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Urticarial vasculitis.
Curr Opin Rheumatol
January 2025
Marmara University School of Medicine, Department of Dermatology, Istanbul, Türkiye.
Article Synopsis
- Urticarial vasculitis (UV) is a rare condition that can range from mild skin issues to serious systemic problems, and recent research focuses on its causes, diagnosis, and treatment options.
- New triggers for UV associated with SARS-CoV-2 and COVID-19 vaccines have been noted, along with a new clinical-dermoscopic method for diagnosis that reduces reliance on skin biopsies.
- Treatments such as antihistamines, corticosteroids, and rituximab show promise for success and long-lasting remission, while epidemiological studies show good survival rates but highlight certain severe health issues that can increase mortality.
Dermoscopy of mycosis fungoides: could it be a confirmatory aid to the clinical diagnosis?
Arch Dermatol Res
November 2024
Professor of dermatology and venereology, Faculty of Medicine, Tanta university, Tanta, Egypt.
Mycosis fungoides (MF) is the most common type of cutaneous T-cell lymphoma that is difficult to be differentiated from other dermatological diseases. Dermoscopy is an easy and non-invasive office procedure that is widely used nowadays in the diagnosis of a wide variety of skin diseases. This prospective study aimed to describe and to differentiate the dermoscopic pattern of different stages and to compare the dermoscopic features observed in different clinical types of mycosis fungoides.
View Article and Find Full Text PDFMyositis: A Rare First Presentation of Systemic Lupus Erythematosus.
Cureus
September 2024
Nephrology, Al-Karama General Hospital, Baghdad, IRQ.
Article Synopsis
- * This case report details an 18-year-old female patient whose SLE first presented with generalized muscle weakness, joint pain, and distinctive rashes indicative of lupus and vasculitis.
- * After extensive testing, she was diagnosed and treated with a combination of medications, leading to significant improvement in her symptoms and muscle strength over time.
Coxsackievirus A6-Induced Atypical Hand-Foot-Mouth Disease.
JAMA Dermatol
July 2024
Department of Dermatology, Kaohsiung Medical University Hospital, Kaohsiung, Taiwan.
Cutaneous Perivascular Hemophagocytosis: A Report of 2 Cases With Emphasis on Clinical and Histological Features.
Am J Dermatopathol
September 2024
Dermatology Clinic, IRCCS San Raffaele Hospital, Vita-Salute San Raffaele University, Milan, Italy.
Cutaneous perivascular hemophagocytosis (CH) is a histological manifestation that manifests as systemic hemophagocytic syndrome, also known as hemophagocytic lymphohistiocytosis, when accompanied by fever, hepatosplenomegaly, liver dysfunction, and cytopenia, and may rarely manifest independently of hemophagocytic lymphohistiocytosis. CH typically presents as purpuric or brownish macules and patches on the extremities, abdomen, and trunks. Histopathologically, the hallmark of CH includes extravasated erythrocytes and karyorrhectic debris phagocytized by histiocytes, associated with dermal capillary ectasia, perivascular infiltration of neutrophils, nuclear dust, and histiocytes without atypia.
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