<?xml version="1.0" encoding="UTF-8"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-10-23T22:58:01Z</responseDate><request verb="GetRecord" identifier="oai:gumushane-rdlopen.rawdatalibrary.net:gumushane/16138" metadataPrefix="oai_dc">https://gumushane-rdlopen.rawdatalibrary.net/oai/request</request><GetRecord><record><header><identifier>oai:gumushane-rdlopen.rawdatalibrary.net:gumushane/16138</identifier><datestamp>2026-10-23T18:25:57Z</datestamp><setSpec>openaire</setSpec><setSpec>driver</setSpec><setSpec>com_gumushane_10000</setSpec><setSpec>col_gumushane_10001</setSpec></header><metadata><oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd"><dc:title>DIAGNOSTIC CHALLENGE OF PRIMARY COLONIC POORLY COHESIVE ADENOCARCINOMA EXHIBITING GASTRIC-TYPE IMMUNOHISTOCHEMISTRY PROFILE AND FOCAL SIGNET-RING DIFFERENTIATION</dc:title><dc:creator>ISSiN, Gizem</dc:creator><dc:creator>Tok, Merve</dc:creator><dc:creator>ÇAgATAY, Diren Vuslat</dc:creator><dc:creator>Gökçe, Oruc Numan</dc:creator><dc:creator>Aytekin, Faruk Onder</dc:creator><dc:subject>primary colonic poorly cohesive adenocarcinoma</dc:subject><dc:subject>gastric-type immunophenotype</dc:subject><dc:subject>signet-ring cell differentiation</dc:subject><dc:subject>MLH1/PMS2 deficiency</dc:subject><dc:subject>PD-L1 expression</dc:subject><dc:description>Colorectal adenocarcinoma infrequently exhibits a diffuse, poorly cohesive architecture and a gastric-type immunophenotype, closely resembling diffuse-type gastric carcinoma and posing a formidable diagnostic challenge. This report describes a 65-year-old woman who presented with non-specific abdominal discomfort and was found by colonoscopy to have a 6.5 cm ulceroinfiltrative lesion in the hepatic flexure. Histologically, the tumor comprised discohesive cells with focal signet-ring morphology, accompanied by extensive lymphovascular and perineural invasion, necrosis, and a marked peritumoral lymphoid response. Immunohistochemical analysis demonstrated a gastric-type profile (CK7+, CK20-, SATB2-, CDX2 weak/focal, MUC5AC+, MUC2-), whereas panels excluding breast, urothelial, M &amp; uuml;llerian, neuroendocrine, and hematolymphoid differentiation were uniformly negative. Comprehensive imaging and endoscopic evaluation excluded an extra-colonic primary malignancy/ carcinoma. Mismatch repair testing revealed loss of MLH1/PMS2 expression with preserved MSH2/MSH6. This case underscores that, in such uncommon colorectal variants, reliance on immunophenotype alone may mislead, and that definitive diagnosis necessitates integrated clinicopathologic correlation, exhaustive sampling, and exclusion of alternative primaries/primary malignancies/carcinomas to confirm a primary colonic poorly cohesive adenocarcinoma with focal signet-ring differentiation.</dc:description><dc:publisher>VESALIUS UNIV MEDICAL PUBL</dc:publisher><dc:date>2025</dc:date><dc:type>Article</dc:type><dc:identifier>https://rdlopen.rawdatalibrary.net/r/gumushane/16138</dc:identifier><dc:identifier>https://doi.org/10.5114/pjp.2025.159280</dc:identifier><dc:identifier>1233-9687</dc:identifier><dc:language>en</dc:language><dc:relation>POLISH JOURNAL OF PATHOLOGY</dc:relation><dc:rights>info:eu-repo/semantics/openAccess</dc:rights><dc:type>info:eu-repo/semantics/article</dc:type><dc:identifier>https://gumushane-rdlopen.rawdatalibrary.net/tr/items/gumushane/16138</dc:identifier></oai_dc:dc></metadata></record></GetRecord></OAI-PMH>