{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Kibbi N"],"funding":["NCI NIH HHS"],"pagination":["417-424"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC10918581"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["160(4)"],"pubmed_abstract":["<h4>Importance</h4>Extramammary Paget disease (EMPD) is a rare, highly recurrent cutaneous malignant neoplasm of unclear origin. EMPD arises most commonly on the vulvar and penoscrotal skin. It is not presently known how anatomic subtype of EMPD affects disease presentation and management.<h4>Objective</h4>To compare demographic and tumor characteristics and treatment approaches for different EMPD subtypes. Recommendations for diagnosis and treatment are presented.<h4>Data sources</h4>MEDLINE, Embase, Web of Science Core Collection, and Cochrane Reviews CENTRAL from December 1, 1990, to October 24, 2022.<h4>Study selection</h4>Articles were excluded if they were not in English, reported fewer than 3 patients, did not specify information by anatomic subtype, or contained no case-level data."],"journal":["JAMA dermatology"],"pubmed_title":["Anatomic Subtype Differences in Extramammary Paget Disease: A Meta-Analysis."],"pmcid":["PMC10918581"],"funding_grant_id":["P30 CA008748"],"pubmed_authors":["Choi JN","Servaes S","Iavazzo C","Kibbi N","Wang JX","Lawrence N","Worley B","Fujisawa Y","Solomon MJ","Aasi SZ","Alam M","Owen JL","Harikumar V","Rossi AM","MacLean AB","Kim JYS","Ross JS","Chandra S","Leitao MM"],"additional_accession":[]},"is_claimable":false,"name":"Anatomic Subtype Differences in Extramammary Paget Disease: A Meta-Analysis.","description":"<h4>Importance</h4>Extramammary Paget disease (EMPD) is a rare, highly recurrent cutaneous malignant neoplasm of unclear origin. EMPD arises most commonly on the vulvar and penoscrotal skin. It is not presently known how anatomic subtype of EMPD affects disease presentation and management.<h4>Objective</h4>To compare demographic and tumor characteristics and treatment approaches for different EMPD subtypes. Recommendations for diagnosis and treatment are presented.<h4>Data sources</h4>MEDLINE, Embase, Web of Science Core Collection, and Cochrane Reviews CENTRAL from December 1, 1990, to October 24, 2022.<h4>Study selection</h4>Articles were excluded if they were not in English, reported fewer than 3 patients, did not specify information by anatomic subtype, or contained no case-level data.","dates":{"release":"2024-01-01T00:00:00Z","publication":"2024 Apr","modification":"2025-04-05T14:39:23.416Z","creation":"2025-04-05T14:39:23.416Z"},"accession":"S-EPMC10918581","cross_references":{"pubmed":["38446447"],"doi":["10.1001/jamadermatol.2024.0001"]}}