Dear Editor,
Tumor necrosis factor alpha (TNF-alpha) inhibitors have proven efficacy in managing various immune-mediated inflammatory conditions. Five TNF-alpha inhibitors are currently available: infliximab, adalimumab, etanercept, certolizumab pegol, and golimumab. Generally, TNF-alpha inhibitors demonstrate favorable tolerability profiles but are linked to specific adverse reactions, notably cutaneous manifestations.1,2 These include injection/infusion-related responses, skin infections, neoplasms, and immunemediated manifestations.2 In this report, we present a rare case of lichen planus pigmentosus potentially triggered by golimumab administration.
A 43-year-old male patient, undergoing golimumab treatment (100 mg monthly) for a year due to a history of ulcerative colitis, presented with a progressive facial hyperpigmentation evolving over six months. The patient, with Fitzpatrick skin phototype IV, worked a desk job and had minimal sun exposure. He denied any prior history of facial or mucosal hyperpigmentation and confirmed no prior usage of topical treatments or daily cosmetic products. On physical examination, diffuse pruritic, brown-colored hyperpigmentation was observed across the face, involving the eyelids but sparing the nasal tip, devoid of scaling or erosions (Fig. 1). The patient exhibited intact mucous membranes and appendages. The dermoscopic evaluation revealed a diffuse grayish-brown hyperpigmentation with a lichenoid pattern encircling follicular openings and isolated bright white rosette-like structures (Fig. 2).
Dermoscopy. Grayish-brown hyperpigmentation witha lichenoid pattern encircling follicular openings and isolated bright white rosette-like structures.
Considering the clinical context and the progressive extension of lesions, a histopathological study was conducted, indicating findings of superficial and periadnexal lymphoplasmacytic dermatitis with a focal lichenoid interface and dermal melanosis, consistent with pigmented lichenoid dermatitis (Fig. 3).
Histopathological examination of the skin biopsy shows features consistent with pigmented lichenoid dermatitis. (A) The epidermis exhibits irregular hyperkeratosis and acanthosis, with a perivascular and perifollicular lymphoplasmacytic infiltrate in the dermis, accompanied by abundant melanophages (Hematoxylin & eosin, ×100). (B) Civatte bodies are also present (Hematoxylin & eosin, ×200).
Further investigation revealed no other known triggers for lichen planus pigmentosus, such as hepatitis B or C virus, mustard oil, henna, nickel, or hair dye. A standard European patch test was performed, which returned negative results. Topical immunomodulatory therapy was initiated and suspecting a cutaneous adverse reaction secondary to golimumab usage, a reassessment by Gastroenterology was warranted. Golimumab was suspended and changed to adalimumab; this decision was influenced by the fact that, in the public health system to which the patient belongs, only TNF-alpha inhibitors (golimumab, adalimumab, infliximab) are economically covered for the treatment of refractory or severe ulcerative colitis. Currently, the patient has been on adalimumab for 4 months. The lesions have shown a slight reduction (Fig. 4); however, the pruritus has significantly diminished, despite the patient discontinuing the topical immunomodulatory therapy without medical guidance.
Facial hyperpigmentation after 4 months of adalimumab therapy, showing a slight reduction following the discontinuation of golimumab.
The majority of documented cases involving immunemediated cutaneous eruptions associated with TNF-alpha inhibitors commonly represent the onset of psoriasis or psoriasiform drug reactions.1 However, albeit rare, there is an increasing number of reports associating TNF-alpha inhibitors with the onset of lichenoid eruption.3 Among these reported cases, the frequency of occurrences was highest with infliximab, followed by etanercept, adalimumab and certolizumab, in decreasing order.4,5 No previously reported cases of a lichenoid eruption attributed to the use of golimumab were found in the English or Spanish literature upon investigation.
The pathophysiology of anti-TNF-alpha-induced lichenoid eruption remains unclear. However, some authors propose that TNF-alpha inhibition in specific genotypes may lead to the upregulation of opposing cytokines, such as interferonalpha. This upregulation could activate T-cells and dendritic cells, triggering an inflammatory response that may induce lichen planus.6
Reporting rare adverse effects of these medications, increasingly used in clinical practice, is crucial to establishing pharmacovigilance registries. These registries help to understand the long-term implications of treatment with TNF-alpha inhibitors, which are increasingly used and currently extend beyond the timeframe of randomized controlled trials.
References
- 1 Lindhaus C, Tittelbach J, Elsner P. Cutaneous side effects of TNF- alpha inhibitors. J Dtsch Dermatol Ges. 2017;15:281-8.
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2 Pasadyn SR, Knabel D, Fernández AP, Warren CB. Cutaneous adverse effects of biologic medications. Cleve Clin J Med. 2020;87:288-99, http://dx.doi.org/10.3949/ccjm.87a.19119
» http://dx.doi.org/10.3949/ccjm.87a.19119 - 3 Oliveira SC, Vasconcelos AHC, Magalhães EPB, Corrêa FJV, Rodrigues CEM. Clinical, histopathological and outcome analysis of five patients with lichenoid eruption following anti-tumor necrosis factor-alpha therapy for ankylosing spondylitis: report of one case and review of the literature. Cureus. 2020;12:e10598.
- 4 Jayasekera PS, Walsh ML, Hurrell D, Parslew RA. Case report of lichen planopilaris occurring in a pediatric patient receiving a tumor necrosis factor a inhibitor and a review of the literature. Pediatr Dermatol. 2016;33:e143-6.
- 5 Kunadia A, Shulman K, Sami N. Certolizumab-induced lichenoid eruption in a patient with rheumatoid arthritis. BMJ Case Rep. 2021;14:e245875.
- 6 Seneschal J, Milpied B, Vergier B, Lepreux S, Schaeverbeke T, Taïeb A. Cytokine imbalance with increased production of interferon-alpha in psoriasiform eruptions associated with antitumour necrosis factor-alpha treatments. Br J Dermatol. 2009;161:1081-8.
Publication Dates
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Publication in this collection
18 Aug 2025 -
Date of issue
2025
History
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Received
22 May 2024 -
Accepted
04 Oct 2024 -
Published
13 Mar 2025








