{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,2]],"date-time":"2026-05-02T12:56:23Z","timestamp":1777726583057,"version":"3.51.4"},"reference-count":8,"publisher":"SAGE Publications","issue":"2","license":[{"start":{"date-parts":[[2025,2,1]],"date-time":"2025-02-01T00:00:00Z","timestamp":1738368000000},"content-version":"unspecified","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by-nc\/4.0\/"}],"content-domain":{"domain":["journals.sagepub.com"],"crossmark-restriction":true},"short-container-title":["J Int Med Res"],"published-print":{"date-parts":[[2025,2]]},"abstract":"<jats:p>Inflammatory linear verrucous epidermal nevus (ILVEN) is a rare type of epidermal nevus characterized by an inflammatory appearance, intense pruritus, and a tendency to be resistant to treatment. We present here, the case of a 7-year-old boy who presented with a widespread inflammatory skin lesion on the right side of his body, with some of the eruption following Blaschko\u2019s lines. He also had an associated contracture in the ipsilateral limb and short stature. Initially, we suspected this may be a rare case of CHILD syndrome in a boy. However, after further investigation, we confirmed the diagnosis as a severe form of ILVEN.<\/jats:p>","DOI":"10.1177\/03000605251318201","type":"journal-article","created":{"date-parts":[[2025,2,14]],"date-time":"2025-02-14T23:24:26Z","timestamp":1739575466000},"update-policy":"https:\/\/doi.org\/10.1177\/sage-journals-update-policy","source":"Crossref","is-referenced-by-count":0,"title":["Unilateral widespread inflammatory linear verrucous epidermal nevus with ipsilateral limb contracture along the lines of Blaschko: A case report"],"prefix":"10.1177","volume":"53","author":[{"given":"Wanxing","family":"Zhang","sequence":"first","affiliation":[{"name":"Department of Dermatology, Tianjin Children\u2019s Hospital (Children\u2019s Hospital, Tianjin University), Tianjin Key Laboratory of Birth Defects for Prevention and Treatment, Tianjin, China"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jiao","family":"Ma","sequence":"additional","affiliation":[{"name":"State Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood Diseases, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin, China"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-2339-5466","authenticated-orcid":false,"given":"Shijun","family":"Shan","sequence":"additional","affiliation":[{"name":"Hangzhou Third People\u2019s Hospital, Liangzhu laboratory, Hangzhou, China"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0009-0009-7432-6031","authenticated-orcid":false,"given":"Haihui","family":"Su","sequence":"additional","affiliation":[{"name":"Department of Dermatology, Tianjin Children\u2019s Hospital (Children\u2019s Hospital, Tianjin University), Tianjin Key Laboratory of Birth Defects for Prevention and Treatment, Tianjin, China"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"179","published-online":{"date-parts":[[2025,2,14]]},"reference":[{"key":"bibr1-03000605251318201","doi-asserted-by":"publisher","DOI":"10.1001\/archderm.1971.04000220043008"},{"key":"bibr2-03000605251318201","doi-asserted-by":"publisher","DOI":"10.1016\/j.jid.2021.02.765"},{"key":"bibr3-03000605251318201","volume-title":"CHILD Syndrome. 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