intraosseous lesion is uncommon. A 43-year-old woman showed a well-circumscribed intraosseous radiolucency involving the maxillary
Natália Galvão Garcia   +4 more
doaj   +1 more source

Desmoplastic Fibroma and Cemento Ossifying Fibroma of The Anterior Maxilla: A Rare Case Report: Desmoplastic Fibroma dan Cemento Ossifying Fibroma: Laporan Kasus Langka

open access: yes, 2021
Tumors located in the maxillofacial part of the body were classified by WHO in 2017 and among these are intraosseous form of fibromatosis known as Desmoplastic and Cemento-ossifying fibromas.
Vera Julia, Eky Nasuri, Victor Pakpahan
core  

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

open access: yesCase 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   +6 more
wiley   +1 more source

[Desmoplastic fibroma].

open access: yesRevue 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   +4 more
openaire   +3 more sources

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

open access: yesBabcock 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   +4 more
doaj   +1 more source

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

open access: yesDental 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   +3 more
doaj   +1 more source

Pathomorphology of Ameloblastomas

open access: yesХірургія 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

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

open access: yes
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   +5 more
core   +1 more source

Odontogenic Fibroma of Maxilla: A Rare Clinical Entity

open access: yesBiomedical 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   +2 more
doaj   +1 more source

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

open access: yesHuman 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   +14 more
wiley   +1 more source

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