Brain Tumor Res Treat.  2019 Apr;7(1):39-43. 10.14791/btrt.2019.7.e24.

Extensive Pachymeningeal Dissemination of Glioblastoma Mimicking Chronic Subdural Hematoma: A Case Report

Affiliations
  • 1Division of Neurooncology and Department of Neurosurgery, Samsung Changwon Hospital, Sungkyunkwan University School of Medicine, Changwon, Korea. yzkim@skku.edu
  • 2Department of Pathology, Samsung Changwon Hospital, Sungkyunkwan University School of Medicine, Changwon, Korea.

Abstract

Meningeal dissemination (MDS) of glioblastoma is rare, although its incidence might have been underestimated. MDS of glioblastoma has a fatal course. Thus, rapid and precise diagnosis of MDS is important for further palliative treatment. Unfortunately, MDS of glioblastoma could be diagnosed at a delayed time, causing failure to treat patient optimally. Herein, we present a case of a 56-year-old male with MDS of glioblastoma mimicking chronic subdural hemorrhage (CSDH) after head trauma due to slip down. During treatment for CSDH, MDS of glioblastoma was not controlled appropriately. The patient succumbed to MDS of glioblastoma at 9 weeks after the date of diagnosis of CSDH which could be an MDS.

Keyword

Glioblastoma; Gliosarcoma; Meningeal dissemination; Mortality

MeSH Terms

Craniocerebral Trauma
Diagnosis
Glioblastoma*
Gliosarcoma
Hematoma, Subdural
Hematoma, Subdural, Chronic*
Humans
Incidence
Male
Middle Aged
Mortality
Palliative Care

Figure

  • Fig. 1 The second MR image at the time of occurrence of progressive hemiparesis on the left side showing increased size of the previous area with high signal intensity in fluid attenuated inversion recovery image (A), and nodular rim enhancement at size of 1 cm×1 cm showing in T1WI axial (B) coronal (C), and sagittal images (D) in the right frontoparietal area.

  • Fig. 2 MR image for regular follow-up showing more extensive peritumoral edema in the fluid attenuated inversion recovery image (A), the low signal intensity suggesting necrosis, irregular shaped unevenly thicken walled mass with internal necrosis, and heterogeneous enhancement on axial (B), coronal (C), and sagittal images (D) in the right frontoparietal area.

  • Fig. 3 Histopathological features showing two biphasic patterns in tumor of epithelioid glial component (upper lane) and cellular spindle mesenchymal component (bottom lane); (H&E staining, ×20) (A). The glial component surrounded by elongated mesenchymal component and the glial area is composed of mild pleomorphic astrocyte (H&E staining, ×20) (B), leading to the diagnosis of gliosarcoma. Immunohistochemistry for GFAP demonstrates positivity in glial component (×20) (C), and the biphasic pattern shows strong reticulin positivity in mesenchymal areas with reticulin negative glial areas (reticulin stain, ×20) (D). H&E: hematoxylin and eosin.

  • Fig. 4 The noncontrast CT scan showing a newly developed subdural fluid collection which is suggestive hematoma at the right hemisphere (A). Repeated CT scan without contrast showing the lining pattern of soft tissue density as well as fluid collection at the right hemisphere (B). Intraoperative findings (C) show that thickened dura matter with attachment of the tumors (➀), whitish colored tumor with a fragile texture and relatively poor vascularity (➁), and the relatively well preserved arachnoid membrane beneath the tumor without destruction nor invasion by the tumor (➂).


Reference

1. Dho YS, Jung KW, Ha J, et al. An updated nationwide epidemiology of primary brain tumors in Republic of Korea, 2013. Brain Tumor Res Treat. 2017; 5:16–23.
Article
2. Louis DN, Perry A, Burger P, et al. International Society of Neuropathology--Haarlem consensus guidelines for nervous system tumor classification and grading. Brain Pathol. 2014; 24:429–435.
Article
3. Ostrom QT, Gittleman H, Truitt G, et al. CBTRUS statistical report: primary brain and other central nervous system tumors diagnosed in the United States in 2011–2015. Neuro Oncol. 2018; 20:suppl_4. iv1–iv86.
Article
4. Louis DN, Perry A, Reifenberger G, et al. The 2016 World Health Organization Classification of Tumors of the Central Nervous System: a summary. Acta Neuropathol. 2016; 131:803–820.
Article
5. Preusser M, de Ribaupierre S, Wöhrer A, et al. Current concepts and management of glioblastoma. Ann Neurol. 2011; 70:9–21.
Article
6. Stupp R, Hegi ME, Mason WP, et al. Effects of radiotherapy with concomitant and adjuvant temozolomide versus radiotherapy alone on survival in glioblastoma in a randomised phase III study: 5-year analysis of the EORTC-NCIC trial. Lancet Oncol. 2009; 10:459–466.
7. Kumar R, Jain R, Tandon V. Thalamic glioblastoma with cerebrospinal fluid dissemination in the peritoneal cavity. Pediatr Neurosurg. 1999; 31:242–245.
Article
8. Salazar OM, Rubin P. The spread of glioblastoma multiforme as a determining factor in the radiation treated volume. Int J Radiat Oncol Biol Phys. 1976; 1:627–637.
Article
9. Macdonald DR, Cascino TL, Schold SC Jr, Cairncross JG. Response criteria for phase II studies of supratentorial malignant glioma. J Clin Oncol. 1990; 8:1277–1280.
Article
10. Bryan P. CSF seeding of intra-cranial tumours: a study of 96 cases. Clin Radiol. 1974; 25:355–360.
Article
11. Saito R, Kumabe T, Jokura H, Shirane R, Yoshimoto T. Symptomatic spinal dissemination of malignant astrocytoma. J Neurooncol. 2003; 61:227–235.
12. Vertosick FT Jr, Selker RG. Brain stem and spinal metastases of supratentorial glioblastoma multiforme: a clinical series. Neurosurgery. 1990; 27:516–521.
Article
13. Lim DA, Cha S, Mayo MC, et al. Relationship of glioblastoma multiforme to neural stem cell regions predicts invasive and multifocal tumor phenotype. Neuro Oncol. 2007; 9:424–429.
Article
14. Lawton CD, Nagasawa DT, Yang I, Fessler RG, Smith ZA. Leptomeningeal spinal metastases from glioblastoma multiforme: treatment and management of an uncommon manifestation of disease. J Neurosurg Spine. 2012; 17:438–448.
Article
15. Kato H, Fujimura M, Kumabe T, Ishioka C, Kanamaru R, Yoshimoto T. PTEN gene mutation and high MIB-1 labeling index may contribute to dissemination in patients with glioblastoma. J Clin Neurosci. 2004; 11:37–41.
Article
16. Korshunov A, Sycheva R, Golanov A, Pronin I. Gains at the 1p36 chromosomal region are associated with symptomatic leptomeningeal dissemination of supratentorial glioblastomas. Am J Clin Pathol. 2007; 127:585–590.
Article
17. Sato A, Sakurada K, Kumabe T, et al. Association of stem cell marker CD133 expression with dissemination of glioblastomas. Neurosurg Rev. 2010; 33:175–183.
Article
18. Arita N, Taneda M, Hayakawa T. Leptomeningeal dissemination of malignant gliomas. Incidence, diagnosis and outcome. Acta Neurochir (Wien). 1994; 126:84–92.
Article
19. Onda K, Tanaka R, Takahashi H, Takeda N, Ikuta F. Cerebral glioblastoma with cerebrospinal fluid dissemination: a clinicopathological study of 14 cases examined by complete autopsy. Neurosurgery. 1989; 25:533–540.
Article
20. Lomax AJ, Yannakou CK, Rosenthal MA. Spinal cord metastasis in a patient treated with bevacizumab for glioblastoma. Target Oncol. 2013; 8:153–155.
Article
21. Bae JS, Yang SH, Yoon WS, Kang SG, Hong YK, Jeun SS. The clinical features of spinal leptomeningeal dissemination from malignant gliomas. J Korean Neurosurg Soc. 2011; 49:334–338.
Article
22. Grah JJ, Katalinic D, Stern-Padovan R, et al. Leptomeningeal and intramedullary metastases of glioblastoma multiforme in a patient reoperated during adjuvant radiochemotherapy. World J Surg Oncol. 2013; 11:55.
Article
23. Taschner CA, Brendecke S, Weyerbrock A, Egger K, Prinz M. Freiburg neuropathology case conference: widespread mass lesions after resection of a glioblastoma multiforme. Clin Neuroradiol. 2012; 22:375–380.
Article
Full Text Links
  • BTRT
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr