Primary ectopic meningioma in the thoracic cavity: A rare case report and review of the literature

BackgroundMeningioma is a common type of intracranial tumor in adults. It rarely arises in the chest, with only a few case reports in the English literature. Here, we report the case of a patient with a primary ectopic meningioma (PEM) located in the thoracic cavity.Case presentationA 55-year-old wo...

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Main Authors: Xu Liu, Jiao Liu, Ting Nai, Yuxia Yang, Yuchang Hu
Format: Article
Language:English
Published: Frontiers Media S.A. 2023-04-01
Series:Frontiers in Oncology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fonc.2023.1149627/full
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author Xu Liu
Xu Liu
Jiao Liu
Ting Nai
Ting Nai
Yuxia Yang
Yuxia Yang
Yuchang Hu
Yuchang Hu
author_facet Xu Liu
Xu Liu
Jiao Liu
Ting Nai
Ting Nai
Yuxia Yang
Yuxia Yang
Yuchang Hu
Yuchang Hu
author_sort Xu Liu
collection DOAJ
description BackgroundMeningioma is a common type of intracranial tumor in adults. It rarely arises in the chest, with only a few case reports in the English literature. Here, we report the case of a patient with a primary ectopic meningioma (PEM) located in the thoracic cavity.Case presentationA 55-year-old woman presented with exercise-induced asthma, chest tightness, intermittent dry cough and fatigue for several months. Computed tomography revealed the presence of a huge mass in the thoracic cavity, with no connection to the spinal canal. Lung cancer and mesothelioma were suspected, and surgery was performed. Grossly, the mass was a grayish-white solid 9.5 cm × 8.4 cm × 5.3 cm in size. The microscopic morphology of the lesion was consistent with that of typical central nervous system meningioma. The pathological subtype was transitional meningioma. The tumor cells were arranged in a fascicular, whorled, storiform and meningithelial pattern, with occasional intranuclear pseudo-inclusions and psammoma bodies. In focal areas tumor cells were considerably dense, and the cells were round or irregular in shape, with less cytoplasm, uniform nuclear chromatin, and visible nucleoli and mitoses (2/10 HPF). By immunohistochemistry, the neoplastic cells showed strong and diffuse staining with vimentin, epithelial membrane antigen and SSTR2 with variable expression of PR, ALK and S100 protein. However, the cells were negative for GFAP, SOX-10, inhibin, CD34, STAT6, smooth muscle actin, desmin, CKpan, D2-40, WT-1, CK5/6 and CD45. The highest proliferation index by Ki-67 was 15%. The abnormal expression of ALK led to the initial misdiagnosis of an inflammatory myofibroblastic tumor. After 12 months of follow-up, no disease progression was observed.ConclusionThe presence of primary ectopic meningiomas in the thoracic cavity is extremely rare, and this tumor is easily misdiagnosed clinically. Imaging is suggested to determine the location and possible differential diagnosis, while the final diagnosis should be via pathological examination. Immunohistochemistry is crucial for disease diagnosis. Owing to our limited knowledge of PEM, its pathogenesis and tissue of origin remain unclear. Clinicians should pay close attention to such potential patients. The present case report may provide insights into the diagnosis and therapy of patients with this tumor.
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spelling doaj.art-5804dc61037541cc8830744727fca8462023-04-11T06:03:17ZengFrontiers Media S.A.Frontiers in Oncology2234-943X2023-04-011310.3389/fonc.2023.11496271149627Primary ectopic meningioma in the thoracic cavity: A rare case report and review of the literatureXu Liu0Xu Liu1Jiao Liu2Ting Nai3Ting Nai4Yuxia Yang5Yuxia Yang6Yuchang Hu7Yuchang Hu8Institute of Pathology, China Three Gorges University, Yichang, ChinaDepartment of Pathology, Yichang Central People’s Hospital, Yichang, ChinaDepartment of Obstetrics, Affiliated Renhe Hospital of China Three Gorges University, Yichang, ChinaInstitute of Pathology, China Three Gorges University, Yichang, ChinaDepartment of Pathology, Yichang Central People’s Hospital, Yichang, ChinaInstitute of Pathology, China Three Gorges University, Yichang, ChinaDepartment of Pathology, Yichang Central People’s Hospital, Yichang, ChinaInstitute of Pathology, China Three Gorges University, Yichang, ChinaDepartment of Pathology, Yichang Central People’s Hospital, Yichang, ChinaBackgroundMeningioma is a common type of intracranial tumor in adults. It rarely arises in the chest, with only a few case reports in the English literature. Here, we report the case of a patient with a primary ectopic meningioma (PEM) located in the thoracic cavity.Case presentationA 55-year-old woman presented with exercise-induced asthma, chest tightness, intermittent dry cough and fatigue for several months. Computed tomography revealed the presence of a huge mass in the thoracic cavity, with no connection to the spinal canal. Lung cancer and mesothelioma were suspected, and surgery was performed. Grossly, the mass was a grayish-white solid 9.5 cm × 8.4 cm × 5.3 cm in size. The microscopic morphology of the lesion was consistent with that of typical central nervous system meningioma. The pathological subtype was transitional meningioma. The tumor cells were arranged in a fascicular, whorled, storiform and meningithelial pattern, with occasional intranuclear pseudo-inclusions and psammoma bodies. In focal areas tumor cells were considerably dense, and the cells were round or irregular in shape, with less cytoplasm, uniform nuclear chromatin, and visible nucleoli and mitoses (2/10 HPF). By immunohistochemistry, the neoplastic cells showed strong and diffuse staining with vimentin, epithelial membrane antigen and SSTR2 with variable expression of PR, ALK and S100 protein. However, the cells were negative for GFAP, SOX-10, inhibin, CD34, STAT6, smooth muscle actin, desmin, CKpan, D2-40, WT-1, CK5/6 and CD45. The highest proliferation index by Ki-67 was 15%. The abnormal expression of ALK led to the initial misdiagnosis of an inflammatory myofibroblastic tumor. After 12 months of follow-up, no disease progression was observed.ConclusionThe presence of primary ectopic meningiomas in the thoracic cavity is extremely rare, and this tumor is easily misdiagnosed clinically. Imaging is suggested to determine the location and possible differential diagnosis, while the final diagnosis should be via pathological examination. Immunohistochemistry is crucial for disease diagnosis. Owing to our limited knowledge of PEM, its pathogenesis and tissue of origin remain unclear. Clinicians should pay close attention to such potential patients. The present case report may provide insights into the diagnosis and therapy of patients with this tumor.https://www.frontiersin.org/articles/10.3389/fonc.2023.1149627/fullprimary ectopic meningiomathoracic cavityimmunohistochemistrydiagnosiscase report
spellingShingle Xu Liu
Xu Liu
Jiao Liu
Ting Nai
Ting Nai
Yuxia Yang
Yuxia Yang
Yuchang Hu
Yuchang Hu
Primary ectopic meningioma in the thoracic cavity: A rare case report and review of the literature
Frontiers in Oncology
primary ectopic meningioma
thoracic cavity
immunohistochemistry
diagnosis
case report
title Primary ectopic meningioma in the thoracic cavity: A rare case report and review of the literature
title_full Primary ectopic meningioma in the thoracic cavity: A rare case report and review of the literature
title_fullStr Primary ectopic meningioma in the thoracic cavity: A rare case report and review of the literature
title_full_unstemmed Primary ectopic meningioma in the thoracic cavity: A rare case report and review of the literature
title_short Primary ectopic meningioma in the thoracic cavity: A rare case report and review of the literature
title_sort primary ectopic meningioma in the thoracic cavity a rare case report and review of the literature
topic primary ectopic meningioma
thoracic cavity
immunohistochemistry
diagnosis
case report
url https://www.frontiersin.org/articles/10.3389/fonc.2023.1149627/full
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