Pelvic mass with isolated supratentorial brain parenchymal metastasis - An unusual presentation of Neuroblastoma: A case report

Swetha Palla , Richa Jain , Vivek Premshankar Tiwari , Nandita Kakkar
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Abstract

Background

Central nervous system (CNS) metastasis in neuroblastoma (NBL) is rare, typically occurring at the time of disease progression or relapse. Isolated CNS metastasis at diagnosis is even rarer and can present a diagnostic challenge. It is generally associated with a poor prognosis, necessitating aggressive treatment.

Case report

We report a case of neuroblastoma with an unusual presentation, featuring a pelvic primary tumor and a solitary brain parenchymal metastasis—both uncommon sites for NBL.

Conclusion

Although CNS metastasis is rare, a high index of suspicion with appropriate diagnostic workup is crucial for early diagnosis. The prognosis in these cases is generally poor, requiring a multidisciplinary treatment approach, including chemotherapy, surgery, and radiotherapy, to improve survival outcomes.
盆腔肿块伴孤立的幕上脑实质转移-神经母细胞瘤的一种不寻常的表现:1例报告
神经母细胞瘤(NBL)的中枢神经系统(CNS)转移是罕见的,通常发生在疾病进展或复发时。孤立的中枢神经系统转移在诊断时更为罕见,并且可以提出诊断挑战。它通常与预后不良有关,需要积极治疗。病例报告我们报告一例神经母细胞瘤,其不寻常的表现为盆腔原发肿瘤和孤立的脑实质转移,这两个部位在NBL中都不常见。结论虽然中枢神经系统转移是罕见的,但高怀疑指数和适当的诊断检查对早期诊断至关重要。这些病例的预后通常较差,需要多学科治疗方法,包括化疗、手术和放疗,以改善生存结果。
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