Sebastian McWilliams

Dr. Sebastian McWilliams

orcid

Research Focus & Metrics

Academic Career Length

11Years (2016-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 January 2022 in RadioGraphics
Verified
Journal Article
Closed access
DRDemetrios A. Raptis
Demetrios A. Raptis
RSRyan Short
Ryan Short
CRCaroline Robb
Caroline Robb
JMJoshua Marlow
Joshua Marlow
MNMuhammad Naeem
Muhammad Naeem
SBSanjeev Bhalla
Sanjeev Bhalla
Pulmonary arteriovenous malformations are frequently encountered in patients with suspected hereditary hemorrhagic telangiectasia and are rarely incidentally detected at routine multidetector CT, a... A pulmonary arteriovenous malformation (PAVM) is a fistulous connection between a pulmonary artery and a pulmonary vein that bypasses the normal pulmonary capillary bed resulting in a right-to-left...

10 November 2016 in American Journal of Neuroradiology
Verified
Journal Article
Open access
PDF file
GPG.J. Palagallo
G.J. Palagallo
SMSebastian McWilliams
Sebastian McWilliams
LSL.A. Sekarski
L.A. Sekarski
ASA. Sharma
A. Sharma
MGM.S. Goyal
M.S. Goyal
AWAndrew J White
Andrew J White
BACKGROUND AND PURPOSE: Brain AVM, cerebral abscess, and ischemic stroke are among the well known neurologic manifestations of hereditary hemorrhagic telangiectasia. However, recently reported data suggest an additional association with malformations of cortical development. The purpose of this study was to determine the prevalence of malformations of cortical development in a population of pediatric patients with hereditary hemorrhagic telangiectasia. MATERIALS AND METHODS: A retrospective review of brain MRIs from 116 pediatric patients was performed. Each patient was referred from our institution9s Hereditary Hemorrhagic Telangiectasia Clinic. Each MRI included a 3D sequence, most frequently MPRAGE. The 3D sequence was evaluated by a neuroradiology fellow, with specific attention to the presence or absence of malformations of cortical development. Positive studies were subsequently reviewed by 2 attending neuroradiologists, who rendered a final diagnosis. RESULTS: Fourteen of 116 (12.1%) patients were found to have a malformation of cortical development. Among these 14, there were 12 cases of polymicrogyria and 2 cases of bifrontal periventricular nodular heterotopia. CONCLUSIONS: Pediatric patients with hereditary hemorrhagic telangiectasia have a relatively high prevalence of malformations of cortical development, typically perisylvian polymicrogyria.

12 January 2018 in Academic Radiology
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Journal Article
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SMSebastian McWilliams
Sebastian McWilliams
CSChristopher Smith
Christopher Smith
YOYaseen Oweis
Yaseen Oweis
KMKareem Mawad
Kareem Mawad
CRConstantine Raptis
Constantine Raptis
VMVincent M. Mellnick
Vincent M. Mellnick

17 August 2016 in Case Reports in Radiology
Verified
Journal Article
Open access
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IAIbtisam Musallam Aljohani
Ibtisam Musallam Aljohani
KAKhalefa Ali Alghofaily
Khalefa Ali Alghofaily
SMSebastian McWilliams
Sebastian McWilliams
MSMnahi Bin Saeedan
Mnahi Bin Saeedan
A tailgut cyst is a rare developmental lesion and usually is located in the retrorectal or presacral space. Extrahepatic hydatid disease has been reported in several locations including the pelvis and it often poses a diagnostic challenge. There are very few reported cases of primary perineal hydatid cysts. We present the multimodality imaging findings of a tailgut cyst and concurrent perineal hydatid disease in a 32-year-old male patient.

1 September 2017 in Journal of the American College of Radiology
Verified
Journal Article
Open access
PWPamela K. Woodard
Pamela K. Woodard
SMSebastian McWilliams
Sebastian McWilliams
DRDemetrios A. Raptis
Demetrios A. Raptis
JHJudd E. Hollander
Judd E. Hollander
HLHarold Litt
Harold Litt
QTQuynh A. Truong
Quynh A. Truong

6 December 2024 in Onco
Verified
Journal Article
Open access
PDF file
SBSimon Louis Barry
Simon Louis Barry
ELEmer Lynch
Emer Lynch
PBPhilip Bredin
Philip Bredin
SMSebastian McWilliams
Sebastian McWilliams
JMjulie elizabeth McCarthy
julie elizabeth McCarthy
SOSeamus O'Reilly
Seamus O'Reilly
Anaplastic thyroid cancer (ATC) is considered to be one of the most virulent, treatment-refractory malignancies. Recent molecular insights into the biology of thyroid cancer have transformed ATC management, and BRAF/MEK targeted therapy is now incorporated into guideline-based multidisciplinary care. We report visceral perforation in the setting of an extreme response to such therapy in a patient with ATC. Molecularly targeted therapy afforded a dramatic but life-threatening response to treatment. This report highlights the complexities of care for the patient and treating clinicians.