Figure 1.
A large and richly annotated cohort of patients with CD reveals a small subset of cases with a form of CD that does not meet UCD or iMCD criteria. A total of 304 cases with sufficient diagnostic radiologic data underwent preliminary review for categorization by probable subtype. Forty-one cases had insufficient documentation to undergo panel review. The remaining cases were categorized probable UCD (n = 63), probable iMCD (n = 168), and probable CD with an undefined subtype (n = 32). After expert panel review for diagnosis adjudication, 46 UCD, 119 iMCD, and 14 CD-undefined cases were panel confirmed. Cases whose CD diagnosis was panel confirmed were significantly more likely to be classified as UCD or iMCD than as CD-undefined (P = .007). IgG4RD, IgG4 related disease; MIS-C, multisystem inflammatory syndrome in children.

A large and richly annotated cohort of patients with CD reveals a small subset of cases with a form of CD that does not meet UCD or iMCD criteria. A total of 304 cases with sufficient diagnostic radiologic data underwent preliminary review for categorization by probable subtype. Forty-one cases had insufficient documentation to undergo panel review. The remaining cases were categorized probable UCD (n = 63), probable iMCD (n = 168), and probable CD with an undefined subtype (n = 32). After expert panel review for diagnosis adjudication, 46 UCD, 119 iMCD, and 14 CD-undefined cases were panel confirmed. Cases whose CD diagnosis was panel confirmed were significantly more likely to be classified as UCD or iMCD than as CD-undefined (P = .007). IgG4RD, IgG4 related disease; MIS-C, multisystem inflammatory syndrome in children.

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