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Cutaneous Rosai – Dorfman disease in a patient with late syphilis and cervical cancer – case report and a review of literature
BACKGROUND: Cutaneous Rosai – Dorfman disease (CRDD) is extremely rare variant of idiopathic histiocytic proliferative disorder, which may manifest as a non-specific macules, papules, plaques or nodules ranging in size and colour from yellow – red to red -brown. CASE PRESENTATION: A 52-year-old fema...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7720066/ https://www.ncbi.nlm.nih.gov/pubmed/33287799 http://dx.doi.org/10.1186/s12895-020-00115-w |
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author | Bielach – Bazyluk, Angelika Serwin, Agnieszka B. Pilaszewicz – Puza, Agata Flisiak, Iwona |
author_facet | Bielach – Bazyluk, Angelika Serwin, Agnieszka B. Pilaszewicz – Puza, Agata Flisiak, Iwona |
author_sort | Bielach – Bazyluk, Angelika |
collection | PubMed |
description | BACKGROUND: Cutaneous Rosai – Dorfman disease (CRDD) is extremely rare variant of idiopathic histiocytic proliferative disorder, which may manifest as a non-specific macules, papules, plaques or nodules ranging in size and colour from yellow – red to red -brown. CASE PRESENTATION: A 52-year-old female presented with three gradually enlarging, reddish - brown nodules on the right upper extremity lasting six months. The patients denied fever, weight loss, malaise. Clinical examination and imaging tests showed no sign of lymphadenopathy. A biopsy specimen of a nodule showed a dense dermal polymorphic infiltrate with numerous histiocytes exhibiting emperipolesis phenomenon. Immunohistochemical staining of the histiocytes showed S-100 protein (+), CD68(+), but CD1a (-). Aforementioned findings were consistent with CRDD characteristics. Additionally, a routine serological screening and confirmatory serological tests for syphilis were positive. Syphilis of unknown duration was diagnosed. The IgG antibodies titre against Chlamydia trachomatis was elevated. An isolated sensory impairment over the right trigeminal nerve was found on neurological consultation. Comprehensive gynaecological assessment was carried out because of patient’s complaints of bleeding after sexual intercourse and led to diagnosis of cervical cancer. The initial therapy with methotrexate was discontinued after three months due to neutropenia. Further therapy with dapson was ineffective, therefore complete surgical excision was recommended. CONCLUSIONS: CRDD is a rare, benign condition especially difficult to diagnose due to lack of general symptoms and lymphadenopathy. Histopathologic examination with immunohistochemical staining, exhibiting characteristic and reproducible findings play a key role in establishing an accurate diagnosis. In the presented case activated histiocytes demonstrated in a lesional skin might be a response to immune dysregulation related to chronic, untreated sexually transmitted infections and cancer. |
format | Online Article Text |
id | pubmed-7720066 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-77200662020-12-07 Cutaneous Rosai – Dorfman disease in a patient with late syphilis and cervical cancer – case report and a review of literature Bielach – Bazyluk, Angelika Serwin, Agnieszka B. Pilaszewicz – Puza, Agata Flisiak, Iwona BMC Dermatol Case Report BACKGROUND: Cutaneous Rosai – Dorfman disease (CRDD) is extremely rare variant of idiopathic histiocytic proliferative disorder, which may manifest as a non-specific macules, papules, plaques or nodules ranging in size and colour from yellow – red to red -brown. CASE PRESENTATION: A 52-year-old female presented with three gradually enlarging, reddish - brown nodules on the right upper extremity lasting six months. The patients denied fever, weight loss, malaise. Clinical examination and imaging tests showed no sign of lymphadenopathy. A biopsy specimen of a nodule showed a dense dermal polymorphic infiltrate with numerous histiocytes exhibiting emperipolesis phenomenon. Immunohistochemical staining of the histiocytes showed S-100 protein (+), CD68(+), but CD1a (-). Aforementioned findings were consistent with CRDD characteristics. Additionally, a routine serological screening and confirmatory serological tests for syphilis were positive. Syphilis of unknown duration was diagnosed. The IgG antibodies titre against Chlamydia trachomatis was elevated. An isolated sensory impairment over the right trigeminal nerve was found on neurological consultation. Comprehensive gynaecological assessment was carried out because of patient’s complaints of bleeding after sexual intercourse and led to diagnosis of cervical cancer. The initial therapy with methotrexate was discontinued after three months due to neutropenia. Further therapy with dapson was ineffective, therefore complete surgical excision was recommended. CONCLUSIONS: CRDD is a rare, benign condition especially difficult to diagnose due to lack of general symptoms and lymphadenopathy. Histopathologic examination with immunohistochemical staining, exhibiting characteristic and reproducible findings play a key role in establishing an accurate diagnosis. In the presented case activated histiocytes demonstrated in a lesional skin might be a response to immune dysregulation related to chronic, untreated sexually transmitted infections and cancer. BioMed Central 2020-12-07 /pmc/articles/PMC7720066/ /pubmed/33287799 http://dx.doi.org/10.1186/s12895-020-00115-w Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Case Report Bielach – Bazyluk, Angelika Serwin, Agnieszka B. Pilaszewicz – Puza, Agata Flisiak, Iwona Cutaneous Rosai – Dorfman disease in a patient with late syphilis and cervical cancer – case report and a review of literature |
title | Cutaneous Rosai – Dorfman disease in a patient with late syphilis and cervical cancer – case report and a review of literature |
title_full | Cutaneous Rosai – Dorfman disease in a patient with late syphilis and cervical cancer – case report and a review of literature |
title_fullStr | Cutaneous Rosai – Dorfman disease in a patient with late syphilis and cervical cancer – case report and a review of literature |
title_full_unstemmed | Cutaneous Rosai – Dorfman disease in a patient with late syphilis and cervical cancer – case report and a review of literature |
title_short | Cutaneous Rosai – Dorfman disease in a patient with late syphilis and cervical cancer – case report and a review of literature |
title_sort | cutaneous rosai – dorfman disease in a patient with late syphilis and cervical cancer – case report and a review of literature |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7720066/ https://www.ncbi.nlm.nih.gov/pubmed/33287799 http://dx.doi.org/10.1186/s12895-020-00115-w |
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