Download full-text PDF |
Source |
|---|
Publication Analysis
Top Keywords
Similar Publications
[A man with grouped papules on his shoulder].
Ned Tijdschr Geneeskd
August 2023
Alrijne Ziekenhuis,afd. Dermatologie, Leiden.
A 58-years old man was seen at the dermatology outpatient clinic because of a spot near his ear. However, during physical examination soft-elastic papules on his left shoulder were visible. As the patient had not undergone additional examination for this, a biopsy was taken.
View Article and Find Full Text PDFSegmental neurofibromatosis with Lisch nodules.
Med J Armed Forces India
March 2021
Professor & Head (Dermatology), SRM Med College & Research Centre, SRM Nagar, TamilNadu, India.
Neurofibromatosis (NF) is an inherited neuroectodermal abnormality that primarily affects the growth of neural tissues, and Riccardi classified it into eight types. Segmental neurofibromatosis, which is a rare form of neurofibromatosis, is classified as type 5. We report a case for very unusual presentation of segmental NF with unilateral lisch nodules and uncommon sites involving the scalp.
View Article and Find Full Text PDFLarge, linear pigmentation anomaly: an unusual dyspigmentation case.
Dermatol Online J
December 2022
Dr Phillip Frost Department of Dermatology, University of Miami, Miami, Florida, USA.
Segmental pigmentation anomalies can be further divided into segmental pigmentation disorder (SPD) complex and café-au-lait macules (CALMs). Both are congenital skin conditions characterized by hyper- or hypopigmentation. Segmental pigmentation disorder is a rare entity, whereas CALMs are common skin lesions that may be associated with various genetic conditions, especially when several are present and the patient has other indicators of a genetic abnormality.
View Article and Find Full Text PDFSynchronous cutaneous malignant peripheral nerve sheath tumor and jejunal gastrointestinal stromal tumor and submucosal angiomyolipoma in type 1 neurofibromatosis: A case report and literature review.
Medicine (Baltimore)
January 2023
Department of Pathology, College of Medicine, Chosun University, Gwangju, Korea.
Rationale: Type 1 neurofibromatosis (NF1) is one of the most prevalent genetic conditions. NF1 is characterized by cutaneous plexiform neurofibromas and café au lait skin pigmentation, and is inherited in an autosomal dominant trait with mutation in the neurofibromin 1 gene on chromosome 17. Neurofibromin is involved in Ras proto-oncogene regulation.
View Article and Find Full Text PDFUnusual Bilateral Distribution of Neurofibromatosis Type 5 on the Distal Upper Extremities.
Cutis
September 2022
Drs. Hemmrich and Mancuso are from the Dr. Kiran C. Patel College of Osteopathic Medicine, Nova Southeastern University, Fort Lauderdale, Florida. Dr. Francis is from the Department of Dermatology, University of Florida College of Medicine, Gainesville.
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!