Xia Qin, Tao Cheng, Zhu Ke-Wei, Zhong Wei-Ye, Li Peng-Lin, Jiang Yi, Mao Min-Zhi
Department of Orthopedics, The Second Xiangya Hospital, Central South University, Changsha 410011, Hunan Province, China.
Department of Pathology, The Second Xiangya Hospital, Central South University, Changsha 410011, Hunan Province, China.
World J Clin Cases. 2020 Feb 6;8(3):614-623. doi: 10.12998/wjcc.v8.i3.614.
Erdheim-Chester disease (ECD) is a rare multi-system or multi-organ histiocytic proliferative disease with diverse clinical manifestations, and the development of the disease is complex, which makes clinical diagnosis and treatment difficult. The characteristic clinical manifestations include multi-organ involvement, especially in the symmetrical diaphysis and metaphysis of the bilateral extremities. ECD with a unilateral talus lesion is extremely rare. Here, we report an unusual case of ECD invading the asymmetric talus and tibia without involving other organs. The patient had good outcome after surgery.
We report a case of a 67-year-old man who was referred to our outpatient department because of left ankle chronic pain for 5 years, which exacerbated after a foot sprain 6 mo previously. We discovered multiple sclerotic lesions of the tibia and talus on his previous X-ray films, which were initially missed in a local hospital. Therefore, enhanced computer computed tomography (CT) and magnetic resonance imaging were performed. These examinations showed multiple lesions in the bone marrow cavity of the left tibia, and cortical sclerosis and osteonecrosis of the left talus. Specimens were collected bone puncture from the two lesions, and a final diagnosis of ECD was confirmed by pathological and immunohistochemical examinations. In addition, other auxiliary examinations including head CT, pulmonary CT, spinal CT, abdominal CT, cardiac ultrasound and thyroid ultrasound showed no obvious abnormalities. The patient underwent surgery for the tibia lesion scraping and talus lesion scraping combined with cement casting. The patient started on a progressive rehabilitation at 4 wk, and felt no pain after surgery. During a 2-year follow-up period, the patient exercised normally without pain, and there were no signs of recurrence.
This study shows that surgery treatment may also achieve good results for ECD patients with only bone involvement.
厄尔德海姆-切斯特病(ECD)是一种罕见的多系统或多器官组织细胞增生性疾病,临床表现多样,疾病发展复杂,导致临床诊断和治疗困难。其特征性临床表现包括多器官受累,尤其是双侧肢体对称的骨干和干骺端。单侧距骨病变的ECD极为罕见。在此,我们报告一例不寻常的ECD病例,其侵犯不对称的距骨和胫骨,未累及其他器官。患者术后预后良好。
我们报告一例67岁男性,因左踝慢性疼痛5年就诊于我院门诊,6个月前足部扭伤后疼痛加剧。此前的X线片显示其胫骨和距骨有多个硬化性病变,当地医院最初漏诊。因此,进行了增强计算机断层扫描(CT)和磁共振成像检查。这些检查显示左胫骨骨髓腔内有多个病变,左距骨皮质硬化和骨坏死。从两个病变部位进行骨穿刺采集标本,经病理和免疫组化检查确诊为ECD。此外,包括头部CT、肺部CT、脊柱CT、腹部CT、心脏超声和甲状腺超声在内的其他辅助检查均未发现明显异常。患者接受了胫骨病变刮除术和距骨病变刮除术并联合骨水泥填充。患者在4周时开始逐步康复训练,术后无疼痛。在2年的随访期内,患者正常活动无疼痛,无复发迹象。
本研究表明,手术治疗对于仅累及骨骼的ECD患者也可能取得良好效果。