先天性颈部神经母细胞瘤伴霍纳综合征。
Congenital cervical neuroblastoma associated with Horner syndrome.
作者信息
Ogita S, Tokiwa K, Takahashi T, Imashuku S, Sawada T
机构信息
Division of Surgery, Children's Research Hospital, Kyoto Prefectural University of Medicine, Japan.
出版信息
J Pediatr Surg. 1988 Nov;23(11):991-2. doi: 10.1016/s0022-3468(88)80001-0.
PMID:3244095
Abstract
A rare case of congenital neuroblastoma of the neck associated with complete Horner syndrome and respiratory distress is described. The case was successfully treated by total excision secondary to chemotherapy. Horner syndrome was of value for early diagnosis of this lesion.
摘要
本文描述了一例罕见的颈部先天性神经母细胞瘤，伴有完全性霍纳综合征和呼吸窘迫。该病例在化疗后通过手术全切成功治愈。霍纳综合征对该病变的早期诊断具有重要价值。
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