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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>6</Volume>
				<Issue>3(summer)</Issue>
				<PubDate PubStatus="epublish">
					<Year>2007</Year>
					<Month>10</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Generalized Lymphadenopathy: A Case Report of Rosai-Dorfman Disease</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>65</FirstPage>
			<LastPage>67</LastPage>
			<ELocationID EIdType="pii">242263</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Soheila</FirstName>
					<LastName>Khalilzadeh</LastName>
<Affiliation>Department of Pediatrics,</Affiliation>

</Author>
<Author>
					<FirstName>Shirin</FirstName>
					<LastName>Karimi</LastName>

						<AffiliationInfo>
						<Affiliation>Department of Clinical Anatomical Pathology,</Affiliation>
						</AffiliationInfo>

						<AffiliationInfo>
						<Affiliation>Mycobateriology Research Center,</Affiliation>
						</AffiliationInfo>

</Author>
<Author>
					<FirstName>Atefeh</FirstName>
					<LastName>Fakharian</LastName>
<Affiliation>Department of Internal
Medicine, NRITLD, Shahid Beheshti University, M.C., TEHRAN-IRAN.</Affiliation>

</Author>
<Author>
					<FirstName>Seyed Shahin</FirstName>
					<LastName>Hakimi</LastName>
<Affiliation>Department of Pediatrics,</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2021</Year>
					<Month>02</Month>
					<Day>12</Day>
				</PubDate>
			</History>
		<Abstract>Sinus histiocytosis with massive lymphadenopathy (SHML), Rosai-Dorfman Disease, is a rare histiocytic syndrome first described by Rosai and Dorfman, seen predominantly in childhood and early adulthood. Even though it is considered a benign disease, fatalities may occur due to cellular infiltrates of SHML. We report a 16–year–old boy with signs of polydypsia, polyuria, weight loss and generalized lymphadenopathy. He had been receiving corticosteroid following the diagnosis of histiocytosis X. Due to hyperglycemia, the patient was admitted with the primary diagnosis of diabetic ketoacidosis and medications were initiated. All paraclinical and immunologic examinations were negative. Axillary lymph node biopsy revealed the diagnosis of Rosai–Dorfman disease. (Tanaffos 2007; 6(3): 65-67)</Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Rosai–Dorfman disease</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Diabetes Mellitus</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">histiocytosis X</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Children</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://www.tanaffosjournal.ir/article_242263_982ac964c46d41c125f5e359b74a6373.pdf</ArchiveCopySource>
</Article>
</ArticleSet>
