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<article xlink="http://www.w3.org/1999/xlink" dtd-version="1.0"><Article><Journal><PublisherName>yemenjmed</PublisherName><JournalTitle>Yemen Journal of Medicine</JournalTitle><PISSN>c</PISSN><EISSN>o</EISSN><Volume-Issue>Volume 2 Issue 2  </Volume-Issue><IssueTopic>Multidisciplinary</IssueTopic><IssueLanguage>English</IssueLanguage><Season>May-August 2023</Season><SpecialIssue>N</SpecialIssue><SupplementaryIssue>N</SupplementaryIssue><IssueOA>Y</IssueOA><PubDate><Year>2023</Year><Month>09</Month><Day>28</Day></PubDate><ArticleType>Article</ArticleType><ArticleTitle>A rare case of childhood interstitial lung disease attributed to desquamative interstitial pneumonia</ArticleTitle><SubTitle/><ArticleLanguage>English</ArticleLanguage><ArticleOA>Y</ArticleOA><FirstPage>112</FirstPage><LastPage>114</LastPage><AuthorList><Author><FirstName>Samiksha</FirstName><LastName>Kamble1</LastName><AuthorLanguage>English</AuthorLanguage><Affiliation/><CorrespondingAuthor>N</CorrespondingAuthor><ORCID/><FirstName>Ketaki</FirstName><LastName>Utpat2</LastName><AuthorLanguage>English</AuthorLanguage><Affiliation/><CorrespondingAuthor>Y</CorrespondingAuthor><ORCID/><FirstName>Gayathri</FirstName><LastName>Amonkar3</LastName><AuthorLanguage>English</AuthorLanguage><Affiliation/><CorrespondingAuthor>Y</CorrespondingAuthor><ORCID/><FirstName>Unnati</FirstName><LastName>Desai2</LastName><AuthorLanguage>English</AuthorLanguage><Affiliation/><CorrespondingAuthor>Y</CorrespondingAuthor><ORCID/></Author></AuthorList><DOI>10.32677/yjm.v2i2.4098</DOI><Abstract>Desquamative interstitial pneumonia is a rare form of interstitial lung disease in children that can be idiopathic but is usually associated with an inborn error of surfactant metabolism. We reported DIP in a thirteen-year-old girl who was referred to our outpatient clinic because of worsening dyspnoea. High-resolution computed tomography showed ground-glass attenuation with honeycombing and intralobular, interstitial septal thickening suggestive of an interstitial lung disease. Transbronchial lung biopsy was performed and histopathology findings were consistent with desquamative interstitial pneumonia. The patient was started on steroid therapy with oxygen support. Unfortunately, she died a month after being diagnosed due to disease progression.</Abstract><AbstractLanguage>English</AbstractLanguage><Keywords>Child interstitial lung disease, Desquamative interstitial pneumonia, Transbronchial lung biopsy</Keywords><URLs><Abstract>https://yemenjmed.com/admin/abstract?id=67</Abstract></URLs><References><ReferencesarticleTitle>References</ReferencesarticleTitle><ReferencesfirstPage>16</ReferencesfirstPage><ReferenceslastPage>19</ReferenceslastPage><References>Clement A, Nathan N, Epaud R, et al. Interstitial lung diseases in children. Orphanet J Rare Dis 2010; 20(5): 1-24.Dinwiddie R, Sharief N, Crawford O. Idiopathic interstitial pneumonitis in children: a national survey in the United Kingdom and Ireland. Pediatr Pulmonol 2002; 34(1):23-9.Fan LL, Kozinetz CA. Factors influencing survival in children with chronic interstitial lung disease. Am J Respir Crit Care Med 1997;156:939-42.Kitazawa H, Kure S. 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