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Drug-induced phospholipidosis of the kidney suspected to be caused by atomoxetine

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dc.contributor.authorChoi, Sung-Eun-
dc.contributor.authorKim, Kee Hyuck-
dc.contributor.authorJung, Minsun-
dc.contributor.authorKie, Jeong Hae-
dc.date.accessioned2026-01-29T07:41:30Z-
dc.date.available2026-01-29T07:41:30Z-
dc.date.created2026-01-28-
dc.date.issued2026-01-
dc.identifier.issn2383-7837-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/210371-
dc.description.abstractFabry disease and drug-induced phospholipidosis (DIP) both exhibit zebra bodies on electron microscopy, complicating differential diagnosis. A 17-year-old male with microscopic hematuria and proteinuria had received atomoxetine (40 mg) for 11 months to treat attention-deficit hyperactivity disorder. Light microscopy showed one glomerulus with perihilar sclerosis and periglomerular fibrosis. Kidney biopsy revealed zebra bodies in podocytes, initially suggesting Fabry disease. However, alpha-galactosidase A enzyme activity was normal on tandem mass spectrometry. Next-generation sequencing of GLA identified only three benign variants. This represents the first reported case of atomoxetine-induced DIP. When zebra bodies are observed, clinicians should consider DIP caused by cationic amphiphilic drugs alongside Fabry disease. Atomoxetine meets the structural criteria for inducing DIP, and awareness of this potential complication is essential.-
dc.languageEnglish-
dc.publisherThe Korean Society of Pathologists-
dc.relation.isPartOfJOURNAL OF PATHOLOGY AND TRANSLATIONAL MEDICINE-
dc.relation.isPartOfJOURNAL OF PATHOLOGY AND TRANSLATIONAL MEDICINE-
dc.titleDrug-induced phospholipidosis of the kidney suspected to be caused by atomoxetine-
dc.typeArticle-
dc.contributor.googleauthorChoi, Sung-Eun-
dc.contributor.googleauthorKim, Kee Hyuck-
dc.contributor.googleauthorJung, Minsun-
dc.contributor.googleauthorKie, Jeong Hae-
dc.identifier.doi10.4132/jptm.2025.12.10-
dc.relation.journalcodeJ01680-
dc.identifier.eissn2383-7845-
dc.identifier.pmid41531328-
dc.subject.keywordLysosomal storage diseases-
dc.subject.keywordFabry disease-
dc.subject.keywordPodocytes-
dc.subject.keywordBiopsy-
dc.subject.keywordAtomoxetine hydrochloride-
dc.contributor.affiliatedAuthorJung, Minsun-
dc.identifier.wosid001658583000001-
dc.citation.volume60-
dc.citation.number1-
dc.citation.startPage124-
dc.citation.endPage128-
dc.identifier.bibliographicCitationJOURNAL OF PATHOLOGY AND TRANSLATIONAL MEDICINE, Vol.60(1) : 124-128, 2026-01-
dc.identifier.rimsid91376-
dc.type.rimsART-
dc.description.journalClass2-
dc.description.journalClass2-
dc.subject.keywordAuthorLysosomal storage diseases-
dc.subject.keywordAuthorFabry disease-
dc.subject.keywordAuthorPodocytes-
dc.subject.keywordAuthorBiopsy-
dc.subject.keywordAuthorAtomoxetine hydrochloride-
dc.subject.keywordPlusRENAL PHOSPHOLIPIDOSIS-
dc.subject.keywordPlusFABRY-DISEASE-
dc.type.docTypeArticle; Early Access-
dc.identifier.kciidART003296594-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClasskci-
dc.relation.journalWebOfScienceCategoryPathology-
dc.relation.journalResearchAreaPathology-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Pathology (병리학교실) > 1. Journal Papers

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