Imaging findings of anaplastic astrocytoma in a child with maple syrup urine disease: a case report

被引:0
作者
Jessie Aw-Zoretic
Nitin R. Wadhwani
Lulla R. Rishi
Maura E. Ryan
机构
[1] Ann & Robert H. Lurie Children’s Hospital,Department of Medical Imaging
[2] Ann & Robert H. Lurie Children’s Hospital,Department of Pathology
[3] Ann & Robert H. Lurie Children’s Hospital,Division of Hematology, Oncology, Neuro
[4] Northwestern University Feinberg School of Medicine,Oncology and Stem Cell Transplant
[5] Northwestern University Feinberg School of Medicine,Department of Radiology
[6] Northwestern University Feinberg School of Medicine,Department of Pathology
来源
Child's Nervous System | 2015年 / 31卷
关键词
Maple syrup urine disease; Anaplastic glioma; MR spectroscopy; Metabolic disorders;
D O I
暂无
中图分类号
学科分类号
摘要
Maple syrup urine disease (MSUD) is an inborn error of branched-chain amino acid metabolism, which usually presents in childhood with encephalopathy due to cerebral edema and dysmyelination. Even with treatment, metabolic stressors may precipitate later episodes of acute decompensation. Changes related to cerebral and white matter edema have been described by magnetic resonance imaging (MRI), and imaging can aid in both initial diagnosis and evaluation of decompensation. To date, there are no published known reports of cancer in patients with MSUD. Here, we present the first case report of an anaplastic astrocytoma in a teenager with MSUD, with a discussion of imaging findings and the use of magnetic resonance spectroscopy (MRS) to help distinguish between tumor and metabolic changes.
引用
收藏
页码:1625 / 1629
页数:4
相关论文
共 50 条
  • [21] Comb-like EEG pattern in maple syrup urine disease: A case report
    Jaafar, Fatima
    Haddad, Laith
    Habanjar, Dima
    Charafeddine, Lama
    Yunis, Khalid
    Karam, Pascale E.
    Obeid, Makram
    SEIZURE-EUROPEAN JOURNAL OF EPILEPSY, 2021, 87 : 21 - 24
  • [22] Anaesthesia in patients with maple syrup urine disease: Case report and perioperative anaesthetic management
    Haberstich P.
    Kindler C.H.
    Schürch M.
    Der Anaesthesist, 2010, 59 (10) : 914 - 917
  • [23] Mirror necrosis of basal ganglia in maple syrup urine disease. A case report
    Jimenez Gonzalez, Yurisandra
    Esquivel Sosa, Leidelen
    Fleites Garcia, Yagima
    Leon de Armas, Yandy
    MEDISUR-REVISTA DE CIENCIAS MEDICAS DE CIENFUEGOS, 2022, 20 (04): : 754 - 759
  • [24] Intermittent Maple Syrup Urine Disease: Two Case Reports
    Axler, Olof
    Holmquist, Peter
    PEDIATRICS, 2014, 133 (02) : E458 - E460
  • [25] Maple syrup urine disease: Diffusion MRI, and proton MR spectroscopy findings
    Sener, R. Nuri
    COMPUTERIZED MEDICAL IMAGING AND GRAPHICS, 2007, 31 (02) : 106 - 110
  • [26] Typical Neuroradiological Diagnosis of Maple Syrup Urine Disease as a Precursor to Clinical Diagnosis A Case Report
    Srinivasan, K. G.
    Ramprabananth, S.
    Ushanandhini, K. P.
    Srividya, S.
    NEURORADIOLOGY JOURNAL, 2009, 22 (05) : 564 - 567
  • [27] CLASSIC MAPLE SYRUP URINE DISEASE IN A 46-DAY-OLD BABY: A CASE REPORT
    Idrees, Zara
    Khushdil, Arshad
    Zakir, Ujala
    Ahmed, Zeeshan
    KHYBER MEDICAL UNIVERSITY JOURNAL-KMUJ, 2018, 10 (01): : 44 - 46
  • [28] Age dependence of diffusion-weighted magnetic resonance imaging findings in maple syrup urine disease encephalopathy
    Sakai, M
    Inoue, Y
    Oba, H
    Ishiguro, A
    Sekiguchi, K
    Tsukune, Y
    Mitomo, M
    Nakamura, H
    JOURNAL OF COMPUTER ASSISTED TOMOGRAPHY, 2005, 29 (04) : 524 - 527
  • [29] Heterozygous liver transplantation for maple syrup urine disease: First European reported case
    Roilides, I.
    Xinias, I.
    Mavroudi, A.
    Ioannou, H.
    Savopoulou, P.
    Imvrios, G.
    PEDIATRIC TRANSPLANTATION, 2016, 20 (06) : 846 - 850
  • [30] Liver transplantation in maple syrup urine disease
    U. Wendel
    J. M. Saudubray
    A. Bodner
    P. Schadewaldt
    European Journal of Pediatrics, 1999, 158 : S060 - S064