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Lentigo maligna – anatomic location as a potential risk factor for recurrences after non‐surgical treatment

BACKGROUND: A higher incidence of lentigo maligna (LM) recurrences on the nose was previously observed in our cohort after non‐surgical treatment. OBJECTIVES: To determine histological parameters that might be related to the previously observed higher incidence of LM recurrences on the nose after no...

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Autores principales: Greveling, K., van der Klok, Th., van Doorn, M.B.A., Noordhoek Hegt, V., Prens, E.P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5363235/
https://www.ncbi.nlm.nih.gov/pubmed/27557425
http://dx.doi.org/10.1111/jdv.13941
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author Greveling, K.
van der Klok, Th.
van Doorn, M.B.A.
Noordhoek Hegt, V.
Prens, E.P.
author_facet Greveling, K.
van der Klok, Th.
van Doorn, M.B.A.
Noordhoek Hegt, V.
Prens, E.P.
author_sort Greveling, K.
collection PubMed
description BACKGROUND: A higher incidence of lentigo maligna (LM) recurrences on the nose was previously observed in our cohort after non‐surgical treatment. OBJECTIVES: To determine histological parameters that might be related to the previously observed higher incidence of LM recurrences on the nose after non‐surgical treatment. METHODS: We randomly selected 22 surgical specimens of LM on the nose and 22 on the cheek. Histopathological analysis was performed on haematoxylin and eosin stained and microphthalmia transcription factor immunohistochemically stained slides. The number of pilosebaceous units (PSU) per mm, maximum depth of atypical melanocytes along the skin appendages and maximum depth of the PSU itself were determined. RESULTS: The nose had a significantly higher density of PSU than the cheek. The atypical melanocytes extended deeper along the PSU on the nose with a mean (SD) depth of 1.29 mm (0.48) vs. a mean depth of 0.72 mm (0.30) on the cheek (P < 0.001). The maximum depth of the PSU on the nose was greater than on the cheek, mean (SD) depth of 2.28 mm (0.41) vs. 1.65 mm (0.82) (P = 0.003). CONCLUSIONS: The higher recurrence risk of LM on the nose after non‐surgical treatment that we previously observed in our cohort is most likely based on a higher density of atypical melanocytes and also their deeper extension into the follicles. These results shed more light on our previous findings and learn that anatomical location is relevant for the risk of recurrence of LM after non‐surgical treatment.
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spelling pubmed-53632352017-04-06 Lentigo maligna – anatomic location as a potential risk factor for recurrences after non‐surgical treatment Greveling, K. van der Klok, Th. van Doorn, M.B.A. Noordhoek Hegt, V. Prens, E.P. J Eur Acad Dermatol Venereol Original Articles and Short Reports Oncology BACKGROUND: A higher incidence of lentigo maligna (LM) recurrences on the nose was previously observed in our cohort after non‐surgical treatment. OBJECTIVES: To determine histological parameters that might be related to the previously observed higher incidence of LM recurrences on the nose after non‐surgical treatment. METHODS: We randomly selected 22 surgical specimens of LM on the nose and 22 on the cheek. Histopathological analysis was performed on haematoxylin and eosin stained and microphthalmia transcription factor immunohistochemically stained slides. The number of pilosebaceous units (PSU) per mm, maximum depth of atypical melanocytes along the skin appendages and maximum depth of the PSU itself were determined. RESULTS: The nose had a significantly higher density of PSU than the cheek. The atypical melanocytes extended deeper along the PSU on the nose with a mean (SD) depth of 1.29 mm (0.48) vs. a mean depth of 0.72 mm (0.30) on the cheek (P < 0.001). The maximum depth of the PSU on the nose was greater than on the cheek, mean (SD) depth of 2.28 mm (0.41) vs. 1.65 mm (0.82) (P = 0.003). CONCLUSIONS: The higher recurrence risk of LM on the nose after non‐surgical treatment that we previously observed in our cohort is most likely based on a higher density of atypical melanocytes and also their deeper extension into the follicles. These results shed more light on our previous findings and learn that anatomical location is relevant for the risk of recurrence of LM after non‐surgical treatment. John Wiley and Sons Inc. 2016-09-19 2017-03 /pmc/articles/PMC5363235/ /pubmed/27557425 http://dx.doi.org/10.1111/jdv.13941 Text en © 2016 The Authors. Journal of the European Academy of Dermatology and Venereology published by John Wiley & Sons Ltd on behalf of European Academy of Dermatology and Venereology. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles and Short Reports Oncology
Greveling, K.
van der Klok, Th.
van Doorn, M.B.A.
Noordhoek Hegt, V.
Prens, E.P.
Lentigo maligna – anatomic location as a potential risk factor for recurrences after non‐surgical treatment
title Lentigo maligna – anatomic location as a potential risk factor for recurrences after non‐surgical treatment
title_full Lentigo maligna – anatomic location as a potential risk factor for recurrences after non‐surgical treatment
title_fullStr Lentigo maligna – anatomic location as a potential risk factor for recurrences after non‐surgical treatment
title_full_unstemmed Lentigo maligna – anatomic location as a potential risk factor for recurrences after non‐surgical treatment
title_short Lentigo maligna – anatomic location as a potential risk factor for recurrences after non‐surgical treatment
title_sort lentigo maligna – anatomic location as a potential risk factor for recurrences after non‐surgical treatment
topic Original Articles and Short Reports Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5363235/
https://www.ncbi.nlm.nih.gov/pubmed/27557425
http://dx.doi.org/10.1111/jdv.13941
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