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Published on: November 15, 2024
Dermatologic toxicity from immune checkpoint blockade therapy with an interstitial granulomatous pattern
Celestine Trinidad1,2, Kelly C Nelson3, Isabella C Glitza Oliva4
1Department of Pathology, University of Texas M.D. Anderson Cancer Center, Houston, Texas.
Abstract:
Immunotherapies targeting cytotoxic T-lymphocyte-associated antigen 4 (CTLA-4) and the programmed cell death 1 (PD-1) receptor and its ligand (PD-L1) have showed significant therapeutic benefit in patients with clinically advanced solid malignancies, including melanoma. However, immune-related adverse events (irAE) are common, and novel dermatologic toxicities continue to emerge as more patients are treated with immunotherapy. Here we describe a patient treated with combination immunotherapy of ipilimumab and pembrolizumab, who developed asymptomatic erythematous patches on both legs. Histopathologic examination revealed a cutaneous interstitial granulomatous dermatitis. Notably, our patient did not require cessation of immunotherapy for these lesions, which subsequently remained stable, while the patient's melanoma remained controlled. This case expands the dermatologic toxicity profile of immune checkpoint blockade, as recognition of such toxicities is critical to optimal patient management.
Insights
Immune checkpoint inhibitors, like ipilimumab and pembrolizumab, can cause skin toxicities. A patient developed granulomatous dermatitis during combination immunotherapy for melanoma, which remained stable without treatment cessation.
Area of Science:
- Oncology
- Dermatology
- Immunology
Background:
- Immune checkpoint inhibitors targeting CTLA-4 and PD-1/PD-L1 pathways offer significant benefits for advanced solid malignancies, including melanoma.
- However, immune-related adverse events (irAEs) are frequent, with emerging dermatologic toxicities requiring careful management.
Observation:
- A patient receiving combination immunotherapy (ipilimumab and pembrolizumab) for advanced melanoma developed asymptomatic erythematous patches on the legs.
- Histopathologic analysis confirmed a diagnosis of cutaneous interstitial granulomatous dermatitis.
Findings:
- The patient's granulomatous dermatitis did not necessitate interruption of immunotherapy.
- Dermatologic lesions remained stable, correlating with effective control of the patient's melanoma.
Implications:
- This case expands the known spectrum of dermatologic toxicities associated with immune checkpoint blockade.
- Recognizing and managing novel irAEs is crucial for optimizing patient care and maintaining therapeutic efficacy in cancer immunotherapy.
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