Literature DB >> 28503387

Rubinstein-Taybi Syndrome Associated with Pituitary Macroadenoma: A Case Report.

Yasamin Olyaei1, J Manuel Sarmiento2, Serguei I Bannykh3, Doniel Drazin2, Robert T Naruse4, Wesley King2.   

Abstract

Rubinstein-Taybi Syndrome (RSTS) is an autosomal dominant disorder that is classically characterized by prenatal and postnatal growth restriction, microcephaly, dysmorphic craniofacial features, broad thumbs and toes, and intellectual disability. We describe the first reported case of a pituitary macroadenoma associated with RSTS. A 39-year-old Caucasian female with a past medical history of RSTS diagnosed at age two was found to have a gadolinium-enhancing pituitary mass on magnetic resonance imaging (MRI) of the brain three years ago during workup for migraine-like headaches. Subsequent serial imaging showed radiographic evidence of growth up to 11.5 x 14.0 x 10.0 mm in size. The pituitary sellar lesion was resected through an endoscopic transnasal transsphenoidal approach and was found to be a thyrotroph adenoma. RSTS is a rare, neurodevelopmental genetic disease where most patients with disabilities survive into adulthood. The disorder is associated with an increased predisposition for development of nervous system tumors, including pituitary adenomas.

Entities:  

Keywords:  pituitary adenoma; rubinstein-taybi syndrome

Year:  2017        PMID: 28503387      PMCID: PMC5426823          DOI: 10.7759/cureus.1151

Source DB:  PubMed          Journal:  Cureus        ISSN: 2168-8184


  24 in total

1.  Identical twin sisters with Rubinstein-Taybi syndrome associated with Chiari malformations and syrinx.

Authors:  Lea Parsley; Gary Bellus; Michael Handler; Anne Chun-Hui Tsai
Journal:  Am J Med Genet A       Date:  2011-09-19       Impact factor: 2.802

Review 2.  Broad thumb-hallux (Rubinstein-Taybi) syndrome 1957-1988.

Authors:  J H Rubinstein
Journal:  Am J Med Genet Suppl       Date:  1990

3.  Rubinstein-Taybi syndrome predisposing to non-WNT, non-SHH, group 3 medulloblastoma.

Authors:  Franck Bourdeaut; Catherine Miquel; Wilfrid Richer; Jacques Grill; Michel Zerah; Camille Grison; Gaelle Pierron; Jeanne Amiel; Clementine Krucker; Francois Radvanyi; Laurence Brugieres; Olivier Delattre
Journal:  Pediatr Blood Cancer       Date:  2013-09-20       Impact factor: 3.167

4.  Cervical spondylolisthesis and other skeletal abnormalities in Rubinstein-Taybi syndrome.

Authors:  M J Robson; L M Brown; W J Sharrard
Journal:  J Bone Joint Surg Br       Date:  1980-08

5.  [Dissecting aneurysm of the anterior cerebral artery with Rubinstein-Taybi syndrome--a case report].

Authors:  Shunsuke Ishizaka; Gouhei Sou; Youichi Morofuji; Kentaro Hayashi; Naoki Kitagawa; Youhei Tateishi; Minoru Morikawa; Kazuhiko Suyama; Izumi Nagata
Journal:  Brain Nerve       Date:  2010-10

6.  Dandy-Walker malformation in Rubinstein-Taybi syndrome: a rare association.

Authors:  Ramesh Agarwal; Rajiv Aggarwal; Madhulika Kabra; Ashok K Deorari
Journal:  Clin Dysmorphol       Date:  2002-07       Impact factor: 0.816

7.  The association of neural axis and craniovertebral junction anomalies with scoliosis in Rubinstein-Taybi syndrome.

Authors:  Carlo Giussani; Angelo Selicorni; Chiara Fossati; Pablo Ingelmo; Francesco Canonico; Andrea Landi; Andrea Trezza; Matteo Riva; Erik P Sganzerla
Journal:  Childs Nerv Syst       Date:  2012-08-23       Impact factor: 1.475

8.  Novel cAMP binding protein-BP (CREBBP) mutation in a girl with Rubinstein-Taybi syndrome, GH deficiency, Arnold Chiari malformation and pituitary hypoplasia.

Authors:  Pierluigi Marzuillo; Anna Grandone; Ruggero Coppola; Domenico Cozzolino; Adalgisa Festa; Federica Messa; Caterina Luongo; Emanuele Miraglia Del Giudice; Laura Perrone
Journal:  BMC Med Genet       Date:  2013-02-23       Impact factor: 2.103

Review 9.  Rubinstein-Taybi syndrome: clinical features, genetic basis, diagnosis, and management.

Authors:  Donatella Milani; Francesca Maria Paola Manzoni; Lidia Pezzani; Paola Ajmone; Cristina Gervasini; Francesca Menni; Susanna Esposito
Journal:  Ital J Pediatr       Date:  2015-01-20       Impact factor: 2.638

10.  Clinical and molecular characterization of Rubinstein-Taybi syndrome patients carrying distinct novel mutations of the EP300 gene.

Authors:  G Negri; D Milani; P Colapietro; F Forzano; M Della Monica; D Rusconi; L Consonni; L G Caffi; P Finelli; G Scarano; C Magnani; A Selicorni; S Spena; L Larizza; C Gervasini
Journal:  Clin Genet       Date:  2014-02-17       Impact factor: 4.438

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