Results 21 to 30 of about 6,163 (220)

Prophylactic intramedullary nailing of the proximal femur in a case of McCune Albright syndrome – A case report & review of literature

Journal of Orthopaedic Reports, 2023
Introduction: Premature puberty, café-au-lait pigmentation, polyostotic fibrous dysplasia, and/or varied endocrine disorders make up the unusual condition known as McCune Albright Syndrome.
Mrinal Mahadev Kambli, Shaswat Mishra, Sagar Bansal, Sachin Khemkar, Sanjeev Ghildiyal, Manish Jain   +5 more
doaj   +1 more source

Polyostotic fibrous dysplasia (McCune-Albright) with rare multiple epiphyseal lesions in association with aneurysmal bone cyst and pathologic fracture

Radiology Case Reports, 2021
Fibrous dysplasia, including McCune-Albright syndrome, is a genetic, non-inheritable benign bone disorder that may involve a single or multiple bone, typically occurring in the diaphysis or the metaphysis of long bones. In very rare instances polyostotic
Alvaro Burdiles, MD, Rodrigo Marín, MD, Ianiv Klaber, MD, Antonieta Solar, MD, Miguel Calderón, MD, Felipe Jara, MD, Fernanda Kara, MD, Diego Bazáes, MD   +7 more
doaj   +1 more source

Clinical Characteristics and Management of Patients With McCune-Albright Syndrome With GH Excess and Precocious Puberty: A Case Series and Literature Review

Frontiers in Endocrinology, 2021
BackgroundMcCune-Albright syndrome is a rare disorder characterized by fibrous dysplasia, café au lait skin spots, and hyperfunctioning endocrinopathies. The coexistence of precocious puberty and growth hormone excess in McCune-Albright syndrome is rare.
Xiao Zhai, Xiao Zhai, Lian Duan, Lian Duan, Yong Yao, Bing Xing, Kan Deng, Linjie Wang, Linjie Wang, Feng Feng, Zhiyong Liang, Hui You, Hongbo Yang, Hongbo Yang, Lin Lu, Lin Lu, Shi Chen, Shi Chen, Renzhi Wang, Hui Pan, Hui Pan, Huijuan Zhu, Huijuan Zhu   +22 more
doaj   +1 more source

Imaging of advanced craniofacial fibrous dysplasia associated with McCune-Albright syndrome: A case report

European Journal of Radiology Open, 2020
The fibrous dysplasia of bone is painless, benign, and slowly progressive bone lesion. It may rarely become aggressive by compression of adjacent organs or malignant transformation.
Lynda N. Bile-Gui, Judicael Ahoury, Raïssa M. Kabas   +2 more
doaj   +1 more source

Pituitary mammosomatotroph tumor with folliculo-stellate and mucin cells in a child with McCune Albright syndrome

Human Pathology: Case Reports, 2019
A pituitary tumor is a common manifestation of the endocrinopathies criterion in McCune Albright syndrome. Herein, we report a 12-year-old male with McCune Albright syndrome, who presented with dysmorphic features and tall stature, then, underwent a ...
Sadeem Al-Subaie, Mussa H. AlMalki, Maqsood Ahmed, Sadeq Al-Dandan   +3 more
doaj   +1 more source

Mazabraud Syndrome Associated with McCune-Albright Syndrome: A Case Report and Literature Review

Case Reports in Oncology, 2023
The Mazabraud syndrome is a rare form of bone fibrous dysplasia associated with intramuscular myxomas. The McCune-Albright syndrome is characterized by the association of dysplasia fibrous bone to one or more extra-osseous manifestations, including café ...
Laurys Boudin, Valeria De Luca, Léna Mescam-Mancini, Vincent Niziers, Delphine Perrot, Jerome Guiramand, Audrey Monneur, Christophe Chagnaud, François Bertucci   +8 more
doaj   +1 more source

Treatment of Girls and Boys with McCune-Albright Syndrome with Precocious Puberty - Update 2017 [PDF]

, 2017
The most common endocrinopathy associated with McCune-Albright Syndrome (MAS) is peripheral precocious puberty (PP) which occurs far more often in girls than in boys.
Eugster, Erica A., Neyman, Anna
core   +1 more source

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

Clinical Case Reports, 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.
Alexandre Michev, Luca Lungarotti, Maria Sole Prevedoni Gorone, Antonia Apicella, Giulia Di Vincenzo, Gian Luigi Marseglia, Ilaria Brambilla   +6 more
doaj   +1 more source

Delayed Diagnosis of McCune–Albright Syndrome

Case Reports in Genetics, 2021
Background. McCune–Albright syndrome (MAS) is a rare heterogeneous genetic disorder that is characterized by a triad of polyostotic fibrous dysplasia (FD), café au lait spots (CAL), and multiple hyperfunctional endocrinopathies.
Bereket Fantahun, Seblewongel Desta
doaj   +1 more source

Hyperthyroidism related to McCune-Albright syndrome: report of two cases and review of the literature [PDF]

, 2008
INTRODUCTION: McCune-Albright syndrome is a sporadic disease clinicaly characterized by polyostotic fibrous dysplasia, café-au-lait cutaneous spots and hyperfunctional endocrinopathies, such as precocious puberty, hyperthyroidism, acromegaly and others ...
Abs R, Albin J, Albright F, Ana Carolina R. Sallum, Andrews SB, Benedict P, Brogan P, Cavanah SFW, Cohen MM Jr, de Sanctis C, Domenech E, D’Armiento M, Fernando D. Leonhardt, Feuillan PP, Feuillan PP, Firat D, Gallacher SJ, Giovanelli G, Halvorsen S, Hamilton CR Jr, Huang TS, Isotani H, Jervis GA, Kim JP, Lair-Milan F, Lawless ST, Lee PA, Leet AI, Mastorakos G, Mastorakos G, Mauras N, McCune DJ, Misaki M, Moldawer M, Márcio Abrahão, Onivaldo Cervantes, Peck FB, Reinaldo K. Yazaki, Richton SM, Riminucci M, Samuel S, Schwindinger WF, Shenker A, Shenker A, Sternberg WH, Summerfeldt P, Tanaka T, Vague J, Weinstein LS, Yettra M, Yoshimoto M, Zangeneh F   +51 more
core   +3 more sources