| Literature DB >> 12892467 |
Mayumi Shimizu1, Toshihide Shimizu, Takashi Adachi, Masaki Nishiuchi, Masato Kanzaki, Takamasa Onuki.
Abstract
Neuroblastoma rarely occurs in adults, in whom prognosis is poor. Here we report on the effective use of multimodal therapy to achieve long-term survival in adult mediastinal neuroblastoma. In a 33-year-old male with severe pain radiating from the left hypochondrium to the back area, no abnormal shadow was detected on first examination; the shadow appeared in chest X-ray only 10 months later when the severe pain recurred. The patient was then referred to our department for further examination. Chest X-rays and chest CT scans revealed a posterior mediastinal mass beside the thoracic vertebrae. Diagnosis was confirmed after surgical resection, which was followed by outpatient adjuvant therapy through radiation and chemotherapy. The patient has survived 8 years and 8 months without recurrence or metastasis.Entities:
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Year: 2003 PMID: 12892467 DOI: 10.1007/bf02719388
Source DB: PubMed Journal: Jpn J Thorac Cardiovasc Surg ISSN: 1344-4964