The haemophilic pseudotumour

The management of the patient with a haemophilic pseudotumour is complex and carries a high rate of potential complications. There are a number of therapeutic alternatives for this dangerous condition: embolization, radiation, percutaneous management, surgical removal and exeresis, and filling of the dead cavity. It is hoped that with the advent of widespread maintenance therapy, pseudotumours will be less common in the future. It is important that they are diagnosed early, and prevention of muscular haematomas is key to reducing their incidence. Untreated, proximal pseudotumours will ultimately destroy soft tissues, erode bone and may produce neurovascular complications. Surgical excision is the treatment of choice but should only be carried out in major haemophilia centres by a multidisciplinary surgical team.

[1]  F. Decataldo,et al.  Long‐term evaluation of a novel surgical approach to the pseudotumour of the ilium in haemophilia: exeresis and transposition of the omentum in the residual cavity , 2000, Haemophilia : the official journal of the World Federation of Hemophilia.

[2]  Heaton,et al.  Iliopsoas haemophiliac pseudotumours with bowel fistulation , 2000, Haemophilia : the official journal of the World Federation of Hemophilia.

[3]  Almagro,et al.  Successful surgical treatment of haemophilic pseudotumour, filling the defect with hydroxyapatite , 2000, Haemophilia : the official journal of the World Federation of Hemophilia.

[4]  Álvarez,et al.  Therapeutic embolization and surgical excision of haemophilic pseudotumour , 1999, Haemophilia : the official journal of the World Federation of Hemophilia.

[5]  Ishiguro,et al.  The surgical treatment of a haeophilic pseudotumour in an extremity: a report of three cases with pathological fractures , 1998, Haemophilia.

[6]  J. R. Horn,et al.  Excision of a haeophilic pseudotumour of the ilium, complicated by fistulation , 1998, Haemophilia : the official journal of the World Federation of Hemophilia.

[7]  N. Sakuragawa [Hemophilic pseudotumor]. , 1998, Ryoikibetsu shokogun shirizu.

[8]  D. Green,et al.  Recombinant factor VIIa in the management of a pseudotumour in acquired haemophilia , 1997, Haemophilia.

[9]  J. M. Matthews,et al.  THE HAEMOPHILIC PSEUDOTUMOUR OR HAEMOPHILIC SUBPERIOSTEAL HAEMATOMA. , 1965, The Journal of bone and joint surgery. British volume.