"Surgical Management of Cyclosporine-Associated Gingival Hyperplasia in Patients with Idiopathic Thrombocytopenic Purpura: A Case Report


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Gürses Z. G., Arpağ O. F.

21st International Hippocrates Congress on Medical and Health Sciences, İstanbul, Türkiye, 13 - 14 Mart 2026, ss.76-77, (Özet Bildiri)

  • Yayın Türü: Bildiri / Özet Bildiri
  • Basıldığı Şehir: İstanbul
  • Basıldığı Ülke: Türkiye
  • Sayfa Sayıları: ss.76-77
  • Hatay Mustafa Kemal Üniversitesi Adresli: Evet

Özet

Surgical Management of Cyclosporine-Associated Gingival Hyperplasia in Patients with Idiopathic Thrombocytopenic Purpura: A Case Report

Abstract

Background: Drug-induced gingival hyperplasia is a significant adverse effect of systemic medications such as cyclosporine, phenytoin, and calcium channel blockers on periodontal tissues. Cyclosporine, commonly used for its immunosuppressive properties, may induce gingival enlargement by increasing fibroblast activity. This study aimed to evaluate the periodontal and surgical management of cyclosporine-induced gingival hyperplasia in the presence of concomitant Idiopathic Thrombocytopenic Purpura (ITP) and to emphasize the importance of a multidisciplinary approach in patients with a high risk of bleeding.

Case Presentation: A 47-year-old female patient presented with complaints of gingival swelling, bleeding, and pain. Her medical history revealed aplastic anemia and ITP. She had been taking cyclosporine (100 mg twice daily) and eltrombopag (50 mg three times daily) for approximately 1.5 years. Clinical examination demonstrated generalized fibrotic gingival hyperplasia affecting mastication, bleeding on probing, and localized suppuration. Oral hygiene instructions and Phase I periodontal therapy were performed. Due to the likelihood of cyclosporine-induced gingival enlargement, a consultation with the relevant physician was conducted; however, modification of the medication regimen was not considered appropriate. Prior to surgery, a hematology consultation was obtained to increase the platelet count to ≥100,000/mm³. Platelet replacement therapy was administered before both surgical sessions, and 2 g of oral amoxicillin was given as prophylaxis 30–60 minutes prior to the procedures. Gingivectomy and gingivoplasty were performed in the maxillary and mandibular arches at two-week intervals, with platelet transfusion administered one day before each surgery. Postoperatively, analgesics and antiseptic mouthwash were prescribed as supportive therapy.

Results: Although initial periodontal therapy resulted in a reduction of inflammation, surgical excision was required due to the extent of the gingival enlargement. The surgical procedures were completed under safe hematological conditions. Postoperative healing was uneventful, and functional as well as esthetic gingival contours were successfully restored.

Conclusion: This case demonstrates that cyclosporine-induced gingival hyperplasia can be safely and effectively managed with a multidisciplinary approach, even in the presence of ITP. Preoperative platelet optimization enhanced surgical safety and resulted in satisfactory clinical outcomes. Regular periodontal follow-up is essential to minimize the risk of recurrence.  

Keywords: Gingival Hyperplasia, Cyclosporine, Thrombocytopenia