Embryonal tumor with multilayered rosettes arising from the internal auditory canal of an adult: Illustrative case with molecular investigations

被引:1
|
作者
Sheriff, Adam [1 ]
Takami, Hirokazu [2 ]
Takayanagi, Shunsaku [2 ,7 ]
Kitagawa, Yosuke [5 ,6 ]
Tanaka, Shota [2 ]
Ikemura, Masako [3 ]
Matsuura, Reiko [2 ]
Matsushita, Yuko [4 ]
Ichimura, Koichi [4 ]
Saito, Nobuhito [2 ]
机构
[1] Kings Coll London, Guys Kings & St Thomas GKT, London, England
[2] Univ Tokyo Hosp, Dept Neurosurg, Tokyo, Japan
[3] Univ Tokyo Hosp, Dept Pathol, Tokyo, Japan
[4] Juntendo Univ, Grad Sch Med, Dept Brain Dis Translat Res, Tokyo, Japan
[5] Harvard Med Sch, Translat Neurooncol Lab, Massachusetts Gen Hosp, Boston, MA USA
[6] Harvard Med Sch, Massachusetts Gen Hosp, Dept Neurosurg, Boston, MA USA
[7] Univ Tokyo Hosp, Dept Neurosurg, 7-3-1 Hongo,Bunkyo Ku, Tokyo 1138655, Japan
关键词
embryonal tumor with multilayered rosettes (ETMR); infratentorial neoplasms; internal auditory canal (IAC); LIN28A expression; primitive neuroectodermal tumors; CENTRAL-NERVOUS-SYSTEM; CLASSIFICATION; DIAGNOSIS;
D O I
10.1111/neup.12951
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Embryonal tumors with multilayered rosettes (ETMRs) are aggressive central nervous system (CNS) tumors that usually occur in young children. Here, we describe the first incidence of ETMR in an adult patient that also originated in the novel location of the internal auditory canal (IAC). The 36-year-old patient initially presented with unsteadiness, diplopia, and tinnitus. The tumor in the IAC was discovered on brain magnetic resonance imaging, and gross total resection was performed followed by pathological and molecular diagnosis. The patient received whole brain and spinal cord radiotherapy after an intracranial recurrence and adjuvant chemotherapy consisting of four cycles of ifosfamide, cisplatin, and etoposide. Progression was rapid; however, the patient survived for 22 months after diagnosis before succumbing to the disease. Molecular investigation revealed a DICER1 mutation at exon 25, and methylation classification categorized the tumor as ETMR, non-C19MC-altered. This case underscores the diverse possible presentations of ETMR, DICER1-mutated and the importance of molecular techniques to characterize and promptly treat atypical ETMR.
引用
收藏
页码:208 / 215
页数:8
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