{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,5]],"date-time":"2026-09-05T15:57:33Z","timestamp":1788623853863,"version":"build-2803163510"},"reference-count":6,"publisher":"Oceanside Publications Inc.","issue":"6","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["allergy asthma proc"],"published-print":{"date-parts":[[2025,11,1]]},"abstract":"<jats:p>We present the case of a 9-year-old girl with a medical history of growth hormone deficiency, Hashimoto\u2019s thyroiditis, failure to thrive, and eosinophilic colitis, and with a new progressive rash. The rash began as erythematous, pruritic papules, which gradually spread and evolved\n into larger, well-circumscribed plaques. Despite treatment with topical corticosteroids and broad antifungal therapy, the rash persisted without improvement. The patient reported no systemic symptoms. On examination, she was well appearing and afebrile, with normal vital signs. Dermatologic\n findings included erythematous, pruritic plaques on the abdomen, perioral area, and lower extremities. No lymphadenopathy or other abnormalities were noted. After a more thorough evaluation, an unexpected diagnosis was made. This case highlights the clinical challenge of diagnosing dermatologic\n conditions in pediatric patients with complex medical histories. Although the presentation was suggestive of atopic dermatitis, the morphology and distribution of the lesions, along with resistance to standard therapy, raised concerns for alternative diagnoses. This case underscores the importance\n of maintaining a broad differential diagnosis when managing chronic or atypical skin eruptions, particularly in patients with multisystem involvement or a history of autoimmune conditions.<\/jats:p>","DOI":"10.2500\/aap.2025.46.250066","type":"journal-article","created":{"date-parts":[[2025,10,29]],"date-time":"2025-10-29T04:32:17Z","timestamp":1761712337000},"page":"512-514","source":"Crossref","is-referenced-by-count":5,"title":["Unmasking the underlying cause: A rash with deeper implications"],"prefix":"10.2500","volume":"46","author":[{"given":"Priyal","family":"Upadhyay","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Juanita","family":"Valdes Camacho","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Adil","family":"Khan","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"David","family":"Kaufman","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"1355","reference":[{"key":"B1","first-page":"20285","article-title":"Novel CARMIL2 loss-of-function variants are associated with pediatric inflammatory bowel disease","volume":"11","author":"Rosa","year":"2021","journal-title":"Sci Rep"},{"key":"B2","doi-asserted-by":"crossref","first-page":"e20220275","DOI":"10.1084\/jem.20220275","article-title":"Human CARMIL2 deficiency underlies a broader immunological and clinical phenotype than CD28 deficiency","volume":"220","author":"L\u00e9vy","year":"2023","journal-title":"J Exp Med"},{"key":"B3","doi-asserted-by":"crossref","first-page":"203","DOI":"10.3389\/fimmu.2018.00203","article-title":"Novel CARMIL2 mutations in patients with variable clinical dermatitis, infections, and combined immunodeficiency","volume":"9","author":"Alazami","year":"2018","journal-title":"Front Immunol"},{"key":"B4","doi-asserted-by":"crossref","first-page":"1004","DOI":"10.1111\/all.15010","article-title":"Evolution and long-term outcomes of combined immunodeficiency due to CARMIL2 deficiency","volume":"77","author":"Kolukisa","year":"2022","journal-title":"Allergy"},{"key":"B5","doi-asserted-by":"crossref","first-page":"884","DOI":"10.3389\/fimmu.2020.00884","article-title":"A novel pathogenic variant in CARMIL2 (RLTPR) causing CARMIL2 deficiency and EBV-associated smooth muscle tumors","volume":"11","author":"Yonkof","year":"2020","journal-title":"Front Immunol"},{"key":"B6","doi-asserted-by":"crossref","first-page":"355","DOI":"10.2500\/aap.2024.45.240051","article-title":"Diagnostic tests for primary immunodeficiency disorders: classic and genetic testing","volume":"45","author":"Klangkalya","year":"2024","journal-title":"Allergy Asthma Proc"}],"container-title":["Allergy and Asthma Proceedings"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.ingentaconnect.com\/content\/ocean\/aap\/2025\/00000046\/00000006\/art00015","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2025,11,1]],"date-time":"2025-11-01T05:22:32Z","timestamp":1761974552000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.ingentaconnect.com\/content\/10.2500\/aap.2025.46.250066"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2025,11,1]]},"references-count":6,"journal-issue":{"issue":"6","published-print":{"date-parts":[[2025,11,1]]}},"alternative-id":["1088-5412(20251101)46:6L.512;1-"],"URL":"https:\/\/doi.org\/10.2500\/aap.2025.46.250066","relation":{},"ISSN":["1088-5412"],"issn-type":[{"value":"1088-5412","type":"print"}],"subject":[],"published":{"date-parts":[[2025,11,1]]}}}