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. 2012 Aug;85(1016):1107–1111. doi: 10.1259/bjr/12938443

Table 1. Six haemophilic pseudotumours of the maxillary bone reported in the literature.

Author Sex (M/F)/age (years) History Symptoms Haemophilia Laterality Imaging findings Treatment Follow-up
de Sousa et al (1995) [1] M/1 Tibia HP, nasal trauma 6 years previously None (incidental finding) A (<1% Factor VIII) Left Radiolucent lesion (CT) Curettage Healing (2 years)
Zheng K (1997) [2] M/26 Tibia HP None (incidental finding) A (11% Factor VIII) Left Radiolucent lesion (radiograph) Curettage Not specified
Stevenson and Keast (2002) [8] M/75 COAD, chronic atrial fibrillation, aortic valve replacement surgery Spontaneous epistaxis No haemophilia Right Soft-tissue mass associated bone expansion and destruction (CT) Curettage, radiotherapy No recurrence (18 months)
Steele et al (2004) [7] M/0.5 None Cheek swelling, eye tearing for 3 weeks A (<1% Factor VIII) Left Hypodense mass with peripheral nodular enhancement (CT), hypointense lesion with hyperintense rim on T1 weighted image (MRI) Curettage, Factor VIII therapy Not specified
Lima et al (2008) [9] M/12 Bone cyst of the radius Spontaneous gingival bleeding for 2 months A (14% Factor VIII) Left Osteolytic lesion with bony cortical preservation, (panoramic radiography and CT) Curettage, Factor VIII therapy No recurrence (9 months)
Xue et al (2011) [10] M/24 None Pain, dysfunction for 1 month A (<5% Factor VIII) Right Soft-tissue lump with erosion bony cortex Replacement therapy Resolution

COAD, chronic obstructive airway disease; F, female; HP, haemophilic pseudotumours; M, male.