Literature DB >> 16444678

Intraocular Langerhans cell histiocytosis in a neonate resulting in bilateral loss of vision.

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.

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Year:  2006        PMID: 16444678     DOI: 10.1002/pbc.20714

Source DB:  PubMed          Journal:  Pediatr Blood Cancer        ISSN: 1545-5009            Impact factor:   3.167


  1 in total

1.  Choroidal neovascular membrane formation and retinochoroidopathy in a patient with systemic langerhans cell histiocytosis: a case report and review of the literature.

Authors:  Aristomenis Thanos; Demetrios Vavvas; Lucy H Young; C Stephen Foster
Journal:  Case Rep Ophthalmol       Date:  2012-04-13
  1 in total

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