Year: 2024
Type: article
Study design: Case Report
Abstract: Iododerma is a rare halogenoderma resulting from exposure to iodinated compounds. We present a case involving a 51‐year‐old Caucasian female with advanced renal disease who developed a hemorrhagic and papulonodular eruption following oral contrast exposure. Cryptococcoid bodies were noted on histopathological evaluation and raised suspicion for the diagnosis of iododerma, which was ultimately confirmed through serum and urine iodine studies. This case highlights a severe presentation of iododerma with important dermatopathology findings.
Source: JEADV Clinical Practice
DOI: 10.1002/jvc2.588
Authors: S. Subhadarshani, L. E. Flowers, C. Logan, K. E. Spicknall, C. Shaughnessy
Institutions: University of Cincinnati, University of Missouri
Language: English
Subfield: Pharmacology
Field: Medicine
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $2,700
OpenAlex ID: W4404762591