Division of Anatomical Pathology, Department of Pathology and Laboratory Medicine, Children and Women's Health Centre of BC, Vancouver, British Columbia, Canada.
Divisions of Neurology and Oncology, Department of Pediatrics, Children and Women's Health Centre of BC, Vancouver, British Columbia, Canada.
Pediatr Dev Pathol. 2020 Aug;23(4):326-331. doi: 10.1177/1093526620912645. Epub 2020 Apr 13.
Embryonal tumor with multilayered rosettes (ETMR) is a rare and highly aggressive embryonal central nervous system tumor that primarily affects young children. It is characterized by (1) amplification of the C19MC miRNA cluster at 19q13.42 and (2) immunohistochemical tumor cell positivity for LIN28A. We describe the case of a 3-year-old girl who presented with a 2-week history of multiple neurological deficits. Based primarily on imaging findings that revealed a large pontine tumor, biopsy was not performed and the patient was clinically diagnosed with a "diffuse intrinsic pontine glioma." She was subsequently treated with radiation and concurrent adjuvant temozolomide, but unfortunately there was minimal response and the patient died 6 months after diagnosis. Autopsy revealed an ETMR that was confirmed via C19MC fluorescence in situ hybridization and LIN28 immunohistochemistry. Although widespread central nervous system dissemination was observed, large portions of the main pontine mass exhibited evidence of extensive glial and neuronal maturation (ie, differentiation). We consider this tissue "maturation" to have been induced by chemotherapy and radiation. Herein, we discuss the importance of antemortem biopsy of intrinsic pontine tumors and the clinical significance of glial and neuronal maturation post therapy in the context of ETMR.
胚胎性肿瘤伴多层菊形团(ETMR)是一种罕见且高度侵袭性的胚胎性中枢神经系统肿瘤,主要影响幼儿。其特征为(1)19q13.42 处 C19MC miRNA 簇扩增,(2)LIN28A 免疫组化肿瘤细胞阳性。我们描述了一例 3 岁女孩的病例,她因多发性神经功能缺损出现 2 周病史。主要基于影像学发现提示大型脑桥肿瘤,未进行活检,临床诊断为“弥漫性内在脑桥胶质瘤”。随后,她接受了放疗和辅助替莫唑胺治疗,但不幸的是,反应甚微,患者在诊断后 6 个月死亡。尸检显示 ETMR,通过 C19MC 荧光原位杂交和 LIN28 免疫组化得到证实。尽管广泛的中枢神经系统播散,但主要脑桥肿块的大部分显示出广泛的胶质和神经元成熟(即分化)的证据。我们认为这种组织的“成熟”是由化疗和放疗诱导的。在此,我们讨论了对内在脑桥肿瘤进行生前活检的重要性,以及在 ETMR 背景下治疗后胶质和神经元成熟的临床意义。