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Interventional treatment of keratoacanthoderma: a case report
This current case report describes a 56-year-old male patient with a skin mass on his lip that had been growing for 1 year. The pathological findings demonstrated that the epidermis was characterized by hyperkeratosis, hyperplasia and hypertrophy and was formed in the shape of a crater. The skin on...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9793027/ https://www.ncbi.nlm.nih.gov/pubmed/36565019 http://dx.doi.org/10.1177/03000605221143287 |
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author | Mei, Dan Song, Lei Gao, Jin-Qi Wu, Jie |
author_facet | Mei, Dan Song, Lei Gao, Jin-Qi Wu, Jie |
author_sort | Mei, Dan |
collection | PubMed |
description | This current case report describes a 56-year-old male patient with a skin mass on his lip that had been growing for 1 year. The pathological findings demonstrated that the epidermis was characterized by hyperkeratosis, hyperplasia and hypertrophy and was formed in the shape of a crater. The skin on both ends had developed into a ball-like growth that resembled a volcanic cone. There was invasive growth of heterotype squamous epithelium and a small number of inflammatory cells infiltrating the dermis. Immunohistochemistry demonstrated an increase in P16 (the focus, +) and the hot spot Ki-67 index. The diagnosis was of tumour-like hyperplasia, malignancy and moderate-to-severe dysplasia confirming that it was keratoacanthoma. The patient underwent surgical resection and was discharged from hospital, but the tumour returned. Paclitaxel and cisplatin were administered intraoperatively and bilateral lingual artery perfusion chemoembolization was undertaken six times. This procedure led to an excellent postoperative recovery and discharge from hospital. Tumour therapy was regarded as successful. The patient’s medical history included acute lymphoblastic leukaemia L1 and long-term immunosuppressant use. After a 6-month period of follow-up, he died from systemic organ failure as a consequence of having too many ailments. |
format | Online Article Text |
id | pubmed-9793027 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-97930272022-12-28 Interventional treatment of keratoacanthoderma: a case report Mei, Dan Song, Lei Gao, Jin-Qi Wu, Jie J Int Med Res Case Reports This current case report describes a 56-year-old male patient with a skin mass on his lip that had been growing for 1 year. The pathological findings demonstrated that the epidermis was characterized by hyperkeratosis, hyperplasia and hypertrophy and was formed in the shape of a crater. The skin on both ends had developed into a ball-like growth that resembled a volcanic cone. There was invasive growth of heterotype squamous epithelium and a small number of inflammatory cells infiltrating the dermis. Immunohistochemistry demonstrated an increase in P16 (the focus, +) and the hot spot Ki-67 index. The diagnosis was of tumour-like hyperplasia, malignancy and moderate-to-severe dysplasia confirming that it was keratoacanthoma. The patient underwent surgical resection and was discharged from hospital, but the tumour returned. Paclitaxel and cisplatin were administered intraoperatively and bilateral lingual artery perfusion chemoembolization was undertaken six times. This procedure led to an excellent postoperative recovery and discharge from hospital. Tumour therapy was regarded as successful. The patient’s medical history included acute lymphoblastic leukaemia L1 and long-term immunosuppressant use. After a 6-month period of follow-up, he died from systemic organ failure as a consequence of having too many ailments. SAGE Publications 2022-12-23 /pmc/articles/PMC9793027/ /pubmed/36565019 http://dx.doi.org/10.1177/03000605221143287 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by-nc/4.0/Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Case Reports Mei, Dan Song, Lei Gao, Jin-Qi Wu, Jie Interventional treatment of keratoacanthoderma: a case report |
title | Interventional treatment of keratoacanthoderma: a case
report |
title_full | Interventional treatment of keratoacanthoderma: a case
report |
title_fullStr | Interventional treatment of keratoacanthoderma: a case
report |
title_full_unstemmed | Interventional treatment of keratoacanthoderma: a case
report |
title_short | Interventional treatment of keratoacanthoderma: a case
report |
title_sort | interventional treatment of keratoacanthoderma: a case
report |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9793027/ https://www.ncbi.nlm.nih.gov/pubmed/36565019 http://dx.doi.org/10.1177/03000605221143287 |
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