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Spectacular Skin Nodules: Cutaneous Necrobiotic Xanthogranuloma Without Paraproteinemia

Necrobiotic xanthogranuloma (NXG) is a very rare, progressive variant of non-Langerhans cell histiocytosis. It is known to be associated with multisystem involvement and paraproteinemias. A 65-year-old female presented with chronic, slowly growing, asymptomatic periorbital nodules. The lesions had r...

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Autores principales: Kadakia, Shimoni, Nadkarni, Nitin, Sonavane, Sham, Ghate, Sunil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3482807/
https://www.ncbi.nlm.nih.gov/pubmed/23112364
http://dx.doi.org/10.4103/0019-5154.100499
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author Kadakia, Shimoni
Nadkarni, Nitin
Sonavane, Sham
Ghate, Sunil
author_facet Kadakia, Shimoni
Nadkarni, Nitin
Sonavane, Sham
Ghate, Sunil
author_sort Kadakia, Shimoni
collection PubMed
description Necrobiotic xanthogranuloma (NXG) is a very rare, progressive variant of non-Langerhans cell histiocytosis. It is known to be associated with multisystem involvement and paraproteinemias. A 65-year-old female presented with chronic, slowly growing, asymptomatic periorbital nodules. The lesions had recurred after local excision elsewhere. No systemic involvement or paraproteinemias were detected. A provisional diagnosis of isolated cutaneous NXG was made which was confirmed by histopathology and immunohistochemistry staining. The lesions were surgically excised with excellent cosmetic and functional results. There was no recurrence over a period of 9 months. To our knowledge, this is the second case of NXG reported from India and the first without any systemic manifestations.
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spelling pubmed-34828072012-10-30 Spectacular Skin Nodules: Cutaneous Necrobiotic Xanthogranuloma Without Paraproteinemia Kadakia, Shimoni Nadkarni, Nitin Sonavane, Sham Ghate, Sunil Indian J Dermatol Case Report Necrobiotic xanthogranuloma (NXG) is a very rare, progressive variant of non-Langerhans cell histiocytosis. It is known to be associated with multisystem involvement and paraproteinemias. A 65-year-old female presented with chronic, slowly growing, asymptomatic periorbital nodules. The lesions had recurred after local excision elsewhere. No systemic involvement or paraproteinemias were detected. A provisional diagnosis of isolated cutaneous NXG was made which was confirmed by histopathology and immunohistochemistry staining. The lesions were surgically excised with excellent cosmetic and functional results. There was no recurrence over a period of 9 months. To our knowledge, this is the second case of NXG reported from India and the first without any systemic manifestations. Medknow Publications & Media Pvt Ltd 2012 /pmc/articles/PMC3482807/ /pubmed/23112364 http://dx.doi.org/10.4103/0019-5154.100499 Text en Copyright: © Indian Journal of Dermatology 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
Kadakia, Shimoni
Nadkarni, Nitin
Sonavane, Sham
Ghate, Sunil
Spectacular Skin Nodules: Cutaneous Necrobiotic Xanthogranuloma Without Paraproteinemia
title Spectacular Skin Nodules: Cutaneous Necrobiotic Xanthogranuloma Without Paraproteinemia
title_full Spectacular Skin Nodules: Cutaneous Necrobiotic Xanthogranuloma Without Paraproteinemia
title_fullStr Spectacular Skin Nodules: Cutaneous Necrobiotic Xanthogranuloma Without Paraproteinemia
title_full_unstemmed Spectacular Skin Nodules: Cutaneous Necrobiotic Xanthogranuloma Without Paraproteinemia
title_short Spectacular Skin Nodules: Cutaneous Necrobiotic Xanthogranuloma Without Paraproteinemia
title_sort spectacular skin nodules: cutaneous necrobiotic xanthogranuloma without paraproteinemia
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3482807/
https://www.ncbi.nlm.nih.gov/pubmed/23112364
http://dx.doi.org/10.4103/0019-5154.100499
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