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Narjess Er-rachdy

Publications (14)

Coexistence of Giant Congenital Melanocytic Nevus and Neurofibromatosis Type 1 among Child : A Rare Association

Narjess Er-rachdy, Ouissal Essadeq, Maha Habibi, Taha Aaboudech, Kaoutar Znati, Laila Benzekri & Nadia Ismaili · Asian Journal of Pediatric Research · 2025

Background: Giant congenital melanocytic nevus (GCMN) are rare pigmented lesions present at birth, often exceeding 20 cm in size, and may be associated with serious complications such as melanoma and neurocutaneous melanosis. Neurofibromatosis type 1 (NF1) is a common phakomatosi...

Open access Research Article 10.9734/ajpr/2025/v15i8466

Anhidrotic Ectodermal Dysplasia: Report of Two Cases

Narjess Er-rachdy, Ouissal Essadeq, Laila Benzekri & Nadia Ismaili · Asian Journal of Pediatric Research · 2025

Background: Anhidrotic ectodermal dysplasia (AED), also referred to as hypohidrotic ectodermal dysplasia, is a rare genetic condition characterized by a triad of hypotrichosis, hypodontia, and hypohidrosis. Case Report: This article reports two illustrative cases: an adolescent a...

Open access Research Article 10.9734/ajpr/2025/v15i7467

Desmoplastic Trichoepithelioma: A Case Report with Familial Context

Narjess Er-rachdy, Ouissal Essadeq, Taha Aaboudech, Kaoutar Znati, Laila Benzekri & Mariame Meziane · Asian Journal of Research in Dermatological Science · 2025

Background: Desmoplastic trichoepithelioma (DTE) is a rare, benign adnexal tumor derived from follicular germinative cells. It predominantly affects young females and commonly presents on the face as annular plaques or papules with a depressed center. The tumor poses diagnostic c...

Open access Research Article 10.9734/ajrdes/2025/v8i1135

Clinical Spectrum of Congenital Ichthyosis in a Moroccan Pediatric Study

Narjess Er-rachdy, Ouissal Essadeq, Laila Benzekri & Nadia Ismaili · Asian Journal of Pediatric Research · 2025

Background: Congenital ichthyoses are rare genetic skin disorders characterized by abnormal keratinization, often present at birth and associated with various extracutaneous manifestations. Material and Methods: We conducted a retrospective 30-month study at a Moroccan university...

Open access Research Article 10.9734/ajpr/2025/v15i7464

Unusual Coexistence of Castleman's Disease and Pityriasis Lichenoides in a Child

Narjess Er-rachdy, Ouissal Essadeq, Taha Aaboudech, Kaoutar Znati, Laila Benzekri & Nadia Ismaili · Asian Journal of Pediatric Research · 2025

Castleman disease is a rare lymphoproliferative disorder, particularly in children. Its association with pityriasis lichenoides has not been previously reported. This report presents a 5-year-old girl born to consanguineous parents, who developed recurrent necrotic and bullous sk...

Open access Research Article 10.9734/ajpr/2025/v15i7462

Clinical Variants of Cutaneous Mastocytosis in Children: Experience from a Single Center

Narjess Er-rachdy, Ouissal Essadeq, Laila Benzekri & Nadia Ismaili · Asian Journal of Pediatric Research · 2025

Background: Cutaneous mastocytosis (CM) is a rare pediatric dermatosis characterized by the abnormal proliferation and accumulation of mast cells in the skin. It typically presents in early childhood and is most often confined to the skin, with a generally favorable prognosis. Ma...

Open access Research Article 10.9734/ajpr/2025/v15i7463

Treating a Co-existence of Hidradenitis Suppurativa and Psoriasis with Secukinumab: A Case Report

Narjess Er-rachdy, Ouissal Essadeq, Syrine Hamada, Mariame Meziane, Nadia Ismaili & Laila Benzekri · Asian Journal of Research in Dermatological Science · 2025

Background: Hidradenitis suppurativa (HS) and psoriasis are chronic inflammatory diseases that may coexist and share IL-17–mediated pathogenic pathways. Secukinumab, an anti–IL-17A monoclonal antibody, is effective in psoriasis and has shown promise in HS. Case report: We report...

Open access Research Article 10.9734/ajrdes/2025/v8i1134

The Trichoscopic Hallmarks of Pressure Alopecia: A Case-based Study

Ouissal Essadeq, Narjess Er-rachdy, Laila Benzekri & Mariame Meziane · Asian Journal of Research in Dermatological Science · 2025

Pressure alopecia is a rare and often underrecognized form of hair loss caused by prolonged ischemia of the scalp. Frequently misdiagnosed, it requires a high index of suspicion  and a careful clinical and dermoscopic assessment. Trichoscopy plays a pivotal role in its diagnosis....

Open access Research Article 10.9734/ajrdes/2025/v8i1133

Juvenile Lichenoid Mycosis Fungoides: A Rare Variant Case Report with Clinical and Dermoscopic Features

Ouissal Essadeq, Narjess Er-rachdy, Meriem Boubekri, Taha Aaboudech, Kaoutar Znati, Laila Benzekri & Nadia Ismaili · Asian Journal of Pediatric Research · 2025

Background: Lichenoid mycosis fungoides is an exceptionally rare entity in children, often posing significant diagnostic challenges due to its atypical presentation and resemblance to benign dermatoses. Case Report: We report a pediatric case of lichenoid mycosis fungoides presen...

Open access Research Article 10.9734/ajpr/2025/v15i6457

The Perils of Drug Reintroduction: A Case of Generalized Bullous Fixed Drug Eruption Due to Cross Reactive NSAIDs

Ouissal Essadeq, Narjess Er-rachdy, Kaoutar Znati, Mariame Meziane, Nadia Ismaili, Karima Senouci & Laila Benzekri · Asian Journal of Research in Dermatological Science · 2025

Background: Generalized Bullous Fixed Drug Eruption (GBFDE) is a severe cutaneous adverse drug reaction that can mimic toxic epidermal necrolysis (TEN). Its prompt recognition is crucial to prevent severe complications and recurrence upon drug re-exposure. Case Report: We report...

Open access Research Article 10.9734/ajrdes/2025/v8i1123

Sclerodermatomyositis Overlap Syndrome with Bullous Lesion: A Rare Presentation

Meryem Elomari Alaoui, Amani Fliti, Narjess Er-rachdy, Mariame Meziane, Nadia Ismaili, Laila Benzekri & Karima Senouci · Asian Journal of Research in Dermatological Science · 2024

Overlap syndrome is diagnosed when at least two classical connective tissue diseases are observed in one patient, which develops simultaneously or sequentially. Sclerodermatomyositis (SDM) is one of the overlapping syndromes, defined by the association of dermatomyositis and scle...

Open access Research Article 10.9734/ajrdes/2024/v7i1106

Comorbidities Associated with Psoriasis: A Single Center Study of Morocco

Amani Fliti, Meryem Elomari Alaoui, Narjess Er-rachdy, Karima Senouci & Mariame Meziane · Asian Journal of Research in Dermatological Science · 2024

Introduction: Psoriasis, a chronic autoimmune inflammatory disease, is recognized as a systemic inflammatory disease with cutaneous and extracutaneous manifestations, often associated with multiple comorbidities. Our study aims to identify the various comorbidities associated wit...

Open access Research Article 10.9734/ajrdes/2024/v7i1105

A Case Report about Coexistence of Pigmented Bowen’s Disease and Cutaneous Capillary Malformation: Unusual Case with Dermatoscopic Findings

Meryem Elomari Alaoui, Amani Fliti, Narjess Er-rachdy, Mariame Meziane, Nadia Ismaili, Laila Benzekri & Karima Senouci · Asian Journal of Research in Dermatological Science · 2024

Capillary malformation and Bowen's disease (BD) or intraepidermal squamous cell carcinoma are two different entities whether clinically, histologically or prognostically. Bowen’s disease or squamous cell carcinoma in situ is a precursor malignant neoplasm restricted to the epider...

Open access Research Article 10.9734/ajrdes/2024/v7i1102

Not Every Chronic Intertrigo is Fungal: Hailey-Hailey Disease Revealed by Dermoscopy

Chourouq Mustapha Eid, Fatima Ezzahraa Sassine, Manal El Beyeg, Taha Yassine Aaboudech, Kaoutar Znati, Narjess Er-rachdy, Laila Benzekri & Mariame Meziane · Asian Journal of Research in Dermatological Science · 2026

Aims: To report a case of Hailey-Hailey disease identified with the aid of dermoscopy in a woman with a darker skin phototype whose chronic flexural intertrigo had repeatedly been misdiagnosed and treated as a fungal infection, and to highlight dermoscopic features that may reduc...

Open access Research Article 10.9734/ajrdes/2026/v9i1173