Salunke Abhijeet Ashok, Vala Pathik Chandrakant, Singh Harpreet, Parwani Rohan, Gandhi Sanjay, Shah Diva
Gujarat Cancer Research Institute, Ahmedabad, Gujarat, India.
V.S. Medical College, Ahmedabad, India.
J Clin Orthop Trauma. 2016 Oct-Dec;7(Suppl 1):61-64. doi: 10.1016/j.jcot.2016.08.001. Epub 2016 Oct 19.
Leiomyoma is a benign tumor of smooth muscle origin and commonly diagnosed in the uterus, gastrointestinal tract, skin, and mucous membranes. To the best of our knowledge, the only reported intraosseous leiomyomas in extremities occurred in the proximal aspect and distal aspect of the femur, in the tibia, and in the ulna. We are not aware of any previous reports of intraosseous leiomyomas in the foot. The radiograph of the intraosseous leiomyoma shows unilocular or multilocular lytic lesion with sclerotic rim. Due to lack of definitive radiological features on magnetic resonance imaging and computed tomography diagnosis of this rare tumor is established with histopathological study and immuno-histochemistry markers. Smooth muscle spindle cells and positive immunohistochemistry markers for muscle cells is hall mark for the diagnosis. The treatment of intraosseous leiomyoma is surgical intervention by excision with wide margin and curettage followed by filling the cavity. The diagnosis of this tumor is challenging due to its extraordinarily rare incidence. Intraosseous leiomyoma should be included in the differential diagnosis of intraosseous lesion with benign radiographic feature. We report of the first published case of primary intraosseous leiomyoma of calcaneum in a 22-year-old male patient.
平滑肌瘤是一种起源于平滑肌的良性肿瘤,常见于子宫、胃肠道、皮肤和黏膜。据我们所知,仅有的关于四肢骨内平滑肌瘤的报道发生在股骨近端和远端、胫骨以及尺骨。我们未发现此前有足部骨内平滑肌瘤的任何报道。骨内平滑肌瘤的X线片显示为单房或多房溶骨性病变,伴有硬化边缘。由于磁共振成像缺乏明确的放射学特征,这种罕见肿瘤的诊断需通过组织病理学研究和免疫组织化学标记物来确立。平滑肌梭形细胞以及肌肉细胞免疫组织化学标记物阳性是诊断的关键特征。骨内平滑肌瘤的治疗是通过广泛切除和刮除进行手术干预,随后填充骨腔。由于其发病率极低,该肿瘤的诊断具有挑战性。骨内平滑肌瘤应纳入具有良性放射学特征的骨内病变的鉴别诊断中。我们报告了首例22岁男性患者跟骨原发性骨内平滑肌瘤的病例。