Dermoscopy and confocal microscopy for different chemotherapy-induced alopecia (CIA) phases characterization: Preliminary study.


Journal

Skin research and technology : official journal of International Society for Bioengineering and the Skin (ISBS) [and] International Society for Digital Imaging of Skin (ISDIS) [and] International Society for Skin Imaging (ISSI)
ISSN: 1600-0846
Titre abrégé: Skin Res Technol
Pays: England
ID NLM: 9504453

Informations de publication

Date de publication:
Mar 2020
Historique:
received: 15 07 2019
accepted: 02 09 2019
pubmed: 27 9 2019
medline: 6 1 2021
entrez: 27 9 2019
Statut: ppublish

Résumé

Chemotherapy-induced alopecia (CIA) affects 65% of patients receiving chemotherapy regimens and is often identified with the massive hair loss stage. Reflectance confocal microscopy (RCM) is a noninvasive technique used in alopecia assessment for disease characterization and state of activity. To describe RCM features of CIA in different timing and identify specific phases of alopecia development. A total of 16 patients treated with chemotherapy underwent dermoscopy and RCM evaluations four times during the observation: 2 and 4-6 weeks after starting and 3 and 6 months after the end of chemotherapy. Ten examinations for each stage were performed. Four phases of CIA have been identified. Initial hair loss showed specific dots not previously described, named CIA dots. massive hair loss phase was characterized by black dots (10/10 pt), CIA dots (8/10 pt) and hair shaft abnormalities. Three months after the end of chemotherapy, during the partial regrowth phase, 10/10 patients showed thin hair in regrowth and 8/10 presented black and yellow dots. At 6 months, normal hair in regrowth appears in all patients (total regrowth phase). Chemotherapy-induced alopecia has to be considered as a dynamic process with specific phases characterized by distinctive dermoscopic and confocal features.

Sections du résumé

BACKGROUND BACKGROUND
Chemotherapy-induced alopecia (CIA) affects 65% of patients receiving chemotherapy regimens and is often identified with the massive hair loss stage. Reflectance confocal microscopy (RCM) is a noninvasive technique used in alopecia assessment for disease characterization and state of activity.
OBJECTIVE OBJECTIVE
To describe RCM features of CIA in different timing and identify specific phases of alopecia development.
METHODS METHODS
A total of 16 patients treated with chemotherapy underwent dermoscopy and RCM evaluations four times during the observation: 2 and 4-6 weeks after starting and 3 and 6 months after the end of chemotherapy. Ten examinations for each stage were performed.
RESULTS RESULTS
Four phases of CIA have been identified. Initial hair loss showed specific dots not previously described, named CIA dots. massive hair loss phase was characterized by black dots (10/10 pt), CIA dots (8/10 pt) and hair shaft abnormalities. Three months after the end of chemotherapy, during the partial regrowth phase, 10/10 patients showed thin hair in regrowth and 8/10 presented black and yellow dots. At 6 months, normal hair in regrowth appears in all patients (total regrowth phase).
CONCLUSIONS CONCLUSIONS
Chemotherapy-induced alopecia has to be considered as a dynamic process with specific phases characterized by distinctive dermoscopic and confocal features.

Identifiants

pubmed: 31556477
doi: 10.1111/srt.12790
doi:

Substances chimiques

Antineoplastic Agents 0

Types de publication

Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

269-276

Informations de copyright

© 2019 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Références

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Auteurs

Chiara Franceschini (C)

Clinical Dermatology Department, San Gallicano Dermatological Institute-IRCCS, Rome, Italy.

Valentina Garelli (V)

Department of Plastic and Reconstructive Surgery, San Gallicano Dermatological Institute-IRCCS, Rome, Italy.

Flavia Persechino (F)

Clinical Dermatology Department, San Gallicano Dermatological Institute-IRCCS, Rome, Italy.
Department of Clinical and Molecular Medicine, "Sapienza" University of Rome, Rome, Italy.

Isabella Sperduti (I)

Biostatistical Unit, Scientific Direction, San Gallicano Dermatological Institute-IRCCS, Rome, Italy.

Gemma Caro (G)

Department of Internal Medicine and Medical Specialties, "Sapienza" University of Rome, Rome, Italy.

Alfredo Rossi (A)

Department of Internal Medicine and Medical Specialties, "Sapienza" University of Rome, Rome, Italy.

Marco Ardigò (M)

Clinical Dermatology Department, San Gallicano Dermatological Institute-IRCCS, Rome, Italy.

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