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Posterior cervical instrumented fusion case complicated by acute generalized erythematous pustulosis.
J Surg Case Rep
March 2025
Department of Neurosurgery, Neurosurgery, The Walton Centre NHS Foundation Trust, Lower Lane, Liverpool L9 7LJ, United Kingdom.
This case report describes the first case of acute generalised erythematous pustulosis (AGEP) following cervical spinal surgery. A 74-year-old male post-operatively developed a painful, exudative bullous rash progressing from the posterior cervical wound site. Initial management with antibiotics for suspected cellulitis failed, leading to further investigation and a diagnosis of AGEP by dermatology.
View Article and Find Full Text PDFPrurigo pigmentosa following laparoscopic sleeve gastrectomy: a case report.
J Surg Case Rep
March 2025
Department of General Surgery, Prince Sultan Military Medical City, Riyadh Makkah Al Mukarramah Road, As Sulimaniyah, Riyadh, 12233, Saudi Arabia.
Prurigo pigmentosa (PP) is a rare dermatological condition with an unclear, often idiopathic etiology, but recent evidence points to a potential link between the disease and metabolic changes, particularly those associated with ketosis. It typically presents as a pruritic, erythematous rash, mainly affecting the trunk and neck, and often features hyperpigmented macules and plaques. The onset of PP has been associated with various factors, including fasting, dieting, and certain metabolic disorders.
View Article and Find Full Text PDFPityriasis Rubra Pilaris Following COVID-19 Infection: A Case of Successful Treatment With Ixekizumab.
Cureus
February 2025
Department of Dermatology, Marshall University Joan C. Edwards School of Medicine, Huntington, USA.
Pityriasis rubra pilaris (PRP) is a rare dermatologic disorder marked by erythema, scaling, pruritus, pain, and follicular hyperkeratosis. It usually appears as red, scaly patches with areas of unaffected skin and is commonly associated with orange-colored palms and soles. While the exact etiology is unknown, emerging evidence points to several contributing factors.
View Article and Find Full Text PDFAnti-nuclear Matrix Protein 2 Antibody-Positive Dermatomyositis Relapse With Preceding Panniculitis.
Cureus
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Department of Rheumatic Diseases, Tokyo Metropolitan Tama Medical Center, Fuchu, JPN.
Dermatomyositis (DM) is an idiopathic inflammatory myopathy characterized by cutaneous lesions such as heliotrope rash, Gottron's papules, and Gottron's sign. Panniculitis is rarely reported as a skin manifestation of DM. Herein, we present a case of anti-nuclear matrix protein 2 antibody (NXP-2)-positive DM relapse with panniculitis in the absence of muscle symptoms.
View Article and Find Full Text PDFPsoriasiform rash possibly induced by oral propranolol in a 12-month-old girl with infantile hemangioma: a case report and literature review.
Dermatol Reports
March 2025
Department of Pediatric Dermatology, King Abdullah Specialized Children's Hospital, Riyadh.
Infantile hemangiomas are the most common soft-tissue tumors in children, with propranolol, a non-cardioselective β-blocker, considered the first-line treatment for complicated cases. β-blockers have been reported to be the most common causative agents for drug-induced psoriasis in adults. In the pediatric population, only one previous case exists.
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