CT and MRI findings in leptomeningeal melanocytosis

Leptomeningeal melanocytosis is a rare cause of seizure in the pediatric population. Shown here is a case of this disease in a 9-year-old male who presented with seizures and minor trauma. Imaging showed progression of leptomeningeal enhancement in the setting of increased seizure activity, and biop...

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Main Authors: Ferzana A. Hossain, BS, Hector J. Marquez, MD, Daniel L. Veltkamp, MD, Sophia Q. Xie, MD, Laura J. Klesse, MD, PhD, Charles F. Timmons, MD, PhD, Cory M. Pfeifer, MD, MS
Format: Article
Language:English
Published: Elsevier 2020-03-01
Series:Radiology Case Reports
Online Access:http://www.sciencedirect.com/science/article/pii/S193004331930367X
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author Ferzana A. Hossain, BS
Hector J. Marquez, MD
Daniel L. Veltkamp, MD
Sophia Q. Xie, MD
Laura J. Klesse, MD, PhD
Charles F. Timmons, MD, PhD
Cory M. Pfeifer, MD, MS
author_facet Ferzana A. Hossain, BS
Hector J. Marquez, MD
Daniel L. Veltkamp, MD
Sophia Q. Xie, MD
Laura J. Klesse, MD, PhD
Charles F. Timmons, MD, PhD
Cory M. Pfeifer, MD, MS
author_sort Ferzana A. Hossain, BS
collection DOAJ
description Leptomeningeal melanocytosis is a rare cause of seizure in the pediatric population. Shown here is a case of this disease in a 9-year-old male who presented with seizures and minor trauma. Imaging showed progression of leptomeningeal enhancement in the setting of increased seizure activity, and biopsy confirmed the diagnosis. The patient received immunotherapy but eventually succumbed to the disease. This case serves as an educational tool to improve awareness of melanocytic proliferation as a differential consideration for leptomeningeal enhancement. Keywords: Leptomeningeal melanocytosis
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spelling doaj.art-915a0b41f83b45468db0dd62457dc3142022-12-22T03:19:37ZengElsevierRadiology Case Reports1930-04332020-03-01153186189CT and MRI findings in leptomeningeal melanocytosisFerzana A. Hossain, BS0Hector J. Marquez, MD1Daniel L. Veltkamp, MD2Sophia Q. Xie, MD3Laura J. Klesse, MD, PhD4Charles F. Timmons, MD, PhD5Cory M. Pfeifer, MD, MS6University of Texas Southwestern Medical Center, 5323 Harry Hines Blvd, Dallas, TX 75390, USAUniversity of Texas Southwestern Medical Center, 5323 Harry Hines Blvd, Dallas, TX 75390, USAUniversity of Texas Southwestern Medical Center, 5323 Harry Hines Blvd, Dallas, TX 75390, USAUniversity of Texas Southwestern Medical Center, 5323 Harry Hines Blvd, Dallas, TX 75390, USAUniversity of Texas Southwestern Medical Center, 5323 Harry Hines Blvd, Dallas, TX 75390, USAUniversity of Texas Southwestern Medical Center, 5323 Harry Hines Blvd, Dallas, TX 75390, USACorresponding author.; University of Texas Southwestern Medical Center, 5323 Harry Hines Blvd, Dallas, TX 75390, USALeptomeningeal melanocytosis is a rare cause of seizure in the pediatric population. Shown here is a case of this disease in a 9-year-old male who presented with seizures and minor trauma. Imaging showed progression of leptomeningeal enhancement in the setting of increased seizure activity, and biopsy confirmed the diagnosis. The patient received immunotherapy but eventually succumbed to the disease. This case serves as an educational tool to improve awareness of melanocytic proliferation as a differential consideration for leptomeningeal enhancement. Keywords: Leptomeningeal melanocytosishttp://www.sciencedirect.com/science/article/pii/S193004331930367X
spellingShingle Ferzana A. Hossain, BS
Hector J. Marquez, MD
Daniel L. Veltkamp, MD
Sophia Q. Xie, MD
Laura J. Klesse, MD, PhD
Charles F. Timmons, MD, PhD
Cory M. Pfeifer, MD, MS
CT and MRI findings in leptomeningeal melanocytosis
Radiology Case Reports
title CT and MRI findings in leptomeningeal melanocytosis
title_full CT and MRI findings in leptomeningeal melanocytosis
title_fullStr CT and MRI findings in leptomeningeal melanocytosis
title_full_unstemmed CT and MRI findings in leptomeningeal melanocytosis
title_short CT and MRI findings in leptomeningeal melanocytosis
title_sort ct and mri findings in leptomeningeal melanocytosis
url http://www.sciencedirect.com/science/article/pii/S193004331930367X
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