Møller J F, Sneppen O
Aarhus Universitetshospital, afsnit for ortopaedisk onkologi og ortopaedkirurgisk afdeling E.
Ugeskr Laeger. 1992 Jul 6;154(28):1968-71.
PABC is a rather rare, non-malignant osteolytic bone disease, affecting children and young people. Most frequently, it is localized to the metaphyses of the long bones. The present material consists of 21 cases, treated in the Orthopaedic Hospital in Aarhus between 1973 and 1991. Nineteen patients were treated with curettage of the cyst followed by bone grafting to the cavity. Six (31%) had recurrences. Five were operated again without any recurrence. The last patient has not yet received any further treatment. Two patients were initially treated by bone resection. No postoperative complications occurred. Curettage of PABC followed by bone grafting is recommended as the treatment of choice, in spite of the recurrence rate mentioned above. Because of the risk of recurrence after this treatment, regular follow-up examinations are necessary until healing has occurred i order to treat a possible local recurrence in time.
青少年前体骨干骺端骨皮质缺损(PABC)是一种相当罕见的非恶性溶骨性骨病,影响儿童和年轻人。最常见的是,它局限于长骨的干骺端。本资料包括1973年至1991年在奥胡斯骨科医院治疗的21例病例。19例患者接受了囊肿刮除术,随后对空腔进行了植骨。6例(31%)复发。5例再次手术,无复发。最后1例患者尚未接受进一步治疗。2例患者最初接受了骨切除术。未发生术后并发症。尽管有上述复发率,但建议首选刮除PABC后植骨治疗。由于这种治疗后有复发风险,在愈合之前需要定期进行随访检查,以便及时治疗可能的局部复发。