Volume 56, Issue 5 pp. 784-787
Patient Report

Parotid lymphangioma associated with facial nerve paralysis

Mitsuyoshi Imaizumi

Mitsuyoshi Imaizumi

Department of Otolaryngology, School of Medicine, Fukushima Medical University, Fukushima, Japan

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Akiko Tani

Akiko Tani

Department of Otolaryngology, School of Medicine, Fukushima Medical University, Fukushima, Japan

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Hiroshi Ogawa

Hiroshi Ogawa

Department of Otolaryngology, School of Medicine, Fukushima Medical University, Fukushima, Japan

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Koichi Omori

Corresponding Author

Koichi Omori

Department of Otolaryngology, School of Medicine, Fukushima Medical University, Fukushima, Japan

Correspondence: Koichi Omori, MD PhD, Department of Otolaryngology, School of Medicine, Fukushima Medical University, 1 Hikarigaoka, Fukushima 960-1295, Japan. Email: [email protected]Search for more papers by this author
First published: 22 October 2014
Citations: 2

Abstract

Parotid lymphangioma is a relatively rare disease that is usually detected in infancy or early childhood, and which has typical features. Clinical reports of facial nerve paralysis caused by lymphangioma, however, are very rare. Usually, facial nerve paralysis in a child suggests malignancy. Here we report a very rare case of parotid lymphangioma associated with facial nerve paralysis. A 7-year-old boy was admitted to hospital with a rapidly enlarging mass in the left parotid region. Left peripheral-type facial nerve paralysis was also noted. Computed tomography and magnetic resonance imaging also revealed multiple cystic lesions. Open biopsy was undertaken in order to investigate the cause of the facial nerve paralysis. The histopathological findings of the excised tumor were consistent with lymphangioma. Prednisone (40 mg/day) was given in a tapering dose schedule. Facial nerve paralysis was completely cured 1 month after treatment. There has been no recurrent facial nerve paralysis for eight years.

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