Synchronous glioblastoma and medulloblastoma in a child with mismatch repair mutation

被引:11
|
作者
Amayiri, Nisreen [1 ]
Al-Hussaini, Maysa [2 ]
Swaidan, Maisa [3 ]
Jaradat, Imad [4 ]
Qandeel, Monther [3 ]
Tabori, Uri [5 ]
Hawkins, Cynthia [6 ]
Musharbash, Awni [7 ]
Alsaad, Khulood [8 ]
Bouffet, Eric [5 ]
机构
[1] King Hussein Canc Ctr, Dept Pediat, Hematol Oncol, Queen Rania Al Abdullah St,POB 1269, Amman 11941, Jordan
[2] King Hussein Canc Ctr, Dept Pathol, Amman 11941, Jordan
[3] King Hussein Canc Ctr, Dept Radiol, Amman 11941, Jordan
[4] King Hussein Canc Ctr, Dept Radiat Oncol, Amman 11941, Jordan
[5] Hosp Sick Children, Dept Pediat, Div Hematol Oncol, Toronto, ON M5G 1X8, Canada
[6] Hosp Sick Children, Div Pathol, Arthur & Sonia Labatt Brain Tumour Res Ctr, 555 Univ Ave, Toronto, ON M5G 1X8, Canada
[7] King Hussein Canc Ctr, Dept Surg Neurosurg, Amman 11941, Jordan
[8] Salmanyia Med Complex, Dept Pediat, Manama, Bahrain
关键词
Glioblastoma; Cis-retinoic acid; Biallelic mismatch repair syndrome; Synchronous tumors; EUROPEAN CONSORTIUM CARE; RETINOIC ACID THERAPY; PILOCYTIC ASTROCYTOMA; 13-CIS-RETINOIC ACID; STEM-CELLS; CHEMOTHERAPY; RADIOTHERAPY; NEUROBLASTOMA; SURVEILLANCE; TEMOZOLOMIDE;
D O I
10.1007/s00381-015-2883-3
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Synchronous primary malignant brain tumors are rare. We present a 5-year-old boy with synchronous glioblastoma and medulloblastoma. Both tumor samples had positive p53 stain and loss of PMS2 and MLH1 stains. The child had multiple caf, au lait spots and a significant family history of cancer. After subtotal resection of both tumors, he received craniospinal radiation with concomitant temozolomide followed by chemotherapy, alternating cycles of cisplatin/lomustine/vincristine with temozolomide. Then, he started maintenance treatment with cis-retinoic acid (100 mg/m(2)/day for 21 days). He remained asymptomatic for 34 months despite a follow-up brain MRI consistent with glioblastoma relapse 9 months before his death. Cis-retinoic acid may have contributed to prolong survival in this child with a probable biallelic mismatch repair syndrome.
引用
收藏
页码:553 / 557
页数:5
相关论文
共 50 条
  • [1] Synchronous glioblastoma and medulloblastoma in a child with mismatch repair mutation
    Nisreen Amayiri
    Maysa Al-Hussaini
    Maisa Swaidan
    Imad Jaradat
    Monther Qandeel
    Uri Tabori
    Cynthia Hawkins
    Awni Musharbash
    Khulood Alsaad
    Eric Bouffet
    [J]. Child's Nervous System, 2016, 32 : 553 - 557
  • [2] Germline POLE mutation in a child with hypermutated medulloblastoma and features of constitutional mismatch repair deficiency
    Lindsay, Holly
    Scollon, Sarah
    Reuther, Jacquelyn
    Voicu, Horatiu
    Rednam, Surya P.
    Lin, Frank Y.
    Fisher, Kevin E.
    Chintagumpala, Murali
    Adesina, Adekunle M.
    Parsons, D. Will
    Plon, Sharon E.
    Roy, Angshumoy
    [J]. COLD SPRING HARBOR MOLECULAR CASE STUDIES, 2019, 5 (05):
  • [3] Descriptive Statistics for Patients with Glioblastoma Associated with Germline Mismatch Repair Gene Mutation
    Cunningham, D.
    Qualls, K. W.
    Brown, S. M.
    Ruff, M.
    Kizilbash, S.
    Uhm, J. H.
    Laack, N. N., II
    Mahajan, A.
    [J]. INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2022, 114 (03): : E70 - E70
  • [4] Uncommon finding in a common tumour - a medulloblastoma with loss of mismatch repair protein expression in a young child
    Kan, A.
    Ku, D.
    Wong, S. T.
    [J]. VIRCHOWS ARCHIV, 2020, 477 : S339 - S339
  • [5] DIFFERENT TYPES OF HYPERMUTATOR PHENOTYPE OF GLIOBLASTOMA ACCORDING TO MUTATION PATTERNS OF MISMATCH REPAIR GENES
    Saito, Kuniaki
    Shimizu, Saki
    Nozaki, Eriko
    Kobayashi, Keiichi
    Sasaki, Nobuyoshi
    Yamagishi, Yuki
    Shiokawa, Yoshiaki
    Nagane, Motoo
    [J]. NEURO-ONCOLOGY, 2019, 21 : 153 - 153
  • [6] Mismatch Repair Mutations in Pediatric Glioblastoma
    Gestrich, Catherine
    Couce, Marta
    Sadri, Navid
    Cohen, Mark
    Elliott, Robin
    [J]. MODERN PATHOLOGY, 2019, 32
  • [7] Mismatch Repair Mutations in Pediatric Glioblastoma
    Gestrich, Catherine
    Couce, Marta
    Sadri, Navid
    Cohen, Mark
    Elliott, Robin
    [J]. LABORATORY INVESTIGATION, 2019, 99
  • [8] COMPOUND HETEROZYGOUS MUTATION OF THE PMS2 GENE IN AN INFANT WITH CONSTITUTIONAL MISMATCH REPAIR DEFICIENCY AND MEDULLOBLASTOMA
    Lukas, Claudia
    Crenshaw, Melissa
    Gonzalez-Gomez, Ignacio
    Potthast, Joseph
    Shimony, Nir
    Jallo, George
    Stapleton, Stacie
    [J]. NEURO-ONCOLOGY, 2018, 20 : 127 - 127
  • [9] MUTATION SIGNATURE ANALYSIS IN AN ULTRAHYPERMUTATED MEDULLOBLASTOMA PREDICTS UNDERLYING GERMLINE POLYMERASE PROOFREADING DEFICIENCY IN A CHILD WITH CLINICAL FEATURES OF CONSTITUTIONAL MISMATCH REPAIR DEFICIENCY SYNDROME
    Lindsay, Holly
    Scollon, Sarah
    Reuther, Jacquelyn
    Voicu, Horatiu
    Rednam, Surya
    Fisher, Kevin
    Chintagumpala, Murali
    Parsons, D. Will
    Adesina, Adekunle
    Plon, Sharon
    Roy, Angshumoy
    [J]. NEURO-ONCOLOGY, 2019, 21 : 82 - 83
  • [10] Analysis of DNA mismatch repair proteins in human medulloblastoma
    Lee, SE
    Johnson, SP
    Hale, LP
    Li, J
    Bullock, N
    Fuchs, H
    Friedman, A
    McLendon, R
    Bigner, DD
    Modrich, P
    Friedman, HS
    [J]. CLINICAL CANCER RESEARCH, 1998, 4 (06) : 1415 - 1419