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一名3岁男孩下颌骨转移性神经母细胞瘤:病例报告

Metastatic neuroblastoma to the mandible in a 3-year-old boy: a case report.

作者信息

Otmani Naima, Khattab Mohamed

机构信息

Pediatric Hemato-Oncology Unit, Children's Hospital Of Rabat, Rabat, Morocco.

出版信息

Med Oral Patol Oral Cir Bucal. 2007 May 1;12(3):E201-4.

Abstract

Although neuroblastoma is a relatively common malignancy of childhood and its dissemination to distant organs is often seen, metastasis to the mandible is rare. A 3-year-old boy which a mandibular soft tissue mass was the initial presenting symptom of disseminated neuroblastoma is reported. The results of biopsy were inconclusive and the differential diagnosis from the imaging studies included lymphoma, soft tissue sarcoma, and osteosarcoma. A metastatic work-up disclosed neuroblastoma of the adrenal gland origin with osseous and bone marrow metastases. Urinary catecolamines were also increased. Regarding the widespread features of the tumor and lack of adequate treatment at this stage of disease, a palliative chemotherapy was conducted, and the patient died one month after starting treatment. This case illustrates that neuroblastoma at a young age, with bone metastases and bone marrow involvement are predictive of the poor outcome of the disease. Therefore, detecting early stage metastasis is one of the essential factors for improving treatment of neuroblastoma patients.

摘要

虽然神经母细胞瘤是儿童期相对常见的恶性肿瘤,且常可见其扩散至远处器官,但转移至下颌骨的情况却很罕见。本文报告了一名3岁男孩,其下颌软组织肿块是播散性神经母细胞瘤的首发症状。活检结果不明确,影像学研究的鉴别诊断包括淋巴瘤、软组织肉瘤和骨肉瘤。进一步的转移灶检查发现肾上腺起源的神经母细胞瘤伴有骨和骨髓转移。尿儿茶酚胺也升高。鉴于肿瘤的广泛特征以及疾病在此阶段缺乏充分治疗,遂进行了姑息化疗,患者在开始治疗后一个月死亡。该病例表明,年幼的神经母细胞瘤患者出现骨转移和骨髓受累提示疾病预后不良。因此,早期发现转移是改善神经母细胞瘤患者治疗效果的关键因素之一。

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