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Langerhans' cell histiocytosis of the temporal bone: successful treatment of sensorineural hearing loss with low-dose radiotherapy

Published online by Cambridge University Press:  13 June 2008

J K Zlodre*
Affiliation:
Department of Otorhinolaryngology, John Radcliffe Hospital, Oxford, UK
A T M Rennie
Affiliation:
Department of Neuroradiology, John Radcliffe Hospital, Oxford, UK
J D Ramsden
Affiliation:
Department of Otorhinolaryngology, John Radcliffe Hospital, Oxford, UK
*
Address for correspondence: Dr J K Zlodre, Department of Otorhinolaryngology, John Radcliffe Hospital, Oxford OX3 9DU, UK. E-mail: [email protected]

Abstract

Objective:

To present the successful treatment of sensorineural hearing loss secondary to Langerhans' cell histiocytosis with low-dose radiotherapy, and also the disparity between radiological resolution of Langerhans' cell histiocytosis lesions and lack of sensorineural hearing loss improvement, accompanied by a review of the literature on otolaryngological manifestations and management of Langerhans' cell histiocytosis.

Case report:

Langerhans' cell histiocytosis is a multisystem disease which frequently causes osseous lesions in the temporal bones. Hearing loss is usually conductive but may be sensorineural with lesions of the petrous temporal bone. We present a case of sensorineural hearing loss secondary to Langerhans' cell histiocytosis affecting the labyrinth and internal auditory meatus, which resolved following radiotherapy. Contralateral sensorineural hearing loss in the same patient, previously treated with chemotherapy, did not resolve despite radiological resolution of the temporal bone lesions.

Conclusion:

We suggest that timely radiotherapy for treatment of sensorineural hearing loss secondary to Langerhans' cell histiocytosis is an appropriate treatment option.

Type
Clinical Records
Copyright
Copyright © JLO (1984) Limited 2008

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