Maxillary pseudotumor as initial manifestation of von Willebrand disease, type 2: Report of a rare case and literature review

Prokopios P. Argyris, Samuel O. Anim, Ioannis G. Koutlas

Research output: Contribution to journalArticlepeer-review

6 Scopus citations

Abstract

Objectives Von Willebrand disease (VWD) is a bleeding disorder associated with inherited defects of von Willebrand factor (VWF). Type 2 N VWD is characterized by impaired FVIII-binding capacity (VWF:FVIIIB). Pseudotumor (PT) represents a serious complication of hemophilia. Case reports of oral PTs in VWD remain scarce. Methods An 11-year-old Caucasian female presented with an expansile gingival mass of the posterior maxilla. Surgical excision of the tumor was performed. Results Histopathologically, the tumor was characterized by cystic spaces filled with hemorrhagic material and dense fibrous connective tissue. Postoperatively, the patient suffered prolonged hemorrhage. Results of blood tests showed decreased levels of FVIII function (FVIII:C) and VWF:FVIIIB. Subsequent gene analysis for type 2 N VWD confirmed heterozygosity for the missense mutation p.Arg816 Trp. A diagnosis of oral PT was rendered. Conclusions Here, we report the clinical, radiographic, and microscopic features of a rare example of oral PT leading to the diagnosis of type 2 N VWD.

Original languageEnglish (US)
Pages (from-to)e27-e31
JournalOral Surgery, Oral Medicine, Oral Pathology and Oral Radiology
Volume121
Issue number2
DOIs
StatePublished - Feb 1 2016

Bibliographical note

Publisher Copyright:
© 2016 Elsevier Inc.

Copyright:
Copyright 2016 Elsevier B.V., All rights reserved.

Fingerprint Dive into the research topics of 'Maxillary pseudotumor as initial manifestation of von Willebrand disease, type 2: Report of a rare case and literature review'. Together they form a unique fingerprint.

Cite this