From the Department of Neurology (M.S., M.V.P., D.D., T.O., J.H.U., A.S., N.P.S., P.J.B.D., C.E.R., C.J.K.), Mayo Clinic, Rochester, MN; Department of Neurology (S.S.), Rambam Health Care Clinic, Haifa, Israel; Department of Neurosurgery (R.J.S.); and Department of Laboratory Medicine and Pathology (C.J.K.), Mayo Clinic, Rochester, MN.
Neurology. 2023 Oct 3;101(14):e1455-e1460. doi: 10.1212/WNL.0000000000207545. Epub 2023 Jul 3.
The objective of this study was to study early-onset radiation-induced neuropathy reviewing neurologic course, steroid response, and available nerve biopsies.
Patients coded with radiation-induced neuropathy within 6 months of radiation were reviewed from January 1,1999, to August 31, 2022. Patients had to have electrodiagnostically confirmed neuropathy localized within or distal to radiation fields. Neurologic course and nerve biopsies were reviewed.
Twenty-eight patients (16 male and 12 female patients, mean age 63.8 years) were identified. The average radiation dose was 4,659 cGy (range 1,000-7,208). Tumor infiltration was not observed on MRI and PET. Postradiation onsets averaged 2 months (range 0-5). Localizations included brachial (n = 4) plexopathies, lumbosacral (n = 12) plexopathies, radiculopathies (n = 10), and mononeuropathies (n = 2). Neuropathic pain (n = 25) and weakness (n = 25) were typical. The clinical courses were subacute monophasic (n = 14), chronic progressive (n = 8), or static (n = 1), and 5 were without follow-up. Nerve biopsies (n = 8) showed an inflammatory ischemic process with perivascular inflammatory infiltrates (n = 7) or microvasculitis (n = 2). Nine patients, 7 with monophasic courses, received steroid burst therapy with symptom improvement in 8. No patients recovered entirely back to baseline.
In contrast to chronic radiation-induced neuropathy, early-onset patients most commonly have painful monophasic courses with residual deficits, possibly steroid responsive. An ischemic inflammatory pathogenesis is suggested.
本研究旨在探讨早期放射性诱导神经病,分析其神经病变过程、类固醇反应和现有的神经活检结果。
回顾 1999 年 1 月 1 日至 2022 年 8 月 31 日期间因放射性诱导神经病而接受治疗的患者。这些患者的神经病变必须通过电诊断确认,且病变位于辐射野内或辐射野远端。对患者的神经病变过程和神经活检结果进行分析。
共纳入 28 名患者(16 名男性和 12 名女性,平均年龄 63.8 岁)。患者的平均辐射剂量为 4659cGy(范围为 1000-7208cGy)。磁共振成像(MRI)和正电子发射断层扫描(PET)未观察到肿瘤浸润。放射后发病时间平均为 2 个月(范围为 0-5 个月)。病变部位包括臂丛(n=4)、腰骶丛(n=12)、神经根病(n=10)和单神经病(n=2)。神经病理性疼痛(n=25)和无力(n=25)是常见症状。临床过程为亚急性单相(n=14)、慢性进展性(n=8)或静止性(n=1),其中 5 例患者未进行随访。神经活检(n=8)显示炎症性缺血性病变,伴血管周围炎症浸润(n=7)或微血管炎(n=2)。9 名患者接受了类固醇冲击治疗,其中 7 名单相病程患者症状改善,8 名患者症状改善。但无患者完全恢复到基线水平。
与慢性放射性诱导神经病不同,早期发病患者的神经病变过程多为单相、疼痛性,伴有残留症状,可能对类固醇治疗有反应。这提示其发病机制可能为缺血性炎症。