Oral Surgery in Patients With Glanzmann Thrombasthenia: A Case Series

Eleonora Segna, Andrea Artoni, Raffaele Sacco, Aldo Bruno Giannì

Research output: Contribution to journalArticlepeer-review


Glanzmann thrombasthenia is a severe defect of platelet function caused by an inherited deficiency or dysfunction of the glycoprotein IIb/IIIa complex, the platelet fibrinogen receptor. Patients with Glanzmann thrombasthenia experience lifelong spontaneous and post-traumatic mucocutaneous bleeding diathesis. Surgery is usually very challenging, requiring close cooperation among surgeons, hematologists, and anesthesiologists. For anatomic reasons, oral surgery is particularly difficult owing to the inherent risk of hemorrhage and the difficulty in achieving local hemostasis. In the present report, we describe 3 successful cases of oral surgery in patients with Glanzmann thrombasthenia and report the surgical and hematologic management of each case.

Original languageEnglish
Pages (from-to)256-259
JournalJournal of Oral and Maxillofacial Surgery
Issue number2
Publication statusPublished - 2017

ASJC Scopus subject areas

  • Surgery
  • Oral Surgery
  • Otorhinolaryngology


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