Results 51 to 60 of about 2,787 (193)

Fibrous Dysplasia of the Palate: Report of a Case and Review of Palatal Swellings

open access: yesCase Reports in Pediatrics, 2012
Fibrous dysplasia is a benign fibroosseous lesion characterised by the replacement of normal bone by excessive proliferation of cellular fibrous connective tissue which is slowly replaced by bone, osteoid, or cementum-like material. It causes bone pain,
Balasundari Shreedhar   +3 more
doaj   +1 more source

Frontal sinus mucocele in association with polyostotic fibrous dysplasia: A case report

open access: yesProceedings of Singapore Healthcare, 2019
Fibrous dysplasia is an uncommon developmental anomaly of bone wherein normal bone marrow is substituted and subsequently expanded by fibro-osseous tissue. Its association with mucocele formation in the paranasal sinuses is extremely rare.
Leslie Timothy Koh   +2 more
doaj   +1 more source

Atualização em etiologia, diagnóstico e manejo da precocidade sexual [PDF]

open access: yes, 2008
Precocious puberty is defined as the development of secondary sexual characteristics before the age of 8 years in girls and 9 years in boys. Gonadotropin-dependent precocious puberty (GDPP) results from the premature activation of the hypothalamic ...
ARNHOLD, Ivo J. P.   +3 more
core   +2 more sources

Clinicopathologic Analysis of Sarcomas in the Oral and Maxillofacial Region: A Systematic Review

open access: yesOral Diseases, EarlyView.
ABSTRACT Objective This study aimed to systematically review primary sarcomas in the oral and maxillofacial region, focusing on patient demographics and sarcoma‐specific characteristics, including clinical presentation, histopathology, treatment approaches, outcomes, and survival rates.
Iara Vieira Ferreira   +7 more
wiley   +1 more source

Fibrous Dysplasia Polyostotic: When Radiology Clarifies the Diagnosis

open access: yesGlobal Pediatric Health
Fibrous dysplasia is a rare non-hereditary congenital condition characterized by 2 main forms: monostotic and polyostotic. Monostotic is the more common form, while polyostotic, often associated with a syndrome, is rarer. The case presented involves a 10-
Ihssane Lahlou PhD   +8 more
doaj   +1 more source

Escondido pelo cabelo - um caso de puberdade precoce [PDF]

open access: yes, 2020
McCune-Albright syndrome (MAS) is one of the conditions causing precocious gonadotropin-independent puberty. It is a rare disease, characterized by two of the three following features: precocious puberty, polyostotic fibrous dysplasia (PFD), and café au ...
Costa, Sara T.   +4 more
core   +1 more source

Melorheostosis: Clinical, radiological, and histopathological features with a literature review

open access: yesPhysiological Reports, Volume 13, Issue 21, November 2025.
Abstract Melorheostosis is a rare sclerosing bone dysplasia that can clinically and radiologically mimic common bone disorders, particularly in atypical presentations. Its heterogeneous manifestations and limited awareness among clinicians frequently contribute to diagnostic delays or misdiagnosis. We report the case of a 34‐year‐old woman with chronic
Elif Koca   +5 more
wiley   +1 more source

Mc Cune Albright syndrome: gynecological perspective [PDF]

open access: yes, 2023
The key features of McCune-Albright syndrome include sexual precocious puberty, polyostotic fibrous dysplasia and café au lait spots. It is associated with hyperfunction of multiple endocrine glands.
Dharani E.   +2 more
core   +2 more sources

An Unusual Complication After Surgical Correction of Shepherd's Crook Deformity in a Young Woman: A Case Report and Literature Review

open access: yesMedicine Advances, Volume 3, Issue 3, Page 193-196, September 2025.
An 18‐year‐old female patient presented with shepherd's crook deformity in the left lower limb and was subsequently diagnosed with MAS according to the genetic analysis. This patient developed acute heart failure in the second morning after proximal femur osteotomy without preoperative cardiovascular abnormality or excessive liquid supplementation in ...
Rongjie Wu, Guangtao Fu
wiley   +1 more source

Osteoid Osteoma of the Occipital Condyle in Adolescents: Surgical Resection Under Navigation

open access: yesClinical Case Reports, Volume 13, Issue 5, May 2025.
ABSTRACT This article reports a 12‐year‐old male with occipital condyle osteoid osteoma, presenting with neck pain and limited motion, unresponsive to conservative treatment. CT revealed a right condylar lesion. Surgical excision via a right paramedian suboccipital incision achieved complete recovery, confirmed by pathology and 3‐month follow‐up.
Yiji Li   +8 more
wiley   +1 more source

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