<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><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>2026-04-18T18:21:04Z</responseDate><request verb="GetRecord" identifier="oai:riubu.ubu.es:10259/10135" metadataPrefix="marc">https://riubu.ubu.es/oai/request</request><GetRecord><record><header><identifier>oai:riubu.ubu.es:10259/10135</identifier><datestamp>2025-02-01T01:05:44Z</datestamp><setSpec>com_10259_6688</setSpec><setSpec>com_10259_5086</setSpec><setSpec>com_10259_2604</setSpec><setSpec>col_10259_6689</setSpec></header><metadata><record xmlns="http://www.loc.gov/MARC21/slim" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dcterms="http://purl.org/dc/terms/" xsi:schemaLocation="http://www.loc.gov/MARC21/slim http://www.loc.gov/standards/marcxml/schema/MARC21slim.xsd">
<leader>00925njm 22002777a 4500</leader>
<datafield tag="042" ind1=" " ind2=" ">
<subfield code="a">dc</subfield>
</datafield>
<datafield tag="720" ind1=" " ind2=" ">
<subfield code="a">Reoyo Pascual, José Felipe</subfield>
<subfield code="e">author</subfield>
</datafield>
<datafield tag="720" ind1=" " ind2=" ">
<subfield code="a">Alonso Alonso, Evelio</subfield>
<subfield code="e">author</subfield>
</datafield>
<datafield tag="720" ind1=" " ind2=" ">
<subfield code="a">Polanco Pérez, Lucía</subfield>
<subfield code="e">author</subfield>
</datafield>
<datafield tag="720" ind1=" " ind2=" ">
<subfield code="a">Álvarez Rico, Miguel Ángel</subfield>
<subfield code="e">author</subfield>
</datafield>
<datafield tag="260" ind1=" " ind2=" ">
<subfield code="c">2024-12</subfield>
</datafield>
<datafield tag="520" ind1=" " ind2=" ">
<subfield code="a">Retrorectal cystic hamartoma (also known as tailgut cyst) is a congenital lesion that originates from debris from the embryonic caudal intestine. Incidentally diagnosed in more than half of cases, the treatment of choice is surgical resection. It is a very rare pathology whose oncological transformation constitutes a true pathological rarity.</subfield>
</datafield>
<datafield tag="024" ind2=" " ind1="8">
<subfield code="a">0093-7754</subfield>
</datafield>
<datafield tag="024" ind2=" " ind1="8">
<subfield code="a">http://hdl.handle.net/10259/10135</subfield>
</datafield>
<datafield tag="024" ind2=" " ind1="8">
<subfield code="a">10.1053/j.seminoncol.2024.10.003</subfield>
</datafield>
<datafield ind1=" " ind2=" " tag="653">
<subfield code="a">Hamartoma</subfield>
</datafield>
<datafield ind1=" " ind2=" " tag="653">
<subfield code="a">Retrorrectal</subfield>
</datafield>
<datafield ind1=" " ind2=" " tag="653">
<subfield code="a">Adenocarcinoma</subfield>
</datafield>
<datafield tag="245" ind1="0" ind2="0">
<subfield code="a">Adenocarcinoma on retrorectal cystic hamartoma: An illustrative image for a very rare diagnosis</subfield>
</datafield>
</record></metadata></record></GetRecord></OAI-PMH>