Blitman Netta M, Levsky Jeffrey M, Villanueva-Siles Esperanza, Thornhill Beverly A
Department of Radiology, Children's Hospital at Montefiore, Montefiore Medical Center, Albert Einstein College of Medicine, Bronx, NY 10467, USA.
Pediatr Radiol. 2007 Sep;37(9):925-8. doi: 10.1007/s00247-007-0535-9. Epub 2007 Jul 12.
Spontaneous subperiosteal hemorrhage is a rare complication of von Recklinghausen's disease. There are few reports describing the MR imaging characteristics of this entity. Our case is unique among these as an underlying plexiform neurofibroma was visualized by MR imaging. We present a 12-year-old child with neurofibromatosis 1 who presented with a rapidly enlarging mass of the fibula. Surgery and pathology revealed subperiosteal hemorrhage into a benign, plexiform neurofibroma. The MR imaging features, pathogenesis and clinical implications of this entity are discussed. Recognition of this disease process and differentiating it from malignant transformation can prevent unnecessary surgery.
自发性骨膜下出血是冯·雷克林豪森病的一种罕见并发症。很少有报告描述该病症的磁共振成像(MR)特征。我们的病例在这些报告中很独特,因为通过MR成像观察到了潜在的丛状神经纤维瘤。我们报告一例12岁患有1型神经纤维瘤病的儿童,其腓骨出现迅速增大的肿块。手术和病理检查显示骨膜下出血进入一个良性丛状神经纤维瘤。本文讨论了该病症的MR成像特征、发病机制及临床意义。认识这一疾病过程并将其与恶性转化相鉴别可避免不必要的手术。