| Literature DB >> 28503387 |
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