Gilder Hannah E, Puffer Ross C, Spinner Robert J, Raghunathan Aditya, Bydon Mohamad
Department of Neurosurgery, Mayo Clinic, Rochester, Minnesota, USA.
Department of Pathology, Mayo Clinic, Rochester, Minnesota, USA.
World Neurosurg. 2018 Sep;117:178-181. doi: 10.1016/j.wneu.2018.06.035. Epub 2018 Jun 14.
It is important to differentiate low-grade malignant peripheral nerve sheath tumors (MPNSTs) from benign nerve sheath tumors as MPNSTs may require a more aggressive treatment strategy during and after initial resection. Loss of expression of the trimethyl histone H3 at the Lys27 position (H3K27-me3) has recently been described in MPNSTs and may help distinguish this tumor from pathologic mimics.
A 43-year-old woman presented with symptoms of radiculopathy and a history of pelvic radiation for cervical cancer 7 years prior. Imaging and surgical pathology were initially consistent with an L5 schwannoma including spindle morphology without mitoses and retained S100 expression. After an aggressive recurrence 11 months later, pathology was consistent with high-grade MPNST including heightened mitotic activity and loss of S100 expression.
After the identification of MPNST, H3K27M me3 immunostaining was applied to both the initial and recurrent pathologic specimens. The initial specimen demonstrated patchy loss of H3K27M me3 expression, more consistent with low-grade MPNST than schwannoma.
This case highlights the role of H3K27M me3 immunostaining to help differentiate MPNSTs that may mimic more benign nerve sheath tumors, especially in patients who have a history of radiation to the region in question.
区分低度恶性外周神经鞘瘤(MPNSTs)与良性神经鞘瘤很重要,因为MPNSTs在初次切除期间及之后可能需要更积极的治疗策略。最近在MPNSTs中发现了赖氨酸27位置的三甲基组蛋白H3(H3K27 - me3)表达缺失,这可能有助于将该肿瘤与病理模拟物区分开来。
一名43岁女性出现神经根病症状,有7年前因宫颈癌接受盆腔放疗史。最初的影像学和手术病理结果与L5神经鞘瘤一致,包括梭形形态、无核分裂且S100表达保留。11个月后出现侵袭性复发,病理结果与高级别MPNST一致,包括有丝分裂活性增强和S100表达缺失。
在确诊为MPNST后,对初始和复发的病理标本均进行了H3K27M me3免疫染色。初始标本显示H3K27M me3表达呈斑片状缺失,与低度MPNST而非神经鞘瘤更相符。
该病例突出了H3K27M me3免疫染色在帮助区分可能模拟更良性神经鞘瘤的MPNSTs中的作用,特别是在有相关区域放疗史的患者中。