| Literature DB >> 16444678 |
Kaan Boztug1, Kwabena Frimpong-Ansah, Vasanta Rao Nanduri, Joanna Lawson, Isabelle Russell-Eggitt, Penelope Brock.
Abstract
Intraocular involvement in Langerhans cell histiocytosis (LCH) is rare. We describe the case of a neonate with congenital disseminated LCH involving skin, liver, spleen, and intraocular structures including uvea and retina. Early and aggressive treatment according to the LCH-II treatment protocol was administered and resulted in remission of the disease. However, despite close follow-up and additional local treatment, involvement of intraocular structures resulted in severe long-term ophthalmological sequelae including complete bilateral loss of vision. Copyright (c) 2006 Wiley-Liss, Inc.Entities:
Mesh:
Year: 2006 PMID: 16444678 DOI: 10.1002/pbc.20714
Source DB: PubMed Journal: Pediatr Blood Cancer ISSN: 1545-5009 Impact factor: 3.167