<?xml version="1.0" encoding="UTF-8"?> <!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.2d1 20170631//EN" "JATS-journalpublishing1.dtd"> <ArticleSet> <Article> <Journal> <PublisherName>journal-jmsr</PublisherName> <JournalTitle>Journal of Medical and Surgical Research</JournalTitle> <PISSN>I</PISSN> <EISSN>S</EISSN> <Volume-Issue>Vol. III, n 2</Volume-Issue> <PartNumber/> <IssueTopic>Multidisciplinary</IssueTopic> <IssueLanguage>English</IssueLanguage> <Season>December 2016</Season> <SpecialIssue>N</SpecialIssue> <SupplementaryIssue>N</SupplementaryIssue> <IssueOA>Y</IssueOA> <PubDate> <Year>-0001</Year> <Month>11</Month> <Day>30</Day> </PubDate> <ArticleType>JMSR Oncology</ArticleType> <ArticleTitle>Juvenile Granulosa Cell Tumor: a Neo-natal Revelation.</ArticleTitle> <SubTitle/> <ArticleLanguage>English</ArticleLanguage> <ArticleOA>Y</ArticleOA> <FirstPage>258</FirstPage> <LastPage>260</LastPage> <AuthorList> <Author> <FirstName>Aboubacar Sidiky</FirstName> <LastName>N'DIAYE</LastName> <AuthorLanguage>English</AuthorLanguage> <Affiliation/> <CorrespondingAuthor>N</CorrespondingAuthor> <ORCID/> <FirstName>Yahdi</FirstName> <LastName>Viche</LastName> <AuthorLanguage>English</AuthorLanguage> <Affiliation/> <CorrespondingAuthor>Y</CorrespondingAuthor> <ORCID/> <FirstName>Nadia</FirstName> <LastName>Cherradi</LastName> <AuthorLanguage>English</AuthorLanguage> <Affiliation/> <CorrespondingAuthor>Y</CorrespondingAuthor> <ORCID/> <FirstName>Rachida</FirstName> <LastName>Dafiri</LastName> <AuthorLanguage>English</AuthorLanguage> <Affiliation/> <CorrespondingAuthor>Y</CorrespondingAuthor> <ORCID/> </Author> </AuthorList> <DOI/> <Abstract>The juvenile granulosa cell tumors of the ovary tumors belong to the group of stroma and sex cord tumors. These are rare tumors representing 1 - 2% of ovarian tumors. These tumors are involved in ovarian hormone function, responsible for the synthesis of hormones (estrogen, corticosteroids), which explains the hormonal dysfunctions associated with these cancers. The juvenile granulosa cell tumors occur in older children, usually before the age of 20 years old, with a maximum frequency in pre puberty. We report an exceptional case of a granulosa tumor in a four- month infant</Abstract> <AbstractLanguage>English</AbstractLanguage> <Keywords>Juvenile Granulosa Cell Tumors, Neo-natal, Tomodensitometry, Immunohistochemistry.</Keywords> <URLs> <Abstract>https://journal-jmsr.net/ubijournal-v1copy/journals/abstract.php?article_id=4787&title=Juvenile Granulosa Cell Tumor: a Neo-natal Revelation.</Abstract> </URLs> <References> <ReferencesarticleTitle>References</ReferencesarticleTitle> <ReferencesfirstPage>16</ReferencesfirstPage> <ReferenceslastPage>19</ReferenceslastPage> <References/> </References> </Journal> </Article> </ArticleSet>