背景:非创伤性骨化性肌炎是一种罕见疾病,其具体发病机制尚不清楚。这种疾病的早期诊断在儿童中是非常困难的,因为难以确定病史和非特异性的早期临床表现。可能导致部分患者得不到及时有效的诊断和治疗。我们报告了儿童非创伤性骨化性肌炎的诊断和治疗,并总结了该疾病的临床特征和诊断治疗。
方法:一名8岁的女孩第一次来到我们医院,右下肢疼痛超过一周。没有外伤或剧烈活动的病史。在体检时,右大腿上没有发现肿块,右下肢活动受限。超声检查显示髋部滑膜炎,建议卧床休息。三天后,孩子的疼痛持续并恶化,伴有发烧和其他不适。她再次来到我们医院,发现右大腿有肿块,表面红肿。图像显示右大腿软组织肿瘤伴钙化。血常规检查显示炎症指标明显增加。在感染的情况下,病人接受了抗生素治疗,疼痛很快缓解了,没有发烧。然而,右大腿肿块持续并硬化。患者在1个多月后接受了切口活检,术后病理显示非创伤性骨化性肌炎。经过大约9个月的观察,肿瘤仍然存在,影响了孩子的生活,然后进行切除。自从后续行动以来,没有复发。
结论:由于难以辨别儿童的病史和多样化的早期表现,儿童非骨化性肌肉疾病的早期诊断比较困难。及时随访、定期影像监测等措施有利于疾病的早期诊断。本病具有一定的自我限制,可以先观察和治疗。如果肿瘤在后期持续存在或影响功能,然后考虑手术。
BACKGROUND: Nontraumatic myositis ossificans is a rare disease whose specific pathogenesis is unclear. Early diagnosis of this disease is very difficult in children because of difficulties in determining medical history and nonspecific early clinical manifestations, which may lead to the failure of timely and effective diagnosis and treatment in some patients. We report the diagnosis and treatment of a child with nontraumatic myositis ossificans and summarize the clinical characteristics and diagnosis and treatment of the disease.
METHODS: An 8-year-old girl first came to our hospital for more than a week with pain in the right lower limb. There was no history of trauma or strenuous activities. On physical examination, no mass on the right thigh was found, and the movement of the right lower extremity was limited. Ultrasonography showed synovitis of the hip, and bed rest was recommended. Three days later, the child\'s pain persisted and worsened, accompanied by fever and other discomforts. She came to our hospital again and a mass was found on the right thigh with redness and swelling on the surface. The images showed a soft tissue tumor on the right thigh with calcification. Routine blood tests revealed that the inflammation index was significantly increased. In
case of infection, the patient was given antibiotics, and the pain was relieved soon after, without fever. However, the right thigh mass persisted and hardened. The patient underwent incision biopsy more than 1 mo later, and the postoperative pathology showed nontraumatic myositis ossificans. After approximately 9 mo of observation, the tumor still persisted, which affected the life of the child, and then resection was performed. Since follow-up, there has been no recurrence.
CONCLUSIONS: Due to the difficulty in discerning a child\'s medical history and the diverse early manifestations, it is difficult to diagnose nonossifying muscle disease in children in its early stage. Measures such as timely follow-up and periodic image monitoring are conducive to early diagnosis of the disease. The disease has a certain degree of self-limitation, and it can be observed and treated first. If the tumor persists in the later stage or affects functioning, then surgery is considered.