腹腔假性囊肿合并脑室腹腔分流:附十二例报告及文献复习。

S J Gaskill, A E Marlin
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引用次数: 90

摘要

据报道,分流并发症的发生率约为26%。假性囊肿是一种不常见但重要的并发症。自1954年Harsh首次提到与分流术相关的脐周囊肿以来,文献中已报道了44例病例。除了我们自己的12个案例外,我们还审查了这些案例。从收集到的一系列病例中,病因和治疗的几个特点变得明显。最常见的表现是腹胀和/或疼痛,而不是分流功能障碍。然后很容易用超声检查进行诊断。在病因学上,很明显,炎症过程是一个常见的诱发因素。在我们的研究中,16%有急性感染,41.6%有脑脊液感染史(6个月至6.2年),16%有中枢神经系统肿瘤,尽管肿瘤细胞未从腹膜囊肿中分离出来。我们对囊肿本身的处理与其他系列报道不同;经脑脊液转移后,发现囊肿自发重吸收,无需切除或抽吸。一旦囊肿重新吸收,腹腔就可以用于分流。这有时需要在腹腔重新利用之前转换到心房或胸膜分流。在3个月到4年的随访中,尽管58%的分流管转化为脑室-腹膜分流管,但没有出现囊肿复发的问题。本文对囊肿和脑积水的治疗模式进行综述。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pseudocysts of the abdomen associated with ventriculoperitoneal shunts: a report of twelve cases and a review of the literature.

Shunt complications are reported to occur at a rate of approximately 26%. One of the less frequent but important complications is that of the pseudocyst. Since Harsh's first mention of a periumbilical cyst associated with a shunt in 1954, 44 cases have been reported in the literature. These are reviewed in addition to 12 cases of our own. From the collected series several features about the etiology and management become apparent. The most common presentation is that of abdominal distension and/or pain rather than shunt malfunction. Diagnosis is then readily made with ultrasonography. Etiologically, it is evident that an inflammatory process is a frequent predisposing factor. In our series 16% had acute infection, 41.6% had a past history of CSF infection (6 months to 6.2 years), and 16% had CNS tumor although tumor cells were not isolated from the peritoneal cysts. Our management of the cyst itself was different from that reported in other series; it was found that the cyst reabsorbed spontaneously without excision or aspiration once the CSF was diverted. The peritoneal cavity could then be used for shunting once the cyst had reabsorbed. This sometimes required conversion to an atrial or pleural shunt before reutilization of the peritoneal cavity. There were no problems with cyst recurrence despite the conversion of 58% of the shunts to ventriculoperitoneal shunts with follow-up ranging from 3 months to 4 years. The mode of management of both the cyst and the hydrocephalus is reviewed.

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