Yeh Ya-Lin, Yeh Shu-I, Cheng Chih-Ting
Department of Orthopedics, Hsinchu Mackay Memorial Hospital, Hsinchu City, Taiwan.
Department of Ophthalmology, Mackay Memorial Hospital, Taipei, Taiwan.
Int J Surg Case Rep. 2017;34:106-109. doi: 10.1016/j.ijscr.2017.03.013. Epub 2017 Mar 16.
Intramuscular hemangioma in the periosteal region is rare. Although comprising less than 1% of all hemangiomas, they represent the most common type of intramuscular tumors. When located adjacent to bone, a periosteal reaction can occur. The deep localization of the hemangioma poses the diagnosis difficult. Only 8% to 19% of cases were diagnosed before surgery according to the literature review.
We present a case of forty-one-year-old female diagnosed with intramuscular hemangioma, mimicking osteoid osteoma, adjacent to the periosteal region of tibia diaphysis treated by surgical excision.
When intramuscular hemangioma occurs nearby a bone structure, it can cause cortical, medullary and periosteal bone changes that are frequently misdiagnosed by plain radiography. Due to their infrequency, deep location, and atypical presentation, these lesions are seldom diagnosed at presentation. The hemangioma of the periosteal region can be locally destructive due to compression exerted on neighboring structures. It does not regress spontaneously, and surgical excision is frequently needed.
Intramuscular hemangioma of periosteal region occurs most commonly adjacent to long bones of the lower limb. They can cause hypertrophic periosteal reactions mimicking a periosteal or parosteal tumor. Although osteoid osteoma was considered in the differential diagnosis, MRI with enhancement should be performed to exclude intramuscular hemangioma. This may avoid unnecessary aggressive en-bloc tumor excisions resulting in bone weakness and prolonged rehabilitation. This case report has been written in line with the SCARE criteria (Agha et al., 2016 [1]).
骨膜区域的肌内血管瘤较为罕见。尽管其在所有血管瘤中占比不到1%,但却是最常见的肌内肿瘤类型。当位于骨骼附近时,可发生骨膜反应。血管瘤的深部定位使诊断困难。根据文献综述,仅8%至19%的病例在手术前得到诊断。
我们报告一例41岁女性,诊断为肌内血管瘤,类似于骨样骨瘤,位于胫骨干骨膜区域附近,接受了手术切除治疗。
当肌内血管瘤发生在骨结构附近时,可引起皮质、髓质和骨膜骨改变,这些改变在X线平片上常被误诊。由于其罕见性、深部定位和非典型表现,这些病变在就诊时很少被诊断出来。骨膜区域的血管瘤可因对邻近结构的压迫而具有局部破坏性。它不会自行消退,通常需要手术切除。
骨膜区域的肌内血管瘤最常发生在下肢长骨附近。它们可引起肥厚性骨膜反应,类似于骨膜或骨旁肿瘤。尽管在鉴别诊断中考虑了骨样骨瘤,但应进行增强MRI检查以排除肌内血管瘤。这可以避免不必要的积极整块肿瘤切除,从而导致骨质薄弱和康复时间延长。本病例报告是按照SCARE标准撰写的(Agha等人,2016 [1])。