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Endolymphatic sac tumor in a 4-year-old boy
被引:25
|作者:
Kupferman, ME
Bigelow, DC
Carpentieri, TF
Bilaniuk, LT
Kazahaya, K
机构:
[1] Childrens Hosp, Div Pediat Otolaryngol, Richard D Wood Ctr, Philadelphia, PA 19104 USA
[2] Univ Penn, Sch Med, Dept Otorhinolaryngol Head & Neck Surg, Philadelphia, PA 19104 USA
[3] Childrens Hosp Philadelphia, Dept Anat & Pathol, Philadelphia, PA 19104 USA
[4] Univ Penn, Sch Med, Dept Radiol, Philadelphia, PA 19104 USA
关键词:
endolymphatic sac tumor;
pediatric;
transcochlear;
D O I:
10.1097/00129492-200409000-00022
中图分类号:
R74 [神经病学与精神病学];
学科分类号:
摘要:
Introduction: Endolymphatic sac tumors (ELST) are rare, low-grade, locally aggressive papillary neoplasms. We present a case of a 4-year-old boy with an ELST, the youngest described in the literature. Case: A boy presented with a right-sided serous otitis media and sudden-onset right facial nerve palsy. An audiogram revealed right-sided profound sensorineural hearing loss. Radiographic imaging demonstrated a 3-cm expansile lytic lesion along the posterior face of the petrous bone. Intervention/Results: The patient initially underwent a right transmastoid-infralabyrinthine biopsy. Pathologic examination revealed a papillary lesion suspicious for an ELST. Subsequently, a transtemporal-transcochlear approach with intra- and extradural resection of the tumor was performed. The facial nerve was dissected and transposed anteriorly and preserved. Histopathologic and immunohistochemical studies confirmed the ELST. At his 6-month follow up, there is no evidence of recurrence and the facial nerve function has returned to Grade 11 palsy. Conclusion: ELST are rare tumors of the temporal bone. This is the youngest case of ELST reported. Presentation, evaluation, and management of ELST is discussed.
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页码:782 / 786
页数:5
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