Department of Neurology, The First People's Hospital of Changde City, Changde, Hunan, China.
Department of Nursing, Changde Vocational Technical College, Changde, Hunan, 415000, China.
Medicine (Baltimore). 2022 Sep 23;101(38):e30768. doi: 10.1097/MD.0000000000030768.
Hereditary neuropathy with liability to pressure palsies (HNPP) is an autosomal dominantly inherited genetic disease characterized by recurrent numbness and limb weakness. HNPP can be easily missed or misdiagnosed because of electrophysiological heterogeneity and atypical clinical symptoms. To date, diagnosis of HNPP remains a challenge for clinicians.
Here, we report the case of a 12-year-old woman diagnosed with HNPP, which was initially diagnosed with Guillain-Barré Syndrome (GBS) and treated with intravenous immunoglobulin (IVIG).
Repeat electrodiagnostic studies and genetic testing confirmed the diagnosis of HNPP.
The patient was treated with neurotrophic drugs and health education, including avoiding maintenance of a certain posture for extended periods, which could damage the peripheral nerves.
The patient was discharged 5 days later. The patient was free from recurrence after 6 months of follow-up.
This case highlights the complexity of HNPP diagnosis and emphasizes the importance of early identification.
遗传性压力易感性神经病(HNPP)是一种常染色体显性遗传的遗传病,其特征是反复出现麻木和四肢无力。由于电生理学的异质性和不典型的临床症状,HNPP 很容易被忽视或误诊。迄今为止,HNPP 的诊断仍然是临床医生面临的挑战。
我们在此报告了一例 12 岁女性 HNPP 患者的病例,该患者最初被诊断为格林-巴利综合征(GBS),并接受了静脉注射免疫球蛋白(IVIG)治疗。
重复电诊断研究和基因检测证实了 HNPP 的诊断。
患者接受了神经营养药物和健康教育的治疗,包括避免长时间保持某种姿势,这可能会损害周围神经。
患者 5 天后出院。经过 6 个月的随访,患者未再复发。
该病例强调了 HNPP 诊断的复杂性,并强调了早期识别的重要性。