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Juvenile xanthogranuloma-diagnostic challenge on fine-needle aspiration cytology

Juvenile xanthogranuloma (JXG) is a rare cutaneous lesion with paucity of literature on its cytological features. We report one such case which on fine-needle aspiration cytology yielded a mixed population of foamy histiocytes, multinucleated giant cells and variable admixture of lymphocytes and eos...

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Autores principales: Bandyopadhyay, Arghya, Gangopadhyay, Mimi, Chakraborty, Subrata
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications Pvt Ltd 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3214472/
https://www.ncbi.nlm.nih.gov/pubmed/22090701
http://dx.doi.org/10.4103/0970-9371.86356
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author Bandyopadhyay, Arghya
Gangopadhyay, Mimi
Chakraborty, Subrata
author_facet Bandyopadhyay, Arghya
Gangopadhyay, Mimi
Chakraborty, Subrata
author_sort Bandyopadhyay, Arghya
collection PubMed
description Juvenile xanthogranuloma (JXG) is a rare cutaneous lesion with paucity of literature on its cytological features. We report one such case which on fine-needle aspiration cytology yielded a mixed population of foamy histiocytes, multinucleated giant cells and variable admixture of lymphocytes and eosinophils causing diagnostic dilemma with other differentials, especially Langerhans cell histiocytosis. However, clinical correlation followed by histopathology confirmed the diagnosis. Hence, JXG has characteristic and diagnostic cytologic features.
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spelling pubmed-32144722011-11-16 Juvenile xanthogranuloma-diagnostic challenge on fine-needle aspiration cytology Bandyopadhyay, Arghya Gangopadhyay, Mimi Chakraborty, Subrata J Cytol Case Report Juvenile xanthogranuloma (JXG) is a rare cutaneous lesion with paucity of literature on its cytological features. We report one such case which on fine-needle aspiration cytology yielded a mixed population of foamy histiocytes, multinucleated giant cells and variable admixture of lymphocytes and eosinophils causing diagnostic dilemma with other differentials, especially Langerhans cell histiocytosis. However, clinical correlation followed by histopathology confirmed the diagnosis. Hence, JXG has characteristic and diagnostic cytologic features. Medknow Publications Pvt Ltd 2011 /pmc/articles/PMC3214472/ /pubmed/22090701 http://dx.doi.org/10.4103/0970-9371.86356 Text en Copyright: © Journal of Cytology 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
Bandyopadhyay, Arghya
Gangopadhyay, Mimi
Chakraborty, Subrata
Juvenile xanthogranuloma-diagnostic challenge on fine-needle aspiration cytology
title Juvenile xanthogranuloma-diagnostic challenge on fine-needle aspiration cytology
title_full Juvenile xanthogranuloma-diagnostic challenge on fine-needle aspiration cytology
title_fullStr Juvenile xanthogranuloma-diagnostic challenge on fine-needle aspiration cytology
title_full_unstemmed Juvenile xanthogranuloma-diagnostic challenge on fine-needle aspiration cytology
title_short Juvenile xanthogranuloma-diagnostic challenge on fine-needle aspiration cytology
title_sort juvenile xanthogranuloma-diagnostic challenge on fine-needle aspiration cytology
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3214472/
https://www.ncbi.nlm.nih.gov/pubmed/22090701
http://dx.doi.org/10.4103/0970-9371.86356
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