Syringomyelia in mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome): imaging findings following bone marrow transplantation

被引:0
|
作者
S. H. Hite
William Krivit
Stephen J. Haines
Chester B. Whitley
机构
[1] Department of Radiology,
[2] Box 292,undefined
[3] University of Minnesota Hospital and Clinic,undefined
[4] 420 Delaware Street SE,undefined
[5] Minneapolis,undefined
[6] MN 55455,undefined
[7] USA,undefined
[8] Department of Pediatrics and Institute for Human Genetics,undefined
[9] University of Minnesota Hospital and Clinic,undefined
[10] Minneapolis,undefined
[11] Minnesota,undefined
[12] USA,undefined
[13] Department of Neurological Surgery,undefined
[14] University of Minnesota Hospital and Clinic,undefined
[15] Minneapolis,undefined
[16] Minnesota,undefined
[17] USA,undefined
来源
Pediatric Radiology | 1997年 / 27卷
关键词
Magnetic Resonance Imaging; Bone Marrow; Bone Marrow Transplant; Marrow Transplant; Imaging Finding;
D O I
暂无
中图分类号
学科分类号
摘要
We present the imaging findings in a patient with mucopolysaccharidosis (MPS) type VI (Maroteaux-Lamy syndrome) who developed holocord syringomyelia. This represents the only reported case of syrinx formation in a child with MPS VI. Clinical, neurologic and spinal magnetic resonance imaging findings are presented. The patient has maintained a stable clinical and neurologic course over the period following allogeneic bone marrow transplant.
引用
收藏
页码:736 / 738
页数:2
相关论文
共 50 条
  • [41] Mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome): assessment of joint mobility and grip and pinch strength
    Cardoso-Santos, Antonio
    Azevedo, Ana C. M. M.
    Fagondes, Simone
    Burin, Maira G.
    Giugliani, Roberto
    Schwartz, Ida V. D.
    JORNAL DE PEDIATRIA, 2008, 84 (02) : 130 - 135
  • [42] CLEARING OF CORNEA AFTER PERFORATING KERATOPLASTY IN MUCOPOLYSACCHARIDOSIS TYPE-VI (MAROTEAUX-LAMY SYNDROME)
    KRIVIT, W
    NEW ENGLAND JOURNAL OF MEDICINE, 1985, 312 (15): : 995 - 995
  • [43] Bone marrow transplantation for Maroteaux-Lamy syndrome (MPS VI): Long-term follow-up
    Herskhovitz, E
    Young, E
    Rainer, J
    Hall, CM
    Lidchi, V
    Chong, K
    Vellodi, A
    JOURNAL OF INHERITED METABOLIC DISEASE, 1999, 22 (01) : 50 - 62
  • [44] MUCOPOLYSACCHARIDOSIS VI (MAROTEAUX-LAMY SYNDROME): DEVELOPMENT OF CLINICAL AND LABORATORY GUIDELINES FOR DIAGNOSIS
    Harmatz, P.
    D'Almeida, V
    Eng, C.
    Fietz, M.
    Burin, M.
    Hendriksz, C.
    Hwu, P.
    Ketteridge, D.
    Lukacs, Z.
    Mendelsohn, N. J.
    Pasquali, M.
    Schenone, A.
    Schoonderwoerd, K.
    Winchester, B.
    Wood, T.
    Giugliani, R.
    JOURNAL OF INHERITED METABOLIC DISEASE, 2011, 34 : S211 - S211
  • [45] METABOLIC DEFECT IN MUCOPOLYSACCHARIDOSIS-VI (MAROTEAUX-LAMY DISEASE)
    CANTZ, M
    SPRANGER, J
    OBRIEN, JF
    KLINISCHE WOCHENSCHRIFT, 1977, 55 (02): : 86 - 86
  • [46] HIGH PREVALENCE OF MENTAL IMPAIRMENT IN A SERIES OF 6 PATIENTS WITH MUCOPOLYSACCHARIDOSIS TYPE VI (MAROTEAUX-LAMY SYNDROME)
    Valayannopoulos, V.
    Barbier, V.
    Boddaert, N.
    Arnoux, J. B.
    Lemerrer, M.
    de Lonlay, P.
    MOLECULAR GENETICS AND METABOLISM, 2009, 98 (1-2) : 80 - 80
  • [47] KERATOPLASTY IN LAYERS IN CONGENITAL MUCOPOLYSACCHARIDOSIS OF MAROTEAUX-LAMY TYPE
    MARKICHEVA, NA
    VESTNIK OFTALMOLOGII, 1985, (06) : 63 - &
  • [48] EMPTY SELLA SYNDROME IN A BOY WITH MUCOPOLYSACCHARIDOSIS TYPE 6 (MAROTEAUX-LAMY)
    MUHLENDAHL, KEV
    BRADAC, GB
    HELVETICA PAEDIATRICA ACTA, 1975, 30 (02) : 185 - 190
  • [49] Anesthesia in a patient with mucopolysaccharidosis type VI (Maroteaux–Lamy syndrome)
    Soon Hak Suh
    Ryu Okutani
    Masato Nakasuji
    Kazuo Nakata
    Journal of Anesthesia, 2010, 24 : 945 - 948
  • [50] Left ventricular aneurysm in a patient with mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome): clinical and pathological correlation
    Oudit, Gavin Y.
    Butany, Jagdish
    Williams, William G.
    Siu, Sam C.
    Clarke, Joe T. R.
    Iwanochko, Robert M.
    CARDIOVASCULAR PATHOLOGY, 2007, 16 (04) : 237 - 240