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A Cross-Sectional Study of the Dermatological Manifestations of Patients with Fabry Disease and the Assessment of Angiokeratomas with Multimodal Imaging

Fabry disease (FD) is a multisystemic X-linked lysosomal storage disease that presents with angiokeratomas (AKs). Our objective was to investigate the clinical and morphologic features of AKs and to present two experimental techniques, multispectral imaging (MSI) and non-linear microscopy (NLM). A t...

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Autores principales: Anker, Pálma, Fésűs, Luca, Kiss, Norbert, Lengyel, Anna, Pinti, Éva, Lihacova, Ilze, Lihachev, Alexey, Plorina, Emilija Vija, Fekete, György, Medvecz, Márta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10378346/
https://www.ncbi.nlm.nih.gov/pubmed/37510112
http://dx.doi.org/10.3390/diagnostics13142368
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author Anker, Pálma
Fésűs, Luca
Kiss, Norbert
Lengyel, Anna
Pinti, Éva
Lihacova, Ilze
Lihachev, Alexey
Plorina, Emilija Vija
Fekete, György
Medvecz, Márta
author_facet Anker, Pálma
Fésűs, Luca
Kiss, Norbert
Lengyel, Anna
Pinti, Éva
Lihacova, Ilze
Lihachev, Alexey
Plorina, Emilija Vija
Fekete, György
Medvecz, Márta
author_sort Anker, Pálma
collection PubMed
description Fabry disease (FD) is a multisystemic X-linked lysosomal storage disease that presents with angiokeratomas (AKs). Our objective was to investigate the clinical and morphologic features of AKs and to present two experimental techniques, multispectral imaging (MSI) and non-linear microscopy (NLM). A thorough dermatological examination was carried out in our 26 FD patients and dermoscopic images (n = 136) were evaluated for specific structures. MSI was used for the evaluation of AKs in seven patients. NLM was carried out to obtain histology samples of two AKs and two hemangiomas. Although AKs were the most common manifestation, the majority of patients presented an atypical distribution and appearance, which could cause a diagnostic challenge. Dermoscopy revealed lacunae (65%) and dotted vessels (56%) as the most common structures, with a whitish veil present in only 25%. Autofluorescence (405 nm) and diffuse reflectance (526 nm) images showed the underlying vasculature more prominently compared to dermoscopy. Using NLM, AKs and hemangiomas could be distinguished based on morphologic features. The clinical heterogeneity of FD can result in a diagnostic delay. Although AKs are often the first sign of FD, their presentation is diverse. A thorough dermatological examination and the evaluation of other cutaneous signs are essential for the early diagnosis of FD.
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spelling pubmed-103783462023-07-29 A Cross-Sectional Study of the Dermatological Manifestations of Patients with Fabry Disease and the Assessment of Angiokeratomas with Multimodal Imaging Anker, Pálma Fésűs, Luca Kiss, Norbert Lengyel, Anna Pinti, Éva Lihacova, Ilze Lihachev, Alexey Plorina, Emilija Vija Fekete, György Medvecz, Márta Diagnostics (Basel) Article Fabry disease (FD) is a multisystemic X-linked lysosomal storage disease that presents with angiokeratomas (AKs). Our objective was to investigate the clinical and morphologic features of AKs and to present two experimental techniques, multispectral imaging (MSI) and non-linear microscopy (NLM). A thorough dermatological examination was carried out in our 26 FD patients and dermoscopic images (n = 136) were evaluated for specific structures. MSI was used for the evaluation of AKs in seven patients. NLM was carried out to obtain histology samples of two AKs and two hemangiomas. Although AKs were the most common manifestation, the majority of patients presented an atypical distribution and appearance, which could cause a diagnostic challenge. Dermoscopy revealed lacunae (65%) and dotted vessels (56%) as the most common structures, with a whitish veil present in only 25%. Autofluorescence (405 nm) and diffuse reflectance (526 nm) images showed the underlying vasculature more prominently compared to dermoscopy. Using NLM, AKs and hemangiomas could be distinguished based on morphologic features. The clinical heterogeneity of FD can result in a diagnostic delay. Although AKs are often the first sign of FD, their presentation is diverse. A thorough dermatological examination and the evaluation of other cutaneous signs are essential for the early diagnosis of FD. MDPI 2023-07-14 /pmc/articles/PMC10378346/ /pubmed/37510112 http://dx.doi.org/10.3390/diagnostics13142368 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Anker, Pálma
Fésűs, Luca
Kiss, Norbert
Lengyel, Anna
Pinti, Éva
Lihacova, Ilze
Lihachev, Alexey
Plorina, Emilija Vija
Fekete, György
Medvecz, Márta
A Cross-Sectional Study of the Dermatological Manifestations of Patients with Fabry Disease and the Assessment of Angiokeratomas with Multimodal Imaging
title A Cross-Sectional Study of the Dermatological Manifestations of Patients with Fabry Disease and the Assessment of Angiokeratomas with Multimodal Imaging
title_full A Cross-Sectional Study of the Dermatological Manifestations of Patients with Fabry Disease and the Assessment of Angiokeratomas with Multimodal Imaging
title_fullStr A Cross-Sectional Study of the Dermatological Manifestations of Patients with Fabry Disease and the Assessment of Angiokeratomas with Multimodal Imaging
title_full_unstemmed A Cross-Sectional Study of the Dermatological Manifestations of Patients with Fabry Disease and the Assessment of Angiokeratomas with Multimodal Imaging
title_short A Cross-Sectional Study of the Dermatological Manifestations of Patients with Fabry Disease and the Assessment of Angiokeratomas with Multimodal Imaging
title_sort cross-sectional study of the dermatological manifestations of patients with fabry disease and the assessment of angiokeratomas with multimodal imaging
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10378346/
https://www.ncbi.nlm.nih.gov/pubmed/37510112
http://dx.doi.org/10.3390/diagnostics13142368
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