Patil Prashant Sadashiv, Gupta Abhaya, Kothari Paras L, Kekre Geeta, Gupta Rahul, Dikshit Vishesh, Mudkhedkar Kedar, Kesan Krishna
Department of Paediatric Surgery, L.T.M.G. Hospital, Sion, Mumbai, Maharashtra, India.
J Pediatr Neurosci. 2016 Apr-Jun;11(2):99-104. doi: 10.4103/1817-1745.187619.
To analyze immediate and long-term results of lipomeningomyelocele (LMM) repair in asymptomatic patients.
Seventeen patients of LMM presented to Department of Paediatric Surgery over a period from 2011 to 2015 were evaluated preoperatively by magnetic resonance imaging of whole spine, and pre- and post-operative Ultrasound of kidney, ureter, bladder, and neurosonogram. Surgical procedure involved total excision of lipoma in 15 patients and near total excision in 2 patients. Division of filum terminale could be done in 15 out of 17 patients. Follow-up varied from 1 to 3.5 years (mean 1.9 years).
This study included 10 (58.8%) patients of lumbosacral LMM, 5 (29.4%) patients of sacral, and 2 (11.7%) patients of thoracolumbar LMM. About 13 (76.4%) patients were operated before 3 months of age, 2 (23.5%) patients were operated between 3 and 6 months, and two patients were operated between 6 and 11 months. None of the patients had bladder/bowel dysfunction preoperatively. Preoperative lower limb power was normal in all patients. Objective improvement in lower limb motor function was observed in 3 (17.6%) patients and three patients had decreased lower limb power. Two patients developed altered sensations and weakness of lower limb about 2.5-3 years after initial LMM repair. They needed repeat detethering of cord. Two patients had fecal pseudoincontinence, whereas one patient developed constipation. Bowel dysfunction was managed by rectal washouts, and oral laxatives were added if required. One (5.8%) patient of lumbosacral LMM and 1 (5.8%) patient of sacral LMM had urinary incontinence postoperatively. This was managed by clean intermittent catheterization with continuous overnight drainage. Conservative management of bladder and bowel dysfunction was effective in all patients till the last follow-up. Two patients developed hydrocephalus after LMM repair for which low-pressure ventriculoperitoneal shunt was inserted. Wound infection occurred in 1 (5.8%) patient, whereas 7 (41.1%) patients developed seroma in wound which responded to repeated aspirations under aseptic precautions.
With total excision of lipoma and division of filum terminale satisfactory outcome for asymptomatic patients of LMM can be achieved. Authors recommend early surgery for LMM even in asymptomatic patients. Patients with residual lipoma and undivided filum terminale should be observed closely for the development of progressive neurological changes.
分析无症状性脂肪脊髓脊膜膨出(LMM)修复的近期和远期效果。
2011年至2015年期间,17例LMM患儿到小儿外科就诊,术前均行全脊柱磁共振成像、肾脏、输尿管、膀胱超声及神经超声检查。手术方式为15例患者行脂肪瘤全切术,2例患者行次全切术。17例患者中有15例可行终丝切断术。随访时间为1至3.5年(平均1.9年)。
本研究包括10例(58.8%)腰骶部LMM患者、5例(29.4%)骶部LMM患者和2例(11.7%)胸腰段LMM患者。约13例(76.4%)患者在3个月龄前接受手术,2例(23.5%)患者在3至6个月龄间接受手术,2例患者在6至11个月龄间接受手术。所有患者术前均无膀胱/肠道功能障碍。所有患者术前下肢肌力均正常。3例(17.6%)患者下肢运动功能有客观改善,3例患者下肢肌力下降。2例患者在初次LMM修复术后约2.5至3年出现下肢感觉改变和无力。他们需要再次行脊髓栓系松解术。2例患者出现粪便假性失禁,1例患者出现便秘。肠道功能障碍通过直肠冲洗处理,必要时加用口服泻药。1例(5.8%)腰骶部LMM患者和1例(5.8%)骶部LMM患者术后出现尿失禁。通过清洁间歇性导尿及持续夜间引流进行处理。直至最后一次随访,所有患者膀胱和肠道功能障碍的保守治疗均有效。2例患者在LMM修复术后出现脑积水,为此行低压脑室腹腔分流术。1例(5.8%)患者发生伤口感染,7例(41.1%)患者伤口出现血清肿,经无菌操作下反复抽吸后好转。
通过脂肪瘤全切及终丝切断术,无症状性LMM患者可获得满意疗效。作者建议即使是无症状性LMM患者也应尽早手术。残留脂肪瘤和未切断终丝的患者应密切观察是否出现进行性神经学改变。