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Primary Dural Mucosa-associated Lymphoid Tissue Lymphoma Mimicking Falx Meningioma: A Case Report

An 85-year-old woman presented with ataxia and deterioration of cognitive functions. She had no history of autoimmune diseases or viral infections. Magnetic resonance imaging showed a solitary mass lesion at the cerebral falx on contrast-enhanced T1-weighted imaging. Gross total resection of the les...

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Autores principales: TAKEUCHI, Issei, TANEI, Takafumi, KUWABARA, Kyoko, KATO, Takenori, NAITO, Takehiro, KOKETSU, Yuta, HIRAYAMA, Kento, HASEGAWA, Toshinori
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japan Neurosurgical Society 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9217145/
https://www.ncbi.nlm.nih.gov/pubmed/35756189
http://dx.doi.org/10.2176/jns-nmc.2021-0426
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author TAKEUCHI, Issei
TANEI, Takafumi
KUWABARA, Kyoko
KATO, Takenori
NAITO, Takehiro
KOKETSU, Yuta
HIRAYAMA, Kento
HASEGAWA, Toshinori
author_facet TAKEUCHI, Issei
TANEI, Takafumi
KUWABARA, Kyoko
KATO, Takenori
NAITO, Takehiro
KOKETSU, Yuta
HIRAYAMA, Kento
HASEGAWA, Toshinori
author_sort TAKEUCHI, Issei
collection PubMed
description An 85-year-old woman presented with ataxia and deterioration of cognitive functions. She had no history of autoimmune diseases or viral infections. Magnetic resonance imaging showed a solitary mass lesion at the cerebral falx on contrast-enhanced T1-weighted imaging. Gross total resection of the lesion involving the dura mater was performed by bifrontal craniotomy. Histological examination showed diffuse infiltration of small lymphocytes and plasma cells. There was also some proliferation of large lymphocytes with folded nuclei, high-density chromatin, and inconspicuous nucleoli. The large atypical B lymphocytes did not demonstrate diffuse dense sheet findings. Meningothelial components were not detected. Immunohistochemistry was positive for pan B-cell antigens. The analysis of the kappa/lambda ratio indicated kappa immunoglobulin light chain-restricted B-cell proliferation. The final histopathological diagnosis was mucosa-associated lymphoid tissue lymphoma. Systemic screening examinations were then performed. Histological findings of the bone marrow showed normal findings without atypical lymphocytes. A chromosomal study of the bone marrow showed 46, XX. 18F fluoro-2-deoxyglucose positron emission tomography showed high accumulations at the left pterygoid muscle and the right transverse processes of the thoracic vertebrae, and mild accumulation at the right ilium bone, which indicated disseminated lesions. One year later, thickening of the dura mater was detected. Therefore, gamma knife surgery was performed. Two years later, she was alive without neurological deterioration, and magnetic resonance imaging showed no evidence of recurrence.
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spelling pubmed-92171452022-06-23 Primary Dural Mucosa-associated Lymphoid Tissue Lymphoma Mimicking Falx Meningioma: A Case Report TAKEUCHI, Issei TANEI, Takafumi KUWABARA, Kyoko KATO, Takenori NAITO, Takehiro KOKETSU, Yuta HIRAYAMA, Kento HASEGAWA, Toshinori NMC Case Rep J Case Report An 85-year-old woman presented with ataxia and deterioration of cognitive functions. She had no history of autoimmune diseases or viral infections. Magnetic resonance imaging showed a solitary mass lesion at the cerebral falx on contrast-enhanced T1-weighted imaging. Gross total resection of the lesion involving the dura mater was performed by bifrontal craniotomy. Histological examination showed diffuse infiltration of small lymphocytes and plasma cells. There was also some proliferation of large lymphocytes with folded nuclei, high-density chromatin, and inconspicuous nucleoli. The large atypical B lymphocytes did not demonstrate diffuse dense sheet findings. Meningothelial components were not detected. Immunohistochemistry was positive for pan B-cell antigens. The analysis of the kappa/lambda ratio indicated kappa immunoglobulin light chain-restricted B-cell proliferation. The final histopathological diagnosis was mucosa-associated lymphoid tissue lymphoma. Systemic screening examinations were then performed. Histological findings of the bone marrow showed normal findings without atypical lymphocytes. A chromosomal study of the bone marrow showed 46, XX. 18F fluoro-2-deoxyglucose positron emission tomography showed high accumulations at the left pterygoid muscle and the right transverse processes of the thoracic vertebrae, and mild accumulation at the right ilium bone, which indicated disseminated lesions. One year later, thickening of the dura mater was detected. Therefore, gamma knife surgery was performed. Two years later, she was alive without neurological deterioration, and magnetic resonance imaging showed no evidence of recurrence. The Japan Neurosurgical Society 2022-05-31 /pmc/articles/PMC9217145/ /pubmed/35756189 http://dx.doi.org/10.2176/jns-nmc.2021-0426 Text en © 2022 The Japan Neurosurgical Society https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives International License.
spellingShingle Case Report
TAKEUCHI, Issei
TANEI, Takafumi
KUWABARA, Kyoko
KATO, Takenori
NAITO, Takehiro
KOKETSU, Yuta
HIRAYAMA, Kento
HASEGAWA, Toshinori
Primary Dural Mucosa-associated Lymphoid Tissue Lymphoma Mimicking Falx Meningioma: A Case Report
title Primary Dural Mucosa-associated Lymphoid Tissue Lymphoma Mimicking Falx Meningioma: A Case Report
title_full Primary Dural Mucosa-associated Lymphoid Tissue Lymphoma Mimicking Falx Meningioma: A Case Report
title_fullStr Primary Dural Mucosa-associated Lymphoid Tissue Lymphoma Mimicking Falx Meningioma: A Case Report
title_full_unstemmed Primary Dural Mucosa-associated Lymphoid Tissue Lymphoma Mimicking Falx Meningioma: A Case Report
title_short Primary Dural Mucosa-associated Lymphoid Tissue Lymphoma Mimicking Falx Meningioma: A Case Report
title_sort primary dural mucosa-associated lymphoid tissue lymphoma mimicking falx meningioma: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9217145/
https://www.ncbi.nlm.nih.gov/pubmed/35756189
http://dx.doi.org/10.2176/jns-nmc.2021-0426
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