Diffuse Leptomeningeal Glioneuronal Tumor in Adults: Case Report and Literature Review

Abstract: Introduction: Diffuse leptomeningeal glioneuronal tumor (DLGNT), a new addition to the 2016 World Health Organization (WHO) classification, is a rare childhood neoplasm presenting with disseminated leptomeningeal enhancement and an occasional intraparenchymal mass. Diagnosis is often impeded by infectious/immunological differentials, necessitating a biopsy to confirm the diagnosis. We report an adult male with DLGNT without hydrocephalus, which is rare in patients with cerebellar masses. Case Presentation: A 56-year-old man presented with headaches, vertigo, diplopia, impaired hearing, and gait imbalance over 6 months. Magnetic resonance imaging showed a cystic right cerebellar mass with its leptomeningeal dissemination but without hydrocephalus. Cerebrospinal fluid analysis revealed elevated proteins with CD56-positive tumor cells. Cerebellar lesion biopsy verified the diagnosis of DLGNT (WHO Grade 3) with KIAA1549::BRAF fusion and 1p deletion. Radiotherapy was prematurely aborted due to clinical deterioration. The patient was subsequently discharged to palliative home care and lost to follow-up. Conclusion: We conducted the first review of all 34 adult DLGNT cases, including ours (one of the oldest), hitherto published in the literature. The majority presented with signs and symptoms of increased intracranial pressure. 52.0% of adult DLGNT patients were alive at follow-up. DLGNT should be considered in the differential diagnoses of diffuse leptomeningeal enhancement in imaging. Further studies comparing pediatric and adult subgroups of DLGNT are needed to evaluate histopathological prognosticators and standardize therapy for both subpopulations.

Standort
Deutsche Nationalbibliothek Frankfurt am Main
Umfang
Online-Ressource
Sprache
Englisch

Erschienen in
Diffuse Leptomeningeal Glioneuronal Tumor in Adults: Case Report and Literature Review ; volume:17 ; number:1 ; year:2024 ; pages:337-343 ; extent:7
Case reports in oncology ; 17, Heft 1 (2024), 337-343 (gesamt 7)

Urheber
de los Reyes-Nabhan, Nova Kristine
Scheil-Bertram, Stefanie
Boppudi, Sangamitra
Carl, Barbara
Jussen, Daniel

DOI
10.1159/000536400
URN
urn:nbn:de:101:1-2406270103494.982678778329
Rechteinformation
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
Letzte Aktualisierung
14.08.2025, 10:57 MESZ

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Beteiligte

  • de los Reyes-Nabhan, Nova Kristine
  • Scheil-Bertram, Stefanie
  • Boppudi, Sangamitra
  • Carl, Barbara
  • Jussen, Daniel

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