# The Development of Sarcoidosis in an Ulcerative Colitis Patient Treated with Vedolizumab: A Case Report and Review of the Literature

**Authors:** John K. Triantafillidis, Konstantinos Malgarinos, Loukas Kaklamanis, Emmanouil Kritsotakis, Victoria Polydorou, Konstantinos Pantos, Konstantinos Sfakianoudis, Agni Pantou, Konstantinos Bramis, Manousos M. Konstantoulakis, Apostolos E. Papalois

PMC · DOI: 10.3390/clinpract16020044 · 2026-02-23

## TL;DR

A patient with ulcerative colitis developed sarcoidosis while on vedolizumab, but the condition stabilized after treatment adjustments.

## Contribution

This case report adds to the limited literature on the coexistence of UC and sarcoidosis during vedolizumab therapy.

## Key findings

- The patient developed systemic sarcoidosis while being treated with vedolizumab for UC.
- Discontinuation of vedolizumab led to UC relapse, but reintroduction resulted in remission.
- Sarcoidosis remained stable despite resuming vedolizumab, suggesting a coincidental rather than causal relationship.

## Abstract

Background: Ulcerative colitis (UC) and sarcoidosis are chronic inflammatory diseases that share immunological pathways but rarely coexist. The increasing use of biologic agents in inflammatory bowel disease (IBD) has raised concerns regarding paradoxical inflammatory manifestations, including sarcoidosis-like reactions. Case presentation: We report the case of a 63-year-old man with long-standing UC treated with vedolizumab who developed systemic sarcoidosis characterized by bilateral hilar lymphadenopathy, mediastinal and abdominal lymph node enlargement, pulmonary involvement, and erythema nodosum. Extensive diagnostic work-up, including imaging and histopathology, confirmed non-necrotizing granulomatous disease consistent with sarcoidosis, while alternative infectious, malignant, and drug-induced causes were excluded. Vedolizumab was temporarily discontinued, leading to UC relapse, and subsequently reintroduced with rapid clinical remission of UC. Discussion: Sarcoidosis remained clinically and radiologically stable despite vedolizumab re-initiation, suggesting a coincidental association rather than a direct causal relationship. This case highlights the diagnostic challenges and therapeutic dilemmas in patients with immune-mediated diseases receiving biologic therapy. Conclusion: The coexistence of UC and sarcoidosis during vedolizumab therapy is rare. Although causality cannot be established, our findings suggest that vedolizumab may be safely continued in selected patients under close multidisciplinary monitoring.

## Linked entities

- **Diseases:** ulcerative colitis (MONDO:0005101), sarcoidosis (MONDO:0008399)

## Full-text entities

- **Genes:** HLA-A (major histocompatibility complex, class I, A) [NCBI Gene 3105] {aka HLAA}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, CD68 (CD68 molecule) [NCBI Gene 968] {aka GP110, LAMP4, SCARD1}
- **Diseases:** Crohn's disease (MESH:D003424), Sarcoidosis (MESH:D012507), COVID-19 (MESH:D000086382), immune dysfunction (MESH:D007154), cough (MESH:D003371), erythema nodosum (MESH:D004893), fungal infections (MESH:D009181), systemic lymphadenopathy (MESH:D006425), immune dysregulation (OMIM:614878), intestinal disease (MESH:D007410), UC (MESH:D003093), Infectious (MESH:D003141), IBD (MESH:D015212), lymphoproliferative disease (MESH:D008232), parenchymal disease (MESH:D017563), granulomas (MESH:D006099), tuberculosis (MESH:D014376), type 1 diabetes (MESH:D003922), systemic (MESH:D015619), bowel inflammation (MESH:D007249), injury to (MESH:D014947), Pulmonary involvement (MESH:C566343), granulomatous (MESH:D013968), granulomatosis (MESH:D015267), Hematological malignancy (MESH:D019337), systemic lupus erythematosus (MESH:D008180), pulmonary sarcoidosis (MESH:D017565), granulomatous disease (MESH:D006105), lymphadenopathy (MESH:D008206), pulmonary infiltrates (MESH:D017254), autoimmune diseases (MESH:D001327), hilar lymphadenopathy (MESH:D018285), immune-mediated diseases (MESH:C567355)
- **Chemicals:** Entyvio (MESH:C543529), Hematoxylin (MESH:D006416), eosin (MESH:D004801), steroid (MESH:D013256), azathioprine (MESH:D001379), mesalamine (MESH:D019804)
- **Species:** Homo sapiens (human, species) [taxon 9606], Cutibacterium acnes (species) [taxon 1747]

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12939528/full.md

---
Source: https://tomesphere.com/paper/PMC12939528