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期刊名:Dermatopathology

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ISSN:2296-3529

e-ISSN:2296-3529

IF/分区:1.7/Q3

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Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Oriana Simonetti,Elisa Molinelli,Valerio Brisigotti et al. Oriana Simonetti et al.
Primary dermal melanoma (PDM) is a rare distinct variant of cutaneous melanoma, predominantly occurring on the extremities of young or middle-aged adults. In comparison to conventional melanoma, PDM is characterized by unexpectedly prolonge...
Gerardo Cazzato,Anna Colagrande,Antonella Cimmino et al. Gerardo Cazzato et al.
Atypical fibroxanthoma-like amelanotic melanoma is a very rare variant of melanoma that can, if not correctly recognized and framed, lead to diagnostic errors that can potentially cause problems of extreme relevance to patients. Correct kno...
Samanta Buchholzer,Raùl Verdeja,Tommaso Lombardi Samanta Buchholzer
Neurofibromatosis type 1 (NF1) is a common genetic disease whose dermatological lesions are at the forefront of its development. Cutaneous manifestations include café au lait spots, intertriginous freckling, and neurofibromas which appear ...
Tejas Vishwanath,Angela Nagpal,Sunil Ghate et al. Tejas Vishwanath et al.
Background: A plethora of diseases manifest as acquired genital lymphangiectasias which clinically manifest as superficial vesicles. They range from infections such as tuberculosis to connective tissue diseases such as sc...
Primali Rukmal Jayasooriya,Chamara Athukorala,Manjula Attygalla et al. Primali Rukmal Jayasooriya et al.
Low-grade myofibroblastic sarcoma (LGMS) is a mesenchymal tumor of myofibroblasts that occurs more frequently in adults. A series of three cases is presented to illustrate that LGMS may also occur within the oral cavity in children and adol...
Roland Aschoff,Nick Zimmermann,Stefan Beissert et al. Roland Aschoff et al.
Contemporarily to the new SARS-CoV-2 mediated COVID-19 pandemic, a rise in patients with acral chilblain lesions has been described. They manifest late after mild disease or asymptomatic exposure to SARS-CoV-2. Their pathogenic evolution is...
Carlos Cuenca-Barrales,José Aneiros-Fernández,Israel Pérez-López et al. Carlos Cuenca-Barrales et al.
Keloids are a difficult-to-treat disease characterized by an imbalance in mechanisms of tissue reparation. We present the case of a middle-aged woman with spontaneous keloids which histologically and clinically improved after UVA-1 photothe...
Yumi Sawada,Yasuo Nakai,Naho Yokota et al. Yumi Sawada et al.
Voriconazole is a triazole antifungal agent used for the prevention and treatment of fungal infections in immunocompromised patients. Prolonged voriconazole therapy may induce phototoxicity and lead to the development of malignant neoplasms...
Yoshiaki Matsushima,Kento Mizutani,Hiroyuki Goto et al. Yoshiaki Matsushima et al.
Inherited epidermolysis bullosa (EB) is a rare genetic skin disorder characterized by epithelial tissue fragility. Recessive dystrophic epidermolysis bullosa (RDEB) is the most severe form, characterized by the presence of blisters, erosion...
Raphaël André,Yasmine Ibrahim,Aurélie Hsieh et al. Raphaël André et al.
Granuloma annulare is an idiopathic granulomatous condition. Clinical variants of granuloma annulare include classical and localized, large erythematous patch, generalized, perforating, and subcutaneous/deep forms. Rarely, granuloma annular...