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骶部塔尔洛夫囊肿是儿童下肢神经根病的罕见病因。

Sacral Tarlov Cyst as a Rare Cause of Lower Limb Radiculopathy in a Child.

作者信息

Venkata Srujana V, Mak David Sk, Esguerra Jonis Michael L, Aw Sze Jet, Ng Lee Ping, Low Sharon Yy

机构信息

Department of Neurosurgery, National Neuroscience Institute, Singapore, SGP.

Neurosurgery, Cebu South Medical Center, Cebu, PHL.

出版信息

Cureus. 2025 Aug 21;17(8):e90660. doi: 10.7759/cureus.90660. eCollection 2025 Aug.

Abstract

Tarlov cysts (TC) are uncommon perineural cysts that may arise anywhere along the spine, especially in the sacral region. To date, symptomatic TCs in children are very rare. Most of these benign lesions tend to be incidental discoveries during neuroimaging for other reasons. Nonetheless, they have been occasionally reported to cause sensorimotor-related neuropathy in the lower back, pelvis, legs, and urogenital system due to direct compression of the adjacent nerve roots. Management of adult TCs is well-described. In contrast, there is a paucity of contemporary literature on symptomatic TCs that are surgically treated in children. We report an unusual case of a paediatric patient who presents with lower limb radiculopathy secondary to large sacral TCs and discuss the management. A previously well 9-year-old female was referred for persistent lower back pain and left leg pain over a period of 2 months. There were no associated bladder or bowel symptoms. Clinical examination demonstrated a positive straight leg raise on the left and reduced sensation along the posterior left thigh, calf, foot dorsum, and toes. Magnetic resonance imaging (MRI) of her spine showed prominent, large perineural cysts surrounding bilateral S1 and the right S2 cauda equina nerve roots. Of note, there was associated bony expansion and scalloping of the sacral canal and corresponding sacral foramina. After a failed trial of conservative treatment, she underwent a laminotomy, wide fenestration, and excision of TCs. Postoperatively, her symptoms improved significantly. At 12 months' follow-up, there was no recurrence of the patient's lower back and leg symptoms. We describe an unusual case of symptomatic sacral TC in a child, whereby surgical treatment is a feasible treatment option in this age group.

摘要

塔尔洛夫囊肿(TC)是一种罕见的神经周围囊肿,可出现在脊柱的任何部位,尤其是骶骨区域。迄今为止,儿童期有症状的塔尔洛夫囊肿非常罕见。这些良性病变大多是在因其他原因进行神经影像学检查时偶然发现的。尽管如此,偶尔也有报道称,由于相邻神经根受到直接压迫,它们会导致下背部、骨盆、腿部和泌尿生殖系统出现与感觉运动相关的神经病变。成人塔尔洛夫囊肿的治疗方法已有详尽描述。相比之下,关于儿童期有症状且接受手术治疗的塔尔洛夫囊肿的当代文献却很少。我们报告了一例不寻常的儿科病例,该患儿因巨大的骶骨塔尔洛夫囊肿出现下肢神经根病,并讨论了其治疗方法。一名此前健康的9岁女性因持续2个月的下背部疼痛和左腿疼痛前来就诊。没有相关的膀胱或肠道症状。临床检查显示左侧直腿抬高试验阳性,左大腿后侧、小腿、足背和脚趾的感觉减退。其脊柱的磁共振成像(MRI)显示双侧S1和右侧S2马尾神经根周围有突出的大神经周围囊肿。值得注意的是,伴有骶管和相应骶孔的骨质膨胀和扇贝样改变。在保守治疗试验失败后,她接受了椎板切开术、广泛开窗术和塔尔洛夫囊肿切除术。术后,她的症状明显改善。在12个月的随访中,患者的下背部和腿部症状没有复发。我们描述了一例儿童期有症状的骶骨塔尔洛夫囊肿的不寻常病例,在这个年龄组中,手术治疗是一种可行的治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/903e/12449843/b7371f2a80b1/cureus-0017-00000090660-i01.jpg

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