Tagliafico Alberto, Resmini Eugenia, Nizzo Raffaella, Derchi Lorenzo E, Minuto Francesco, Giusti Massimo, Martinoli Carlo, Ferone Diego
Department of Radiology R, University of Genova, Viale Benedetto XV, 6, I-16132 Genova, Italy.
Eur J Endocrinol. 2008 Oct;159(4):369-73. doi: 10.1530/EJE-08-0327. Epub 2008 Jul 16.
Acromegalic patients may complain of sensory disturbances in their hands. Cubital tunnel syndrome, the ulnar nerve neuropathy at the cubital tunnel (UCT), in acromegalic patients has never been reported.
To describe and assess the prevalence of UCT in acromegalic patients and the effects of 1 year of therapy on UCT.
We examined prospectively 37 acromegalic patients with no history of polyneuropathy, acute trauma at the elbow, no diabetes or hypothyroidism with clinical examination, nerve conduction studies (NCS), and high-resolution ultrasound (US). A control group was made by 50 volunteers. The local ethics committee approved the study and written informed consent was obtained from all subjects involved in the study.
Clinical history, physical examination, NCS, and US were used to diagnose UCT at the beginning of the study and after 1 year.
In 8 of 37 patients, a diagnosis of UCT was made at the beginning of the study reflecting a prevalence of 21%. After 1 year, 5 of 8 (62.5%) patients reported clinical and NCS improvements and evident US reduction of nerve cross-sectional area (CSA; 16.7+/-2.9 mm(2) vs 12.2+/-3.1 mm(2); P<0.001). In 3 of 8 (37.5%) patients, the UCT was unchanged. Ulnar nerve CSA was significantly increased in acromegalic patients with UCT (16.7+/-2.9 mm(2) vs 11.1+/-2.3 mm(2); P<0.047).
Ulnar neuropathy could occur in acromegalic patients and can improve in 62% of cases with disease control. Due to the different management and therapeutic approach, it would be important to make differential diagnosis between cubital and carpal tunnel syndrome in acromegaly.
肢端肥大症患者可能会抱怨手部感觉障碍。在肢端肥大症患者中,肘管综合征(即尺神经在肘管处的神经病变,UCT)从未有过报道。
描述并评估肢端肥大症患者中肘管综合征的患病率以及1年治疗对肘管综合征的影响。
我们前瞻性地检查了37例无多神经病病史、肘部无急性创伤、无糖尿病或甲状腺功能减退的肢端肥大症患者,进行了临床检查、神经传导研究(NCS)和高分辨率超声(US)检查。由50名志愿者组成对照组。当地伦理委员会批准了该研究,并获得了所有参与研究的受试者的书面知情同意书。
在研究开始时和1年后,使用临床病史、体格检查、NCS和US来诊断肘管综合征。
在37例患者中的8例中,研究开始时诊断为肘管综合征,患病率为21%。1年后,8例患者中的5例(62.5%)报告临床症状和NCS有所改善,且超声显示神经横截面积明显减小(16.7±2.9mm²对12.2±3.1mm²;P<0.001)。8例患者中的3例(37.5%)肘管综合征无变化。患有肘管综合征的肢端肥大症患者的尺神经横截面积显著增加(16.7±2.9mm²对11.1±2.3mm²;P<0.047)。
肢端肥大症患者可能发生尺神经病变,62%的病例在疾病得到控制后可改善。由于管理和治疗方法不同,在肢端肥大症中区分肘管综合征和腕管综合征进行鉴别诊断很重要。