Key result
Fluoxetine induced a delayed-onset leukocytoclastic vasculitis in a 74-year-old woman seven months after treatment initiation, which resolved upon discontinuation and recurred upon rechallenge.
Case Report (n=1)
This case highlights the potential for delayed-onset, cross-reactive leukocytoclastic vasculitis with SSRIs, which can be successfully managed by switching to an SNRI like venlafaxine.
May prompt vigilance for rare delayed SSRI vasculitis; single case leaves open class effect and switch strategies.
We report a case of leukocytoclastic vasculitis (LCV) in a 74-year-old woman, occurring seven months after the initiation of fluoxetine therapy for generalized anxiety disorder (GAD). The cutaneous lesions resolved upon discontinuation of fluoxetine but recurred promptly upon rechallenge. Notably, subsequent exposure to paroxetine, another selective serotonin reuptake inhibitor (SSRI) previously tolerated by the patient, also elicited a similar but less severe rash, suggesting cross-sensitization. Transition to venlafaxine, a serotonin-norepinephrine reuptake inhibitor (SNRI), led to complete and sustained resolution of the skin lesions. This case highlights three key clinical points: the potential for delayed-onset cutaneous adverse reactions to SSRIs even after months of uneventful treatment; the occurrence of cross-reactive hypersensitivity among SSRIs; and the importance of considering alternative antidepressant classes with distinct pharmacological profiles in patients with SSRI-associated vasculitis.
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Qin et al. (2026) conducted a case report in Generalized anxiety disorder (n=1). Fluoxetine was evaluated on Development of leukocytoclastic vasculitis. Fluoxetine induced a delayed-onset leukocytoclastic vasculitis in a 74-year-old woman seven months after treatment initiation, which resolved upon discontinuation and recurred upon rechallenge.
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