Results 51 to 60 of about 11,759 (256)

Aggressive Multiple Central Giant Cell Granulomas of the Jaws

Case Reports in Dentistry, Volume 2023, Issue 1, 2023., 2023
Central giant cell granuloma (CGCG) is considered a benign intraosseous lesion with a varied range of clinical features in two subtypes, including aggressive and non‐aggressive lesions. This study presents a 9‐year‐old boy with multiple bilateral CGCG in the mandible without any systemic disease or specific syndrome.
Farnoush Mohammadi, Hoorieh Bashizadehfakhar, Sara Aliasghari, Zahra Gholamhoseini, Pia L. Jornet   +4 more
wiley   +1 more source

Secondary amenorrhea in a case of gonadotropin independent precocious puberty: McCune-Albright syndrome [PDF]

, 2021
Precocious puberty may be gonadotropin dependent or gonadotropin independent and due to a myriad of causes including syndromic association. McCune-Albright syndrome (MAS) is a rare disorder, characterized by the triad of precocious puberty, polyostotic ...
Jayaraman, Sangumani, Natarajan, Sundari, Nazirudeen, Roshan, Subbiah, Sridhar, Vasanthiy, Vasanthiy   +4 more
core   +2 more sources

The West China Hospital radiographic classification for fibrous dysplasia in femur and adjacent bones: A retrospective analysis of 205 patients

Orthopaedic Surgery, Volume 14, Issue 9, Page 2096-2108, September 2022., 2022
The explanation of this classification from I to V. Cases presentation for each Type. Objective This study aims to investigate the reliability and clinical outcome of a newly developed classification system for patients with fibrous dysplasia (FD) of the femur and adjacent bones, optimizing its evaluation and management. Methods A total of 205 patients
Yitian Wang, Yi Luo, Li Min, Yong Zhou, Jie Wang, Yuqi Zhang, Minxun Lu, Hong Duan, Chongqi Tu   +8 more
wiley   +1 more source

A case report of McCune–Albright syndrome with hepatic manifestations

Clinical Case Reports, Volume 10, Issue 7, July 2022., 2022
Abstract McCune–Albright syndrome is a non‐hereditary disease characterized by café‐au‐lait skin spots, fibrous dysplasia of bone, and endocrinopathies. We report a boy with a history of repeated hospitalizations from birth due to severe jaundice and hyperthyroidism. At the age of 2 years, he suffered from a proximal left femoral fracture.
Mohammad Haddadi, Elahe Lal Kheirkhah, Mojgan Ansari, Samieh Ahmadzade, Zeinab Taraz, Saeid Yazdi   +5 more
wiley   +1 more source

Clinicopathological and genetic study of a rare occurrence: Malignant transformation of fibrous dysplasia of the jaws

Molecular Genetics &Genomic Medicine, Volume 10, Issue 1, January 2022., 2022
Whole exome sequencing revealed the underlying genetic mechanisms of osteosarcoma arising from fibrous dysplasia of the jaws. Significant somatic single nucleotide variations, including TP53, ROS1 AND CHD8, as well as large amounts of somatic copy number alterations were demonstrated.
Ruirui Shi, Xuefen Li, Jianyun Zhang, Feng Chen, Ming Ma, Yanrui Feng, Tiejun Li   +6 more
wiley   +1 more source

Monostotic fibrous dysplasia in a 10-year-old patient

BLDE University Journal of Health Sciences, 2021
Fibrous dysplasia is a rare congenital bone disorder which manifests as a localized defect in osteoblastic differentiation and maturation with the replacement of normal bone with an abnormal scar-like fibrous connective tissue.
Gayatri Nayanar, Mamatha G S. Reddy
doaj   +1 more source

Pediatric Benign Fibro‐Osseous Lesions of the Nose and Paranasal Sinuses: A Tertiary Hospital Experience

International Journal of Otolaryngology, Volume 2022, Issue 1, 2022., 2022
Background. Pediatric benign fibro‐osseous lesions of the nose and paranasal sinuses are considered rare neoplastic entities. These fibro‐osseous lesions are difficult to accomplish owing to the multifaceted anatomy of the skull base in addition to the closeness to neurovascular configurations. Objective.
Dalia Al Arfaj, Haifa Lafi Alenzi, Ali Almomen, Musab Bakri, Francesco Gazia   +4 more
wiley   +1 more source

Epidemiological and Clinical Characteristics of Fibrous Dysplasia of Bone

Zhongliu Fangzhi Yanjiu, 2022
Objective To describe the epidemiological and clinical characteristics of fibrous dysplasia of bone admitted to a single center in the past 30 years.
XU Hairong, LI Yuan, SHAN Huachao, YU Feng, NIU Xiaohui   +4 more
doaj   +1 more source

Safety of therapy with and withdrawal from denosumab in fibrous dysplasia and McCune‐Albright syndrome: an observational study

Journal of Bone and Mineral Research, Volume 36, Issue 9, Page 1729-1738, September 2021., 2021
ABSTRACT Denosumab (Dmab) treatment can benefit patients with fibrous dysplasia/McCune‐Albright syndrome (FD/MAS) by suppressing the receptor activator of nuclear factor κB ligand (RANKL)‐mediated increased bone resorption. However, limited data of two pediatric cases indicate that a rebound phenomenon may occur after withdrawal.
Maartje E. Meier, Stance N. Clerkx, Elizabeth M. Winter, Alberto M. Pereira, Annenienke C. van de Ven, Michiel A.J. van de Sande, Natasha M. Appelman‐Dijkstra   +6 more
wiley   +1 more source

Scoliosis with peculiar radiological features in a patient with McCune‐Albright syndrome

Clinical Case Reports, Volume 9, Issue 7, July 2021., 2021
Patients with McCune‐Albright Syndrome (MAS) should always attend regular follow‐up. Beside the endocrinological aspects, the screening must take into account osteoarticular complications such as scoliosis, even in patients without fibrous dysplasia. Abstract Patients with McCune‐Albright Syndrome (MAS) should always attend regular follow‐up.
Alexandre Michev, Luca Lungarotti, Maria Sole Prevedoni Gorone, Antonia Apicella, Giulia Di Vincenzo, Gian Luigi Marseglia, Ilaria Brambilla   +6 more
wiley   +1 more source