Download full-text PDF |
Source |
|---|---|
| http://dx.doi.org/10.1684/ejd.2010.1178 | DOI Listing |
Publication Analysis
Top Keywords
Similar Publications
Diagnosis and Differential Diagnosis of Poikiloderma of Civatte: A Dermoscopy Cohort Study.
Dermatol Pract Concept
January 2023
Department of Dermatology, Medical University of Graz, Graz, Austria.
Article Synopsis
- Poikiloderma of Civatte (PC) is a common skin condition primarily affecting peri-menopausal women, characterized by skin changes on the neck and face, with limited existing research on its dermoscopic features.
- The study analyzed 28 patients with PC using a dermoscope, revealing specific patterns like reticular and vessel formations, which can aid in diagnosis.
- The findings indicate that dermoscopy offers a reliable way to distinguish PC from similar skin issues, enhancing both diagnosis and potential treatment plans.
Dermoscopy of acquired pigmentary disorders: a comprehensive review.
Int J Dermatol
January 2022
Keck School of Medicine of University of Southern California, Los Angeles, California, USA.
Article Synopsis
- Dermoscopy is gaining traction not only for diagnosing skin cancers but also for evaluating various pigmentary disorders, as recent studies have shown its effectiveness in this area.
- A comprehensive review of literature from PubMed examined numerous pigmentary conditions, including melasma, vitiligo, and several others, to explore their unique dermoscopic features.
- The findings suggest that dermoscopy can help clinicians differentiate between these disorders, which can be challenging to diagnose clinically and may cause significant emotional distress for patients.
Severe epidermolysis bullosa/Kindler syndrome-like phenotype of an autoinflammatory syndrome in a child.
Clin Exp Dermatol
June 2021
Histopathology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
A 5-year-old boy presented with generalized cutaneous erosions, severe scarring, depigmentation and contractures affecting major joints. The lesions had initially affected his ears, nose, feet, and the genital and ocular mucosa, leading to significant depigmentation, scarring, contractures and mutilation. The whole of the trunk and limbs were involved at the time of presentation, with the exception of some islands of spared skin on the proximal thighs, legs, nipples and external genitalia.
View Article and Find Full Text PDFAcquired Brachial Cutaneous Dyschromatosis: A Rarely Recognized Condition.
Dermatol Pract Concept
January 2021
Dermatology Unit, Hospital Universitario Severo Ochoa, Leganés, Spain.
Acquired Brachial Cutaneous Dyschromatosis in a Middle Aged Male.
Ann Dermatol
June 2018
Department of Dermatology, Ewha Womans University School of Medicine, Seoul, Korea.
Article Synopsis
- Acquired brachial cutaneous dyschromatosis (ABCD) is a skin disorder characterized by gray-brown patches on the upper forearms that are chronic and asymptomatic.
- A case study describes a 40-year-old male with multiple brown macules on his arms, with no history of hypertension, medication use, or sun exposure.
- Histological analysis revealed skin changes consistent with ABCD, and it emphasized the need to differentiate this condition from other pigmentary disorders like poikiloderma of Civatte and melasma.
Want AI Summaries of new PubMed Abstracts delivered to your In-box?
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!