Dheer Sachin, Gekas Pamela, Schick Faith, Karanjia Homyar, Taweel Nicholas
Department of Radiology, Thomas Jefferson University, 111 South 10 Street, Philadelphia, PA 19103.
Department of Podiatry, Rothman Institute, 925 Chestnut Street, Philadelphia, PA 19107.
Radiol Case Rep. 2021 Aug 8;16(10):3016-3019. doi: 10.1016/j.radcr.2021.07.020. eCollection 2021 Oct.
The authors present an unusual case of a leiomyosarcoma of the distal tibia. Leiomyosarcoma tumors typically originate from smooth muscle tissue. It is rare for it to derive from bone and even rarer to be found in a bone of the lower limb. Given this extreme rarity in addition to nonspecific findings on plain film radiographs and magnetic resonance imaging (MRI), biopsy was needed in this case. It was only through immunochemistry staining that a definitive diagnosis was made. As such, this case is an illustrative example of an aggressive, though rare, primary lesion of the bone which should be considered in the differential diagnosis of a lytic intramedullary lesion. This case also highlights the need for careful evaluation of imaging features suggesting a potentially aggressive lesion requiring appropriate work up in a timely fashion.
作者报告了一例罕见的胫骨远端平滑肌肉瘤病例。平滑肌肉瘤通常起源于平滑肌组织。它起源于骨骼极为罕见,在下肢骨骼中发现更是罕见。鉴于这种极端罕见性,再加上X线平片和磁共振成像(MRI)上的非特异性表现,该病例需要进行活检。只有通过免疫化学染色才能做出明确诊断。因此,该病例是一个具有侵袭性但罕见的原发性骨病变的典型例子,在溶骨性髓内病变的鉴别诊断中应予以考虑。该病例还强调了需要仔细评估提示潜在侵袭性病变的影像学特征,并及时进行适当的检查。