A Case Report of Eosinophilic Annular Erythema Treated with Dapsone and Associated Changes in Serum Thymus and Activation Levels [0.03%]
有关使用戊酸吡哌酯治疗 eosinophilic 环状红斑一例的报告及其对血清胸腺生成活化调节蛋白水平的影响
Toshiyuki Sato,Akihiko Asahina,Yoshimasa Nobeyama
Toshiyuki Sato
Introduction: Eosinophilic annular erythema (EAE) is an inflammatory dermatosis characterized clinically by pruritic annular erythematous lesions and histopathologically by eosinophilic dermal infiltration, usually withou...
Diagnostic Challenge in Diagnosing Atypical Pityriasis Rosea: A Case Report [0.03%]
pityriasis rosea非典型诊断病例报告
Madeline N Pham,Benjamin Henry Taylor Bridges,Meghan Rosenquist
Madeline N Pham
Introduction: Pityriasis rosea is a self-limited inflammatory skin condition most commonly associated with systemic active viral infection, particularly human herpesvirus (HHV)-6 and HHV-7. Generally appearing as a herald...
Co-Occurrence of En Coup de Sabre, Parry-Romberg Syndrome, and Hemimasticatory Spasm: A Case Report [0.03%]
额部线状瘢痕伴半面萎缩及三叉神经支配侧咀嚼肌痉挛综合征患者一例报告
Pooja Chaurasia,Asharbh Raman,Yugal K Sharma et al.
Pooja Chaurasia et al.
Introduction: En coup de sabre (ECDS) and Parry-Romberg syndrome (PRS) are rare, localised scleroderma subtypes, often considered to be overlapping variants of morphea. Hemimasticatory spasm (HMS), a distinct rare neuromu...
Hair Shaft Normalization and Hair Growth in SPINK5-Syndromic Epidermal Differentiation Disorder (Netherton Syndrome) while on Treatment with Dupilumab: A Novel Therapeutic Approach for Trichorrhexis Invaginata - A Case Report [0.03%]
SPINK5综合征性表皮分化障碍病（内特赫顿综合征）使用杜普利尤玛治疗时的毛发正常化和生长——一例卷发症（Trichorrhexis invaginata）治疗新方法的病例报告
Adriana Rendon,Niklas Negele,Knut Schäkel
Adriana Rendon
Introduction: SPINK5-syndromic epidermal differentiation disorder (also known as Netherton syndrome [NS]) is a severe chronic genetic disorder characterized by skin inflammation, severe atopy, and trichorrhexis invaginata...
Isolated Sclerodactyly Associated with Silica Exposure in a Stonemason: A Case Report [0.03%]
一例石匠因硅尘暴露导致的孤立性皮肤 sclerosis 病例报告
Vijay Selva,Arabella Wallett
Vijay Selva
Introduction: Sclerodactyly is commonly associated with systemic sclerosis (SSc), occurring alongside Raynaud's phenomenon and disease-specific autoantibodies. The combination of occupational silica exposure and SSc is kn...
When Conventional Therapy Fails: Interleukin-36 Inhibition for Severe Hydroxychloroquine-Induced Acute Generalized Exanthematous Pustulosis in Systemic Lupus Erythematosus - A Case Report [0.03%]
当常规治疗失败时：抗IL-36治疗系统性红斑狼疮患者羟氯喹诱导的严重急性广泛性发疱性皮病的一例报告
Lu Yang,Jiayi Ying,Xiuxiu Wang et al.
Lu Yang et al.
Introduction: Acute generalized exanthematous pustulosis (AGEP) is a rare but severe cutaneous adverse drug reaction characterized by the sudden onset of widespread sterile pustules on an erythematous and edematous base, ...
Isabel Gainza Apraiz,Laura Blanch Rius,Angela Gainza Apraiz et al.
Isabel Gainza Apraiz et al.
Introduction: Purpura fulminans (PF) is a rare and life-threatening thrombohemorrhagic disorder characterized by rapidly progressive purpuric skin lesions caused by dermal microvascular thrombosis and disseminated intrava...
Acquired Digital Arteriovenous Malformation of the Toe Showing Tendency to Clinically Regress after Skin Biopsy: A Case Report [0.03%]
一例趾部获得性数字动静脉畸形临床呈自发消退倾向的病例报告
Yoshihito Mima,Masako Yamamoto,Ken Iozumi
Yoshihito Mima
Introduction: Acquired digital arteriovenous malformation (ADAVM) is a rare vascular anomaly characterized by direct arteriovenous shunts, typically occurring on the digits and often associated with trauma. Toe-localized ...
Cholesterotic Fibrous Histiocytoma: A Rare Variant of a Common Presentation: A Case Report [0.03%]
胆固醇性纤维组织细胞瘤：一种常见疾病的罕见变异型：一例报告
Conall James McKinney,Kris Holte,David Alderdice
Conall James McKinney
Introduction: Here, we report a case of a 48-year-old man with a longstanding firm, asymptomatic nodule on the left upper arm who presented to clinic with a 1 year history of the lesion slowly enlarging to a size of 15 mm...
Allopurinol-Induced DRESS Syndrome in Patients with Pre-Existing Chronic Kidney Disease: A Case Report and Comprehensive Literature Review [0.03%]
慢性肾脏病患者发生别嘌呤醇致DRESS综合征的病例报告和文献复习
Ashraf Ahmed,Alaa Abdelhamid,Hidaya Al-Tamimi et al.
Ashraf Ahmed et al.
Introduction: Drug reaction with eosinophilia and systemic symptoms (DRESS) syndrome is a rare, potentially life-threatening hypersensitivity reaction that can be triggered by allopurinol, with increased risk in patients ...