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Ulcus vulvae acutum - A rare case [PDF]
JDVI (Journal of General Procedural Dermatology & Venereology Indonesia), 2019 Background: Ulcus vulvae acutum, also known as Lipschütz ulcer, is a rare condition characterized by multiple, painful, and acute genital ulceration in young women without venereal infections, associated with systemic symptoms like malaise, fever, and ...
Irene Dorthy Santoso +7 more
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Case Reports in Dermatology, 2020 Eosinophilic pustular folliculitis (EPF) (Ofuji disease) is a chronic, noninfectious pruritic cutaneous disorder of unknown etiology. No official guidelines are available for its treatment.
Claudio Marasca +3 more
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Dermatologica Sinica, 2016 Extramammary Paget's disease (EMPD) is a rare intraepidermal carcinoma and predominantly involves apocrine gland-bearing areas, such as anogenital regions and axillae.
Chi-Hung Wu, Chen-Yi Wu
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Dystrophic epidermolysis bullosa associated with non-syndromic hypodontia
Indian Dermatology Online Journal, 2013 Epidermolysis bullosa (EB) is a genetic disease associated with fragility and bullous lesions of the skin and mucous membranes. There are various patterns of inheritance and histopathology. The disease is associated with systemic and oral manifestations,
Sonali Sharma, Sumit Bedi
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Facial lupus vulgaris neglected for 50 years
Journal of Dermatology and Dermatologic Surgery, 2018 Tuberculosis (TB) is still a problem in the developed and underdeveloped countries, and cutaneous TB is a small part of extrapulmonary forms. Lupus vulgaris (LV) is the most common form of cutaneous TB among Western populations. In Morocco, scrofuloderma
Naoufal Hjira +5 more
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Surgical options in hidradenitis suppurativa
Journal of Dermatology and Dermatologic Surgery, 2019 Hidradenitis suppurativa is a chronic, debilitating disease managed by both medications and surgical therapies. The purpose of this study is to determine the indications for surgical therapies and compare the various surgical options for the treatment of
Sree S Kolli +5 more
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A case of adult-onset Still′s disease presenting with urticated plaques and acute myopericarditis
Indian Journal of Dermatology, 2013 Adult onset Still′s disease (AOSD) is a systemic inflammatory disorder of unknown etiology characterized by spiking fever, evanescent skin rash, arthralgia or arthritis, involvement of various organs, and predominantly neutrophilic leucocytosis.
Noor Hanif Said +2 more
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Anais Brasileiros de Dermatologia, 2009 FUNDAMENTOS: Formas moderada e grave de psoríase requerem fototerapia e/ou medicações sistêmicas. Tanto UVB banda estreita quanto fototerapia UVA com psoralênicos (PUVA) podem ser utilizadas no tratamento dessas formas de psoríase, sendo comprovada a ...
Ida Duarte +3 more
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Anais Brasileiros de Dermatologia, 2012 We present a female patient observed with painful violaceous plaques with central bullae and pustules on the lower limbs, rapidly transformed into ulcers, associated with bloody diarrhea, recurrent oral erosions and hyperthermia in the previous 3 months.
Pedro Andrade +2 more
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Acral acanthosis nigricans in a case of scleroderma
Indian Journal of Dermatology, 2015 Acanthosis nigricans (AN) is a dermatosis characterized by velvety, papillomatous, brownish-black, hyperkeratotic plaques, typically on the intertriginous surfaces and neck.
Mahendra M Kura, Swapnil A Sanghavi
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