Deafness due to bilateral endolymphatic sac tumours in a case of von Hippel Lindau syndrome

被引:30
作者
Kempermann, G
Neumann, HPH
Scheremet, R
Volk, B
Mann, W
Gilsbach, J
Laszig, R
机构
[1] ALBERT LUDWIGS UNIV KLIN,NEUROZENTRUM,DEPT NEUROPATHOL,FREIBURG,GERMANY
[2] ALBERT LUDWIGS UNIV KLIN,DEPT HYPERTENS & NEPHROL,FREIBURG,GERMANY
[3] ALBERT LUDWIGS UNIV KLIN,DEPT OTOLARYNGOL,FREIBURG,GERMANY
[4] ALBERT LUDWIGS UNIV KLIN,NEUROZENTRUM,DEPT NEUROSURG,FREIBURG,GERMANY
[5] UNIV KLIN,DEPT OTOLARYNGOL,MAINZ,GERMANY
[6] KLIN RWTH,DEPT NEUROSURG,AACHEN,GERMANY
关键词
inner ear; thyroid carcinoma;
D O I
10.1136/jnnp.61.3.318
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
A case of bilateral endolymphatic sac tumours is reported. In a patient with von Hippel-Lindau syndrome, tumour growth in the right cerebellopontine angle caused deafness. The tumour was removed and classified as a metastasis from a thyroid carcinoma. However, on thyroidectomy no primary neoplasm could be found. Eight years later a similar tumour was operated on in the left petrosal bone. Histological appearance, immunocytochemical findings, and the clinical context gave evidence that the tumours had to be reclassified as endolymphatic sac tumours-extremely rare entities. The report supports the hypothesis, suggested by the few earlier case reports, that endolymphatic sac tumours could be one of the inherent tumour manifestations in von Hippel-Lindau syndrome.
引用
收藏
页码:318 / 320
页数:3
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