Erysipeloid cutaneous leishmaniasis: a study of 40 cases of an unusual variant.


Journal

International journal of dermatology
ISSN: 1365-4632
Titre abrégé: Int J Dermatol
Pays: England
ID NLM: 0243704

Informations de publication

Date de publication:
Nov 2022
Historique:
revised: 26 04 2022
received: 18 12 2021
accepted: 28 04 2022
pubmed: 25 5 2022
medline: 19 10 2022
entrez: 24 5 2022
Statut: ppublish

Résumé

Erysipeloid cutaneous leishmaniasis (ECL) is known as the chronic form of cutaneous leishmaniasis (CL). However, keeping its clinical presentation in view, there is a need to revisit this form of the disease. To describe ECL in view of clinical features and treatment modalities. We include a case series seen in Sfax (Southern Tunisia) from January 2017 to January 2021. All patients clinically suggestive and laboratory confirmed with a diagnosis of CL were registered. Patients of all age groups and of either gender having cutaneous lesions resembling erysipela on the face were included in the study. Different demographic features of the patients and clinical aspects were identified. Descriptive statistics were used for analysis. Of 1300 registered patients with CL, 40 (3%) were diagnosed as ECL. Ages ranged from 15 to 65 years, and duration of lesions varied from 15 to 180 days. All patients had lesions over the face. Clinically, a painful infiltrated inflammatory placard of the central facial area with a butterfly shape was observed in 14 cases, as well as zones of the cheekbone (11 cases), cheekbone and nose (5 cases), cheekbone and eyelid (8 cases), and cheekbone with ear (2 cases). Several therapeutic methods were prescribed with a sufficient result with no recurrence. ECL is a rare presentation that typically occurs on the face, looking like erysipelas, in patients who are native from an endemic region of CL.

Sections du résumé

BACKGROUND BACKGROUND
Erysipeloid cutaneous leishmaniasis (ECL) is known as the chronic form of cutaneous leishmaniasis (CL). However, keeping its clinical presentation in view, there is a need to revisit this form of the disease.
AIMS OBJECTIVE
To describe ECL in view of clinical features and treatment modalities.
METHODS METHODS
We include a case series seen in Sfax (Southern Tunisia) from January 2017 to January 2021. All patients clinically suggestive and laboratory confirmed with a diagnosis of CL were registered. Patients of all age groups and of either gender having cutaneous lesions resembling erysipela on the face were included in the study. Different demographic features of the patients and clinical aspects were identified. Descriptive statistics were used for analysis.
RESULTS RESULTS
Of 1300 registered patients with CL, 40 (3%) were diagnosed as ECL. Ages ranged from 15 to 65 years, and duration of lesions varied from 15 to 180 days. All patients had lesions over the face. Clinically, a painful infiltrated inflammatory placard of the central facial area with a butterfly shape was observed in 14 cases, as well as zones of the cheekbone (11 cases), cheekbone and nose (5 cases), cheekbone and eyelid (8 cases), and cheekbone with ear (2 cases). Several therapeutic methods were prescribed with a sufficient result with no recurrence.
CONCLUSION CONCLUSIONS
ECL is a rare presentation that typically occurs on the face, looking like erysipelas, in patients who are native from an endemic region of CL.

Identifiants

pubmed: 35609142
doi: 10.1111/ijd.16278
doi:

Types de publication

Case Reports Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1380-1384

Informations de copyright

© 2022 the International Society of Dermatology.

Références

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Auteurs

Chaima Kouki (C)

Department of Dermatology, University of Sfax, Sfax, Tunisia.

Abdelrahmen Masmoudi (A)

Department of Dermatology, University of Sfax, Sfax, Tunisia.

Nadine Kammoun (N)

Department of Dermatology, University of Sfax, Sfax, Tunisia.

Khadija Sellami (K)

Department of Dermatology, University of Sfax, Sfax, Tunisia.

Ines Saguem (I)

Anatompathology Department, Hospital of Habib Bourguiba, Sfax, Tunisia.

Emna Bahloul (E)

Department of Dermatology, University of Sfax, Sfax, Tunisia.

Sonia Boudaya (S)

Department of Dermatology, University of Sfax, Sfax, Tunisia.

Fatma Chikhrouhou (F)

Parasitology Department, Hospital of Habib Bourguiba, Sfax, Tunisa.

Meriem Amouri (M)

Department of Dermatology, University of Sfax, Sfax, Tunisia.

Madiha Mssedi (M)

Department of Dermatology, University of Sfax, Sfax, Tunisia.

Ali Ayedi (A)

Parasitology Department, Hospital of Habib Bourguiba, Sfax, Tunisa.

Tahya Boudawara (T)

Anatompathology Department, Hospital of Habib Bourguiba, Sfax, Tunisia.

Hamida Turki (H)

Department of Dermatology, University of Sfax, Sfax, Tunisia.

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