Download full-text PDF |
Source |
|---|---|
| http://dx.doi.org/10.1016/j.ciresp.2021.02.009 | DOI Listing |
Publication Analysis
Top Keywords
Similar Publications
Sentinel Lymph Node Biopsy in Atypical Spitz Tumor: A Systematic Review.
J Clin Med
May 2024
Soft-Tissue, Peritoneum and Melanoma Surgical Oncology Unit, Veneto Institute of Oncology IOV-IRCCS, 35128 Padova, Italy.
Background: Atypical Spitz tumor (AST) is an intermediate category among Spitz melanocytic neoplasms. Sentinel node biopsy (SNB) has been proposed in the clinical management of AST patients, but this approach remains the subject of debate. This systematic review aims to summarize the available evidence on SNB procedures in AST patients.
View Article and Find Full Text PDFIn vitro culture and tissue-derived specific expression of melanocytes from ovary of adult Silky Fowl.
Poult Sci
April 2024
Hainan Sanya Research Institute, Seed Laboratory & Sanya Research Institute, Hainan, China; State Key Laboratory of Animal Biotech Breeding, Breeding and Reproduction of the Ministry of Agriculture & National Engineering Laboratory for Animal Breeding, China Agricultural University, Beijing, China. Electronic address:
Article Synopsis
- * Melanocytes were successfully purified and cultured from ovarian tissues using a collagenase and trypsin-EDTA mixture, and RNA sequencing analysis was performed to compare gene expression in ovarian vs. peritoneal melanocytes.
- * Results showed that ovarian melanocytes express higher levels of genes linked to sexual hormone production and melanogenesis, while peritoneal melanocytes are more involved in metabolic processes, suggesting the function of melanocytes varies by tissue origin and developmental stage.
Persistent Intracranial Hypertension and Severe Hypoglycorrhachia in an Adult With Giant Congenital Melanocytic Naevi.
Cureus
December 2023
Department of Internal Medicine (Neurology), School of Medical Sciences, Universiti Sains Malaysia, Kubang Kerian, MYS.
A 29-year-old female, with giant congenital melanocytic naevi (GCMN) presented with a-year history of symptoms and signs of intracranial hypertension. Investigations revealed raised cerebrospinal fluid (CSF) pressure and severe hypoglycorrhachia (low CSF glucose) without pleocytosis. Initial contrast-enhanced brain MRI was normal, but a repeat MRI after a year showed meningeal enhancement with mild communicating hydrocephalus.
View Article and Find Full Text PDFMissense mutation of NRAS is associated with malignant progression in neurocutaneous melanosis.
Acta Neuropathol Commun
January 2024
Department of Neurosurgery, Brain Research Institute, Niigata University, 1-757 Asahimachi, Chuo-ku, 951-8585, Niigata, Japan.
Neurocutaneous melanosis (NCM) is a rare congenital neurocutaneous syndrome characterized by congenital melanocytic nevus of skin and abnormal proliferation of leptomeningeal melanocytes. Early acquisition of post-zygotic somatic mutations has been postulated to underlie the pathogenesis of NCM. The pathogenesis of NCM remains to be fully elucidated, and treatment options have not been established.
View Article and Find Full Text PDFWant 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!