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Journal articles on the topic 'Cerebral pseudotumor mimicking meningioma'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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1

Louw, Deon, Garnette Sutherland, William Halliday, and John Kaufmann. "Meningiomas mimicking cerebral schwannoma." Journal of Neurosurgery 73, no. 5 (1990): 715–19. http://dx.doi.org/10.3171/jns.1990.73.5.0715.

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✓ A brain tumor with histological features reminiscent of schwannoma with underlying meningioangiomatosis was subjected to electron microscopic and immunohistochemical analysis, which confirmed the neoplasm as a meningioma. This prompted reexamination of a similar tumor, described in a previous publication as a cerebral schwannoma, with identical immunohistochemical techniques. The results obtained favored alteration of this diagnosis to that of meningioma. This experience has led the authors to recommend the use of immunohistochemistry techniques when evaluating unusual intracranial neoplasms

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2

Anazi, Abdulrahman Al, and Wissam Al Issawi. "Extra-axial Primary Intracranial Cerebral Lymphoma Mimicking Meningioma." Neurosurgery Quarterly 19, no. 3 (2009): 214–16. http://dx.doi.org/10.1097/wnq.0b013e3181a482bc.

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3

Adam, Danil, Ioana Hornea, Cristiana Moisescu, Dragos Iftimie, and Toma Papacocea. "Microcystic meningioma mimicking an arachnoid cyst." Romanian Neurosurgery 29, no. 3 (2015): 279–84. http://dx.doi.org/10.1515/romneu-2015-0037.

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Abstract Microcystic meningioma is a particular morphopathological form of benign meningiomas, with different imaging characteristics compared to other forms of meningiomas. It is presented the case of an 80 year old woman with repeated head injuries, initially operated for a right fronto-temporo-parietal pericerebral fluid collection. After four years, the patient returned with headache, confusional status, somnolence, symptoms wich appeared after a new head injury. Cerebral CT scan revealed a hypodense lesion in the right sylvian fissure of 5.7/3.5 cm, without perilesional edema, which was i

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4

H, Bekralas, Habchi N, Bouallag M, Boulaouad W, Oumchiche W, and Djaafer M. "Diagnosis Error of a Tuberculoma: Case Report and Review of the Literature." Neuroscience and Neurological Surgery 4, no. 1 (2019): 01–02. http://dx.doi.org/10.31579/2578-8868/049.

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Among the diagnoses to be mentioned before a brain tumor, that of tuberculosis, has retained a significant place in the developing countries. The extra axial form poses a real problem of differential diagnosis especially with meningioma. We report a case of a cerebral tuberculoma mimicking meningioma. A histological study is necessary in order to make a correct diagnosis and plan an adequate and early medical procedure.

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5

HM, Alkhalil, Benaguida H, Djibadje H, et al. "Brain Meningioma Mimicking Eclampsia: A Report of Two Cases." International Journal of Medical and Pharmaceutical Case Reports 17, no. 3 (2024): 15–18. http://dx.doi.org/10.9734/ijmpcr/2024/v17i3385.

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Seizures occurring during pregnancy and postpartum may lead to the suspicion of eclampsia. However, it is essential to conduct paraclinical examinations (brain CT scan and brain MRI) to rule out cerebral expansive processes. In this main article, we report two cases of patients admitted for eclampsia, in whom a diagnosis of meningioma was made. Based on the observations, we discuss the different entities of this pathology with data from the literature.

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6

Foo, Jinny Y., Gregory K. Davis, and Mark A. Brown. "Frontal lobe meningioma mimicking preeclampsia: A case study." Obstetric Medicine 10, no. 4 (2017): 192–94. http://dx.doi.org/10.1177/1753495x17701847.

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We report a case of a left frontal lobe meningioma presenting in a woman with proteinuric preeclampsia in her first term pregnancy. The patient had a background of antepartum migraines that resolved in the second trimester of pregnancy. Postpartum, she required urgent surgery and sustained convulsions after surgery. She had no residual disease and has had another successful pregnancy. This case highlights the importance of cerebral imaging in the context of an atypical clinical course of preeclampsia. Although headaches are common in pregnancy and usually benign, other, more serious, diagnoses

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7

Kasliwal, Manish K., Ashish Suri, Deepak K. Gupta, Vaishali Suri, Arvind Rishi, and Bhawani S. Sharma. "Sphenoid wing inflammatory pseudotumor mimicking a clinoidal meningioma: case report and review of the literature." Surgical Neurology 70, no. 5 (2008): 509–13. http://dx.doi.org/10.1016/j.surneu.2007.07.075.

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8

Han, Moon-Soo, Kyung-Sub Moon, Kyung-Hwa Lee, Woo-Youl Jang, Seul-Kee Kim, and Shin Jung. "Intracranial Inflammatory Pseudotumor Associated with Idiopathic Hypertrophic Pachymeningitis Mimicking Malignant Tumor or High-Grade Meningioma." World Neurosurgery 134 (February 2020): 372–76. http://dx.doi.org/10.1016/j.wneu.2019.10.172.

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9

Shrestha, Neha, Oshan Shrestha, Ayeshna Gurung, and Sameen Khatiwada. "An Intriguing Case of Angiomatous Meningioma Mimicking a Hemorrhagic Metastasis." Journal of Nobel Medical College 13, no. 1 (2024): 100–103. http://dx.doi.org/10.3126/jonmc.v13i1.68122.

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Meningiomas comprise a family of neoplasms derived from the meningothelial cells of the arachnoid mater. Peritumoural cerebral oedema can be prominent with certain histological subtypes, such as secretory, angiomatous/microcystic, lymphoplasmacyte-rich, and high-grade meningiomas. We report one such case presenting in our institute that showed well defined blood density hyperdense lesion of size 3.1x2.9x3.4 cm with marked perilesional edema in right parafalcinefronto-parietal lobe and was thought to be a hemorrhagic metastatic lesion or a primary glioma on CT as well as MRI scans. The histopat

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10

Cucu, A. I., Dana Mihaela Turliuc, Anca Sava, Gabriela Florenţa Dumitrescu, Ş. Turliuc, and Claudia Florida Costea. "Falx cerebri tuberculoma mimicking en plaque meningioma – case report." Romanian Neurosurgery 30, no. 2 (2016): 209–13. http://dx.doi.org/10.1515/romneu-2016-0032.

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Abstract Background: The involvement of falx cerebri in tuberculosis is extremely rare, with only three cases reported so far in the literature. The diagnosis is most often difficult to establish, given the location of the lesion, making surgical intervention necessary for a definite histopathologic diagnosis. Methods: We present the case of a 49-year old female patient who was admitted for a right jacksonian seizure, followed by a right crural monoparesis, without a history of tuberculosis. The lesion mimicked a falx cerebri en plaque meningioma in the imaging tests. Results: A complete surgi

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11

Abujarir, Raed Hassan, Ali Ayyad, Ahmad Sotouhy, Essam Bozom, Ahmed Shaaban, and Aisha Al Kubaissi. "Convexity Dura-Based Cerebral Cavernous Malformation Mimicking Meningioma: A Case Report and Literature Review." Asian Journal of Neurosurgery 17, no. 01 (2022): 120–26. http://dx.doi.org/10.1055/s-0042-1749109.

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AbstractCavernous angioma, cavernoma, cavernous hemangioma, also called cerebral cavernous malformation (when present in the brain), are benign vascular malformations, usually intraparenchymal; however, a few reported cases are in the extra-axial location—as middle cranial fossa, near the cavernous sinuses, and in the cerebellopontine angle—and are rarely reported as dura-based convexity lesion resembling meningioma. We report a giant dura-based, convexity, a cerebral cavernous malformation. We wish to notify the case as occurring at a rare location and a large-sized cerebral cavernous malform

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12

Casey, A. T. H., and A. J. Moore. "A traumatic giant posterior cerebral artery aneurysm mimicking a tentorial edge meningioma." British Journal of Neurosurgery 8, no. 1 (1994): 97–99. http://dx.doi.org/10.3109/02688699409002401.

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13

Choi, Joo Won, Richard Ho, Yi Jonathan Zhang, et al. "A rare case of solitary, isolated dural metastasis from hepatocellular carcinoma mimicking a meningioma." Surgical Neurology International 14 (November 10, 2023): 398. http://dx.doi.org/10.25259/sni_733_2023.

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Background: Distinguishing an isolated metastatic dural tumor from a meningioma on imaging is challenging and may lead to a delay in treatment. Here, we present the first known case of isolated, solitary dural metastasis from hepatocellular carcinoma (HCC) mimicking a meningioma. Case Description: A 64-year-old male with a history of liver cirrhosis presented with a 5.8 cm enhancing left parafalcine hemorrhagic dural-based mass extending across the midline. Cerebral angiography revealed a distal left anterior pseudoaneurysm, and tumor contrast blush with feeders from the left ophthalmic and ri

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14

Guettabi, Khadija, Jihad Echnin, Abdelkoudouss Laaidi, et al. "Chordoma of the Sellar Region Mimicking Meningioma: A Literature Review and Illustrative Case." European Journal of Medical and Health Sciences 5, no. 4 (2023): 27–29. http://dx.doi.org/10.24018/ejmed.2023.5.4.1785.

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Background: Chordoma is a rare malignant tumor that accounts for 1-4% of primary malignant bone tumors arising primarily in the axial skeleton and primarily affects adults. It seems to have difficulty with diagnosis and treatment. Case description: A 63-year-old man with a history of diabetes treated with oral antidiabetic medication and hypertension. Presented with two years of bilateral decrease in visual acuity. Neurological examination revealed left ptosis, divergent strabismus, and higher cerebral function disorders. Brain MRI revealed a sellar and suprasellar lesion evokes a sellar menin

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15

Adhikari, Ganesh, Ajit Shrestha, Bipin Kumar Yadav, Sandip Rauniyar, and Saujan Dulal. "MISLEADING PARAFALCINE MASS: A CASE REPORT." Journal of Chitwan Medical College 13, no. 2 (2023): 122–24. http://dx.doi.org/10.54530/jcmc.1284.

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A parafalcine mass can be misdiagnosed with Giant intracranial aneurysm because of lack of specific radiological features. Giant aneurysm are rare comprising of 5 % of all intracranial aneurysm and commonly located on internal carotid artery and middle cerebral artery. A case which we describe, located on left distal anterior cerebral artery, is rare. A 53 old male presented with weakness in right lower limb associated with headache and dysarthria. On examination, Power of rt lower limb was 3/5 with normal vitals. On CT imaging, findings showed midline frontal parafalcine well defined mass wit

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16

Castro-Gomez, Sergio, Julius Binder, Arndt-Hendrik Schievelkamp, and Michael Thomas Heneka. "CNS Superficial Siderosis Mimicking a Motor Neuron Disease." Brain Sciences 12, no. 11 (2022): 1558. http://dx.doi.org/10.3390/brainsci12111558.

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Superficial siderosis of the central nervous system (SS-CNS) is a rare condition characterized by a hemosiderin accumulation along the subpial surfaces and arises from an intermittent chronic bleeding in the subarachnoid space usually as a result of a chronic subarachnoid hemorrhage by trauma, vascular malformations, CNS tumors, or cerebral amyloid angiopathy (CAA). We present a 61-year-old male with a 12-year history of limb weakness, muscle wasting, cramps, clumsiness, progressive unsteady gait, and fine motor impairments. His medical history included the resection of a left parietal meningi

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17

Wajima, Daisuke, Shuta Aketa, and Taiji Yonezawa. "Supratentorial convexity schwannoma unrelated to cranial nerves: Case report and review of the literature." Surgical Neurology International 11 (June 6, 2020): 143. http://dx.doi.org/10.25259/sni_193_2020.

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Background: Intracranial schwannoma not related to cranial nerves is rare entity, and difficult to be diagnosed preoperatively. Here, we experienced a case of convexity schwannoma mimicking convexity meningioma, and discuss about the characteristics of such cases based on the past published reports. Case Description: A 48-year-old man presented with a sudden onset of seizures. Brain magnetic resonance image (MRI) revealed a small mass lesion in the peripheral aspect of the right parieto-frontal lobe. The mass was isointense on T1-weighted and hyperintense on T2-weighted MRI, with homogenous en

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18

Hajtovic, Sabastian, Edward Yu, Alexander Bershadskiy, Raphael Sacho, and Ronit Gilad. "Primary intracranial marginal zone B-cell lymphoma of mucosa-associated lymphoid tissue arising in the lateral ventricle: Case report and review of pathogenesis." Surgical Neurology International 13 (April 29, 2022): 181. http://dx.doi.org/10.25259/sni_54_2022.

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Background: Primary central nervous system lymphoma (PCNSL) is an aggressive extranodal subtype of nonHodgkin’s lymphoma. Ventricle-predominant PCNSL, arising in the CNS ventricular system, is a rare entity. In over 90% of cases, PCNSL is classified as diffuse large B-cell lymphoma. Rarely, PCNSL may be classified as marginal zone B-cell lymphoma (MZBCL) of mucosa-associated lymphoid tissue (MALT). Taken together, a primary MALT-type MZBCL arising in a cerebral ventricle is an extremely rare presentation. Case Description: A 69-year-old female presented with a persistent left frontal headache

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19

Jouanneau, Emmanuel, Rafael Alfonso Guzman Tovar, Claude Desuzinges, et al. "Very Late Frontal Relapse of Medulloblastoma Mimicking a Meningioma in an Adult: Usefulness of 1H Magnetic Resonance Spectroscopy and Diffusion-perfusion Magnetic Resonance Imaging for Preoperative Diagnosis: Case Report." Neurosurgery 58, no. 4 (2006): E789. http://dx.doi.org/10.1227/01.neu.0000204878.10591.71.

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Abstract OBJECTIVE AND IMPORTANCE: We present a rare case of very long-term medulloblastoma relapse in an adult patient and discuss the pattern of recurrence and metabolic imaging of the tumor. CLINICAL PRESENTATION: A 45-year-old man was referred for evaluation of a frontobasal midline tumor 21 years after treatment of a cerebellar medulloblastoma by surgery followed by chemotherapy and craniospinal radiotherapy. Magnetic resonance images were suggestive of a meningioma. Several hypotheses were discussed, such as other radio-induced tumors, sarcomas, high-grade gliomas, or lymphomas (previous

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20

Martha, Lilia Tena-Suck1* Ana Laura Calderón Garcidueñas1 Javier Alcocer2 Rafael Diaz Martínez2 Citlaltepetl Salinas-Lara1 Carlos Sánchez-Garibay1. "Meningeal Actinomyces Mimicking Meningioma, Case Report." October 7, 2022. https://doi.org/10.5281/zenodo.7183647.

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<strong>Background:</strong> Human actinomycosis, a chronic, granulomatous infectious disease, has been recognized for a long time. Actinomyces sp. Is a commensal, filamentous, gram-positive, acid-fast-negative bacteria that can cause pyogranulomatous inflammation in animals and humans. In Central Nervous System (CNS) affection is a rare presentation disease and is usually due to extension from infected lesions or seeding from distant sites.   Histologically, is characterized by a severe pyogranulomatous meningoencephalitis with intralesional filamentous bacteria that were also visib

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21

Ge, Rong, Jun Yang, Xiangang Yin, and Jingya Wang. "Case report: Meningioma associated with meningioangiomatosis mimicking invasive meningioma." Frontiers in Neurology 14 (June 28, 2023). http://dx.doi.org/10.3389/fneur.2023.1200827.

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Meningioangiomatosis (MA) is a rare malformation or hamartomatous lesion in the central nervous system, characterized by a plaque-like mass within the leptomeninges and cerebral cortex. An even rarer condition is MA complicated with meningiomas. We herein report a case of meningioma associated with MA that might be erroneously interpreted as a higher-grade lesion or an invasion by preoperative radiologic and postoperative histological examinations.

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22

Joudar, Imane, Siham Nasri, Narjisse Aichouni, Imane Kamaoui, and Imane Skiker. "A cerebral lymphoma mimicking a meningioma: Case report." Annals of Medicine & Surgery, August 7, 2023. http://dx.doi.org/10.1097/ms9.0000000000001126.

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Introduction: Cerebral lymphoma is a rare and aggressive brain tumor. It accounts for 1% of all non-Hodgkin’s lymphomas (NHL), and 2% of all brain tumors. Untreated brain lymphoma has a very poor prognosis, with an overall life expectancy of around 1.5 months Case presentation: We report the case of a 35-year-old patient, with no previous pathological history, who presented for 3 weeks with deafness and recently aggravated otalgia. in MRI brain imaging revealed a formation initially suggestive of an aggressive meningioma, and in whom the histological study of the operative specimen was in favo

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23

El Abbassi, I., H. Benaaguida, M. Jalal, A. Lamrissi, and S. Bouhya. "Cerebral meningioma during pregnancy mimicking eclampsia: About a rare case." International Journal of Surgery Case Reports, September 2023, 108786. http://dx.doi.org/10.1016/j.ijscr.2023.108786.

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24

Liu, Xiaohai, Renzhi Wang, Mingchu Li, and Ge Chen. "IgG4-Related Inflammatory Pseudotumor Involving the Clivus: A Case Report and Literature Review." Frontiers in Endocrinology 12 (April 30, 2021). http://dx.doi.org/10.3389/fendo.2021.666791.

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IgG4-related inflammatory pseudotumors are very uncommon and are characterized histologically by the presence of inflammatory swellings with increasing IgG4-positive plasma cells and lymphocytes infiltrating the tissues. As reports of intracranial IgG4-related pseudotumors are very rare, we report a case of an IgG4-related inflammatory pseudotumor involving the clivus mimicking meningioma. A 46-year-old male presented with intermittent headache for 2 years and a sudden onset of dysphagia and dysphonia of 7 days’ duration along with lower limb weakness. Enhanced magnetic resonance imaging (MRI)

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25

Sumi, Koichiro, Naoki Otani, Fumi Mori, Shun Yamamuro, Hideki Oshima, and Atsuo Yoshino. "Venous hypertension caused by a meningioma involving the sigmoid sinus: case report." BMC Neurology 21, no. 1 (2021). http://dx.doi.org/10.1186/s12883-021-02144-5.

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Abstract Background Intracranial venous hypertension has been associated with a few cases of meningioma secondary to compression of the venous sinus. This is the rare case of small meningioma involving the sigmoid sinus leading to intracranial venous hypertension mimicking venous thrombosis. Case presentation A 39-year-old woman suffered visual dysfunction due to bilateral papilledema. Noncontrast head computed tomography (CT) showed no intracranial space-occupying lesions or hydrocephalus. Cerebrospinal fluid examination revealed high opening pressure. Various image inspections such as three-

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