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Published on: September 14, 2010
Coexistent granulomatous vasculitis and leukaemia cutis in a patient with resolving herpes zoster
M Elgoweini1, K Blessing, R Jackson
1Department of Pathology, North Glasgow University Hospitals NHS Trust, Glasgow, UK. mahaelgoweini@doctors.org.uk
Abstract:
An 80-year-old man presented with a 6-month history of indurated tender purple papules. These had coalesced to form plaques with some central scarring and a dermatomal distribution on the left arm, immediately following herpes zoster (HZ) infection at this site. The patient had a 5-year history of small lymphocytic lymphoma (SLL), which was being managed conservatively under a 'watch and wait' protocol. On histological examination of a skin biopsy, marked interstitial granulomas and prominent granulomatous vasculitis were seen, supporting the clinical impression of a post-HZ granulomatous reaction. In addition, there was a dense monoclonal small B-cell lymphocytic infiltrate indicating koebnerization by SLL (a finding that has not been reported previously with concurrent postherpetic granulomatous vasculitis). Although benign pseudolymphomas occur in postherpetic cases, this case shows that even in association with benign vasculitic features true lymphomas can occur. Furthermore, this case highlights the importance of immunocytochemistry, molecular studies and clinicopathological correlation.
Insights
This study reports a rare case of small lymphocytic lymphoma (SLL) koebnerization presenting as granulomatous vasculitis following herpes zoster (HZ) infection. It emphasizes the need for thorough investigation to differentiate benign reactions from true lymphomas.
Area of Science:
- Dermatology
- Oncology
- Pathology
Background:
- Small lymphocytic lymphoma (SLL) is a low-grade B-cell lymphoma.
- Herpes zoster (HZ) is a viral infection causing a painful rash.
- Postherpetic granulomatous reactions can mimic other skin conditions.
Observation:
- An 80-year-old man with SLL developed indurated purple papules and plaques post-HZ infection.
- Skin biopsy revealed granulomatous vasculitis and a monoclonal B-cell infiltrate.
- The findings suggest SLL koebnerization in the context of a post-HZ reaction.
Findings:
- Concurrent granulomatous vasculitis and SLL koebnerization post-HZ is a novel finding.
- Distinguishing benign pseudolymphomas from true lymphomas is crucial.
- Histopathology, immunocytochemistry, and molecular studies are vital for diagnosis.
Implications:
- This case underscores the importance of clinicopathological correlation in complex dermatological presentations.
- It highlights that true lymphomas can occur even with seemingly benign vasculitic features.
- Accurate diagnosis is essential for appropriate management of SLL and post-HZ complications.
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