<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>12(6)</volume><submitter>Benesch MGK</submitter><pubmed_abstract>Signet ring cell adenocarcinomas (SRCCs) are a rare histological subtype of adenocarcinomas with a poor prognosis, typically due to advanced disease at diagnosis. A signet ring cell, mimicking its moniker, contains abundant intracytoplasmic mucin that pushes the nucleus to the periphery. In these cancers, this cell feature comprises more than 50% of the tumor. Despite predilection for the gastrointestinal tract, and in particular the stomach, primary SRCCs are also described in other sites, typically in case reports. This literature, however, lacks a standardized overview of the SRCC disease entity. Using a retrospective cohort approach, we summarize the clinicodemographic and mortality outcomes of SRCCs in thirteen primary sites, comprising 95% of all SRCCs in the Surveillance, Epidemiolo</pubmed_abstract><journal>Cancers</journal><pagination>E1544</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7352645</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Epidemiology of Signet Ring Cell Adenocarcinomas.</pubmed_title><pmcid>PMC7352645</pmcid><pubmed_authors>Mathieson A</pubmed_authors><pubmed_authors>Benesch MGK</pubmed_authors></additional><is_claimable>false</is_claimable><name>Epidemiology of Signet Ring Cell Adenocarcinomas.</name><description>Signet ring cell adenocarcinomas (SRCCs) are a rare histological subtype of adenocarcinomas with a poor prognosis, typically due to advanced disease at diagnosis. A signet ring cell, mimicking its moniker, contains abundant intracytoplasmic mucin that pushes the nucleus to the periphery. In these cancers, this cell feature comprises more than 50% of the tumor. Despite predilection for the gastrointestinal tract, and in particular the stomach, primary SRCCs are also described in other sites, typically in case reports. This literature, however, lacks a standardized overview of the SRCC disease entity. Using a retrospective cohort approach, we summarize the clinicodemographic and mortality outcomes of SRCCs in thirteen primary sites, comprising 95% of all SRCCs in the Surveillance, Epidemiolo</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Jun</publication><modification>2025-04-22T19:30:38.302Z</modification><creation>2025-04-06T02:48:50.443Z</creation></dates><accession>S-EPMC7352645</accession><cross_references><pubmed>32545410</pubmed><doi>10.3390/cancers12061544</doi></cross_references></HashMap>