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A CASE OF MULTIPLE MYELOMA PRESENTING AS A BULLOUS DERMATOSIS

Multiple myeloma is a malignant plasma cell proliferative disorder that produces a monoclonal immunoglobulin protein. The skin involvement and the development of bullous disease are rarely seen features in multiple myeloma. We present a 55-year-old man with a longstanding, large, tense bullous erupt...

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Autores principales: Gül, Ülker, Kiliç, Arzu, Gönül, Müzeyyen, Çakmak, Seray Külcü, Heper, Aylin Okçu
Formato: Texto
Lenguaje:English
Publicado: Medknow Publications 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2763721/
https://www.ncbi.nlm.nih.gov/pubmed/19881994
http://dx.doi.org/10.4103/0019-5154.41653
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author Gül, Ülker
Kiliç, Arzu
Gönül, Müzeyyen
Çakmak, Seray Külcü
Heper, Aylin Okçu
author_facet Gül, Ülker
Kiliç, Arzu
Gönül, Müzeyyen
Çakmak, Seray Külcü
Heper, Aylin Okçu
author_sort Gül, Ülker
collection PubMed
description Multiple myeloma is a malignant plasma cell proliferative disorder that produces a monoclonal immunoglobulin protein. The skin involvement and the development of bullous disease are rarely seen features in multiple myeloma. We present a 55-year-old man with a longstanding, large, tense bullous eruption and hypertrophic scars over his body accompanied recently with weight loss and fatique. He had no response to the previous treatments, which included oral glucocorticoids and dapsone. Histologic examination of the lesions revealed subepidermal bullae, while no immunoflourescence staining was observed. In a further detailed labarotory examination, multiple myeloma was detected. After the treatment of multiple myeloma with chemotherapy, the lesions regressed. Patients with longstanding, recurrent, unusual bullous eruption should be investigated for the development of multiple myeloma.
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spelling pubmed-27637212009-10-29 A CASE OF MULTIPLE MYELOMA PRESENTING AS A BULLOUS DERMATOSIS Gül, Ülker Kiliç, Arzu Gönül, Müzeyyen Çakmak, Seray Külcü Heper, Aylin Okçu Indian J Dermatol Case Report Multiple myeloma is a malignant plasma cell proliferative disorder that produces a monoclonal immunoglobulin protein. The skin involvement and the development of bullous disease are rarely seen features in multiple myeloma. We present a 55-year-old man with a longstanding, large, tense bullous eruption and hypertrophic scars over his body accompanied recently with weight loss and fatique. He had no response to the previous treatments, which included oral glucocorticoids and dapsone. Histologic examination of the lesions revealed subepidermal bullae, while no immunoflourescence staining was observed. In a further detailed labarotory examination, multiple myeloma was detected. After the treatment of multiple myeloma with chemotherapy, the lesions regressed. Patients with longstanding, recurrent, unusual bullous eruption should be investigated for the development of multiple myeloma. Medknow Publications 2008 /pmc/articles/PMC2763721/ /pubmed/19881994 http://dx.doi.org/10.4103/0019-5154.41653 Text en © Indian Journal of Dermatology http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Gül, Ülker
Kiliç, Arzu
Gönül, Müzeyyen
Çakmak, Seray Külcü
Heper, Aylin Okçu
A CASE OF MULTIPLE MYELOMA PRESENTING AS A BULLOUS DERMATOSIS
title A CASE OF MULTIPLE MYELOMA PRESENTING AS A BULLOUS DERMATOSIS
title_full A CASE OF MULTIPLE MYELOMA PRESENTING AS A BULLOUS DERMATOSIS
title_fullStr A CASE OF MULTIPLE MYELOMA PRESENTING AS A BULLOUS DERMATOSIS
title_full_unstemmed A CASE OF MULTIPLE MYELOMA PRESENTING AS A BULLOUS DERMATOSIS
title_short A CASE OF MULTIPLE MYELOMA PRESENTING AS A BULLOUS DERMATOSIS
title_sort case of multiple myeloma presenting as a bullous dermatosis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2763721/
https://www.ncbi.nlm.nih.gov/pubmed/19881994
http://dx.doi.org/10.4103/0019-5154.41653
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