Results 41 to 50 of about 12,028 (243)

Fibrous dysplasia: rare manifestation in the temporal bone

Brazilian Journal of Otorhinolaryngology, 2022
Introduction: Fibrous dysplasia is a benign disorder, in which normal bone is replaced by fibrosis and immature bone trabeculae, showing a similar distribution between the genders, and being more prevalent in the earlier decades of life.
Thaís de Carvalho Pontes-Madruga, Halana Valéria Carneiro Filgueiras, Daniel Marcus San da Silva, Leonardo Sales da Silva, José Ricardo Gurgel Testa   +4 more
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

Radioiodine treatment in McCune-Albright syndrome with hyperthyroidism

Indian Journal of Endocrinology and Metabolism, 2012
McCune-Albright syndrome (MAS) is a sporadic disease characterized by polyostotic fibrous dysplasia, "café-au-lait" spots and hyperfunctional endocrinopathies.
Dhritiman Chakraborty, Bhagwant Rai Mittal, Raghava Kashyap, Kuruva Manohar, Anish Bhattacharya, Anil Bhansali   +5 more
doaj   +1 more source

Fibrocartilaginous dysplasia: What do we know so far?

Radiology Case Reports, 2023
Fibrocartilaginous dysplasia has been described as a rare variant of fibrous dysplasia. This lesion will appear in imaging as ground glass matrix similar to fibrous dysplasia, but it will also show rings and arcs calcifications. In turn, this can lead to
Asma Alshalan, MD, Yasser Asiri, MD, Ayed AlGarni, MD, Bader Tayara, MD   +3 more
doaj   +1 more source

Delayed Diagnosis of McCune-Albright Syndrome in Adulthood Revealed by Spinal Fibrous Dysplasia: Report of 2 Cases. [PDF]

JCEM Case Rep
McCune-Albright syndrome (MAS) is a rare genetic disorder characterized by fibrous dysplasia of bone, café-au-lait skin pigmentation, and endocrine abnormalities. Adult presentation with spinal fibrous dysplasia, although previously reported, is uncommon
Rouach V, Yacobi-Bach M, Raz N, Druckman I, Greenman Y, Shemesh E.   +5 more
europepmc   +2 more sources

Management of fibro-osseous lesions of the craniofacial area: presentation of 19 cases and review of the literature [PDF]

, 2013
Introduction: Fibro-osseous lesions constitute a rare benign type of pathology with a non-odontogenic lineage that affect the craniofacial area. According to Waldrom's classification, these lesions are divided into: fibrous dysplasia (FD), cemento ...
Baquero Ruiz de la Hermosa, María del Carmen, Barea, José, Delhom, J., Floría García, Luis Miguel, Mínguez Martínez, Ignacio, Risueño Mata, Presentación, Suárez Soto, Aldo   +6 more
core   +1 more source

Sarcomatous transformation (Leiomyosarcoma) in polyostotic fibrous dysplagia

Indian Journal of Endocrinology and Metabolism, 2013
Malignant changes in polyostotic fibrous dysplasia are very rare. Most common malignancies reported are osteosarcoma and fibrosarcoma, chondrosarcoma and malignant fibrous histiocytoma. Here, we report a previously diagnosed case of fibrous dysplasia who
M K Garg, Reena Bhardwaj, Srishti Gupta, Navdeep Mann, Sandeep Kharb, Aditi Pandit   +5 more
doaj   +1 more source

Burosumab treatment of a child with McCune-Albright syndrome/polyostotic fibrous dysplasia: challenges and benefits. [PDF]

JBMR Plus
Fibrous dysplasia/McCune–Albright syndrome (FD/MAS) is a rare condition caused by a mutation in the GNAS locus. Apart from endocrinopathies, some cases are characterized by excessive fibroblast growth factor 23 (FGF23) production from abnormal fibro ...
Sakka SD, Georgakopoulou D, Doulgeraki A, Krieg AH, Anastasopoulos J, Szinnai G, Kanaka-Gantenbein C.   +6 more
europepmc   +2 more sources

Evolução da displasia fibrosa óssea na síndrome de McCune Albright [PDF]

, 1999
McCune Albright syndrome is a rare disorder characterized by polyostotic fibrous dysplasia, café-au-lait spots and some endocrine hyperfunction, mostly precocious puberty.
Dias-da-Silva, Magnus Régios [UNIFESP], Farhat, Helena L. [UNIFESP], Lazaretti-Castro, Marise [UNIFESP], Verreschi, Ieda Therezinha do Nascimento [UNIFESP]   +3 more
core   +2 more sources

Facial palsy and Valsalva-induced vertigo in a patient with temporal bone cystic fibrous dysplasia

Interdisciplinary Neurosurgery, 2022
A 29-year-old woman, known with polyostotic fibrous dysplasia, presented with facial palsy, vertigo, and ipsilateral neck pain. Radiology revealed a large temporal bone cyst, extruding intracranially, eroding the labyrinth and Fallopian canal ...
Glen J.F. Kemps, Maud P.M. Tijssen, Raymond van de Berg, Jérôme J. Waterval, Dirk H.P.M. Kunst   +4 more
doaj   +1 more source