Genç D Bahar, Özkan M Alp, Büyükgebiz Atilla
Anadolu Medical Center, Pediatric Oncology, Kocaeli, Turkey.
J Clin Res Pediatr Endocrinol. 2012 Sep;4(3):160-3. doi: 10.4274/jcrpe.712.
Fibrous dysplasia (FD) is categorized as either monostotic or polyostotic and may occur as a component of McCune-Albright syndrome (MAS). Imaging findings can mimic neoplastic diseases. We present a case of MAS initially suspected to have neoplastic disease. A 9-year-old girl was admitted to pediatric emergency with ataxia. Upon hospitalization, an extradural mass was seen on cranial magnetic resonance imaging (MRI) and the bone survey showed lytic lesions in the long bones. The patient was referred to the pediatric oncology department with a presumptive diagnosis of Langerhans cell histiocytosis or metastatic tumor. Further investigations demonstrated that the patient had MAS and coexisting postinfectious cerebellitis. The findings in this patient demonstrate that the radiographic findings and the clinical presentation of FD and MAS may be similar to those of malignant diseases.
骨纤维异常增殖症(FD)分为单骨型或多骨型,可能作为McCune-Albright综合征(MAS)的一部分出现。影像学表现可模仿肿瘤性疾病。我们报告一例最初怀疑患有肿瘤性疾病的MAS病例。一名9岁女孩因共济失调入住儿科急诊。住院期间,头颅磁共振成像(MRI)显示硬膜外肿块,骨骼检查显示长骨有溶骨性病变。该患者被转诊至儿科肿瘤科,初步诊断为朗格汉斯细胞组织细胞增多症或转移性肿瘤。进一步检查表明该患者患有MAS并伴有感染后小脑炎。该患者的检查结果表明,FD和MAS的影像学表现及临床表现可能与恶性疾病相似。