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McCune-Albright syndrome with gigantism and hyperprolactinemia [PDF]

Journal of Endocrinological Investigation, 1987
We describe the case of a 38-year-old man with typical Mc Cune-Albright syndrome and the unusual combination of both growth-hormone and prolactin hypersecretion. The patient was extremely tall, which is unusual in Mc Cune-Albright syndrome, suggesting that he did not have precocious fusion of the epiphysis, a common finding in this syndrome ...
Perri G, Bagnolesi P, F. Pacini, A Cilotti, Aldo Pinchera   +4 more
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McCune-Albright Syndrome With Hyperthyroidism

Archives of Pediatrics & Adolescent Medicine, 1966
COEXISTENCE of endocrinopathies in polyostotic fibrous dysplasia has been well established.1In girls, the association of skeletal fibrous dysplasia, sex precocity, and skin pigmentation has been accorded the eponym of McCune-Albright syndrome.2,3In boys, however, concomitant sex precocity has been rarely noted and evidence of hyperthyroidism has been ...
Gary A. Lulejian, Matthew M. Steiner, Fereydoun Zangeneh   +2 more
openaire   +2 more sources

McCune–Albright Syndrome

2019
McCune–Albright syndrome (MAS) is a rare, non-hereditable genetic disorder classically defined by a clinical presentation of bone (fibrous dysplasia), skin (cafe-au-lait macules), and/or endocrine abnormalities. Sporadic occurrence of an activating mutation in the GNAS gene creates a mosaic tissue environment marked with normal and mutated cells ...
Beth A Brillante, Lori C. Guthrie
openaire   +2 more sources

Gigantism Associated with McCune-Albright's Syndrome

Hormone and Metabolic Research, 1985
The case of a 16 year-old boy with McCune-Albright's syndrome which is rarely accompanied by gigantism was studied endocrinologically. The stimulation of growth hormone (GH) release by hypoglycemia, the decline of elevated GH by hyperglycemia and a little lower somatostatin like immunoreactivity (SLI) may support abnormalities of hypothalamic function,
H. Nakagawa, A. Nagasaka, T. Sugiura, K. Nakagawa, Y. Yabe, N. Nihei, M. Hirooka, M. Itoh, A. Nakai, T. Ohyama, T. Aono, J. Gerich   +11 more
openaire   +3 more sources

Sarcomatous transformation in the McCune–Albright syndrome

Oral and Maxillofacial Surgery, 2011
McCune-Albright syndrome is a relatively rare disease characterized by the trio of fibrous dysplasia, café-au-lait pigmentation, and endocrine disturbances. It predominantly affects females and may be associated with sarcomatous degeneration in 0.4% to 4% of the cases.This article reports on the case of a 24-year-old female patient who had presented a ...
Vítor Yamashiro Rocha Soares, Luiz Augusto Nascimento, Aline Marques dos Santos, André Luís de Queiroz, Pedro Ivo Machado Pires de Araújo   +4 more
openaire   +3 more sources

Mazabraud syndrome associated with McCune-Albright syndrome

Journal of Orthopaedic Science, 2011
Abstract Mazabraud syndrome (MS) is characterized by the combination of skeletal fibrous dysplasia (FD) and intramuscular myxoma(s) [1]. It is a rare syndrome. To the best of our knowledge, 80 cases of MS have been reported since the first description by Henschen in 1926 [2-5]. MS is frequently associated with McCune-Albright syndrome (MAS). MAS is a
Yoko Ishihara, Yasuyuki Kitagawa, Hiromoto Ito, Nobuhito Fujii, Mikihiko Hayashi, Yong Kim   +5 more
openaire   +3 more sources

EFFICACY AND SAFETY OF BISPHOSPHONATE THERAPY IN MCCUNE-ALBRIGHT SYNDROME-RELATED POLYOSTOTIC FIBROUS DYSPLASIA: A SINGLE-CENTER EXPERIENCE.

Endocrine Practice, 2019
OBJECTIVE Fibrous dysplasia (FD) is a rare disorder characterized by pain, deformity, and pathologic fractures. McCune-Albright syndrome (MAS) includes a combination of FD, hyperfunctional endocrinopathy, and/or café-au-lait pigmentation.
Yabing Wang, O. Wang, Yan Jiang, Mei Li, W. Xia, Xun‐wu Meng, X. Xing   +6 more
semanticscholar   +1 more source

[Research progress on the pathogenic mechanisms, diagnosis and treatment of McCune-Albright syndrome].

Zhonghua yu fang yi xue za zhi [Chinese journal of preventive medicine]
McCune-Albright syndrome is a rare chimeric disorder due to mutations in the postzygotic GNAS gene. It belongs to the group of guanine nucleotide-binding protein diseases, affecting a wide range of individuals.
D. Mu, H. Q. Liu
semanticscholar   +1 more source

HYPERPROLACTINAEMIA IN A PATIENT WITH THE McCUNE‐ALBRIGHT SYNDROME

BJOG: An International Journal of Obstetrics & Gynaecology, 1979
SummaryA patient is presented with the syndrome of polyostotic fibrous dysplasia and precocious puberty (McCune‐Albright Syndrome). In adult life she developed hyperprolactinaemia with galactorrhoea and amenorrhoea; there was also evidence of excessive secretion of growth hormone.
D. Carr, A. R. Manners, I. K. Mathie, C. Colman   +3 more
openaire   +3 more sources

McCune-Albright Syndrome

Journal of Pediatric Endocrinology and Metabolism, 2007
Alan Daneman, Denis Daneman
openaire   +4 more sources