中华骨科杂志2024,Vol.44Issue(15) :1034-1039.DOI:10.3760/cma.j.cn121113-20240219-00102

青少年股骨远端血管性血友病假瘤一例报告及文献复习

Vascular haemophilic pseudotumour of the distal femur in an adolescent:a case report and literature review

张润康 彭爽 吴计通 田川 梁亮 韩登鹏 梁振明 吴少科
中华骨科杂志2024,Vol.44Issue(15) :1034-1039.DOI:10.3760/cma.j.cn121113-20240219-00102

青少年股骨远端血管性血友病假瘤一例报告及文献复习

Vascular haemophilic pseudotumour of the distal femur in an adolescent:a case report and literature review

张润康 1彭爽 1吴计通 1田川 2梁亮 3韩登鹏 1梁振明 4吴少科4
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作者信息

  • 1. 广东医科大学研究生院,湛江 524000
  • 2. 广东医科大学附属医院儿科,湛江 524000
  • 3. 广东医科大学附属医院血液科,湛江 524000
  • 4. 广东医科大学附属医院骨科,湛江 524000
  • 折叠

摘要

报告1例青少年股骨血管性血友病(von willebrand disease,VWD)3型假瘤.男,12岁,无明显外伤史下因右膝关节活动后乏力并疼痛2个月就诊.基因学检查在患者血管性血友病因子(von willebrand factor,VWF)基因发现两处复合杂合,关联疾病"VWD 3型"与患者临床表现吻合.实验室检查提示凝血因子Ⅷ(FⅧ)活性为2.8%,FⅧ抑制物检测阴性;进一步检测VWF活性为1%,去氨加压素输注试验(1 h和4 h)VWF<1%,VWF抗原<3%.影像学检查示右侧股骨远端干骺端有一个溶骨性病灶,股骨前方骨皮质吸收不连续,内、外侧及后方骨皮质变薄并可见明显的硬化带,远端瘤腔侵及股骨远端骨骺,未发现病变周围有骨膜反应.多学科会诊后诊断为青少年股骨VWD3型假瘤.患者既往未规律补充凝血因子,膝关节无明显外伤史.术前通过输注冷沉淀维持VWF水平在80%以上,行病灶清理及自体腓骨、同种异体骨植骨术.术后随访至5个月,膝关节功能恢复良好.假瘤是遗传性出血性疾病一个罕见但严重的临床表现,多见于血友病患者.VWD的骨骼-肌系统假瘤罕见,以往仅有上、下颌骨假瘤的文献报道.MRI在血友病性假瘤诊断中有着非常重要的价值,增强扫描后显示周缘有强化而中央无强化,是血友病性假瘤的特征性表现.手术是治疗出血性疾病假瘤的首选,且是最彻底、有效的治疗方法.围手术期充分的准备是手术成功的前提,贯穿整个治疗过程的多学科会诊和制定个性化治疗方案具有重要作用.

Abstract

This case report presents an adolescent patient with type 3 pseudotumor associated with vascular hemophil-ia(von willebrand disease,VWD)of the femur.The patient experienced weakness and pain in the right knee joint for two months following physical activity,with no apparent history of trauma.Genetic testing identified two compound heterozygous mutations in the von willebrand factor(VWF)gene,consistent with a diagnosis of"VWD type 3".Laboratory results revealed a Factor Ⅷ activity of 2.8%,a negative Factor Ⅷ inhibitor test,VWF activity of 1%,and VWF antigen levels below 3%.The desmopressin infusion test(1 hours and 4 hours)showed VWF levels of less than 1%.Imaging studies revealed an osteo-lytic lesion in the right distal femoral epiphysis,characterized by discontinuous cortical resorption in the anterior femur,thin-ning of the medial,lateral,and posterior cortex,prominent sclerotic bands,and extension of the tumor into the distal femoral epiphysis without periosteal reaction.After multidisciplinary consultation,the diagnosis of VWD type 3 pseudotumor of the fe-mur was confirmed.The patient had no history of coagulation factor supplementation and no significant knee trauma.Preopera-tively,the VWF level was maintained above 80%with cryoprecipitate infusion.The lesion was surgically debrided,followed by bone grafting with autologous fibula and allograft bone.Postoperative follow-up at 5 months showed good recovery of knee func-tion.Pseudotumor is a rare but serious manifestation of inherited bleeding disorders,predominantly observed in hemophiliacs.Skeletal muscle system pseudotumor in VWD is exceptionally rare,with previous reports limited to the maxilla and mandible.MRI is crucial for the diagnosis of hemophilic pseudotumor,with characteristic findings of peripheral enhancement without cen-tral enhancement on enhanced scans.Surgery remains the preferred and effective treatment,with adequate perioperative prepa-ration being essential for success.In this case,a multidisciplinary approach was critical in developing a personalized treatment plan,contributing significantly to the patient's positive outcome.

关键词

股骨/血管性血友病,3型/青少年/病例报告/假瘤

Key words

Femur/von Willebrand disease,type 3/Adolescent/Case reports/Pseudotumor

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出版年

2024
中华骨科杂志
中华医学会

中华骨科杂志

CSTPCDCSCD北大核心
影响因子:2.137
ISSN:0253-2352
参考文献量20
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