<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>15</volume><submitter>Tang M</submitter><pubmed_abstract>&lt;h4>Objective&lt;/h4>To investigate the clinicopathological features, and mutations of NRAS, KRAS, BRAF and MAP2K1 genes in extranodal Rosai-Dorfman disease (RDD).&lt;h4>Methods&lt;/h4>The clinic opathological features of 27 patients with extranodal RDD were retrospectively analyzed, and the NRAS, KRAS, BRAF and MAP2K1 genes mutation were detected by Sanger sequencing.&lt;h4>Results&lt;/h4>The male to female ratio was 1.7:1. The average age was 46.9 years. There were skin lesions in 12 cases (44.4%) and head and neck lesions in 8 cases (29.6%). Microscopically, those patients with skin RDD had lesions characterized by clear and dark intervals and obvious emperipolesis, while in other parts, the background was more complex. About 21.1% (4/19) had mutations, including 3 mutations in NRAS 2 exon and 1 mutat</pubmed_abstract><journal>Journal of inflammation research</journal><pagination>2775-2787</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9064053</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Clinicopathological and Gene Mutation Analysis of 27 Cases with Extranodal Rosai-Dorfman Disease.</pubmed_title><pmcid>PMC9064053</pmcid><pubmed_authors>Tang M</pubmed_authors><pubmed_authors>Yang XT</pubmed_authors><pubmed_authors>Gu XZ</pubmed_authors><pubmed_authors>Wu PC</pubmed_authors></additional><is_claimable>false</is_claimable><name>Clinicopathological and Gene Mutation Analysis of 27 Cases with Extranodal Rosai-Dorfman Disease.</name><description>&lt;h4>Objective&lt;/h4>To investigate the clinicopathological features, and mutations of NRAS, KRAS, BRAF and MAP2K1 genes in extranodal Rosai-Dorfman disease (RDD).&lt;h4>Methods&lt;/h4>The clinic opathological features of 27 patients with extranodal RDD were retrospectively analyzed, and the NRAS, KRAS, BRAF and MAP2K1 genes mutation were detected by Sanger sequencing.&lt;h4>Results&lt;/h4>The male to female ratio was 1.7:1. The average age was 46.9 years. There were skin lesions in 12 cases (44.4%) and head and neck lesions in 8 cases (29.6%). Microscopically, those patients with skin RDD had lesions characterized by clear and dark intervals and obvious emperipolesis, while in other parts, the background was more complex. About 21.1% (4/19) had mutations, including 3 mutations in NRAS 2 exon and 1 mutat</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2025-05-18T12:05:28.321Z</modification><creation>2025-04-05T20:38:56.561Z</creation></dates><accession>S-EPMC9064053</accession><cross_references><pubmed>35518839</pubmed><doi>10.2147/JIR.S365098</doi></cross_references></HashMap>