Results 21 to 30 of about 11,902 (188)

Desmoplastic Fibroma Recurrence Associated with Tuberous Sclerosis in a Young Patient [PDF]

Case Reports in Dentistry, 2018
Case Report. A nine-year-old patient with a diagnosis of tuberous sclerosis (with no pathological record) that showed calcifications at the brain level. Besides, the case showed the Vogt triad (epilepsy, mental retardation, and sebaceous adenoma).
A. M. Espinoza-Coronado, J. P. Loyola-Rodríguez, J. H. Olvera-Delgado, J. O. García-Cortes, J. F. Reyes-Macías   +4 more
doaj   +2 more sources

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

Rev Bras Ortop (Sao Paulo)
Desmoplastic fibroma; Orthopedic; TibiaFibroma desmoplásico; Ortopedia; TibiaFibroma desmoplàstic; Ortopèdia; TíbiaDesmoplastic fibroma of bone is a very uncommon, benign but locally aggressive fibrogenic tumor.
Pujol O, Castellanos S, Carrasco MG, Garzón A, Romagosa C, Vélez R.   +5 more
europepmc   +2 more sources

Hyperparathyroidism-Jaw Tumor Syndrome Associated to a CDC73 Gene Pathogenic VARIANT and a Nonossifying Desmoplastic Fibroma of the Mandible. [PDF]

Case Rep Endocrinol
Most cases of primary hyperparathyroidism (PHPT) are sporadic and are caused by parathyroid adenomas. Hereditary forms may occur in up to 10% of PHPT patients and are more frequent in younger patients. The hyperparathyroidism‐jaw tumor (HPT‐JT) syndrome is characterized by PHPT in up to 95% of patients and ossifying fibromas in the jaw in 25%–50%.
Elena C, Andrea C, Di Giovanni F, Alessandra L, Mirella F, Antonella M.   +5 more
europepmc   +2 more sources

A Case of Desmoplastic Fibroma of the Thoracic Spine with Incomplete Paralysis of both Lower Limbs [PDF]

Spine Surgery and Related Research
Takafumi Yayama, Kanji Mori, Shunichi Miyahara, Hideki Saito, Yuya Chosei, Tomohiro Mimura, Kosuke Kumagai, Shinji Imai   +7 more
doaj   +2 more sources

Desmoplastic fibroma of the temporal bone

Otolaryngology Case Reports, 2021
Background: Desmoplastic fibroma is a benign osseous neoplasm most often affecting the facial skeleton when presenting in the head and neck region. Involvement of the temporal bone is rare.
Masanari G. Kato, Varun V. Varadarajan, Ashly Cordero Rivera, Jameson K. Mattingly   +3 more
doaj   +1 more source

Desmoplastic fibroma of the occipital bone in adult female: A case report

Interdisciplinary Neurosurgery, 2021
Desmoplastic fibroma is a primary locally aggressive bone tumor which is exceedingly rare in the cranial bones. We report the first case of occipital bone desmoplastic fibroma.
Mohamed Kh. Elbadawy, Mahmoud M. Taha, Tarek H. AbdelBary   +2 more
doaj   +1 more source

Desmoplastic fibroma of the maxilla in a 5-year-old patient with Tuberous Sclerosis Complex (TSC): Case report and review of the literature

Oral and Maxillofacial Surgery Cases
The following case report details the presentation of a left maxillary painless expansile lesion in a five-year-old female that was proven to be desmoplastic fibroma (DF) of the maxilla, which was treated via a conservative excision. Given the paucity of
Hunter Watson, Sarah Glass, Yotom Rabinowitz, Daniel Hawkins   +3 more
doaj   +2 more sources

Rare Desmoplastic Fibroma in Ramus and Mandibular Angle: Presentation of a Case Report With Review of Literature

Acta Medica Iranica, 2020
Desmoplastic fibroma is a rare, benign fibrous tumor of bone which is locally aggressive. The mandible is the most prevalent affected of the facial bones.
Azadehzeinab Titidej, Maryam Jolehar
doaj   +1 more source

Clinical analysis of 8 cases of desmoplastic fibroma of the jaw

口腔疾病防治, 2022
Objective To improve the dentist's understanding of desmoplastic fibroma of the jaw, we investigated the clinical manifestations, pathological features, treatment and prognosis of this disease.
HU Mingjing, WANG Zhiyong
doaj   +1 more source

Desmoplastic Fibroma : Mandible [PDF]

Medical Journal Armed Forces India, 2004
Desmoplastic fibroma of bone has been described as a rare, locally aggressive, benign lesion that histologically resembles a desmoid tumour of the soft tissue. It was initially described in 1958 by Jaffe, who separated it as a distinct entity from other intraosseous fibrous tumours.
V K, Shukul, S, Saxena, B G, Shankar
openaire   +2 more sources