In vivo Diagnosis of Primary Cutaneous Amyloidosis -the Role of Reflectance Confocal Microscopy.

cutaneous amyloidosis in vivo non-invasive reflectance confocal microscopy

Journal

Diagnostics (Basel, Switzerland)
ISSN: 2075-4418
Titre abrégé: Diagnostics (Basel)
Pays: Switzerland
ID NLM: 101658402

Informations de publication

Date de publication:
27 Jun 2019
Historique:
received: 17 05 2019
revised: 20 06 2019
accepted: 24 06 2019
entrez: 30 6 2019
pubmed: 30 6 2019
medline: 30 6 2019
Statut: epublish

Résumé

Primary cutaneous amyloidosis (PCA) is a form of localized amyloidosis. It is characterized by the deposition of a fibrillar material in the superficial dermis, without affecting other systems or organs. The diagnosis can be made clinically, but usually a skin biopsy is performed in order to exclude other skin diseases with similar appearance. Reflectance confocal microscopy (RCM) is a novel imaging tool that enables in vivo characterization of various skin changes with a high, quasi-microscopic resolution. This technique might have an important role in the differential diagnosis of cutaneous amyloidosis, by the in vivo assessment of epidermal changes and dermal amyloid deposition. Moreover, it is completely non-invasive and can be safely repeated on the same skin area. However, to date, there is only one published paper presenting the confocal features of primary cutaneous amyloidosis. Hereby, we describe the in vivo RCM features of PCA lesions from a patient with diabetes and correlate them with histologic findings. This strengthens the clinical usefulness of in vivo RCM examination for the non-invasive diagnosis of cutaneous amyloidosis, especially in patients that might associate diseases with impaired wound healing.

Identifiants

pubmed: 31252549
pii: diagnostics9030066
doi: 10.3390/diagnostics9030066
pmc: PMC6787715
pii:
doi:

Types de publication

Case Reports

Langues

eng

Subventions

Organisme : Unitatea Executiva pentru Finantarea Invatamantului Superior, a Cercetarii, Dezvoltarii si Inovarii
ID : project no. 61PCCDI⁄2018 PN-III-P1-1.2-PCCDI-2017-0341

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Auteurs

Ana-Maria Ionescu (AM)

First Department of Dermatology, Colentina Clinical Hospital, 020125 Bucharest, Romania.
Dermatology Research Laboratory, "Carol Davila" University of Medicine and Pharmacy, 050474 Bucharest, Romania.

Mihaela-Adriana Ilie (MA)

Dermatology Research Laboratory, "Carol Davila" University of Medicine and Pharmacy, 050474 Bucharest, Romania.
Department of Biochemistry, "Carol Davila" University of Medicine and Pharmacy, 050474 Bucharest, Romania.

Virginia Chitu (V)

First Department of Dermatology, Colentina Clinical Hospital, 020125 Bucharest, Romania.
Department of Dermatology, "Carol Davila" University of Medicine and Pharmacy, 050474 Bucharest, Romania.

Andrei Razvan (A)

Department of Pathology, Colentina Clinical Hospital, 020125 Bucharest, Romania.

Daniela Lixandru (D)

Department of Biochemistry, "Carol Davila" University of Medicine and Pharmacy, 050474 Bucharest, Romania.

Cristiana Tanase (C)

Department of Biochemistry-Proteomics, "Victor Babes" National Institute of Pathology, 050096 Bucharest, Romania.

Daniel Boda (D)

Dermatology Research Laboratory, "Carol Davila" University of Medicine and Pharmacy, 050474 Bucharest, Romania.
Department of Dermatology, "Prof. N. Paulescu" National Institute of Diabetes, Nutrition and Metabolic Diseases, 011233 Bucharest, Romania.

Constantin Caruntu (C)

Department of Dermatology, "Prof. N. Paulescu" National Institute of Diabetes, Nutrition and Metabolic Diseases, 011233 Bucharest, Romania. costin.caruntu@gmail.com.
Department of Physiology, "Carol Davila" University of Medicine and Pharmacy, 050474 Bucharest, Romania. costin.caruntu@gmail.com.

Sabina Zurac (S)

Department of Dermatology, "Carol Davila" University of Medicine and Pharmacy, 050474 Bucharest, Romania.
Department of Pathology, Colentina Clinical Hospital, 020125 Bucharest, Romania.

Classifications MeSH