Shekhar Anshu, Korlhalli Suresh, Murgod Gururaj
Department of Orthopaedics, S. D. M. College of Medical Sciences and Hospital, Sattur, Dharwad, India.
Department of Orthopaedics, Karnataka Institute of Medical Sciences and Hospital, Hubli, Karnataka, India.
Indian J Orthop. 2015 May-Jun;49(3):365-8. doi: 10.4103/0019-5413.156229.
Ewing's sarcoma is the second most common malignant primary bone tumor of childhood and adolescence affecting mainly the diaphysis of long bones and flat bones. This tumor is extraordinarily rare in small bones of the hand and presents as a swelling with atypical radiological features of cystic and lytic lesion with scant periosteal reaction. The common differential diagnosis include osteomyelitis, tuberculosis, enchondroma and benign tumors. Moreover, skip metastasis to adjacent bones is even rarer. The prognosis of this condition is greatly influenced by the presence of metastasis at presentation, further emphasizing the importance of early diagnosis. Multimodality treatment using surgery, radiotherapy and chemotherapy is currently recommended though no consensus exists. We report a case of Ewing's sarcoma of the little finger proximal phalanx which was initially missed and developed skip metastasis to several metacarpals within 4 months.
尤因肉瘤是儿童和青少年中第二常见的原发性恶性骨肿瘤,主要影响长骨骨干和扁骨。这种肿瘤在手的小骨中极为罕见,表现为肿胀,具有囊性和溶骨性病变的非典型放射学特征,骨膜反应稀少。常见的鉴别诊断包括骨髓炎、结核、内生软骨瘤和良性肿瘤。此外,跳跃性转移至相邻骨骼的情况更为罕见。该疾病的预后在很大程度上受就诊时是否存在转移的影响,这进一步凸显了早期诊断的重要性。目前推荐采用手术、放疗和化疗的多模式治疗,不过尚未达成共识。我们报告一例小指近节指骨尤因肉瘤病例,该病例最初被漏诊,4个月内出现跳跃性转移至多个掌骨。