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Y-J Hwang,H-S Kho Y-J Hwang
Of the five new cases, four with gastrointestinal stromal tumours developed oral lichenoid lesions (OLLs), and one with chronic myeloid leukaemia (CML) developed oral hyperpigmentation (OHP). Of the total 50 patients, 26 were male and 24 were female, and age ranged from 29 to 86 years.
Ahoud Jazzar,Hebah AlDehlawi Ahoud Jazzar
Background: Oral-pigmented lesions have raised aesthetic concerns, leading to multiple depigmentation techniques. This systematic review and network meta-analysis aimed to assess the efficacy of different treatments for o...
Desiana Radithia,Ajiravudh Subarnbhesaj,Nurina-Febriyanti Ayuningtyas et al. Desiana Radithia et al.
This review aimed to estimate the prevalence of oral hyperpigmentation which affect individual quality of life as a side effect of HAART....The pooled prevalence of oral hyperpigmentation in HAART patients was 25% (95% CI: 11%, 38%; I2: 99%). Subgroup analysis based on geographical location showed varied result may be due to the type and duration of HAART used in study population....The most widely used type of ARV was from the NRTI group (n=7) and the study with the shortest duration showed the lowest oral hyperpigmentation prevalence (n=7)....Conclusions: There is an increased prevalence of oral hyperpigmentation by the use of HAART. Future study should investigate the correlation between HAART duration and the degree of oral hyperpigmentation.
Anna Danielly Almeida do Nascimento,Débora Maria Porto,Aurora Karla de Lacerda Vidal Anna Danielly Almeida do Nascimento
Objective: The objective of this study was to report and discuss oral hyperpigmentation associated with HFS caused by the use of capecitabine, which is still poorly described in the literature.
Éder Gerardo Dos Santos-Leite,Lorena Vieira Sacramento,Alessandra Monteiro Santana et al. Éder Gerardo Dos Santos-Leite et al.
Hand-foot syndrome (HFS) is a common adverse effect of anticancer therapy. It is known to cause dermatological symptoms including acral erythema and dysesthesia of the palms and soles of the feet, swelling, pain, itching, and scaling. Some ...
Florica Sandru,Aida Petca,Mihai Cristian Dumitrascu et al. Florica Sandru et al.
Peutz-Jeghers syndrome (PJS), a rare autosomal dominant serine/threonine kinase 11 (STK11)/ liver kinase B1 (LKB1) gene-related genodermatosis, is characterized by oral hyperpigmentation (OHP); multiple gastro-intestinal mucosal benign hamartomatous polyps causing local bleeding, occlusion, intussusception
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