No identifiable primary, only metastases: Case report of a small round blue cell tumor consistent with Ewing sarcoma presenting with multisystem spread in a young woman

Document Type

Case Report

Department

Medical College Pakistan; Radiology

Abstract

Ewing sarcoma is the second most common malignant bone tumor in children and adolescents but remains rare and highly aggressive. We present the case of a 31-year-old woman with widespread metastatic disease suggestive of Ewing sarcoma, including lung, spinal, and brain involvement at presentation; however, no dominant primary lesion was identified despite extensive imaging. The patient’s clinical course was complicated by neuropathic pain, seizures, and severe treatment-related infections. She was managed with multi-agent chemotherapy and supportive care but ultimately left against medical advice due to socioeconomic constraints. This case illustrates the diagnostic and therapeutic challenges of Ewing sarcoma in low-resource settings and underscores the importance of early detection, molecular confirmation, and multidisciplinary management.

Comments

Pagination and issue are not provided by the author/publisher.

Publication (Name of Journal)

Clin Med Insights Case Rep

DOI

10.1177/11795476261457179

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