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Cancer and hidradenitis suppurativa.
Clin Dermatol
December 2024
DermSurgery Associates, Sugar Land, Texas, USA.
Article Synopsis
- * Factors like smoking, prolonged lesions, and certain treatments (like TNF-alpha inhibitors) may increase the risk of developing squamous cell carcinoma in these patients.
- * There is a need for careful monitoring of new or rapidly changing lesions in hidradenitis suppurativa patients, as they can mimic or hide underlying cancers, necessitating prompt medical evaluation.
An algorithmic approach towards diagnosis of patients with hereditary reticulate pigmentary disorders: a narrative review.
Clin Exp Dermatol
December 2024
Department of Dermatology, Venereology and Leprology, Postgraduate Institute of Medical Education and Research, Sector 12, Chandigarh, India.
Article Synopsis
- * A literature review was conducted to develop a user-friendly diagnostic algorithm to help clinicians identify these disorders and determine appropriate genetic testing.
- * The research included a comprehensive search of databases, resulting in 625 relevant articles that discuss the different diseases and contributed to forming a clear approach for provisional diagnosis based on specific clinical factors.
Inherited Reticulate Pigmentary Disorders.
Genes (Basel)
June 2023
Department of Dermatology, College of Medicine, Kaohsiung Medical University, Kaohsiung 807, Taiwan.
Article Synopsis
- Reticulate pigmentary disorders (RPDs) are skin conditions that can be either inherited or acquired, featuring areas of hyperpigmentation or hypopigmentation.
- There are several inherited types of RPDs, with varying pigmentation patterns and additional symptoms, including DSH, DUH, and RAK primarily affecting East Asian populations, while DDD is more common in Caucasians.
- The article examines the different clinical, histological, and genetic characteristics of these inherited RPDs.
Haber's Syndrome: A Case Report.
Cureus
February 2023
Dermatology, King Abdulaziz Hospital, Makkah, SAU.
Haber's syndrome is an autosomal dominant, rare genodermatosis characterized by photosensitive, persistent facial erythema associated with reticulated hyperpigmentation. We present a case of an eight-year-old healthy Saudi girl who presented with facial erythema and generalized reticulated hyperpigmentation. Systematic review and laboratory studies were unremarkable.
View Article and Find Full Text PDFFollicular Dowling-Degos Disease and Blepharophimosis-Ptosis-Epicanthus Inversus Syndrome: A Chance or Significant Association.
Indian J Dermatol
January 2021
Department of Dermatology, Venereology and Leprosy King George's Medical University (KGMU), Lucknow, Uttar Pradesh, India E-mail:
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