Results 61 to 70 of about 6,987 (215)

Fibroma cemento-osificante gingival mandibular: presentación de un caso [PDF]

, 2004
Presentamos el caso clínico de una mujer con un fibroma cemento- osificante gigante dependiente de la encía mandibular de 20 años de evolución. El fibroma cemento-osificante es un tumor poco frecuente, clasificado dentro de las lesiones fibroóseas ...
Crespo Pinilla, J.I., Espeso Ferrero, A., Galdeano Arenas, M., Verrier Hernández, Alberto, Álvarez Otero, Rafael   +4 more
core   +1 more source

Cementoblastoma in the Maxilla: A Case Report [PDF]

, 2009
The cementoblastoma is a rare, benign odontogenic tumour. It is generally asymptomatic and usually occurs in young adults. It is more common in males.
Balmer, Colette, Barker, Gillian L, Begley, Anne   +2 more
core   +1 more source

An Unusual Case of Periapical Cemento‐Osseous Dysplasia

Clinical Case Reports, Volume 13, Issue 10, October 2025.
ABSTRACT Periapical cemento‐osseous dysplasia (PCOD) is a benign fibro‐osseous condition often discovered incidentally during radiographic examinations. Accurate diagnosis is crucial to prevent unnecessary treatment. Conservative management with regular monitoring is typically sufficient, as illustrated in this case involving a 62‐year‐old female ...
Emanuel Harouni, Elham Radan, Parish Sedghizadeh   +2 more
wiley   +1 more source

LABRAD : Vol 42, Issue 1 - March 2016 [PDF]

, 2016
Biochemical Bone Profiles Available at Clinical Laboratoryof Aga Khan University Hospital Ionized Calcium Determination in Clinical Labortory Parathyroid Hormone Disorders and Issues of Testing Tubular Maximum Reabsorption Rate of Phosphate to Glomerular
Aga Khan University Hospital, Karachi,
core   +1 more source

novel insights into the genetics and pathophysiology of adrenocortical tumors [PDF]

, 2015
International audienceAdrenocortical tumors (ACTs) are typically unilateral and can be classified as benign adrenocortical adenomas (ACAs) or malignant adrenocortical cancers (ACCs).
Drougat, Ludivine, Lefèvre, Lucile, Omeiri, Hanin, Ragazzon, Bruno   +3 more
core   +7 more sources

Novel report of an osteogenic tumor in a late Jurassic Mamenchisaurid from Thailand

Journal of Anatomy, Volume 247, Issue 3-4, Page 699-711, September/October 2025.
Here we describe a pathology in an ulna of a Late Jurassic mamenchisaurid from Thailand. We use anatomical descriptions, CT scanning, and bone histology to identify the pathology as an osteogenic tumor. Abstract Here we report on an osseous abnormality and multiple fractures in an ulna of a subadult basal Eusauropod (Mamenchisauridae) from the Late ...
Siripat Kaikaew, Suravech Suteethorn, Anusuya Chinsamy   +2 more
wiley   +1 more source

Osteoid-osteoma and osteoblastoma with rare localization – presentation of 4 clinical cases

Journal of the Bulgarian Orthopaedics and Trauma Association, 2023
Osteoid-osteoma and osteoblastoma are the two most common representatives of benign bone-forming tumors. Although both tumors are well known to the orthopedic community in Bulgaria, there are several rare localizations that would present difficulties in
Kircho Patrikov, Yordan Ivanov
doaj   +2 more sources

Cervical Osteoblastoma: A Rare Primary Spinal Tumor

Nepal Journal of Neuroscience, 2016
Osteoblastoma is a rare and benign osteoid producing primary bone tumor that affects mainly the long bones. It makes 5% of spinal tumors, mostly arising within the posterior elements of the spine within the second and 3rd decades of life.
Gopal Sedain , Ram K Shrestha , Mohan R Sharma   +2 more
doaj   +1 more source

Unveiling Hybrid Ameloblastoma: Uncommon Variant With Unique Diagnostic Challenges

Clinical Case Reports, Volume 13, Issue 8, August 2025.
ABSTRACT Ameloblastoma is a benign tumor originating from odontogenic tissue and has various histological subtypes. It accounts for approximately 18% of all odontogenic tumors. Hybrid ameloblastoma represents a combination of histopathological features from both desmoplastic ameloblastoma and conventional ameloblastoma, likely arising from the varying ...
Dilasha Dhungel, Varun Rastogi, Sandhya Chaurasia, Priyambada Karna   +3 more
wiley   +1 more source

Abnormal DNA Methylation Profile Suggests the Extension of the Clinical Spectrum of the SETD2 ‐Related Disorders to a Syndromic Multiple Tumor Phenotype

American Journal of Medical Genetics Part A, Volume 197, Issue 7, July 2025.
ABSTRACT SETD2 has an essential role in epigenetic regulation. SETD2 pathogenic variants cause neurodevelopmental disorders (SETD2‐NDDs) that most commonly include various degrees of intellectual disability and behavioral disorders, macrocephaly, brain malformations, and generalized overgrowth.
Marie Lucain, Antonio Vitobello, Bekim Sadikovic, Juliette Albuisson, Léa Gaudillat, Martin Chevarin, Julien Maraval, Christel Thauvin‐Robinet, Jennifer Kerkhof, Christophe Philippe, Sophie Nambot, Laurence Faivre   +11 more
wiley   +1 more source