| Congenital Hypertrophy of the Retinal Pigment Epithelium in Familial Colonic Polyposis. |
|
Jeong Ho Lee, Jong Min Kim, Suk Dong Kim |
|
Department of Ophthalmology, Holy Family Hospital, The Catholic University of Korea. |
| 가족성 대장 용종증에 동반된 선천성 망막색소상피 비대증 |
|
이정호(Jeong Ho Lee),김종민(Jong Min Kim),김석동(Suk Dong Kim) |
|
|
|
|
| Abstract |
|
Congenital hypertrophy of the retinal pigment epithlium(CHRPE)is a well-circumscribed, flat, pigmented fundus lesion that is presented solitary or grouped. It is the most common extracolonic manifestation of familial adenomatous polyposis(FAP). Unfortunately, there is no phenotypic biochemical abnormality or serological marker which indicates whether or not a family member will be affected FAP. However, most of patients with polyposis have CHRPE which is usually multiple and bilateral, The presence of CHRPE in a family member should therefore arouse suspicion of increased risk of polyposis. We experienced one case of familial adenomatous polyposis that showed no extracolonic manifestation except multiple, bilateral fundus lesions. A prophylactic total colectomy was performed. So we report it with the review of literature of clinical value of CHRPE as a predictive congenital marker of FAP. |
| Key Words:
Congenital hypertrophy of the retinal pigment epithelium(CHRPE);Familial adenomatous polyposis(FAP) |
|
PDF Links
Download Citation
