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腰椎非脊髓纵裂性硬脊膜内脂肪瘤与囊肿的罕见共存——病例报告及文献综述

A rare coexistence of a non-dysraphic intradural lipoma and a cyst in the lumbar spine - A case report and literature review.

作者信息

Khaddam Hala, Shbani Abdulrahman, Yousef Obai, Hussein Ali, Salman Iyas, Salman Issam

机构信息

Faculty of Medicine, Tartous University, Tartous, Syria.

Faculty of Medicine, Tartous University, Tartous, Syria.

出版信息

Int J Surg Case Rep. 2024 Nov;124:110379. doi: 10.1016/j.ijscr.2024.110379. Epub 2024 Oct 1.

Abstract

INTRODUCTION

Spinal intradural lipomas are rare entities, particularly when not associated with spinal dysraphism. Their diagnosis is often delayed due to their slow growth and presentation in dorsal components. Although the association between lipomas and cysts has been previously noted, the coexistence of lipomas with fluid-filled cysts is exceedingly rare. We present a case that highlights the presentation, management, and outcomes of a patient with the unusual coexistence of these two lesions in the lumbar region.

CASE REPORT

An eight-year-old female presented to our outpatient neurology clinic with complaints of weakness and severe pain in her lower limbs, accompanied by urinary retention and lumbar focal hypertrichosis. Magnetic resonance imaging (MRI) of the spine revealed a lipoma alongside a cyst at the level of the first two lumbar vertebrae. A subtotal resection of both lesions was performed; the cyst was drained, revealing a clear fluid, while the lipoma was partially resected due to significant adhesions to the spine. The patient achieved full recovery within a few days, as confirmed by neurological and radiological evaluations.

CLINICAL DISCUSSION

The origin of non-dysraphic lipomas remains unclear, with several congenital theories proposed to explain their formation. While associations with various anomalies and cysts have been documented, the coexistence of intradural fluid-filled cysts is exceptionally uncommon. This case presents several potential explanations for this phenomenon. Typically, lipomas are asymptomatic until they cause signs of cord compression. However, the presence of associated entities can lead to earlier symptom onset. Surgical intervention often involves subtotal resection due to severe tumor adhesions, which can yield satisfactory outcomes despite the presence of residual tumor postoperatively.

CONCLUSION

The occurrence of an intradural fluid-filled cyst in conjunction with a lipoma is rare and may represent an arachnoid cyst or a form of weakened spinal dysraphism linked to the controversial formation of lipomas. Illustrating this association is crucial, as the adhesions and indistinct boundaries between these lesions and the spinal cord complicate complete excision, necessitating subtotal resection, which appears to favor better outcomes.

摘要

引言

脊髓硬膜内脂肪瘤较为罕见,尤其是不伴有脊髓发育异常时。由于其生长缓慢且多表现于背部结构,其诊断常常延迟。尽管此前已注意到脂肪瘤与囊肿之间的关联,但脂肪瘤与充满液体的囊肿同时存在的情况极为罕见。我们报告一例病例,突出显示了一名患者在腰椎区域这两种病变异常并存时的临床表现、治疗及预后情况。

病例报告

一名8岁女性因下肢无力和剧痛就诊于我院门诊神经科,伴有尿潴留和腰部局部多毛症。脊柱磁共振成像(MRI)显示在第一、二腰椎水平有一个脂肪瘤和一个囊肿。对这两种病变进行了次全切除;囊肿引流后,流出清亮液体,而脂肪瘤因与脊柱粘连严重,仅部分切除。经神经学和影像学评估证实,患者在数天内完全康复。

临床讨论

非发育异常性脂肪瘤的起源尚不清楚,已提出多种先天性理论来解释其形成。虽然已记录到与各种异常和囊肿的关联,但硬膜内充满液体的囊肿并存情况极为罕见。本病例对此现象提出了几种可能的解释。通常,脂肪瘤在引起脊髓压迫体征之前是无症状的。然而,相关病变的存在可导致症状更早出现。由于肿瘤粘连严重,手术干预通常涉及次全切除,尽管术后存在残留肿瘤,但仍可取得满意的效果。

结论

硬膜内充满液体的囊肿与脂肪瘤同时出现的情况罕见,可能代表蛛网膜囊肿或与有争议的脂肪瘤形成相关的一种脊髓发育异常形式。阐明这种关联至关重要,因为这些病变与脊髓之间的粘连和边界不清使完全切除变得复杂,需要进行次全切除,而这似乎有利于取得更好的预后。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5daa/11489829/b9c5dd6e3478/gr1.jpg

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