Results 71 to 80 of about 5,567 (230)

Clinically aggressive central giant cell granulomas in two patients with neurofibromatosis 1 [PDF]

open access: yes, 2006
Background Neurofibromatosis 1 (NF1) is an autosomal dominantly inherited disorder caused by a spectrum of mutations affecting the Nf1 gene. Affected patients develop benign and malignant tumors at an increased frequency.
Edwards, Paul C.   +5 more
core   +1 more source

Gingival Squamous Cell Carcinoma: Diagnostic Challenges and Clinical Implications

open access: yesClinical Case Reports, Volume 14, Issue 5, May 2026.
ABSTRACT Oral squamous cell carcinoma (OSCC) is one of the highly invasive malignancies globally, accounting for the vast majority of all oral cancers, that is, more than 90%. Carcinomas of the gingiva represent a distinct subgroup of OSCC, constituting approximately 12% of all OSCC cases. These neoplasms might mimic the inflammatory and reactive state
Gitanjali Subedi   +5 more
wiley   +1 more source

Florid cement-osseous dysplasia of maxilla and mandible: a rare clinical case

open access: yesBrazilian Journal of Oral Sciences, 2015
Cemento-osseous dysplasia is a group of disorders known to originate from periodontal ligament tissues. Florid cemento-osseous dysplasia clearly appears to be a form of bone and/or cementoid tissues restricted to jaw bones.
Chandramani B. More   +2 more
doaj   +1 more source

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

open access: yes, 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.   +4 more
core   +1 more source

Pseudotumoural soft tissue lesions of the hand and wrist: a pictorial review [PDF]

open access: yes, 2011
: Mimickers of soft tissue tumours in the hand and wrist are more frequent than true neoplastic lesions. Pseudotumours belong to a large and heterogeneous group of disorders, varying from normal anatomical variants, cystic lesions, post-traumatic lesions,
Filip M. Vanhoenacker   +4 more
core   +1 more source

Vascularized Cardiac Tissue Engineering: From Advances in Biofabrication to Translational Applications

open access: yesAdvanced Science, Volume 13, Issue 23, 23 April 2026.
This review presents a process‐oriented framework for vascularized cardiac tissue engineering, highlighting how the coordinated design of cells, biomaterials, and biofabrication strategies enables the functional development or vascularized myocardium for disease modelling and drug discovery.
Yang Liu   +9 more
wiley   +1 more source

Desmoplastic ameloblastoma of maxilla: a case report [PDF]

open access: yes, 2010
Ameloblastoma is the most common neoplasm affecting the jaws, arising from the odontogenic epithelium. Despite its locally aggressive nature, it is considered to be benign.
Alex, Sheeba   +4 more
core   +1 more source

Fibro-Osseous Lesions of the Maxillofacial Bones [PDF]

open access: yesHead and Neck Pathology, 2013
Fibro-osseous lesions of the maxillofacial bones should be classified based on their radiographic growth pattern. This method can simplify this category of lesions, which have considerable overlapping histologic features. These neoplasms can be grouped into three categories: (a) fibrous dysplasia; (b) ossifying fibroma; (c) and osseous dysplasia ...
openaire   +2 more sources

Multisystem Sarcoidosis Presenting With Hypercalcemia, Lytic Bone Lesion, and Mesenteric Panniculitis in Chronic Kidney Disease

open access: yesClinical Case Reports, Volume 14, Issue 4, April 2026.
The clinical photograph shows bilateral leg swelling with right‐sided predominance and cutaneous changes. CT images (A–C) demonstrate abdominal and retroperitoneal lymphadenopathy, and image D shows a hypodense lytic spinal lesion, suggesting multifocal disease involving the abdomen, retroperitoneum, and spine.
Aishwarya Holi   +5 more
wiley   +1 more source

OMICS Profiling Identifies Signatures of Senescence in Osteogenesis Imperfecta Osteoblasts Counteracted by 4‐PBA

open access: yesJournal of Cellular and Molecular Medicine, Volume 30, Issue 7, April 2026.
ABSTRACT Mutations in collagen I are the most common cause of osteogenesis imperfecta (OI), leading to delayed protein folding and structurally abnormal molecules. While some aberrant collagen is secreted into the extracellular matrix (ECM), impairing bone quality, a significant fraction is retained intracellularly, disrupting osteoblast homeostasis. 4‐
Roberta Besio   +7 more
wiley   +1 more source

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