Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Michelle Bain"'
Publikováno v:
JAAD Case Reports, Vol 45, Iss , Pp 44-46 (2024)
Externí odkaz:
https://doaj.org/article/02cad1f35e51452b847fdf2127f4a9d0
Publikováno v:
Journal of the Dermatology Nurses' Association. 14:256-260
Publikováno v:
SKIN The Journal of Cutaneous Medicine. 5:426-429
Congenital melanocytic nevi with halo phenomenon in children is a rare clinical finding. We report two cases of children who developed depigmentation within medium-size congenital melanocytic nevi. Clinicians should be suspicious when confronted with
Autor:
Tanya Magana, Isabelle M. Sanchez, Taryn Murray, Stephanie Kuschel, Gerard Nuovo, Marylee Braniecki, Michelle Bain
Publikováno v:
Annals of diagnostic pathology. 60
An 11-year-old female presented with multiple oral lesions for several months. Histopathological findings suggested focal epithelial hyperplasia (FEH), also known as Heck disease. FEH is strongly associated with Human papillomavirus (HPV), especially
Autor:
Kayla St Claire, Marylee Braniecki, Michelle Bain, Ryan Bunney, Maria M. Tsoukas, Kurt A. Ashack
Publikováno v:
Clinics in Dermatology. 38:223-234
Langerhans cell histiocytosis (LCH) is an uncommon but serious inflammatory neoplasia that affects many organs, including the skin. Though uncommon, it should remain high on a clinician's differential diagnosis in treatment-resistant cases of conditi
Publikováno v:
Pediatric dermatologyREFERENCES. 39(3)
Immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) syndrome is a rare genetic disorder that typically presents in the first year of life with severe diarrhea, autoimmune endocrine disorder, and inflammatory dermatitis, most common
Publikováno v:
International journal of dermatologyReferences.
Publikováno v:
Journal of Clinical Images and Medical Case Reports. 2
Palisaded Neutrophilic And Granulomatous Dermatitis (PNGD) is a rare inflammatory cutaneous eruption associated with underlying systemic disease, commonly Systemic Lupus Erythematosus (SLE), rheumatoid arthritis, or Anti-Neutrophilic Cytoplasmic Auto
Publikováno v:
Clinical Case Reports
Key Clinical Message Pallister–Killian syndrome (PKS) is a rare, sporadic, multisystem developmental disorder characterized by craniofacial dysmorphic features. We report a case of a two‐year‐old boy with PKS to highlight the cutaneous findings
Publikováno v:
Dermatology online journal. 25(5)
Cidofovir is an antiviral nucleotide analogue with relatively new treatment capacities for dermatological conditions, specifically verruca vulgaris caused by human papilloma virus infection. In a 10-year old boy with severe verruca vulgaris recalcitr