Yanchar N L, Chou S
Division of Pediatric General Surgery, Children's Hospital of Eastern Ontario, Ottawa, Canada.
Pediatr Surg Int. 2000;16(5-6):451-3. doi: 10.1007/s003830050041.
Cervical neuroblastoma (CNB) is relatively rare, accounting for less than 5% of these tumors. Because it arises from the cervical sympathetic chain, complete resection will leave the child with Horner's syndrome in a high proportion of cases. Advances in technology have allowed for the development of diagnostic and imaging modalities more specific to the disease. One of these has been the advent of radiolabeled meta-iodobenzylguanidine (MIBG) to assess the primary tumor and focal metastatic involvement. This nuclide is also taken up by normal salivary-gland tissue; this may be altered, however, in the presence of sympathetic denervation. We present a case of a primary CNB associated with Horner's syndrome, which led to confusion in interpretation of the subsequent MIBG scan. We alert the reader to potential pitfalls in the use of this examination in this disease entity.
颈部神经母细胞瘤(CNB)相对罕见,占此类肿瘤的比例不到5%。由于它起源于颈部交感神经链,在大多数情况下,完整切除会使患儿出现霍纳综合征。技术的进步使得针对该疾病的更具特异性的诊断和成像方式得以发展。其中之一是放射性标记的间碘苄胍(MIBG)的出现,用于评估原发性肿瘤和局灶性转移灶。这种核素也会被正常唾液腺组织摄取;然而,在存在交感神经去神经支配的情况下,这种情况可能会发生改变。我们报告一例与霍纳综合征相关的原发性CNB病例,该病例导致后续MIBG扫描结果的解读出现混淆。我们提醒读者在该疾病实体中使用此项检查时可能存在的潜在陷阱。