{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,2,28]],"date-time":"2026-02-28T22:02:09Z","timestamp":1772316129116,"version":"3.50.1"},"reference-count":13,"publisher":"Springer Science and Business Media LLC","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2026,2,28]]},"DOI":"10.7759\/cureus.104450","type":"journal-article","created":{"date-parts":[[2026,2,28]],"date-time":"2026-02-28T21:37:11Z","timestamp":1772314631000},"source":"Crossref","is-referenced-by-count":0,"title":["Juvenile Xanthogranuloma Mimicking Other Dermal Nodules: A Diagnostic Challenge in an Infant"],"prefix":"10.7759","author":[{"given":"Rashed  A","family":"Alhusaini","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Alsadat","family":"Mosbeh","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Abeer","family":"Albazali","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","reference":[{"key":"ref1","doi-asserted-by":"publisher","DOI":"10.1016\/S0190-9622(97)80207-1","article-title":"Juvenile xanthogranuloma","volume":"36","author":"Hernandez-Martin A","year":"1997","unstructured":"Hernandez-Martin A, Baselga E, Drolet BA, Esterly NB. Juvenile xanthogranuloma. J Am Acad Dermatol. 1997, 36:355-67. 10.1016\/S0190-9622(97)80207-1","journal-title":"J Am Acad Dermatol"},{"key":"ref2","doi-asserted-by":"publisher","DOI":"10.1002\/pbc.20246","article-title":"Uncommon histiocytic disorders: the non-Langerhans cell histiocytoses","volume":"45","author":"Weitzman S","year":"2005","unstructured":"Weitzman S, Jaffe R. Uncommon histiocytic disorders: the non-Langerhans cell histiocytoses. Pediatr Blood Cancer. 2005, 45:256-64. 10.1002\/pbc.20246","journal-title":"Pediatr Blood Cancer"},{"key":"ref3","doi-asserted-by":"publisher","DOI":"10.1097\/01.pas.0000147395.01229.06","article-title":"Juvenile xanthogranuloma in childhood and adolescence: a clinicopathologic study of 129 patients from the kiel pediatric tumor registry","volume":"29","author":"Janssen D","year":"2005","unstructured":"Janssen D, Harms D. Juvenile xanthogranuloma in childhood and adolescence: a clinicopathologic study of 129 patients from the kiel pediatric tumor registry. Am J Surg Pathol. 2005, 29:21-8. 10.1097\/01.pas.0000147395.01229.06","journal-title":"Am J Surg Pathol"},{"key":"ref4","doi-asserted-by":"publisher","DOI":"10.1016\/j.ad.2020.07.004","article-title":"Juvenile xanthogranuloma: an entity with a wide clinical spectrum","volume":"111","author":"Hern\u00e1ndez-San Mart\u00edn MJ","year":"2020","unstructured":"Hern\u00e1ndez-San Mart\u00edn MJ, Vargas-Mora P, Aranibar L. Juvenile xanthogranuloma: an entity with a wide clinical spectrum. Actas Dermosifiliogr (Engl Ed). 2020, 111:725-33. 10.1016\/j.ad.2020.07.004","journal-title":"Actas Dermosifiliogr (Engl Ed)"},{"key":"ref5","doi-asserted-by":"publisher","DOI":"10.1111\/pde.13437","article-title":"Risk of intraocular and other extracutaneous involvement in patients with cutaneous juvenile xanthogranuloma","volume":"35","author":"Samuelov L","year":"2018","unstructured":"Samuelov L, Kinori M, Chamlin SL, et al.. Risk of intraocular and other extracutaneous involvement in patients with cutaneous juvenile xanthogranuloma. Pediatr Dermatol. 2018, 35:329-35. 10.1111\/pde.13437","journal-title":"Pediatr Dermatol"},{"key":"ref6","doi-asserted-by":"publisher","DOI":"10.1016\/0190-9622 (93)70259-v","article-title":"Unusual aspects of juvenile xanthogranuloma","volume":"2","author":"Caputo R","year":"1993","unstructured":"Caputo R, Grimalt R, Gelmetti C, Cottoni F. Unusual aspects of juvenile xanthogranuloma. J Am Acad Dermatol. 1993, 2:868-70. 10.1016\/0190-9622 (93)70259-v","journal-title":"J Am Acad Dermatol"},{"key":"ref7","doi-asserted-by":"publisher","DOI":"10.1182\/blood-2014-05-577825","article-title":"Mutually exclusive recurrent somatic mutations in MAP2K1 and BRAF support a central role for ERK activation in LCH pathogenesis","volume":"124","author":"Chakraborty R","year":"2014","unstructured":"Chakraborty R, Hampton OA, Shen X, et al.. Mutually exclusive recurrent somatic mutations in MAP2K1 and BRAF support a central role for ERK activation in LCH pathogenesis. Blood. 2014, 124:3007-15. 10.1182\/blood-2014-05-577825","journal-title":"Blood"},{"key":"ref8","doi-asserted-by":"publisher","DOI":"10.1111\/j.1600-0560. 1995.tb01415.x","article-title":"Juvenile xanthogranuloma: a clinical, histopathologic and immunohistochemical study","volume":"1995","author":"Sang\u00fceza OP","year":"1995","unstructured":"Sang\u00fceza OP, Salmon JK, White Jr CR, Beckstead JH. Juvenile xanthogranuloma: a clinical, histopathologic and immunohistochemical study. J Cutan Pathol. 1995, 1995:327-35. 10.1111\/j.1600-0560. 1995.tb01415.x","journal-title":"J Cutan Pathol"},{"key":"ref9","doi-asserted-by":"publisher","DOI":"10.1097\/00000478-200305000-00003","article-title":"Juvenile xanthogranulomas in the first two decades of life: a clinicopathologic study of 174 cases with cutaneous and extracutaneous manifestations","volume":"27","author":"Dehner LP","year":"2003","unstructured":"Dehner LP. Juvenile xanthogranulomas in the first two decades of life: a clinicopathologic study of 174 cases with cutaneous and extracutaneous manifestations. Am J Surg Pathol. 2003, 27:579-93. 10.1097\/00000478-200305000-00003","journal-title":"Am J Surg Pathol"},{"key":"ref10","doi-asserted-by":"publisher","DOI":"10.29333\/ejgm\/82897","article-title":"Juvenile nasopharyngeal angiofibroma","volume":"7","author":"Garca MF","year":"2010","unstructured":"Garca MF, Ari Yuca S, Yuca K. Juvenile nasopharyngeal angiofibroma. Eur J Gen Med. 2010, 7:419-25. 10.29333\/ejgm\/82897","journal-title":"Eur J Gen Med"},{"key":"ref11","doi-asserted-by":"publisher","DOI":"10.29333\/ejgm\/82225","article-title":"Juvenile granulosa cell tumor and high blood Ca-125 levels in children with Pseudo-Meigs syndrome","volume":"10","author":"Ciftci I","year":"2013","unstructured":"Ciftci I, Pirgon MO, Unlu Y. Juvenile granulosa cell tumor and high blood Ca-125 levels in children with Pseudo-Meigs syndrome. Eur J Gen Med. 2013, 10:239-42. 10.29333\/ejgm\/82225","journal-title":"Eur J Gen Med"},{"key":"ref12","doi-asserted-by":"publisher","DOI":"10.1016\/j.jaad.2006.06.010","article-title":"Aggressive histiocytic disorders that can involve the skin","volume":"56","author":"Newman B","year":"2007","unstructured":"Newman B, Hu W, Nigro K, Gilliam AC. Aggressive histiocytic disorders that can involve the skin. J Am Acad Dermatol. 2007, 56:302-16. 10.1016\/j.jaad.2006.06.010","journal-title":"J Am Acad Dermatol"},{"key":"ref13","doi-asserted-by":"publisher","DOI":"10.29333\/ejgm\/12029","article-title":"Juvenile xanthogranuloma: a case report and literature review","volume":"19","author":"Yusnita Y","year":"2022","unstructured":"Yusnita Y, Muhammad J, Ahmad I, Kew CH, Teoh PY, Hamzah NH. Juvenile xanthogranuloma: a case report and literature review. Electron J Gen Med. 2022, 19:em380. 10.29333\/ejgm\/12029","journal-title":"Electron J Gen Med"}],"container-title":["Cureus"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.cureus.com\/articles\/439857-juvenile-xanthogranuloma-mimicking-other-dermal-nodules-a-diagnostic-challenge-in-an-infant","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2026,2,28]],"date-time":"2026-02-28T21:37:12Z","timestamp":1772314632000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.cureus.com\/articles\/439857-juvenile-xanthogranuloma-mimicking-other-dermal-nodules-a-diagnostic-challenge-in-an-infant"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2026,2,28]]},"references-count":13,"URL":"https:\/\/doi.org\/10.7759\/cureus.104450","relation":{},"ISSN":["2168-8184"],"issn-type":[{"value":"2168-8184","type":"print"}],"subject":[],"published":{"date-parts":[[2026,2,28]]}}}