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@MISC{Lohmann:908193,
author = {Lohmann, Philipp and Piroth, Marc D and Sellhaus, Bernd and
Geisler, Stefanie and Oros-Peusquens, Ana-Maria and
Mohlberg, Hartmut and Amunts, Katrin and Shah, Nadim J and
Galldiks, Norbert and Langen, Karl-Josef},
title = {{NIMG}-78. {FIRST} {TIME} {CORRELATION} {OF} {FET} {PET},
{MRI} {AND} {POST}-{MORTEM} {WHOLE}-{BRAIN} {HISTOPATHOLOGY}
{IN} {A} {PROGRESSIVE} {GLIOBLASTOMA}},
issn = {1523-5866},
reportid = {FZJ-2022-02446},
year = {2017},
abstract = {BACKGROUND Amino acid PET using
O-(2-[18F]fluoroethyl)-L-tyrosine (FET) provides important
additional information on the extent of viable tumor tissue
of glioblastoma compared with MRI. Especially after
radiochemotherapy, progression of contrast enhancement in
MRI can be equivocal and may represent either true tumor
progression or treatment-related changes. We present the
first case comparing post-mortem whole-brain histopathology
in progressive glioblastoma with dynamic in vivo FET PET and
MRI.METHODSA 61-year-old glioblastoma patient underwent
initially partial resection and died eleven weeks after
completion of chemoradiation with concurrent temozolomide.
Three days before the patient died, a follow-up FET PET and
MRI scan indicated local tumor progression within the
irradiation field. An autopsy was performed at 48 h hours
after death and the tumor bearing brain was preserved. After
fixation in formalin and paraffin embedding, the brain
tissue was cut into 3500 coronal sections (20 micrometers).
Representative sections were stained using GFAP and cresyl
violet. An experienced neuropathologist identified areas of
neoplastic tissue, astrogliosis and necrosis. In vivo FET
PET, MRI and histopathology were co-registered and compared
by three experienced physicians.RESULTSIncreased FET uptake
(tumor-to-brain ratio = 2.3) in the area of equivocal
contrast enhancement on MRI correlated very well with vital
tumor cells and showed tracer kinetics typical for malignant
gliomas (early peak followed by constant descent). An area
of reactive astrogliosis showed only moderate FET uptake
(tumor-to-brain ratio = 1.5) and tracer kinetics usually
observed in benign lesions (constantly increasing). Necrotic
areas showed neither enhanced FET uptake nor contrast
enhancement in MRI.CONCLUSIONSThis case report documents for
the first time the correct imaging of a progressive
glioblastoma by FET PET, thereby confirming findings from
previous studies. FET PET significantly contributes to the
correct identification of neoplastic tissue and, thus, to a
better differentiation of tumor progression and
treatment-related changes.},
cin = {INM-4 / INM-11 / INM-1 / INM-3},
ddc = {610},
cid = {I:(DE-Juel1)INM-4-20090406 / I:(DE-Juel1)INM-11-20170113 /
I:(DE-Juel1)INM-1-20090406 / I:(DE-Juel1)INM-3-20090406},
pnm = {5253 - Neuroimaging (POF4-525)},
pid = {G:(DE-HGF)POF4-5253},
typ = {PUB:(DE-HGF)4},
doi = {10.1093/neuonc/nox168.650},
url = {https://juser.fz-juelich.de/record/908193},
}