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1.
J Cutan Med Surg ; : 12034754241235965, 2024 Feb 26.
Artigo em Inglês | MEDLINE | ID: mdl-38409743
2.
J Cutan Med Surg ; : 12034754241230689, 2024 Feb 05.
Artigo em Inglês | MEDLINE | ID: mdl-38314743
4.
Photodiagnosis Photodyn Ther ; 44: 103738, 2023 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-37558191

RESUMO

Hailey-Hailey disease (HHD) is a rare genetic benign condition resulting in blisters predominantly on the skin folds. The inheritance is autosomal dominant with complete penetrance, but a variable expressivity in affected family members. It can be triggered by a vast variety of factors such as sweating, weight gain, infection, trauma, pregnancy, and ultraviolet radiation, but the major cause of the disease is a mutation in the ATP2C1 gene. The lesions are typically distributed symmetrically within intertriginous regions such as the retroarticular folds, axillae, inguinal, and perianal regions and presents as flaccid vesicles and blisters on erythematous skin, giving rise to erosions, fissures, and vegetations. There is no specific therapy for HHD. The therapeutic approach to HHD involves the control of exacerbating factors, secondary infections, and cutaneous inflammation. Because of the rarity of the disease, evidence of efficacy for topical or systemic therapies is mainly based on small observational studies, case reports, and clinical experience. We present a case of HHD successfully treated by photodynamic therapy (PDT) with a topical liposomal chlorin photosensitizer.


Assuntos
Pênfigo Familiar Benigno , Fotoquimioterapia , Humanos , Pênfigo Familiar Benigno/tratamento farmacológico , Pênfigo Familiar Benigno/genética , Pênfigo Familiar Benigno/patologia , Vesícula/tratamento farmacológico , Raios Ultravioleta , ATPases Transportadoras de Cálcio/genética , ATPases Transportadoras de Cálcio/uso terapêutico , Fotoquimioterapia/métodos , Fármacos Fotossensibilizantes/uso terapêutico
5.
Dermatol Reports ; 12(2): 8372, 2020 Sep 23.
Artigo em Inglês | MEDLINE | ID: mdl-33408829

RESUMO

Buschke-Löwenstein tumor is known to manifest not only in sexually active people and adolescents exposed to violence or drugs, but also in people who do not have any predisposing factors or bad habits. Several studies have shown that in the majority of children with anogenital warts, HPV can be transmitted asexually by hetero- inoculation or through infected objects. To our knowledge, there are currently few reports on BLT in HPV-negative patients in the literature. In our case, the patient presented early, with multiple slow growing warts, no history of alcohol intake, drug use or smoking and no HPV infection, which makes this case unique and important.

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