Ocular Manifestations of Congenital Insensitivity to Pain With Anhidrosis - 18/08/11
, Shima Fukuoka, MD a, Tomohiko Usui, MD a, Norihiko Honda, MD a, Ryuichi Ideta, MD a, Makiko Ochiai, OD a, Satoru Yamagami, MD b, Makoto Araie, MD a, Yutaka Awaya, MD c
Inquiries to Shiro Amano, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-8655 JapanRésumé |
Purpose |
To describe ocular manifestations in Japanese patients with congenital insensitivity to pain with anhidrosis (CIPA), focusing particularly on the status of the ocular surface.
Design |
Observational case series.
Methods |
Eighteen patients with CIPA underwent applicable ophthalmologic examinations, including visual acuity, refraction, slit-lamp examination, fundus examination, tear breakup time, Schirmer 1 test, corneal sensitivity, and corneal topography.
Results |
Superficial punctate keratopathy (SPK) was observed at the interpalpebral area in 23 (64%) of 36 eyes. Corneal opacity was observed in three eyes (8.3%). Tear breakup time was below the lower limit of the normal range in all examined eyes, and the value of Schirmer 1 test was above the lower limit of the normal range in most of the examined eyes.
Conclusions |
Superficial punctate keratopathy is observed in most cases of CIPA, which might predispose patients to corneal infection. Investigation of dry eye in patients with CIPA will provide unique opportunities to explore the critical roles of the autonomic sympathetic nervous system as well as the sensory nervous system in the physiology of tear production.
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Vol 141 - N° 3
P. 472-477 - mars 2006 Retour au numéro
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