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41 results on '"Neuman, Jeremy"'

11. A rare case of laryngeal cleft in association with VACTERL and malrotation

Author

Stern Jonathan, Koshy June, Chen Jesse, and Neuman Jeremy

Subjects
lcsh:Medical physics. Medical radiology. Nuclear medicine, medicine.medical_specialty, lcsh:R895-920, Fistula, Radiography, Malrotation, Tracheoesophageal fistula, Laryngeal cleft, 030218 nuclear medicine & medical imaging, 03 medical and health sciences, 0302 clinical medicine, Lumbar, Rare case, VACTERL, medicine, Radiology, Nuclear Medicine and imaging, Pediatric, business.industry, Incidence (epidemiology), Laryngotracheoesophageal cleft, medicine.disease, Radiology, medicine.symptom, Imperforate anus, business, 030217 neurology & neurosurgery
Abstract

We report a rare case of a neonatal girl who presented with coughing and dyspnea immediately after feeds. At birth, she was noted to have an imperforate anus with a posterior fourchette fistula from which she was stooling. Initial imaging with radiography showed a normal bowel gas pattern; however, lumbar vertebral anomalies were noted. An upper GI series was performed and revealed a laryngeal cleft and malrotation. Ultrasound confirmed malrotation with an abnormal SMA-SMV relationship. Since laryngeal cleft is a rare condition and may not be known to most radiologists, its incidence is likely underestimated. It is important to note the association of laryngeal clefts with VACTERL and malrotation. In addition, it is essential not to confuse a laryngeal cleft with a tracheoesophageal fistula since the management differs. Keywords: Laryngeal cleft, Laryngotracheoesophageal cleft, VACTERL, Malrotation

Published
2018

16. Another Case of Multilevel Cervical Disconnection Syndrome Presenting as Neonatal Encephalopathy

Author

Brady, Kaylan M., Blau, Jonathan A., Serras, Spencer J., Neuman, Jeremy T., and Sidlow, Richard

Subjects
Article Subject
Abstract

Multilevel cervical disconnection syndrome (MCDS) is a rare malformation of the cervical spine previously documented in two toddlers. We present a case of a newborn first thought to have hypoxic-ischemic encephalopathy who was subsequently diagnosed with MCDS. The possibility of in utero presentation of the syndrome in this patient and the categorization of this syndrome in the spectrum of basilar skull/upper cervical malformation syndromes is discussed.

Published
2018
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20. Aortitis

Author

Sanghvi, Snaha, primary, Neuman, Jeremy, additional, Greenstein, Josh, additional, and Hahn, Barry, additional

Published
2018
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25. MOESM1 of Modeling Focal Epileptic Activity in the Wilsonâ Cowan Model with Depolarization Block

Author

Meijer, Hil, Tahra Eissa, Kiewiet, Bert, Neuman, Jeremy, Schevon, Catherine, Emerson, Ronald, Goodman, Robert, McKhann, Guy, Marcuccilli, Charles, Tryba, Andrew, Cowan, Jack, Gils, Stephan, and Drongelen, Wim

Subjects
Physics::Fluid Dynamics, Nonlinear Sciences::Chaotic Dynamics, Computer Science::Symbolic Computation, Nonlinear Sciences::Pattern Formation and Solitons, Computer Science::Distributed, Parallel, and Cluster Computing
Abstract

Full one parameter bifurcation diagrams. (PDF 106 KB)

Published
2015
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26. Occipital mass in antenatal sonography.

Author

Rhodes, Adam, Neuman, Jeremy, and Blau, Jonathan

Subjects
*PREMATURE labor, *CESAREAN section, *FETAL movement, *FETAL MRI, *PREGNANCY
Abstract

Biophysical profile (BPP) with ultrasound performed for a 32-year-old G5P3013 admitted at 31 weeks gestation with preterm, premature rupture of membranes (PPROM) noted an extracalvarial mass concerning for an encephalocele. Fetal MRI demonstrated edema over the occiput with no definable lesion visualized. Preterm labor requiring Cesarean delivery resulted in a live male neonate at 33 weeks gestation. An occipital mass was observed on neonatal physical exam. Postnatal ultrasound and MRI were consistent with cephalohematoma. This was surprising given the lack of vaginal delivery. We hypothesize that the occiput was positioned against the maternal ischial tuberosity and developed chronic trauma secondary to normal fetal movement over time, resulting in a cephalohematoma. Postnatal imaging confirmed this diagnosis as the mass gradually decreased and ultimately resolved. Although other etiologies are possible, this case emphasizes the need to consider cephalohematoma in the differential of CNS masses during pregnancy without abdominal trauma and/or vaginal delivery. [ABSTRACT FROM AUTHOR]

Published
2019
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27. Canal of Nuck cyst masquerading as a testicle in a neonate: A case report and review of the literature

Author

Grossman, Lelah, Horowitz, Mark, Neuman, Jeremy, Sidlow, Richard, Grossman, Lelah, Horowitz, Mark, Neuman, Jeremy, and Sidlow, Richard

Abstract

Canal of Nuck cysts/hydroceles are rare occurrences in females of all age groups. We describe a case of a female neonate presenting with a labial mass which sonographically resembled a testicle. Upon surgical exploration, it was found to be a hydrocele of the canal of Nuck. We also review the literature on canal of Nuck cysts/hydroceles in the pediatric age group.

Published
2016

31. Extra-Intestinal Crohn's Disease and Pyoderma Gangrenosum as a Diagnostic Dilemma: Case Report

Author

Kaur, Dominder, Cacciotti, Chantel, Webb, Ryan L, Neuman, Jeremy, Vaiselbuh, Sarah, Kaur, Dominder, Cacciotti, Chantel, Webb, Ryan L, Neuman, Jeremy, and Vaiselbuh, Sarah

Abstract

Extra-intestinal manifestations such as pyoderma gangrenosum and pulmonary nodules in Crohn's disease are rarely reported in the pediatric population. We report a 17-year-old female who presented with fulminant pyoderma gangrenosum and pulmonary nodules, as a diagnostic challenge. A review of treatment for Crohn's disease and pyoderma gangrenosum are discussed.

Published
2013

39. Another Case of Multilevel Cervical Disconnection Syndrome Presenting as Neonatal Encephalopathy

Author

M. Brady, Kaylan, A. Blau, Jonathan, J. Serras, Spencer, T. Neuman, Jeremy, and Sidlow, Richard

Abstract

Multilevel cervical disconnection syndrome (MCDS) is a rare malformation of the cervical spine previously documented in two toddlers. We present a case of a newborn first thought to have hypoxic-ischemic encephalopathy who was subsequently diagnosed with MCDS. The possibility of in utero presentation of the syndrome in this patient and the categorization of this syndrome in the spectrum of basilar skull/upper cervical malformation syndromes is discussed.

Published
2018
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41. Rare association of progressive congenital extrahepatic portosystemic shunt with development of multifocal hepatocellular carcinoma.

Author

Landau E, Shilo D, Rolnick B, and Neuman J

Abstract

The association between the Abernethy malformation, a rare vascular anomaly in which the portal blood is diverted into the systemic circulation, and development of hepatic tumours is well established. We present a case of multifocal hepatocellular carcinoma (HCC) in the presence of extrahepatic portosystemic shunt with a diminutive portal vein (Type 2 Abernethy malformation). Abdominal ultrasound performed on a 72-year-old female presenting with elevated liver function tests found a 5.6 cm right hepatic lobe mass. Subsequent CT and MRI examinations demonstrated multifocal lesions. A diminutive portal vein was present (transverse diameter of 7 mm) with a large tortuous complex shunt (maximum transverse diameter 2.0 cm) arising at the portal vein bifurcation with branches connecting to the left renal vein and inferior vena cava. Review of a CT examination performed 10 years ago demonstrated a normal-sized portal vein (transverse diameter of 1.5 cm) with a smaller calibre portosystemic shunt (maximum transverse diameter 9 mm). To our knowledge, this is one of the first reports to demonstrate the evolution of progressive portosystemic shunting and the development of HCC.

Published
2016
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