Background: H syndrome is a rare autosomal recessive, multisystem non-Langerhans cell histiocytosis associated with biallelic pathogenic variants in SLC29A3. Published data from North Africa remain limited, and phenotypic variability may complicate clinical recognition. Case Pres...
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Research Article10.9734/ajrdes/2026/v9i1165
Background: Bullous erythema multiforme (EM) major is an uncommon mucocutaneous disorder, and its association with Parvovirus B19 is exceptionally rare. This report describes an immunocompetent adult with Parvovirus B19 DNA detected locally in blister fluid after common infectiou...
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Research Article10.9734/ajrdes/2026/v9i1163
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...
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Research Article10.9734/ajrdes/2024/v7i1105
Aims: Pachyonychia congenita is a rare genodermatosis related to mutations in the genes encoding keratins. Illustrations of such a typical case of this uncommon condition have rarely been seen in the literature, hence the interest of our case report. Case Report: An 11-year-old g...
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Research Article10.9734/ajpr/2023/v12i1232
Aims: To describe a rare case of paraneoplastic pemphigus (PNP) occurring in a patient with synchronous pulmonary and gastric mucosa-associated lymphoid tissue (MALT) lymphoma and to summarise the diagnostic and therapeutic considerations documented in this case. Presentation of...
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Research Article10.9734/ajrdes/2026/v9i1166
Aims: Solitary nodular calcinosis of Winer is a rare and benign form of localized idiopathic cutaneous calcinosis. Its dermoscopic features may be useful for early diagnosis, but have never been described in the literature to our knowledge. Case Report: A 5-year-old child present...
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Research Article10.9734/ajpr/2023/v12i1231
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...
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Research Article10.9734/ajrdes/2025/v8i1123
Introduction: Eosinophils, play major roles in the pathogenesis of various dermatoses (atopic dermatitis, bullous pemphigoid, drug reaction with eosinophilia and systemic symptoms (DRESS)…). Hypereosinophilia in pemphigus has not been well documented in the literature, hence we i...
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Research Article10.9734/ajrdes/2024/v7i1104
Introduction: Pemphigus is a group rare heterogeneous of intraepidermal autoimmune chronic bullous dermatoses associated with a high risk of morbidity and mortality. Despite its rarity, this condition persists as the most prevalent among bullous dermatoses in the Maghreb, includi...
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Research Article10.9734/ajrdes/2024/v7i1101
Introduction: Psoriasis is an immune cell-mediated inflammatory skin disease, characterized by the formation of scaly, indurated, erythematous plaques. Psoriasis comorbidities and symptoms affect the choice of treatments. Secukinumab is a fully human monoclonal anti-body that sel...
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Research Article10.9734/ajrdes/2024/v7i1100
Introduction: Dermatological emergency is defined as any acute dermatological disorder that develops and worsens in less than 5 days. Aims of Study: The aim of our study is to identify the main dermatological emergencies consultations, establish a demographic and clinical profil...
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Research Article10.9734/ajrdes/2024/v7i199
Aims: Folliculotropic mycosis fungoides (FMF) is an uncommon variant of mycosis fungoides, rarely described in children. This type of lymphoma is particularly unresponsive to treatment and has a poor prognosis. Paradoxically, it can be clinically confused with conditions as benig...
The present study reports the appearance of lichen lesions with genital and nail involvement 2 months after the onset of a Stevens-Johnson syndrome (SJS) associated with lamotrigine use. A chronic inflammatory disorder called lichen planus (LP) most frequently affects middle-aged...
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...
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Research Article10.9734/ajrdes/2024/v7i1106
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...
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Research Article10.9734/ajrdes/2024/v7i1102
Marwa Asermouh, Chaimae Ait Khabba, Sektaoui Soukaina, Sabrine Derqaoui, Znati Kaoutar, Mariame Meziane, Nadia Ismaili, Laila Benzekri & Karima Senouci·Asian Journal of Research in Dermatological Science·2023
Aims: The reported association of Plummer-Vinson syndrome and some autoimmune diseases, including pemphigus -association described for the first time-, raises the hypothesis of the autoimmune origin of this syndrome. On the other hand, this unexpected association represents a the...