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ArticleCase reports in oncology

Olfactory Groove Meningioma Detected 10 Months after Cranial Radiotherapy in a Metastatic Ewing Sarcoma Survivor: A Case Report.

Ahmad M Al Malla, Ahmad Al-Bitar, Anas Bitar, Maher Saifo

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Article in Case reports in oncology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

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4 authors.

Ahmad M Al MallaFaculty of Medicine, Damascus University, Damascus, Syrian Arab Republic.
Ahmad Al-BitarFaculty of Medicine, Damascus University, Damascus, Syrian Arab Republic.
Anas BitarFaculty of Medicine, Damascus University, Damascus, Syrian Arab Republic.
Maher SaifoDepartment of Oncology, Faculty of Medicine, Damascus University, Damascus, Syrian Arab Republic.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Secondary intracranial neoplasms are a well-recognized late complication of cranial radiotherapy. Among these, meningiomas are the most frequently reported radiation-associated tumors. However, olfactory groove meningiomas (OGMs) are uncommon, and their development after cranial irradiation with a very short latency remains exceptionally rare. Case Presentation: A 38-year-old woman with Ewing sarcoma of the right thigh and brain metastases underwent multimodal treatment of surgical resection, VDC-IE chemotherapy, and subsequent cranial radiotherapy (54 Gy in 27 fractions). Retrospective review of pre-radiotherapy brain MRI showed no lesion in the olfactory groove region. Ten months after completing treatment, she presented with progressive headache, recurrent vomiting, and generalized seizures. Brain CT and MRI revealed a well-circumscribed, homogeneously enhancing extra-axial mass centered at the olfactory groove, with dural attachment and compression of the frontal lobes. Gross-total microsurgical resection was achieved through a right-sided pterional craniotomy. Histopathological examination confirmed a WHO grade I meningioma with diffuse SSTR2A expression, focal epithelial membrane antigen positivity, and a Ki-67 labeling index of 2%-3%. Immunohistochemistry was negative for CD99 and FLI1, excluding metastatic Ewing sarcoma. The postoperative course was uneventful, and follow-up imaging at 1 year showed no evidence of recurrence. Conclusion: This case highlights a rare early-onset OGM arising after cranial radiotherapy in a metastatic Ewing sarcoma survivor. Although the unusually short latency interval precludes definitive causal attribution, the temporal association, absence of a preexisting lesion on pre-radiotherapy imaging, and distinct histopathological profile support consideration of a radiation-associated origin. Long-term neuro-oncologic surveillance remains essential in patients treated with cranial irradiation.

Indexed as

Cranial radiotherapyEwing sarcomaOlfactory groove meningiomaRadiation-associated meningiomaSecondary intracranial tumor

Identifiers

PMID42494800
PMCPMC13395415

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