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題 名 | Primary Cervical Neuroblastoma in Infants=頸部原發性神經母細胞瘤 |
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作 者 | 戴仲甫; 李國森; 陳一豪; | 書刊名 | 臺灣醫學會雜誌 |
卷 期 | 96:7 1997.07[民86.07] |
頁 次 | 頁561-564 |
分類號 | 415.9 |
關鍵詞 | 頸部; 原發性神經母細胞瘤; Cervical neuroblastoma; |
語 文 | 英文(English) |
英文摘要 | Although neuroblastoma is a relatively common malignancy of childhood, it is rarely of cervical origin. We encountered two cases of primary cervical neuroblastoma in infants. The first case was in a newborn who presented with noisty breathing, dyspnea, and choling on feeding soon after birth. Physical examination disclosed a left retropharyngeal mass near the midline causing aerodigestive compromise. Magnetic resonance imaging showed a well-defined hyperintense mass in the corresponding region. The infant underwent complete surgical excision of the mass 1 month after birth. The pathology report confirmed neuroblastoma. Horner's syndrome developed soon after surgery but resovled spontaneously within 6 months. No recurrence was noted during a 3-year follow-up period. The second patient, a 5-month-old female, presented with stridor and shortness of breath of 2-weeks' duration due to a right cervical mass. Magnetic resonance imaging showed a parapharyngeal mass suggestive of neuroblastoma. Complete surgical excision was done at the expense of sacrificing the sympathetic nerve trunk. The pathologic diagnosis was moderately differentiated neuroblastoma. No recurrence was noted when the patient was seen 2 years after surgery, although right-sided Horner's syndrome persisted. Surgical intervention can result in a good prognosis for low stage cervical neuroblastomas; however, long-term follow-up is important. |
本系統中英文摘要資訊取自各篇刊載內容。