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Atypical Congenital Hypertrophy of the Retinal Pigment Epithelium in Gardner's Syndrome
Journal of the Korean Ophthalmological Society ; : 2509-2513, 2000.
Article in Korean | WPRIM | ID: wpr-85533
ABSTRACT
Congenital hypertrophy of the retinal pigment epithelium (CHRPE)is a well circumscribed, flat, pigmented fundus lesion that have a variety of shapes. It is the most common extracolonic manifestation of Gardner's syndrome. The number and shape of CHRPE should arouse suspicion of increased risk of polyposis.We experienced one case of Gardner's syndrome in a family history of colonic carcinoma that showed atypical congenital hypertrophy of the retinal pigment epithelium, osteoma, epidermal cyst and polyposis combined with colonic carcinoma.A total colectomy and ileostomy were performed.So we reported it with the review of literature of clinical value of CHRPE as a predictive marker of Gardner's syndrome.
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Full text: Available Index: WPRIM (Western Pacific) Main subject: Osteoma / Retinaldehyde / Gardner Syndrome / Ileostomy / Colectomy / Colon / Epidermal Cyst / Retinal Pigment Epithelium / Hypertrophy Type of study: Prognostic study Limits: Humans Language: Korean Journal: Journal of the Korean Ophthalmological Society Year: 2000 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Osteoma / Retinaldehyde / Gardner Syndrome / Ileostomy / Colectomy / Colon / Epidermal Cyst / Retinal Pigment Epithelium / Hypertrophy Type of study: Prognostic study Limits: Humans Language: Korean Journal: Journal of the Korean Ophthalmological Society Year: 2000 Type: Article