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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>National Research Institute of Tuberculosis and Lung Disease (NRITLD), Shahid Beheshti University of Medical Sciences, Tehran, Iran</PublisherName>
				<JournalTitle>TANAFFOS (Respiration)</JournalTitle>
				<Issn>1735-0344</Issn>
				<Volume>1</Volume>
				<Issue>3(summer)</Issue>
				<PubDate PubStatus="epublish">
					<Year>2002</Year>
					<Month>10</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Infantile Histiocytosis X: Case Report</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>57</FirstPage>
			<LastPage>61</LastPage>
			<ELocationID EIdType="pii">241574</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Mohammad Reza</FirstName>
					<LastName>Boloorsaz</LastName>
<Affiliation>Department of Pediatrics,</Affiliation>

</Author>
<Author>
					<FirstName>Abbas</FirstName>
					<LastName>Mir-Afsharieh</LastName>
<Affiliation>Department of Clinical Anatomical Pathology</Affiliation>

</Author>
<Author>
					<FirstName>Kian</FirstName>
					<LastName>Khodadad</LastName>
<Affiliation>Oncology Unit, NRITLD, Shaheed Beheshti University of
Medical Sciences and Health Services, TEHRAN-IRAN</Affiliation>

</Author>
<Author>
					<FirstName>Makan</FirstName>
					<LastName>Sadr</LastName>
<Affiliation>Department of Pediatrics,</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2021</Year>
					<Month>01</Month>
					<Day>07</Day>
				</PubDate>
			</History>
		<Abstract>Langerhans cell histiocytosis (LCH) is a disease of unknown etiology that presents in three forms: Letterer- Siwe disease, Hand-Schuller-Christian disease, and Eosinophilic Granuloma. It is a multifocal disease that usually affects several organs and unifocal forms are rare. Pulmonary involvement occurs in approximately 40% of cases and almost always in young adults. Lungs are rarely affected in infant patients. This report presents a 15-month-old male infant that was admitted for cyanosis and respiratory distress. Diagnostic work up revealed a primary pulmonary histiocytosis and the treatment made a significant improvement of signs and symptoms by the time of discharge. (Tanaffos 2002; 1(3): 57-61)</Abstract>
<ArchiveCopySource DocType="pdf">https://www.tanaffosjournal.ir/article_241574_ab4f4c5e769789dcc4228bdacdfecdc6.pdf</ArchiveCopySource>
</Article>
</ArticleSet>
