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Malignant pilomatricoma of the cheek in an infant

Malignant pilomatricoma (pilomatrical carcinoma) is a rare, locally occurring malignant tumor with a high rate of recurrence in the case of incomplete excision. This tumor has two characteristics. First, recurrences of pilomatrical carcinoma are common; second, distant metastasis is rare, but if it...

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Autores principales: Kim, Yang Seok, Na, Young Cheon, Huh, Woo Hoe, Kim, Ji Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Cleft Palate-Craniofacial Association 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6325331/
https://www.ncbi.nlm.nih.gov/pubmed/30613091
http://dx.doi.org/10.7181/acfs.2018.02138
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author Kim, Yang Seok
Na, Young Cheon
Huh, Woo Hoe
Kim, Ji Min
author_facet Kim, Yang Seok
Na, Young Cheon
Huh, Woo Hoe
Kim, Ji Min
author_sort Kim, Yang Seok
collection PubMed
description Malignant pilomatricoma (pilomatrical carcinoma) is a rare, locally occurring malignant tumor with a high rate of recurrence in the case of incomplete excision. This tumor has two characteristics. First, recurrences of pilomatrical carcinoma are common; second, distant metastasis is rare, but if it occurs, it is very fatal. It has characteristic features of high mitotic counts, cellular atypia, and local invasion. Although fine needle aspiration and excisional biopsy could help to confirm this tumor diagnosis, pathologic findings are critical. Pilomatricomas have some characteristic features in histological aspect, such as epithelial islands of basaloid cells and shadow cells or ghost cell. Also, various types of immunohistochemical staining are used to confirm the diagnosis. Despite the lack of clear surgical criteria, treatment is a wide local excision with histologically clear resection margins with or without adjuvant radiotherapy.
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spelling pubmed-63253312019-01-11 Malignant pilomatricoma of the cheek in an infant Kim, Yang Seok Na, Young Cheon Huh, Woo Hoe Kim, Ji Min Arch Craniofac Surg Case Report Malignant pilomatricoma (pilomatrical carcinoma) is a rare, locally occurring malignant tumor with a high rate of recurrence in the case of incomplete excision. This tumor has two characteristics. First, recurrences of pilomatrical carcinoma are common; second, distant metastasis is rare, but if it occurs, it is very fatal. It has characteristic features of high mitotic counts, cellular atypia, and local invasion. Although fine needle aspiration and excisional biopsy could help to confirm this tumor diagnosis, pathologic findings are critical. Pilomatricomas have some characteristic features in histological aspect, such as epithelial islands of basaloid cells and shadow cells or ghost cell. Also, various types of immunohistochemical staining are used to confirm the diagnosis. Despite the lack of clear surgical criteria, treatment is a wide local excision with histologically clear resection margins with or without adjuvant radiotherapy. Korean Cleft Palate-Craniofacial Association 2018-12 2018-12-27 /pmc/articles/PMC6325331/ /pubmed/30613091 http://dx.doi.org/10.7181/acfs.2018.02138 Text en Copyright © 2018 The Korean Cleft Palate-Craniofacial Association This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Kim, Yang Seok
Na, Young Cheon
Huh, Woo Hoe
Kim, Ji Min
Malignant pilomatricoma of the cheek in an infant
title Malignant pilomatricoma of the cheek in an infant
title_full Malignant pilomatricoma of the cheek in an infant
title_fullStr Malignant pilomatricoma of the cheek in an infant
title_full_unstemmed Malignant pilomatricoma of the cheek in an infant
title_short Malignant pilomatricoma of the cheek in an infant
title_sort malignant pilomatricoma of the cheek in an infant
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6325331/
https://www.ncbi.nlm.nih.gov/pubmed/30613091
http://dx.doi.org/10.7181/acfs.2018.02138
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