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Langerhans cell histiocytosis with presentation as orbital disease

Langerhans cell histiocytosis (LCH) is an uncommon multisystem disease with an abnormal polyclonal proliferation of Langerhans cells that invade various organs. In rare instances, the affection of the orbit is the only and the first symptom. We report an unusual case of an 18-month-old male who pres...

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Autores principales: Bhanage, Ashok B., Katkar, Anand D., Ghate, Prajakta S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4489065/
https://www.ncbi.nlm.nih.gov/pubmed/26167225
http://dx.doi.org/10.4103/1817-1745.159197
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author Bhanage, Ashok B.
Katkar, Anand D.
Ghate, Prajakta S.
author_facet Bhanage, Ashok B.
Katkar, Anand D.
Ghate, Prajakta S.
author_sort Bhanage, Ashok B.
collection PubMed
description Langerhans cell histiocytosis (LCH) is an uncommon multisystem disease with an abnormal polyclonal proliferation of Langerhans cells that invade various organs. In rare instances, the affection of the orbit is the only and the first symptom. We report an unusual case of an 18-month-old male who presented with orbital disease as the first symptom, in the form of chronic presentation of periorbital swelling (2 months duration) with acute inflammation (1-week duration) giving a suspicion of orbital cellulitis. Histopathology after radical excision confirmed the diagnosis of LCH and was advised initial therapy as per Histiocyte Society Evaluation and Treatment Guidelines (2009) but was lost to follow-up only reappearing with progression (multisystem LCH with risk organ involvement) and developed progressive active disease on treatment after 5 weeks. He was treated with salvage therapy for risk patients achieving complete remission.
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spelling pubmed-44890652015-07-12 Langerhans cell histiocytosis with presentation as orbital disease Bhanage, Ashok B. Katkar, Anand D. Ghate, Prajakta S. J Pediatr Neurosci Case Report Langerhans cell histiocytosis (LCH) is an uncommon multisystem disease with an abnormal polyclonal proliferation of Langerhans cells that invade various organs. In rare instances, the affection of the orbit is the only and the first symptom. We report an unusual case of an 18-month-old male who presented with orbital disease as the first symptom, in the form of chronic presentation of periorbital swelling (2 months duration) with acute inflammation (1-week duration) giving a suspicion of orbital cellulitis. Histopathology after radical excision confirmed the diagnosis of LCH and was advised initial therapy as per Histiocyte Society Evaluation and Treatment Guidelines (2009) but was lost to follow-up only reappearing with progression (multisystem LCH with risk organ involvement) and developed progressive active disease on treatment after 5 weeks. He was treated with salvage therapy for risk patients achieving complete remission. Medknow Publications & Media Pvt Ltd 2015 /pmc/articles/PMC4489065/ /pubmed/26167225 http://dx.doi.org/10.4103/1817-1745.159197 Text en Copyright: © Journal of Pediatric Neurosciences http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Bhanage, Ashok B.
Katkar, Anand D.
Ghate, Prajakta S.
Langerhans cell histiocytosis with presentation as orbital disease
title Langerhans cell histiocytosis with presentation as orbital disease
title_full Langerhans cell histiocytosis with presentation as orbital disease
title_fullStr Langerhans cell histiocytosis with presentation as orbital disease
title_full_unstemmed Langerhans cell histiocytosis with presentation as orbital disease
title_short Langerhans cell histiocytosis with presentation as orbital disease
title_sort langerhans cell histiocytosis with presentation as orbital disease
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4489065/
https://www.ncbi.nlm.nih.gov/pubmed/26167225
http://dx.doi.org/10.4103/1817-1745.159197
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