Clinical, radiological and pathological features of temporomesial tumors in the adult. A single center experience from 15 years

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Clinical, radiological and pathological features of temporomesial tumors in the adult. A single center experience from 15 years. / Meyer, Hanno S; Wiestler, Benedikt; Hönikl, Lisa S; Delbridge, Claire; Ketterer, Carl; Gempt, Jens; Meyer, Bernhard.

in: FRONT ONCOL, Jahrgang 13, 28.08.2023, S. 1236269.

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@article{7765a69ed16740169bf82879c70f1ab3,
title = "Clinical, radiological and pathological features of temporomesial tumors in the adult. A single center experience from 15 years",
abstract = "INTRODUCTION: The mesial temporal lobe plays a distinct role in epileptogenesis, and tumors in this part of the brain potentially have specific clinical and radiological features. Differentiating high-grade from lower-grade tumors or non-neoplastic lesions can be challenging, preventing the decision for early resection that can be critical in high-grade tumors.METHODS: A brain tumor database was analyzed retrospectively to identify patients with temporomesial tumors. We determined clinical features (age, sex, symptoms leading to clinical presentation) as well as neuroradiological (tumor location and the presence of contrast enhancement on initial magnetic resonance imaging (MRI)) and neuropathological findings.RESULTS: We identified 324 temporal tumors. 39 involved the mesial temporal lobe. 77% of temporomesial tumors occured in males, and 77% presented with seizures, regardless of tumor type or grade. In patients 50 years or older, 90% were male and 80% had glioblastoma (GBM); there was no GBM in patients younger than 50 years. 50% of GBMs lacked contrast enhancement. Male sex was significantly associated with GBM. In both contrast-enhancing and non-enhancing tumors, age of 50 years or older was also significantly associated with GBM.CONCLUSION: In middle-aged and older patients with a mesial temporal lobe tumor, GBM is the most likely diagnosis even when there is no MRI contrast enhancement. Prolonged diagnostic workup or surveillance strategies should be avoided and early resection may be justified in these patients.",
author = "Meyer, {Hanno S} and Benedikt Wiestler and H{\"o}nikl, {Lisa S} and Claire Delbridge and Carl Ketterer and Jens Gempt and Bernhard Meyer",
note = "Copyright {\textcopyright} 2023 Meyer, Wiestler, H{\"o}nikl, Delbridge, Ketterer, Gempt and Meyer.",
year = "2023",
month = aug,
day = "28",
doi = "10.3389/fonc.2023.1236269",
language = "English",
volume = "13",
pages = "1236269",
journal = "FRONT ONCOL",
issn = "2234-943X",
publisher = "Frontiers Media S. A.",

}

RIS

TY - JOUR

T1 - Clinical, radiological and pathological features of temporomesial tumors in the adult. A single center experience from 15 years

AU - Meyer, Hanno S

AU - Wiestler, Benedikt

AU - Hönikl, Lisa S

AU - Delbridge, Claire

AU - Ketterer, Carl

AU - Gempt, Jens

AU - Meyer, Bernhard

N1 - Copyright © 2023 Meyer, Wiestler, Hönikl, Delbridge, Ketterer, Gempt and Meyer.

PY - 2023/8/28

Y1 - 2023/8/28

N2 - INTRODUCTION: The mesial temporal lobe plays a distinct role in epileptogenesis, and tumors in this part of the brain potentially have specific clinical and radiological features. Differentiating high-grade from lower-grade tumors or non-neoplastic lesions can be challenging, preventing the decision for early resection that can be critical in high-grade tumors.METHODS: A brain tumor database was analyzed retrospectively to identify patients with temporomesial tumors. We determined clinical features (age, sex, symptoms leading to clinical presentation) as well as neuroradiological (tumor location and the presence of contrast enhancement on initial magnetic resonance imaging (MRI)) and neuropathological findings.RESULTS: We identified 324 temporal tumors. 39 involved the mesial temporal lobe. 77% of temporomesial tumors occured in males, and 77% presented with seizures, regardless of tumor type or grade. In patients 50 years or older, 90% were male and 80% had glioblastoma (GBM); there was no GBM in patients younger than 50 years. 50% of GBMs lacked contrast enhancement. Male sex was significantly associated with GBM. In both contrast-enhancing and non-enhancing tumors, age of 50 years or older was also significantly associated with GBM.CONCLUSION: In middle-aged and older patients with a mesial temporal lobe tumor, GBM is the most likely diagnosis even when there is no MRI contrast enhancement. Prolonged diagnostic workup or surveillance strategies should be avoided and early resection may be justified in these patients.

AB - INTRODUCTION: The mesial temporal lobe plays a distinct role in epileptogenesis, and tumors in this part of the brain potentially have specific clinical and radiological features. Differentiating high-grade from lower-grade tumors or non-neoplastic lesions can be challenging, preventing the decision for early resection that can be critical in high-grade tumors.METHODS: A brain tumor database was analyzed retrospectively to identify patients with temporomesial tumors. We determined clinical features (age, sex, symptoms leading to clinical presentation) as well as neuroradiological (tumor location and the presence of contrast enhancement on initial magnetic resonance imaging (MRI)) and neuropathological findings.RESULTS: We identified 324 temporal tumors. 39 involved the mesial temporal lobe. 77% of temporomesial tumors occured in males, and 77% presented with seizures, regardless of tumor type or grade. In patients 50 years or older, 90% were male and 80% had glioblastoma (GBM); there was no GBM in patients younger than 50 years. 50% of GBMs lacked contrast enhancement. Male sex was significantly associated with GBM. In both contrast-enhancing and non-enhancing tumors, age of 50 years or older was also significantly associated with GBM.CONCLUSION: In middle-aged and older patients with a mesial temporal lobe tumor, GBM is the most likely diagnosis even when there is no MRI contrast enhancement. Prolonged diagnostic workup or surveillance strategies should be avoided and early resection may be justified in these patients.

U2 - 10.3389/fonc.2023.1236269

DO - 10.3389/fonc.2023.1236269

M3 - SCORING: Journal article

C2 - 37700844

VL - 13

SP - 1236269

JO - FRONT ONCOL

JF - FRONT ONCOL

SN - 2234-943X

ER -