Blau syndrome is one of the sporadic auto inflammatory disorders recapitulating early-onset granulomatous inflammation of the skin, joints, and eyes. This hereditary condition is caused by a mutation in the NOD2/CARD15 gene, leading to an imbalance of the innate immune response....
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Research Article10.9734/ajrdes/2024/v7i1108
Figilo Ibeinmo Moses, Dasetima D. Altraide, Amaewhule Mary Nnenda, Amadi Ekechi Stella, Ajirenike Rita Nkiru, Chikeka Chimaroke Ukachi & Ogbu Christian·Asian Journal of Research in Dermatological Science·2024
Pyoderma Gangrenosum (PG) is an Uncommon Neutrophilic Dermatoses that presents as Auto-Inflammatory and Ulcerative Disorder of the Skin. It has an estimated incidence of 3-10 cases per million people per year. It is more common in the young and middle-aged people , average age of...
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Research Article10.9734/ajrdes/2024/v7i1107
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
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
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
Introduction: folliculitis decalvans (FD) and lichen planopilaris (LPP) are two primary cicatricial alopecias (neutrophilic and "lymphocytic," respectively) recently associated in a phenotypic spectrum. The "folliculitis decalvans and lichen planopilaris" phenotypic spectrum FDLP...
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Research Article10.9734/ajrdes/2024/v7i1103
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...
Open access
Research Article10.9734/ajrdes/2024/v7i199