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1.
JBJS Case Connect ; 10(4): e20.00378, 2020 12 10.
Artigo em Inglês | MEDLINE | ID: mdl-33463999

RESUMO

CASE: Stiff-person syndrome (SPS) presents with progressive muscle rigidity, postural instability, and periodic debilitating spasms. Reports of axial hyperextension exist, but kyphotic deformities have not been described. We surgically treated a patient with debilitating SPS and severe cervicothoracic hyperkyphosis with posterior spinal fusion and instrumentation. At 1-year follow-up, the patient displayed better upright gait and forward gaze, 18° cervical lordosis, and improved patient-reported outcome scores. CONCLUSION: SPS can lead to extreme spinal deformity and disease, including hyperkyphosis of the cervicothoracic spine, and can successfully be managed with a multidisciplinary team and a posterior-only correction with spinal instrumentation and fusion.


Assuntos
Vértebras Cervicais/cirurgia , Cifose/etiologia , Espondilolistese/etiologia , Rigidez Muscular Espasmódica/complicações , Vértebras Cervicais/diagnóstico por imagem , Humanos , Cifose/diagnóstico por imagem , Cifose/cirurgia , Laminectomia , Masculino , Pessoa de Meia-Idade , Osteotomia , Espondilolistese/diagnóstico por imagem , Espondilolistese/cirurgia , Rigidez Muscular Espasmódica/diagnóstico por imagem , Rigidez Muscular Espasmódica/terapia , Tomografia Computadorizada por Raios X
2.
Cureus ; 9(4): e1151, 2017 Apr 11.
Artigo em Inglês | MEDLINE | ID: mdl-28503387

RESUMO

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.

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