Djuričić Goran, Milošević Zorica, Radović Tijana, Milčanović Nataša, Djukić Predrag, Radulovic Marko, Sopta Jelena
Department of Radiology, University Children's Hospital, Belgrade, School of Medicine, University of Belgrade, Tiršova 10, 11000, Belgrade, Republic of Serbia.
Institute of Oncology and Radiology of Serbia, School of Medicine, University of Belgrade, Pasterova 14, 11000, Belgrade, Republic of Serbia.
BMC Med Imaging. 2018 Dec 19;18(1):54. doi: 10.1186/s12880-018-0297-x.
This is the first reported case of a primary intraosseous angioleiomyoma and the second case of a primary leiomyoma of the rib, irrespective of age. Angioleiomyomas mostly occur in patients of advanced age, in any part of the body, particularly the lower extremities and present as painful, slow-growing nodules in the dermis, subcutaneous fat or deep fascia. Other localizations, especially bone, are considered extremely rare, as well as their occurrence in paediatric patients.
A 10-year-old girl was admitted to the orthopaedic surgery department for further assessment of a pain localized in the posterior part of the right hemithorax. After magnetic resonance imaging (MRI) and surgical biopsy, intraosseus angioleiomyoma of the fourth rib was diagnosed by histopathology examination. Atypical costal localization of this type of a benign tumour presents diagnostic difficulty, especially in children. The differential diagnoses included cartilaginous tumours, Ewing sarcoma, fibrous dysplasia, Langerhans cell histiocytosis, intraosseous haemangioma and metastatic tumours. We report a detailed diagnostic procedure including MRI, selective angiography and histopathologic examination.
Diagnosis of intraosseous angioleiomyoma is difficult due to the extreme rarity of this tumour and absence of pathognomonic radiological signs. Although very rarely identified in bones and young age group, radiographers and reporting doctors should be aware of this possible angioleiomyoma presentation and supported by the provided detailed diagnostic information.
这是首例原发性骨内血管平滑肌瘤的报道病例,也是第二例肋骨原发性平滑肌瘤病例,年龄不限。血管平滑肌瘤多见于老年患者,可发生于身体任何部位,尤其是下肢,表现为真皮、皮下脂肪或深筋膜内疼痛性、生长缓慢的结节。其他部位,尤其是骨骼,以及在儿科患者中的发生,被认为极为罕见。
一名10岁女孩因右半胸后部疼痛入院接受骨科手术进一步评估。经磁共振成像(MRI)和手术活检后,通过组织病理学检查诊断为第四肋骨骨内血管平滑肌瘤。这种类型的良性肿瘤在肋骨的非典型定位存在诊断困难,尤其是在儿童中。鉴别诊断包括软骨肿瘤、尤因肉瘤、骨纤维异常增殖症、朗格汉斯细胞组织细胞增多症、骨内血管瘤和转移性肿瘤。我们报告了包括MRI、选择性血管造影和组织病理学检查在内的详细诊断过程。
由于骨内血管平滑肌瘤极为罕见且缺乏特征性放射学征象,其诊断困难。尽管在骨骼和年轻年龄组中很少见,但放射技师和报告医生应了解这种可能的血管平滑肌瘤表现,并参考所提供的详细诊断信息。