Presentation of Two Cases with Early Extracranial Metastases from Glioblastoma and Review of the Literature
Hindawi Publishing Corporation
Case Reports in Oncological Medicine
Volume 2016, Article ID 8190950, 5 pages
http://dx.doi.org/10.1155/2016/8190950
Case Report
Presentation of Two Cases with Early Extracranial Metastases
from Glioblastoma and Review of the Literature
Maria Dinche Johansen,1 Per Rochat,2 Ian Law,3 David Scheie,4
Hans Skovgaard Poulsen,1,5 and Aida Muhic5
1
Department of Radiation Biology, The Finsen Center, Rigshospitalet, Blegdamsvej 9, 2100 Copenhagen, Denmark
Department of Neurosurgery, The Neurocenter, Rigshospitalet, Blegdamsvej 9, 2100 Copenhagen, Denmark
3
Department of Clinical Physiology, Nuclear Medicine and PET, Center of Diagnostic Investigation, Rigshospitalet, Blegdamsvej 9,
2100 Copenhagen, Denmark
4
Department of Pathology, Center of Diagnostic Investigation, Rigshospitalet, Blegdamsvej 9, 2100 Copenhagen, Denmark
5
Department of Oncology, The Finsen Center, Rigshospitalet, Blegdamsvej 9, 2100 Copenhagen, Denmark
2
Correspondence should be addressed to Maria Dinche Johansen;
Received 17 February 2016; Revised 12 April 2016; Accepted 18 April 2016
Academic Editor: Didier Frappaz
Copyright © 2016 Maria Dinche Johansen et al. This is an open access article distributed under the Creative Commons Attribution
License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly
cited.
Extracranial metastases from glioblastoma are rare. We report two patients with extracranial metastases from glioblastoma. Case 1
concerns a 59-year-old woman with multiple metastases that spread early in the course of disease. What makes this case unusual
is that the tumor had grown into the falx close to the straight sinus and this might be an explanation to the early and extensive
metastases. Case 2 presents a 60-year-old man with liver metastasis found at autopsy, and, in this case, it is more difficult to find
an explanation. This patient had two spontaneous intracerebral bleeding incidents and extensive bleeding during acute surgery
with tumor removal, which might have induced extracranial seeding. The cases presented might have hematogenous spreading in
common as an explanation to extracranial metastases from GBM.
1. Introduction
Glioblastoma (GBM) is the most frequent adult primary
tumor of the central nervous system with median survival of
14.6 months in patients with newly diagnosed glioblastoma.
The majority of patients experience local progression within
the central nervous system [1].
Extracranial metastases (ECMs) are uncommon events
seen in these patients, and most patients metastasize to only
one or two extracranial foci [2]. Most frequent localization of
ECM is regional lymph nodes, mostly cervical, lungs, liver,
and bone [2, 3]. The rarity of ECM makes epidemiological
analysis challenging, but it has been suggested that the
median time from diagnosis to detection of ECM is 8.5
months and the time from ECM to death is 1.5 months [2].
A study has found that 20% of GBM patients have circulating
tumor cells in peripheral blood, pointing out the ability to
escape the central nervous system [4]. This combined with
longer survival time should increase the awareness of ECM.
Here, we report two cases that demonstrate the ability
of GBM to metastasize in one case to multiple organs
simultaneously.
2. Case Presentations
2.1. Case 1. This case presents a 59-year-old woman with
a history of type 2 diabetes, hypertension, and tobacco
consumption (20 cigarettes per day for 45 years). The patient
visited an ophthalmologist due to three months of blurred
vision and two months of headache. This revealed impaired
vision (right sided homonymous hemianopsia) and memory
and concentration difficulties. Contrast enhanced CT and
MRI of the brain showed a 4 × 5 × 4 cm solitaire left sided
occipital tumor with midline shift. At this point, helical CT
2
Case Reports in Oncological Medicine
(a)
(b)
(c)
Figure 1: Case 1. (a) Preoperative post-contrast enhanced T1 weighted MRI showing the localization of the tumor in close proximity to
the falx. (b) Fused FDG PET/CT scanning at liver level 5 months after diagnosis of GBM showing multiple metabolically active metastases
(blue) and inactive liver cyst (white). (c) Frontal maximum intensity projection (MIP) image of whole body FDG PET scanning identifying
disseminated metastatic spread to lymph nodes (green), lungs (red), bone (purple), and liver (blue). Physiological excretion to intestines,
kidneys, and the bladder.
of thorax and abdomen was inconspicuous. The patient was
treated with corticosteroids.
Two weeks later macro radical tumor resection was
achieved using Gliolan when the patient underwent left
sided occipital craniotomy. During surgery, there was copious venous bleeding. Early postoperative post-contrast T1
weighted MRI showed no measurable tumor. Postoperatively the patient suffered from right sided hemianopsia.
Histological examination revealed a cellular astrocytic glioma
with pleomorphic nuclei, numerous mitoses, microvascular
proliferation, pseudopalisading necrosis, and thrombosed
vessels. Upon immunohistochemical examination, the tumor
cells stained positive for GFAP, p53 (pronounced and strong
in almost all tumor cells), map2, and olig2. Immunohistochemical stainings did not reveal IDH1- or ATRX-mutations.
Ki67 was high. These findings were compatible with glioblastoma, WHO grade IV. PCR-analysis revealed an average O6 methylguanine-DNA methyltransferase (MGMT) promoter
methylation of 18%. PET scanning using the radiolabeled
amino acid analog O-(2-18 F-fluoroethyl)-L-tyrosine (FET)
performed at radiation treatment planning revealed a few
mL of active tissue close to the cortex. The patient received
radiotherapy, 2 Gy/5 days per week, for a total dose of 60 Gy
with concomitant chemotherapy (temozolomide 75 mg/m2
per day) for six weeks. This was followed by adjuvant
chemotherapy temozolomide; the first dose was administered
at 150 mg/m2 for five days and second and third cycles were
administered at 200 mg/m2 for five days. Routine surveillance MRI from the start of the second series of adjuvant
chemotherapy found no sign of tumor recurrence. Clinically,
however, the patient complained about circumscribed pain
on the right abdominal side and on the right side of her neck.
This was examined at a local hospital with ultra sound, whole
body FDG PET/CT scanning (Figures 1(b) and 1(c)) and three
biopsies of the cervical lymph nodes. There were no signs of
local recurrence at the resection cavity on brain MRI.
The biopsies were examined by pathologists at the local
hospital and reexamined by neuropathologists who specialize in neurooncology. Microscopic examination revealed
pronounced tumor necrosis. Tumor cells were large and
epithelioid with vesicular nuclei with prominent nucleoli
(Figure 2(a)). Spindled cells were also observed. There were
numerous mitoses. The tumor cells stained positive for S100, vimentin, CD56, and GFAP (Figure 2(b)). T (...truncated)