Division of Neurosciences, Northwest Community Healthcare, Arlington Heights, IL; and.
Loyola University Chicago Stritch School of Medicine, Maywood, IL.
J Clin Neuromuscul Dis. 2021 Jun 1;22(4):192-199. doi: 10.1097/CND.0000000000000355.
Novel antibodies to trisulfated heparin disaccharide (TS-HDS) and fibroblast growth factor receptor 3 (FGFR-3) have been recently described in otherwise cryptogenic small fiber neuropathy (SFN) cases. Our goal was to further describe clinical features in such cases and to analyze treatment responses.
In a retrospective analysis, 40 cases of cryptogenic SFN in a university neuropathy clinic were identified. Of these, TS-HDS and FGFR-3 cases were identified, and clinical features and treatment responses were analyzed.
In this cohort, 95% were women, and 55% had either TS-HDS or FGFR-3 antibodies (77% of these had TS-HDS). Of the seropositive group, 41% had a nonlength dependent epidermal nerve fiber density on skin punch biopsy (OR = 1.80). In the seropositive group, 82% had neuropathic pain as their primary symptom (OR = 1.73). Also 32% of seropositive patients reported widespread pain (OR = 1.63). 63% of seropositive cases presented acutely (OR = 11.0). In the seropositive group, 23% had an initial erroneous diagnosis (OR = 1.47). Eight seropositive patients improved on intravenous immunoglobulin treatment, with a 42% reduction in pain scores (P = 0.02), a 44% reduction in the Utah Neuropathy Score, and improved epidermal nerve fiber density post-treatment.
TS-HDS and FGFR-3 antibodies may be present in a high proportion of cryptogenic SFN cases with acute onset, nonlength dependent pathology, and primary neuropathic and widespread pain. They are often misdiagnosed as other conditions including fibromyalgia. These cases may be responsive to immune treatment, especially with intravenous immunoglobulin.
最近在其他隐源性小纤维神经病(SFN)病例中描述了针对三硫酸肝素二糖(TS-HDS)和成纤维细胞生长因子受体 3(FGFR-3)的新型抗体。我们的目标是进一步描述此类病例的临床特征,并分析治疗反应。
在大学神经病诊所的回顾性分析中,确定了 40 例隐源性 SFN 病例。在这些病例中,确定了 TS-HDS 和 FGFR-3 病例,并分析了临床特征和治疗反应。
在该队列中,95%为女性,55% 具有 TS-HDS 或 FGFR-3 抗体(其中 77% 具有 TS-HDS)。在血清阳性组中,41% 的皮肤活检显示非长度依赖性表皮神经纤维密度(OR = 1.80)。在血清阳性组中,82% 的患者以神经病理性疼痛为主要症状(OR = 1.73)。此外,32% 的血清阳性患者报告广泛疼痛(OR = 1.63)。63%的血清阳性病例表现为急性起病(OR = 11.0)。在血清阳性组中,23% 的患者存在初始误诊(OR = 1.47)。8 例血清阳性患者接受静脉注射免疫球蛋白治疗后有所改善,疼痛评分降低 42%(P = 0.02),犹他州神经病评分降低 44%,治疗后表皮神经纤维密度改善。
TS-HDS 和 FGFR-3 抗体可能存在于高比例的具有急性发作、非长度依赖性病理、主要为神经病理性和广泛疼痛的隐源性 SFN 病例中。它们经常被误诊为其他疾病,包括纤维肌痛。这些病例可能对免疫治疗有反应,尤其是静脉注射免疫球蛋白。