Objective: To highlight a case from 1960 connecting endolymphatic sac tumour and von Hippel-Lindau disease. Case report: In 1960, a 24-year-old woman presented with unilateral hearing loss, pulsatile tinnitus and a mass visible on otoscopy. The patient underwent surgical biopsy, which was complicated by haemorrhage, and ultimately resulted in death. At autopsy, a destructive temporal bone neoplasm with cystic and papillary architecture was observed that had eroded into the otic capsule. Intra-abdominal lesions consistent with von Hippel-Lindau disease were also observed, and the surgeon postulated a connection between endolymphatic sac tumour and von Hippel-Lindau disease. Method: A review of the literature was carried out using PubMed. Conclusion: Endolymphatic sac tumours are rare neoplasms of the temporal bone that can occur sporadically or as part of von Hippel-Lindau disease. The connection between endolymphatic sac tumour and von Hippel-Lindau disease was first proposed in 1988 and formalised in 1997. We believe that this case represents the first documented connection between endolymphatic sac tumour and von Hippel-Lindau disease.
CITATION STYLE
Bellairs, J. A., & Gluth, M. B. (2018). A histopathological connection between a fatal endolymphatic sac tumour and von Hippel-Lindau disease from 1960. Journal of Laryngology and Otology, 132(1), 75–78. https://doi.org/10.1017/S0022215117001888
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