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Scar sarcoidosis on a finger mimicking a rapidly growing soft tissue tumour: a case report

BACKGROUND: Scar sarcoidosis is a rare and uncommon but specific cutaneous manifestation of sarcoidosis. In general it arises in pre-existing scars deriving from mechanical traumas. As most surgeons dealing with scars might not be aware of cutaneous sarcoidosis and its different types of appearance...

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Autores principales: Henrichs, Marcel-Philipp, Streitbürger, Arne, Gosheger, Georg, Surke, Carsten, Dierkes, Christian, Hardes, Jendrik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3515508/
https://www.ncbi.nlm.nih.gov/pubmed/23031186
http://dx.doi.org/10.1186/1756-0500-5-545
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author Henrichs, Marcel-Philipp
Streitbürger, Arne
Gosheger, Georg
Surke, Carsten
Dierkes, Christian
Hardes, Jendrik
author_facet Henrichs, Marcel-Philipp
Streitbürger, Arne
Gosheger, Georg
Surke, Carsten
Dierkes, Christian
Hardes, Jendrik
author_sort Henrichs, Marcel-Philipp
collection PubMed
description BACKGROUND: Scar sarcoidosis is a rare and uncommon but specific cutaneous manifestation of sarcoidosis. In general it arises in pre-existing scars deriving from mechanical traumas. As most surgeons dealing with scars might not be aware of cutaneous sarcoidosis and its different types of appearance the appropriate staging and treatment might be missed or at least delayed. To our knowledge this is the first case in literature of scar sarcoidosis on a finger. CASE PRESENTATION: We present a case of a 33-year-old carpenter who developed scar sarcoidosis on his right index finger 4 years after the tendon of the long digital flexor got accidentally cut by an angle grinder. He was referred due to a swelling of the finger suspected to be a malignant soft tissue tumour. The circumference of the affected finger had almost doubled, adding up to 94 mm. Incision biopsy revealed typical noncaseating granulomas. Further investigation showed a systemic extent of the disease with involvement of the lung. A systemic treatment with oral steroids led to an almost full regression of the swelling with restoration of function and resolution of lung infiltrates. CONCLUSION: In case of a suspicious and/or progressive swelling a definite diagnosis should be achieved by biopsy within a short time to enable a proper treatment. If scar sarcoidosis is proven further investigation is necessary to exclude a systemical involvement. A surgical treatment of the swelling is not indicated.
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spelling pubmed-35155082012-12-06 Scar sarcoidosis on a finger mimicking a rapidly growing soft tissue tumour: a case report Henrichs, Marcel-Philipp Streitbürger, Arne Gosheger, Georg Surke, Carsten Dierkes, Christian Hardes, Jendrik BMC Res Notes Case Report BACKGROUND: Scar sarcoidosis is a rare and uncommon but specific cutaneous manifestation of sarcoidosis. In general it arises in pre-existing scars deriving from mechanical traumas. As most surgeons dealing with scars might not be aware of cutaneous sarcoidosis and its different types of appearance the appropriate staging and treatment might be missed or at least delayed. To our knowledge this is the first case in literature of scar sarcoidosis on a finger. CASE PRESENTATION: We present a case of a 33-year-old carpenter who developed scar sarcoidosis on his right index finger 4 years after the tendon of the long digital flexor got accidentally cut by an angle grinder. He was referred due to a swelling of the finger suspected to be a malignant soft tissue tumour. The circumference of the affected finger had almost doubled, adding up to 94 mm. Incision biopsy revealed typical noncaseating granulomas. Further investigation showed a systemic extent of the disease with involvement of the lung. A systemic treatment with oral steroids led to an almost full regression of the swelling with restoration of function and resolution of lung infiltrates. CONCLUSION: In case of a suspicious and/or progressive swelling a definite diagnosis should be achieved by biopsy within a short time to enable a proper treatment. If scar sarcoidosis is proven further investigation is necessary to exclude a systemical involvement. A surgical treatment of the swelling is not indicated. BioMed Central 2012-10-02 /pmc/articles/PMC3515508/ /pubmed/23031186 http://dx.doi.org/10.1186/1756-0500-5-545 Text en Copyright ©2012 Henrichs et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Henrichs, Marcel-Philipp
Streitbürger, Arne
Gosheger, Georg
Surke, Carsten
Dierkes, Christian
Hardes, Jendrik
Scar sarcoidosis on a finger mimicking a rapidly growing soft tissue tumour: a case report
title Scar sarcoidosis on a finger mimicking a rapidly growing soft tissue tumour: a case report
title_full Scar sarcoidosis on a finger mimicking a rapidly growing soft tissue tumour: a case report
title_fullStr Scar sarcoidosis on a finger mimicking a rapidly growing soft tissue tumour: a case report
title_full_unstemmed Scar sarcoidosis on a finger mimicking a rapidly growing soft tissue tumour: a case report
title_short Scar sarcoidosis on a finger mimicking a rapidly growing soft tissue tumour: a case report
title_sort scar sarcoidosis on a finger mimicking a rapidly growing soft tissue tumour: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3515508/
https://www.ncbi.nlm.nih.gov/pubmed/23031186
http://dx.doi.org/10.1186/1756-0500-5-545
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