Institute of Sports Medicine, Beijing Key Laboratory of Sports Injuries, Peking University Third Hospital, Beijing, China.
Medicine (Baltimore). 2022 Nov 11;101(45):e31715. doi: 10.1097/MD.0000000000031715.
Low-grade myofibroblastic sarcoma (LGMS) is an atypical type of tumor composed of myofibroblasts. LGMS in the femoral head neck junction is extremely rare and no case treated by hip arthroscopy was reported.
We reported a case of LGMS in the femoral head neck junction treated by hip arthroscopy. A 30-year-old female was admitted to our hospital with discomfort and pain after left hip sprained one year prior. Physical examination revealed swelling of the left hip and magnetic resonance images showed a soft tissue mass in the femoral head neck junction.
Via microscopy of pathological specimens, spindle cell proliferative lesions, atypia of some cells, and mitotic figures/pathological mitotic figures of some cells were observed. Immunohistochemistry revealed positive for smooth muscle actin, focally positive for CD34 and CD68, while negative for S-100, desmin, and anaplastic lymphoma kinase. The imaging, histomorphological and immunohistochemical features suggested a final diagnosis of LGMS of the proximal femur.
This patient underwent hip arthroscopy for excision of the soft tissue mass.
The clinical and imaging follow-up at 6 months postoperatively showed that surgery had achieved good clinical outcomes.
To the best of our knowledge, this is the first case report of LGMS in the femoral head neck junction treated by hip arthroscopy. Beyond the present case, other 120 cases from 58 literatures (1998-2022) are reviewed and discussed. The age of LGMS patients ranged from 11 months to 77 years and the male-to-female ratio was approximately 1.28:1. The location distribution of previously reported LGMS cases and the present case was as follows: Head&neck (45.90%), trunk (30.33%), and extremity (23.77%). Hip arthroscopic excision of LGMS may achieve relatively good clinical outcomes.
低度恶性肌纤维母细胞瘤(LGMS)是一种由肌纤维母细胞组成的非典型肿瘤。股骨头颈交界处的 LGMS 极为罕见,且尚无经髋关节镜治疗的病例报道。
我们报告了一例经髋关节镜治疗的股骨头颈交界处 LGMS 病例。一名 30 岁女性,一年前左髋扭伤后出现不适和疼痛,来我院就诊。体格检查发现左髋肿胀,磁共振成像显示股骨头颈交界处软组织肿块。
通过病理标本显微镜观察,观察到梭形细胞增生性病变、部分细胞异型性和有丝分裂/部分细胞病理性有丝分裂。免疫组织化学显示平滑肌肌动蛋白阳性,局灶性 CD34 和 CD68 阳性,而 S-100、结蛋白和间变性淋巴瘤激酶阴性。影像学、组织形态学和免疫组织化学特征提示最终诊断为股骨近端 LGMS。
该患者接受髋关节镜切除软组织肿块。
术后 6 个月的临床和影像学随访显示手术取得了良好的临床效果。
据我们所知,这是首例经髋关节镜治疗的股骨头颈交界处 LGMS 病例报告。除本例外,还回顾和讨论了来自 58 篇文献(1998-2022 年)的其他 120 例病例。LGMS 患者的年龄从 11 个月至 77 岁不等,男女比例约为 1.28:1。以前报道的 LGMS 病例和本病例的位置分布如下:头颈部(45.90%)、躯干(30.33%)和四肢(23.77%)。髋关节镜切除 LGMS 可能获得相对较好的临床效果。