Section 3 of 4
Discussion
Dhiren R. Rajagopal, Dipti Anand, and Melissa D. Babcock · about 2 minutes
Herpes zoster reactivation following intra-articular corticosteroid injection is uncommon, and cutaneous small-vessel vasculitis represents a rare manifestation of VZV infection. Although each has been described independently, to our knowledge, their coexistence following intra-articular corticosteroid administration in an immunocompetent patient has not been previously reported.
A potential explanation for herpes zoster reactivation in our patient is the immunomodulatory effect of corticosteroids. Despite their localized administration, intra-articular corticosteroid injections can produce systemic effects,8 including transient suppression of T-cell-mediated immunity and cytokine signaling, thereby facilitating reactivation of latent VZV, even in otherwise immunocompetent individuals. The absolute risk of herpes zoster, however, remains low among otherwise healthy individuals receiving corticosteroids. For example, a large population-based cohort study demonstrated an incidence of approximately 15 cases per 1000 person-years among healthy patients receiving systemic corticosteroids.3 Consistent with this, reports of herpes zoster following intra-articular corticosteroid injection are exceedingly limited. To our knowledge, only 2 such cases have been described in the literature: 1 case of localized herpes zoster following intra-articular knee injection in an 80-year-old man with multiple comorbidities, and 1 case of Ramsay Hunt syndrome after bilateral intra-articular knee injections in a 55-year-old woman without significant comorbidities.4,5
Our findings also suggest that localized trauma may represent an additional contributing factor. Consistent with this, a large case–control study of over 80,000 Medicare beneficiaries demonstrated that recent physical trauma was associated with 3.4-fold higher odds of herpes zoster, with even stronger associations observed following cranial trauma (25-fold higher odds).9 Local trauma may play a role in viral reactivation through stimulation of sensory nerves with subsequent reactivation within the corresponding dorsal root ganglion, coupled with localized immune dysregulation.
In addition to trauma-related triggers, host immune status may influence the severity and clinical manifestations of VZV infection. In 1 case series of 5 patients with VZV-associated segmental leukocytoclastic vasculitis, four were immunocompromised (including patients with sarcoidosis, mycosis fungoides, and glomerular disease), and notably, 4 cases demonstrated involvement of the lower extremities, similar to our patient.10 However, 1 patient in this series was immunocompetent with involvement of the lower extremity, highlighting that such presentations may also occur in the absence of systemic immunosuppression, consistent with our findings. Proposed mechanisms of VZV-associated vasculitis include immune complex–mediated vascular injury, dysregulated immune responses with autoreactive cell activation, and direct viral involvement of the endothelium leading to vascular remodeling.10
This case expands the clinical spectrum of VZV reactivation and suggests that even localized corticosteroid administration may be sufficient to precipitate both viral reactivation and secondary vasculitic manifestations in immunocompetent individuals. In patients presenting with unusual cutaneous findings following intra-articular corticosteroid injection, consideration of VZV infection is warranted, and histopathologic evaluation with viral testing can help establish the diagnosis. Prompt recognition is critical, as early initiation of antiviral therapy may improve outcomes and prevent disease progression. Although topical corticosteroids do not have an established role in the routine management of herpes zoster, they may be considered for symptomatic relief in select cases with associated inflammatory vasculitic changes, with careful clinical judgment.
Given the widespread use of intra-articular corticosteroid injections, awareness of this rare complication is important to avoid misdiagnosis and delayed antiviral therapy.