Complex Conjunctival Choristoma in Linear Nevus Sebaceous Syndrome: A case report.
- Author:
Jinyoung YOO
;
Jae Kyung KOH
;
Seok Jin KANG
;
Byung Kee KIM
- Publication Type:Case Report
- Keywords:
Choristoma;
Nevus sebaceus
- MeSH:
Atrophy;
Biopsy;
Cartilage;
Child;
Choristoma*;
Choroid;
Humans;
Infant;
Intellectual Disability;
Karyotype;
Lacrimal Apparatus;
Male;
Neurocutaneous Syndromes;
Nevus*;
Nevus, Sebaceous of Jadassohn;
Ophthalmology;
Optic Atrophy;
Parturition;
Pregnancy;
Scalp;
Seizures;
Skin;
Subarachnoid Space
- From:Korean Journal of Pathology
2000;34(9):680-684
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Linear nevus sebaceous syndrome is an uncommon neurocutaneous disorder characterized by nevus sebaceus, seizures, and mental retardation, and is often accompanied by ocular anormalies. We recently experienced a case of conjunctival choristoma associated with linear nevus sebaceous syndrome in a 17-month-old boy. The child was the product of a full-term uncomplicated pregnancy and normal delivery with normal karyotype of 46, XY. He was noted at birth to have a conjunctival mass on the right eye and linear nevi over the midline facial region and right temporoparietal scalp. Ophthalmologic examination revealed optic atrophy, peripapillary staphyloma, macular hypogenesis, and osseous choristoma of the choroid. A computed tomography scan demonstrated widening of the subarachnoid space and moderate atrophy of the cerebral and cerebellar hemispheres. He has been followed by ophthalmology and completely free of seizures since birth. The patient underwent excision of the conjunctival mass and biopsies of the skin lesion at 17 months of age. Histologic examination of the skin biopsies was characteristic for the linear sebaceous nevus of Jadassohn. Histologic findings of the conjunctival lesion showed a complex choristoma that contained lacrimal gland tissue and cartilage.
