Dermoscopic–Histopathological Correlation of Eccrine Poroma: An Observational Study

Background: Eccrine poroma (EP) is a benign adnexal neoplasm that can be pigmented in 17% of cases. Four histopathological variants of EP exist. Dermoscopically, EP can mimic many other skin neoplasms. Objectives: To provide a dermoscopic–histopathological correlation of EP, classifying the clin...

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Autores principales: Marco A. Chessa, Annalisa Patrizi, Carlotta Baraldi, Pier Alessandro Fanti, Alessia Barisani, Sabina Vaccari
Formato: article
Lenguaje:EN
Publicado: Mattioli1885 2019
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spelling oai:doaj.org-article:352204eff2ee439290e0c4b39e9219c42021-11-17T08:29:09ZDermoscopic–Histopathological Correlation of Eccrine Poroma: An Observational Study10.5826/dpc.0904a072160-9381https://doaj.org/article/352204eff2ee439290e0c4b39e9219c42019-10-01T00:00:00Zhttp://dpcj.org/index.php/dpc/article/view/842https://doaj.org/toc/2160-9381 Background: Eccrine poroma (EP) is a benign adnexal neoplasm that can be pigmented in 17% of cases. Four histopathological variants of EP exist. Dermoscopically, EP can mimic many other skin neoplasms. Objectives: To provide a dermoscopic–histopathological correlation of EP, classifying the clinical and dermoscopic features of EPs on the basis of their histopathological subtype, in an attempt to better characterize these entities. Patients and Methods: A single-center retrospective study was conducted. Clinical data were collected; patients were classified on the basis of the 4 histopathological variants of EPs. Dermoscopic images were reviewed. A dermoscopic–histopathological correlation was performed, and the results were compared with literature data. Results: Twenty-six lesions were included, both pigmented and nonpigmented. Three of the 4 histopathological variants were identified. Different dermoscopic features were observed for each distinct histopathological subtype of EP. The lesions mimicked different types of other skin neoplasms, in particular: nonpigmented hidroacanthoma simplex resembled nonmelanoma skin cancer; pigmented hidroacanthoma simplex appeared like a seborrheic keratosis or a solar lentigo; EPs sensu stricto presented as pink nodules if nonpigmented and were similar to seborrheic keratosis if pigmented; dermal duct tumors appeared as pigmented nodular lesions. Conclusions: Distinct dermoscopic features appeared to be recurrent in each histopathological variant. Dermoscopy can provide important clues for the diagnosis of EP; the final diagnosis is allowed by histopathology. To achieve a correct diagnosis of EP, because of its clinical and dermoscopic variability, surgical excision is recommended. Marco A. ChessaAnnalisa PatriziCarlotta BaraldiPier Alessandro FantiAlessia BarisaniSabina VaccariMattioli1885articleeccrineporomadermoscopyhistopathologydiagnosisDermatologyRL1-803ENDermatology Practical & Conceptual, Vol 9, Iss 4 (2019)
institution DOAJ
collection DOAJ
language EN
topic eccrine
poroma
dermoscopy
histopathology
diagnosis
Dermatology
RL1-803
spellingShingle eccrine
poroma
dermoscopy
histopathology
diagnosis
Dermatology
RL1-803
Marco A. Chessa
Annalisa Patrizi
Carlotta Baraldi
Pier Alessandro Fanti
Alessia Barisani
Sabina Vaccari
Dermoscopic–Histopathological Correlation of Eccrine Poroma: An Observational Study
description Background: Eccrine poroma (EP) is a benign adnexal neoplasm that can be pigmented in 17% of cases. Four histopathological variants of EP exist. Dermoscopically, EP can mimic many other skin neoplasms. Objectives: To provide a dermoscopic–histopathological correlation of EP, classifying the clinical and dermoscopic features of EPs on the basis of their histopathological subtype, in an attempt to better characterize these entities. Patients and Methods: A single-center retrospective study was conducted. Clinical data were collected; patients were classified on the basis of the 4 histopathological variants of EPs. Dermoscopic images were reviewed. A dermoscopic–histopathological correlation was performed, and the results were compared with literature data. Results: Twenty-six lesions were included, both pigmented and nonpigmented. Three of the 4 histopathological variants were identified. Different dermoscopic features were observed for each distinct histopathological subtype of EP. The lesions mimicked different types of other skin neoplasms, in particular: nonpigmented hidroacanthoma simplex resembled nonmelanoma skin cancer; pigmented hidroacanthoma simplex appeared like a seborrheic keratosis or a solar lentigo; EPs sensu stricto presented as pink nodules if nonpigmented and were similar to seborrheic keratosis if pigmented; dermal duct tumors appeared as pigmented nodular lesions. Conclusions: Distinct dermoscopic features appeared to be recurrent in each histopathological variant. Dermoscopy can provide important clues for the diagnosis of EP; the final diagnosis is allowed by histopathology. To achieve a correct diagnosis of EP, because of its clinical and dermoscopic variability, surgical excision is recommended.
format article
author Marco A. Chessa
Annalisa Patrizi
Carlotta Baraldi
Pier Alessandro Fanti
Alessia Barisani
Sabina Vaccari
author_facet Marco A. Chessa
Annalisa Patrizi
Carlotta Baraldi
Pier Alessandro Fanti
Alessia Barisani
Sabina Vaccari
author_sort Marco A. Chessa
title Dermoscopic–Histopathological Correlation of Eccrine Poroma: An Observational Study
title_short Dermoscopic–Histopathological Correlation of Eccrine Poroma: An Observational Study
title_full Dermoscopic–Histopathological Correlation of Eccrine Poroma: An Observational Study
title_fullStr Dermoscopic–Histopathological Correlation of Eccrine Poroma: An Observational Study
title_full_unstemmed Dermoscopic–Histopathological Correlation of Eccrine Poroma: An Observational Study
title_sort dermoscopic–histopathological correlation of eccrine poroma: an observational study
publisher Mattioli1885
publishDate 2019
url https://doaj.org/article/352204eff2ee439290e0c4b39e9219c4
work_keys_str_mv AT marcoachessa dermoscopichistopathologicalcorrelationofeccrineporomaanobservationalstudy
AT annalisapatrizi dermoscopichistopathologicalcorrelationofeccrineporomaanobservationalstudy
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AT pieralessandrofanti dermoscopichistopathologicalcorrelationofeccrineporomaanobservationalstudy
AT alessiabarisani dermoscopichistopathologicalcorrelationofeccrineporomaanobservationalstudy
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