Literature DB >> 21864117

A singular case of congenital self-healing histiocytosis with skin, liver and atypical eye involvement.

Fulvio Parentin1, Giovanna Ventura, Serena Pastore, Valentina Kiren, Chiara Bibalo, Stefano Pensiero, Loredana Lepore.   

Abstract

PURPOSE: To describe a rare case of congenital self-healing Langerhans cell histiocytosis (CSHLCH) presenting with atypical eye involvement.
DESIGN: Case report.
METHODS: A female newborn presented with purpuric lesions over the trunk, limbs, and face. Liver ultrasonography revealed hypoechogenic lesions with blurred borders. Biomicroscopy showed right posterior synechiae with fibrinoid deposits on the lens. At 7 months she presented with right acute glaucoma.
RESULTS: Biomicroscopy showed the presence of inflammatory pseudo-membrane covering the anterior surface of the lens, iris, and iridocorneal angle. Ab externo trabeculotomy was performed; access to the anterior chamber with capsulorrhexis forceps permitted a peeling of the pseudo-membrane with normalization of the intraocular pressure. Histologic examination of the membrane revealed an inflammatory tissue with CD1a and S-100 positive histiocytic cells.
CONCLUSIONS: This is the first case of CSHLCH describing acute glaucoma secondary to a pseudo-inflammatory membrane with typical histiocytic cells, occluding the iridocorneal angle.

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Year:  2011        PMID: 21864117     DOI: 10.3109/09273948.2010.605538

Source DB:  PubMed          Journal:  Ocul Immunol Inflamm        ISSN: 0927-3948            Impact factor:   3.070


  1 in total

1.  Case for diagnosis. Hashimoto-Pritzker disease.

Authors:  Virginia Vinha Zanuncio; Luciana Rabelo de Carvalho; Antônio Carlos Martins Guedes; Cláudia Márcia Resende Silva; Bernardo Gontijo
Journal:  An Bras Dermatol       Date:  2013 Nov-Dec       Impact factor: 1.896

  1 in total

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