# A Patient With Granuloma Annulare and Lichen Planus Treated With Apremilast: A Case Report

**Authors:** Emre Sarıkaya, Meltem Türkmen, Selcen Kundak, Sümeyye Ekmekci

PMC · DOI: 10.1155/carm/6883705 · 2025-08-06

## TL;DR

A 55-year-old woman with granuloma annulare and lichen planus showed significant improvement after treatment with apremilast, a drug that reduces inflammatory cytokines.

## Contribution

This case report presents apremilast as a potential treatment for granuloma annulare and lichen planus.

## Key findings

- Apremilast led to almost complete resolution of granuloma annulare and lichen planus in a patient.
- Apremilast inhibits inflammatory cytokines like TNF-α and IFN-γ, which are implicated in both diseases.

## Abstract

Granuloma annulare (GA) is an inflammatory and granulomatous dermatosis characterized by annular erythematous papules/plaques frequently localized in acral regions. Proinflammatory cytokines such as tumor necrosis factor-alpha (TNF-α) and interferon-gamma (IFN-γ), which are released by T helper 1 (Th1) lymphocytes inducing macrophages, are thought to play a role in its pathogenesis. Lichen planus (LP) is an inflammatory dermatosis characterized by pruritic scaly purple papules, often on the wrists and ankles, and can also affect mucosa, hair, and nails. T-cell-mediated proinflammatory cytokines such as IFN-γ and TNF-α, which are released by macrophages upon Th1 stimulation, have been implicated in the pathogenesis of LP, as in GA. A new treatment option is needed in the treatment of these diseases due to suboptimal results and adverse side-effect profiles with conventional treatments. Apremilast is a phosphodiesterase-4 (PDE4) inhibitor and inhibits the production of various inflammatory mediators such as IFN-γ, TNF-α, IL-2, IL-5, IL-8, IL-12, and leukotriene B4. This molecule has three Food and Drug Administration (FDA) approved indications: moderate to severe plaque psoriasis, psoriatic arthritis, and oral ulcers associated with Behcet's disease. Apremilast exhibits a favorable side-effect profile compared to conventional treatments and is a good treatment option with its ability to reduce cytokines implicated in the pathogenesis of GA and LP. Here, we report the case of a 55-year-old woman in whom apremilast treatment led to an almost complete resolution of her GA and LP.

## Linked entities

- **Proteins:** TNF (tumor necrosis factor), IFNG (interferon gamma), IL2 (interleukin 2), IL5 (interleukin 5), CXCL8 (C-X-C motif chemokine ligand 8), IL12 (Interleukin 12 level)
- **Chemicals:** apremilast (PubChem CID 10151715)
- **Diseases:** granuloma annulare (MONDO:0006554), lichen planus (MONDO:0006572), psoriatic arthritis (MONDO:0011849)

## Full-text entities

- **Genes:** CD68 (CD68 molecule) [NCBI Gene 968] {aka GP110, LAMP4, SCARD1}, PDE4A (phosphodiesterase 4A) [NCBI Gene 5141] {aka DPDE2, PDE4, PDE46}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, IL2 (interleukin 2) [NCBI Gene 3558] {aka IL-2, TCGF, lymphokine}, IL12B (interleukin 12B) [NCBI Gene 3593] {aka CLMF, CLMF2, IL-12B, IMD28, IMD29, NKSF}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}, CABIN1 (calcineurin binding protein 1) [NCBI Gene 23523] {aka CAIN, KB-318B8.7, PPP3IN}, IL5 (interleukin 5) [NCBI Gene 3567] {aka EDF, IL-5, TRF}, CXCL8 (C-X-C motif chemokine ligand 8) [NCBI Gene 3576] {aka GCP-1, GCP1, IL8, LECT, LUCT, LYNAP}
- **Diseases:** GA (MESH:D016460), oral ulcers (MESH:D019226), sarcoidosis (MESH:D012507), gastrointestinal side effects (MESH:D064420), necrobiosis lipoidica (MESH:D009335), hyperpigmentation (MESH:D017495), lupus (MESH:D008180), psoriasis (MESH:D011565), papular lesions (MESH:C565924), erythema annulare (MESH:C562461), psychiatric disease (MESH:D001523), tuberculosis (MESH:D014376), itchy skin rash (MESH:D005076), eye disease (MESH:D005128), psoriatic arthritis (MESH:D015535), papules (MESH:D000169), Behcet's disease (MESH:D001528), granuloma ring (MESH:D006099), LP (MESH:D008010), hyperkeratosis (MESH:D017488), mycosis fungoides (MESH:D009182), tinea (MESH:D014005), collagen (MESH:D003095), itching (MESH:D011537), granulomatous inflammation (MESH:D007249), allergy (MESH:D004342), granulomatous dermatosis (MESH:D012871), Wickham striae (MESH:D057896)
- **Chemicals:** pentoxifylline (MESH:D010431), tetracycline (MESH:D013752), leukotriene B4 (MESH:D007975), dapsone (MESH:D003622), isotretinoin (MESH:D015474), cAMP (MESH:D000242), vitamin E (MESH:D014810), hydroxychloroquine (MESH:D006886), retinoids (MESH:D012176), rifampicin (MESH:D012293), ofloxacin (MESH:D015242), Apremilast (MESH:C505730), steroids (MESH:D013256), hydroxyurea (MESH:D006918), minocycline (MESH:D008911), nicotinamide (MESH:D009536), allopurinol (MESH:D000493), zidovudine (MESH:D015215), cyclosporine (MESH:D016572)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12349983/full.md

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Source: https://tomesphere.com/paper/PMC12349983