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
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