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<Article>
<Journal>
				<PublisherName>Shahid Sadoughi University of Medical Sciences</PublisherName>
				<JournalTitle>Journal of Integrated Maternal and Pediatric Care</JournalTitle>
				<Issn>3134-0792</Issn>
				<Volume>7</Volume>
				<Issue>2</Issue>
				<PubDate PubStatus="epublish">
					<Year>2025</Year>
					<Month>10</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Histopathological Spectrum of Duodenal Biopsies in Seropositive Pediatric Celiac Disease: A Retrospective Study from Yazd, Iran</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>58</FirstPage>
			<LastPage>63</LastPage>
			<ELocationID EIdType="pii">452</ELocationID>
			
<ELocationID EIdType="doi">10.18502/wjpn.v7i2.20446</ELocationID>
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Maryam</FirstName>
					<LastName>Vajihinejad</LastName>
<Affiliation>Department of Pathology, School of Medicine, Shahid Sadoughi Hospital, Shahid  Sadoughi University of Medical Sciences, Yazd, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Monireh</FirstName>
					<LastName>Sadri</LastName>
<Affiliation>Department of Pathology, School of Medicine, Shahid Sadoughi Hospital, Shahid  Sadoughi University of Medical Sciences, Yazd, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Saadat</FirstName>
					<LastName>Eslami</LastName>
<Affiliation>Department of Pathology, School of Medicine, Shahid Sadoughi Hospital, Shahid  Sadoughi University of Medical Sciences, Yazd, Iran</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2025</Year>
					<Month>11</Month>
					<Day>11</Day>
				</PubDate>
			</History>
		    <Abstract>Background: Celiac disease (CD) is an immune-mediated enteropathy triggered by gluten, with a global prevalence of approximately 1%. It is strongly associated with HLA-DQ2 and HLA-DQ8 haplotypes. Serological markers, particularly anti-tissue transglutaminase (tTG) immunoglobulin A (IgA), play a pivotal role in screening and diagnosis. This study aimed to evaluate the clinicopathological characteristics of duodenal biopsy specimens from patients with elevated serum tTG IgA levels.Methods: This retrospective cross-sectional study analyzed 213 pediatric patients (age ≤16 years) with elevated anti-tTG IgA levels who underwent duodenal biopsy at Shahid Sadoughi Hospital, Iran (2016-2020). Demographic, clinical, and histopathological data were collected from medical records. Duodenal biopsies were classified using the Marsh-Oberhuber system. Statistical analysis was performed using SPSS version 22.Results: The cohort Included 131 females (61.5%) and 82 males (38.5%), with a mean age of 5.9 years. Abdominal pain (58.7%) and failure to thrive (39%) were the most common clinical manifestations. Histopathological analysis revealed Marsh 3 lesions in 77% of cases (3a: 25.8%, 3b: 39.9%, 3c: 11.3%), while mild changes (Marsh 1-2) were observed in 23%. No significant association was found between Marsh classification and gender (P = 0.36).Conclusion: Elevated anti-tTG IgA levels strongly predict severe mucosal damage in pediatric celiac disease, indicating that serology-based diagnosis could potentially reduce the need for invasive biopsies. Establishing validated antibody thresholds may allow for less invasive diagnostic approaches.                                                                                                                           </Abstract>
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			<Object Type="keyword">
			<Param Name="value">Celiac disease</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">anti-tTG IgA</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Duodenal</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">biopsy</Param>
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			<Object Type="keyword">
			<Param Name="value">Pediatrics</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">histopathology</Param>
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<ArchiveCopySource DocType="pdf">https://jimpc.ssu.ac.ir/article_452_9431c87f273e507e6040fcb07dcb4509.pdf</ArchiveCopySource>
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