Journal of Pediatric Neurology 2021; 19(04): 259-263
DOI: 10.1055/s-0040-1716547
Case Report

Diffuse Leptomeningeal Glioneuronal Tumor in a 4.5-year-old Girl: A Case Report and Review of the Literature

Anna Gabryś
1   Faculty of Medicine, Jagiellonian University Medical College, Kraków, Poland
,
Julia Kuzaj
1   Faculty of Medicine, Jagiellonian University Medical College, Kraków, Poland
,
Dominika Pawełczak
1   Faculty of Medicine, Jagiellonian University Medical College, Kraków, Poland
,
Katarzyna Seliga
2   Molecular and Translational Oncology, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland
,
Agnieszka Jelińska
3   Jagiellonian University Medical College, Kraków, Poland
,
Andrzej Tysarowski
4   Department of Pathology and Laboratory Medicine, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland
2   Molecular and Translational Oncology, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland
,
Wiesława Grajkowska
5   Department of Pathology, Children's Memorial Health Institute, Warsaw, Poland
,
Stanisław Kwiatkowski
6   Jagiellonian University Medical College, Clinic of Children's Neurosurgery, Kraków, Poland
› Institutsangaben

Abstract

Diffuse leptomeningeal glioneuronal tumor (DLGNT) is an entity introduced in 2016 World Health Organization classification of tumors of the central nervous system. The tumor occurs very rarely. Due to the lack of specific clinical and radiological features, biopsy is necessary to be performed and histological and immunohistochemical testing is essential to reach the diagnosis. A 4.5-year-old girl presented with a history of headache, vomiting, and right eye convergent squint. Imaging revealed multiple enhancing lesions located supra- and infratentorially and intramedullary. Histopathological examination demonstrated diffused growth of neoplastic cells. Molecular testing revealed KIAA1549-BRAF fusion and the diagnosis of DLGNT was stated.



Publikationsverlauf

Eingereicht: 08. Juli 2020

Angenommen: 09. August 2020

Artikel online veröffentlicht:
14. September 2020

© 2020. Thieme. All rights reserved.

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Rüdigerstraße 14, 70469 Stuttgart, Germany

 
  • References

  • 1 Wesseling P, Capper D. WHO 2016 classification of gliomas. Neuropathol Appl Neurobiol 2018; 44 (02) 139-150
  • 2 Gardiman MP, Fassan M, Orvieto E. et al. Diffuse leptomeningeal glioneuronal tumors: a new entity? Brain pathology ISSN 2008: 1015-6305
  • 3 Fiaschi P, Badaloni F, Cagetti B. et al. Disseminated oligodendroglial-like leptomeningeal tumor in the adult: case report and review of the literature. World Neurosurg 2018; 114: 53-57
  • 4 Chen W, Kong Z, Fu J. et al. Diffuse leptomeningeal glioneuronal tumour with hydrocephalus as an initial symptom: a case-based update. Child's Nerv Syst 36 (03) 459-468
  • 5 Dyson K, Rivera-Zengotita M, Kresak J. et al. FGFR1 N546K and H3F3A K27M mutations in a diffuse leptomeningeal tumour with glial and neuronal markers. Histopathology 2016; 69 (04) 704-707
  • 6 Karlowee V, Kolakshyapati M, Amatya VJ. et al. Diffuse leptomeningeal glioneuronal tumor (DLGNT) mimicking Whipple's disease: a case report and literature review. Childs Nerv Syst 2017; 33 (08) 1411-1414
  • 7 Tiwari N, Tamrazi B, Robison N, Krieger M, Ji J, Tian D. Unusual radiological and histological presentation of a diffuse leptomeningeal glioneuronal tumor (DLGNT) in a 13-year-old girl. Childs Nerv Syst 2019; 35 (09) 1609-1614
  • 8 Lee JK, Ko HC, Choi JG, Lee YS, Son BC. A case of diffuse leptomeningeal glioneuronal tumor misdiagnosed as chronic tuberculous meningitis without brain biopsy. Case Rep Neurol Med 2018; 2018: 1391943
  • 9 Yamasaki T, Sakai N, Shinmura K. et al. Anaplastic changes of diffuse leptomeningeal glioneuronal tumor with polar spongioblastoma pattern. Brain Tumor Pathol 2018; 35 (04) 209-216
  • 10 Aguilera D, Castellino RC, Janss A. et al. Clinical responses of patients with diffuse leptomeningeal glioneuronal tumors to chemotherapy. Childs Nerv Syst 2018; 34 (02) 329-334
  • 11 Nambirajan A, Suri V, Kedia S. et al. Paediatric diffuse leptomeningeal tumor with glial and neuronal differentiation harbouring chromosome 1p/19q co-deletion and H3.3 K27M mutation: unusual molecular profile and its therapeutic implications. Brain Tumor Pathol 2018; 35 (03) 186-191
  • 12 Cho HJ, Myung JK, Kim H. et al. Primary diffuse leptomeningeal glioneuronal tumors. Brain Tumor Pathol 2015; 32 (01) 49-55
  • 13 Schwetye KE, Kansagra AP, McEachern J, Schmidt RE, Gauvain K, Dahiya S. Unusual high-grade features in pediatric diffuse leptomeningeal glioneuronal tumor: comparison with a typical low-grade example. Hum Pathol 2017; 70: 105-112
  • 14 Lyle MR, Dolia JN, Fratkin J, Nichols TA, Herrington BL. Newly identified characteristics and suggestions for diagnosis and treatment of diffuse leptomeningeal glioneuronal/neuroepithelial tumors: a case report and review of the literature. Child Neurol Open 2015; 2 (01) X14567531
  • 15 Xu H, Chen F, Zhu H, Luo L, Zhang R. Diffuse leptomeningeal glioneuronal tumor in a Chinese adult: a novel case report and review of literature. Acta Neurol Belg 2020; 120 (02) 247-256
  • 16 Rodriguez FJ, Schniederjan MJ, Nicolaides T, Tihan T, Burger PC, Perry A. High rate of concurrent BRAF-KIAA1549 gene fusion and 1p deletion in disseminated oligodendroglioma-like leptomeningeal neoplasms (DOLN). Acta Neuropathol 2015; 129 (04) 609-610
  • 17 Tiwari S, Yadav T, Pamnani J. et al. Diffuse leptomeningeal glioneuronal tumor: a unique leptomeningeal tumor entity. World Neurosurg 2020; 135: 297-300
  • 18 Abongwa C, Cotter J, Tamrazi B, Dhall G, Davidson T, Margol A. Primary diffuse leptomeningeal glioneuronal tumors of the central nervous system: report of three cases and review of literature. Pediatr Hematol Oncol 2020; 37 (03) 248-258