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<!DOCTYPE ArticleSet PUBLIC "-//NLM//DTD PubMed 2.7//EN" "https://dtd.nlm.nih.gov/ncbi/pubmed/in/PubMed.dtd">
<ArticleSet>
<Article>
<Journal>
				<PublisherName></PublisherName>
				<JournalTitle>Journal of Education and Health Promotion</JournalTitle>
				<Issn>2277-9531</Issn>
				<Volume>7</Volume>
				<Issue>3</Issue>
				<PubDate PubStatus="epublish">
					<Year>2017</Year>
					<Month>06</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Cytologic diagnosis of atypical teratoid rhabdoid tumor based on touch imprint study: Report of a case with review of literature</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>1</FirstPage>
			<LastPage>4</LastPage>
			<ELocationID EIdType="pii">26528</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>.</FirstName>
					<LastName>Mansoureh Shokripour</LastName>
<Affiliation>Department of Pathology,
School of Medicine, Shiraz
University of Medical
Sciences,</Affiliation>

</Author>
<Author>
					<FirstName>.</FirstName>
					<LastName>Negar Azarpira</LastName>
<Affiliation>Transplant
Research Centre, Shiraz
University of Medical
Sciences</Affiliation>

</Author>
<Author>
					<FirstName>.</FirstName>
					<LastName>Navid Omidifar</LastName>
<Affiliation>Department of Pathology,
School of Medicine, Shiraz
University of Medical
Sciences
Clinical
Education Center, Shiraz
University of Medical
Sciences, Shiraz, Iran</Affiliation>

</Author>
<Author>
					<FirstName>.</FirstName>
					<LastName>Bita Paknia</LastName>
<Affiliation>Department of Pathology,
School of Medicine, Shiraz
University of Medical
Sciences</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2023</Year>
					<Month>01</Month>
					<Day>23</Day>
				</PubDate>
			</History>
		<Abstract>Atypical teratoid rhabdoid tumor (ATRT) is a rare malignant tumor with gloom destiny. Our case was&lt;br /&gt;a 4‑year‑old boy with a temporal lobe tumor that was then became evident of ATRT with recurrent&lt;br /&gt;happening. In a retrospective review of all cytologic slides, we found unique rhabdoid cells that are&lt;br /&gt;morphologically evident cells for ATRT in both times. Unfortunately, the cells were overlooked at the&lt;br /&gt;first time. We conclude if the pathologist is experienced to see rhabdoid cells noticing these cells is&lt;br /&gt;highly helpful for diagnosis ATRT, especially in frozen sectioning.&lt;br /&gt;&lt;br /&gt;</Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Atypical teratoid rhabdoid tumor</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Cytology</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">diagnosis </Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://jehp.mui.ac.ir/article_26528_2b12a84466d35eee6f84649d1c0ac8a5.pdf</ArchiveCopySource>
</Article>
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