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Childs Nerv Syst. 2019 Feb 15. doi: 10.1007/s00381-019-04074-7. [Epub ahead of print]

Unusual radiological and histological presentation of a diffuse leptomeningeal glioneuronal tumor (DLGNT) in a 13-year-old girl.

Author information

1
Department of Pathology and Laboratory Medicine, Children's Hospital Los Angeles, Los Angeles, CA, 90027, USA.
2
Department of Radiology, Neuroradiology, Children's Hospital Los Angeles, Los Angeles, CA, 90027, USA.
3
Department of Pediatrics, Neuro-oncology, Children's Hospital Los Angeles, Los Angeles, CA, 90027, USA.
4
Department of Surgery, Neurosurgery, Children's Hospital Los Angeles, Los Angeles, CA, 90027, USA.
5
Department of Pathology and Laboratory Medicine, Children's Hospital Los Angeles, Los Angeles, CA, 90027, USA. ditian118@gmail.com.

Abstract

Diffuse leptomeningeal glioneuronal tumors (DLGNTs) are newly recognized as an entity in the 2016 revision of the WHO Classification of tumors of the central nervous system. They typically present as diffuse leptomeningeal infiltrates along the neuraxis with focal and superficial involvement of the parenchyma. Here, we report a DLGNT with unusual radiological and histological features. A 13-year-old girl presented with scoliosis and back pain. Magnetic resonance imaging demonstrated a syrinx from C2 to T11 and an intramedullary mass from T6 to T9-10. No leptomeningeal involvement was recognized. Histological examination of the gross total resection specimen revealed a low-grade neuroepithelial neoplasm predominantly infiltrating the spinal cord and only focally involving the leptomeninges. Chromosome microarray identified co-deletion of the short arm of chromosome 1 and the long arm of chromosome 19 as well as fusion of the KIAA1549 and BRAF genes. Next-generation sequencing demonstrated wild-type alleles at the mutational hotspots of IDH1 (R132) and IDH2 (R140 and R172). In contrast to most reported DLGNTs, the tumor described in this manuscript was characterized by a predominant parenchymal component and only minor leptomeningeal involvement both radiographically and histologically. Our case, therefore, expands the spectrum of radiological and histopathological features of this new entity. It also highlights the critical role of molecular genetic testing in establishing the diagnosis of DLGNT in unusual cases.

KEYWORDS:

1p/19q co-deletion; BRAF; Diffuse leptomeningeal glioneuronal tumors (DLGNT); KIAA1549-BRAF fusion; Scoliosis; Syrinx

PMID:
30770994
DOI:
10.1007/s00381-019-04074-7

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