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Syringocystadenoma Papilliferum of the Anogenital Area and Buttocks: A Report of 16 Cases, Including Human Papillomavirus Analysis and HRAS and BRAF V600 Mutation Studies
AM. Konstantinova, L. Kyrpychova, J. Nemcova, M. Sedivcova, M. Bisceglia, H. Kutzner, M. Zamecnik, E. Sehnalkova, M. Pavlovsky, K. Zateckova, S. Shvernik, Z. Spurkova, M. Michal, K. Kerl, DV. Kazakov,
Language English Country United States
Document type Journal Article
- MeSH
- Tubular Sweat Gland Adenomas genetics pathology virology MeSH
- Anal Canal pathology MeSH
- Adult MeSH
- Buttocks pathology MeSH
- Papillomavirus Infections epidemiology MeSH
- Middle Aged MeSH
- Humans MeSH
- Adolescent MeSH
- Young Adult MeSH
- Mutation MeSH
- Genital Neoplasms, Male genetics pathology MeSH
- Sweat Gland Neoplasms genetics pathology virology MeSH
- Genital Neoplasms, Female genetics pathology virology MeSH
- Papillomaviridae MeSH
- Proto-Oncogene Proteins B-raf genetics MeSH
- Proto-Oncogene Proteins p21(ras) genetics MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Adolescent MeSH
- Young Adult MeSH
- Male MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
Syringocystadenoma papilliferum (SCAP) is a benign tumor most commonly located on the head and neck area often associated with nevus sebaceus. In its usual location, the human papillomavirus (HPV) DNA and mutations in the RAS/mitogen-activated protein kinase signaling pathway have been detected in SCAP. We studied 16 cases of SCAP in the anogenital areas and buttock where this neoplasm is rare and attempted to find out whether SCAP in these sites have different histopathological and molecular biological features. It seems that there is no significant difference between the morphology of anogenital SCAP and SCAP in other locations. Several tumors in our cohort demonstrated features resembling those seen in warts, but HPV DNA was not found in these lesions. On the contrary, we identified DNA of HPV high-risk types in some tumors without HPV-related morphology. Our study confirms the role of HRAS and BRAF V600 mutations in the pathogenesis of SCAP, including SCAP in the anogenital areas and buttock.
Agel Laboratory of Pathology Novy Jicin Czech Republic
Anatomic Pathology School of Biomedical Sciences Etromapmax Pole Lesina Italy
Bioptical Laboratory Pilsen Czech Republic
Department of Dermatology University Hospital Zurich Zurich Switzerland
Department of Pathology Bulovlka Hospital Prague Czech Republic
Department of Pathology Regional Hospital Decin Decin Czech Republic
Department of Pathology Regional Hospital Most Czech Republic
Department of Pathology Silesian Hospital Opava Czech Republic
Dermatopathologische Gemeinschaftspraxis Friedrichshafen Germany
References provided by Crossref.org
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- $a Konstantinova, Anastasia M $u Department of Pathology, Clinical Research and Practical Center for Specialized Oncological Care, Saint-Petersburg, Russia. Department of Pathology, Medical Faculty, Saint-Petersburg State University, Saint Petersburg, Russia. Department of Pathology, Saint-Petersburg Medico-Social Institute, Saint Petersburg, Russia.
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- $a Syringocystadenoma papilliferum (SCAP) is a benign tumor most commonly located on the head and neck area often associated with nevus sebaceus. In its usual location, the human papillomavirus (HPV) DNA and mutations in the RAS/mitogen-activated protein kinase signaling pathway have been detected in SCAP. We studied 16 cases of SCAP in the anogenital areas and buttock where this neoplasm is rare and attempted to find out whether SCAP in these sites have different histopathological and molecular biological features. It seems that there is no significant difference between the morphology of anogenital SCAP and SCAP in other locations. Several tumors in our cohort demonstrated features resembling those seen in warts, but HPV DNA was not found in these lesions. On the contrary, we identified DNA of HPV high-risk types in some tumors without HPV-related morphology. Our study confirms the role of HRAS and BRAF V600 mutations in the pathogenesis of SCAP, including SCAP in the anogenital areas and buttock.
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