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Your search keyword '"Jesse A. Taylor"' showing total 12 results
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12 results on '"Jesse A. Taylor"'

1. The Expanded Forehead Flap for Resurfacing of Multi-unit Congenital Nevi of the Face

Author

Meagan Wu, MA, Matthew E. Pontell, MD, Benjamin B. Massenburg, MD, Jinggang J. Ng, MA, Dominic J. Romeo, MA, Jordan W. Swanson, MD, MSc, Jesse A. Taylor, MD, and Scott P. Bartlett, MD

Subjects
Surgery, RD1-811
Abstract

Summary:. The forehead flap is a timeless and robust reconstructive option for complex facial defects. In accordance with aesthetic subunit principles, it has traditionally been used to resurface defects affecting a single cervicofacial region, most commonly the nose or periorbital unit. In this article, we present three cases of congenital nevi treated with expanded forehead flap reconstruction of the nasal, periorbital, and cheek units in early childhood. This series demonstrates an approach that, while violating facial units, limits total scar burden and optimizes aesthetic and functional results. With precise staging and execution, this reconstructive technique allows for a single flap to resurface multi-unit defects in the pediatric population with excellent long-term results.

Published
2024
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7. Delayed Postnatal Synostosis without Spheno-occipital Synchondrosis Fusion: A Curious Case of Apert Syndrome

Author

Jinggang J. Ng, MA, Benjamin B. Massenburg, MD, Meagan Wu, MA, Dominic J. Romeo, MA, Jordan W. Swanson, MD, Jesse A. Taylor, MD, and Scott P. Bartlett, MD

Subjects
Surgery, RD1-811
Abstract

Summary:. Apert syndrome classically presents with craniosynostosis at birth, most commonly of the bilateral coronal sutures, which may lead to cephalocranial disproportion and elevated intracranial pressure, the latter of which is associated with optic atrophy, visual loss, and developmental delays. A small number of patients with syndromic craniosynostosis demonstrate open sutures at birth; however, all previously reported patients of this subtype have been reported to develop premature suture fusion in the early postnatal period and/or require cranial vault expansion for increased intracranial pressure. Here, we report on a patient with Apert syndrome who did not have closed sutures at birth, and only began to demonstrate unilateral coronal suture fusion between ages 4 and 6 years, yet neither developed phenotypic signs of craniosynostosis nor evidence of intracranial hypertension. Moreover, despite demonstrating patency of the spheno-occipital synchondrosis, the patient developed progressive midface hypoplasia, requiring a subcranial Le Fort 3 advancement with external distraction at age 9. Now at skeletal maturity, this patient has a normal cranial shape and will likely never require cranial vault surgery for functional or aesthetic concerns. We are not aware of any prior reports of a patient with Apert syndrome who did not require intracranial surgery over long-term follow-up.

Published
2024
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8. D53. The Spectrum of Severity in Metopic Craniosynostosis: An Analysis of the Largest Cohort to Date using Craniorate™ Machine Learning Algorithm

Author

Angel Dixon, BA, Anne Glenney, BA, Nicolás Kass, BA, Joseph Mocharnuk, BS, Casey Zhang, BS, Erin Anstadt, MD, Lucas A. Dvoracek, MD, Megan Pencek, MD, Wenzheng Tao, BS, Ross Whitaker, PhD, Lisa R. David, MD, MBA, Michael Golinko, MD, Michael Alperovich, MD, Christopher M. Runyan, MD, PhD, Jesse A. Taylor, MD, Jordan Swanson, MD, and Jesse Goldstein, MD

Subjects
Surgery, RD1-811
Published
2024
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12. SP43. The Spectrum Of Severity In Metopic Craniosynostosis: An Analysis Of The Largest Cohort To Date Using Craniorate™ Machine Learning Algorithm

Author

Nicolás M. Kass, BA, Angel Dixon, BA, Anne Glenney, BS, Joseph Mocharnuk, BS, Erin Anstadt, MD, Lucas Dvoracek, MD, Megan Pencek, MD, Wenzheng Tao, MS, Ross Whitaker, PhD, Lisa R. David, MD, MBA, Michael Golinko, MD, Jesse A. Taylor, MD, Jordan W. Swanson, MD, and Jesse Goldstein, MD

Subjects
Surgery, RD1-811
Published
2024
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