An Official publication of The Asian Congress of Neurological Surgeons (AsianCNS)

Search Article
Home About us Editorial board Search Ahead of print Current issue Archives Submit article Instructions Advertise Subscribe Contacts Login  Facebook Tweeter
  Users Online: 2903 Home Print this page Email this page Small font sizeDefault font sizeIncrease font size  

   Table of Contents      
CASE REPORT
Year : 2019  |  Volume : 14  |  Issue : 3  |  Page : 935-937

Patent persistent fibrous tract in a patient with disconnected lumboperitoneal shunt


1 Department of Neurosurgery, National Academy of Medical Sciences, Bir Hospital, Kathmandu, Nepal; Department of Neurosurgery, Banbuntane Hotokukai Hospital, Fujita Health University, Nagoya, Japan
2 Department of Neurosurgery, Chiba Kashiwa Tanaka Hospital, Kashiwa, Japan
3 Department of Neurosurgery, Banbuntane Hotokukai Hospital, Fujita Health University, Nagoya, Japan

Date of Web Publication2-Aug-2019

Correspondence Address:
Rajan Kumar Sharma
Department of Neurosurgery, National Academy of Medical Sciences, Bir Hospital, Kathmandu, Nepal

Login to access the Email id

Source of Support: None, Conflict of Interest: None


DOI: 10.4103/ajns.AJNS_91_19

Rights and Permissions
  Abstract 


Disconnection of proximal or distal catheter is seen more frequently in the complication of the lumboperitoneal (LP) shunt. A connective tissue sheath that forms around the peritoneal catheter of silicone shunt tubing is a normal biological response to foreign material. The literature did not establish whether the disconnected LP shunt can allow passage of cerebrospinal fluid (CSF) through the disconnected portion. However, proof of the passage of CSF through these sheaths has been reported in only one published study to date. We present a case of a young patient with disconnected LP shunt who reported patent persistent fibrous tract around the tube shunt. In conclusion, asymptomatic patients with shunt disconnection should be evaluated with shuntography for patency of fibrous sheath before removal of the shunt to avoid the possible complications.

Keywords: Malfunction, patent persistent fibrous tract, rare


How to cite this article:
Sharma RK, Takagi K, Yamada Y, Kawase T, Kato Y. Patent persistent fibrous tract in a patient with disconnected lumboperitoneal shunt. Asian J Neurosurg 2019;14:935-7

How to cite this URL:
Sharma RK, Takagi K, Yamada Y, Kawase T, Kato Y. Patent persistent fibrous tract in a patient with disconnected lumboperitoneal shunt. Asian J Neurosurg [serial online] 2019 [cited 2019 Dec 12];14:935-7. Available from: http://www.asianjns.org/text.asp?2019/14/3/935/263981




  Introduction Top


There is a huge advancement in the evaluation and the treatment of hydrocephalus over several years after the introduction of the effective cerebrospinal fluid (CSF) shunting methods.[1] Despite the development and improvement of these diversion methods, there are various complications of the shunt system such as catheter occlusion, disconnection, migration, fracture, and outgrowth.[2],[3],[4] When there are mechanical problems with the shunt but the patients are asymptomatic or minimally symptomatic and the cranial computed tomography (CT) scan does not reveal an active ventricular dilatation, the decision of treatment becomes difficult. It has postulated that patent fibrous tract allows passage of the CSF through disconnected outgrowth distal catheter.[5],[6] It has been asserted that in these situations, CSF passes through the fibrous sheath around the catheter, but this has not been definitively proved in previous reports. We present here a case of a 17-year-old boy who had lumboperitoneal (LP) shunt done for the postoperative pseudomeningocele which occurred postsuboccipital decompression for Arnold–Chiari type I malformation. The patient had a disconnection of the LP shunt and was asymptomatic, so the LP shunt was removed. Later, the patient developed symptoms of increased intracranial pressure (ICP) and we had to place LP shunt again.


  Case Report Top


A 17-year-old man was performed LP shunt at 12 years old due to pseudomeningocele from suboccipital decompression in Arnold–Chiari type I malformation [Figure 1]a and [Figure 1]b. LP shunt revision was performed 8 months after because of shunt malfunction. He recovered so completely that he again started his favorite sports (Kendo; Japanese fencing). He frequently bent his back while performing Kendo. Then, he complained about low back pain after revision. Radiographic studies demonstrated that the proximal catheter disconnected [Figure 2] and CSF could not aspirate from the flushing device. The LP shunt removal was performed, and subcutaneous mass from CSF collection was observed after the closing of the proximal fibrous tract by tobacco-bag suture [Figure 3]. Collagen fibers, fat tissue, and small vessels were also observed in that fibrous tract [Figure 4]. The patient complained about a severe headache after the procedure. The lumbar puncture revealed the high pressure of 40 cmH2O. The patient had undergone CT scan and found that there is disconnection of the LP shunt. We found subcutaneous mass containing CSF, and after removal of this fibrous tract, the patient became symptomatic which suggest that the fibrous tract is still functioning. It is clinicoradiological assessment of the function of the fibrous tract. The emergency LP shunt was done and symptoms of the patient disappear instantly [Figure 5]. The patient recovered completely and showed no signs of shunt malfunction. This also denotes that when the patient is young and indulges in excessive sports activities, there is a high chance of shunt malfunction with the LP shunt as we could see in this case. Ventriculoatrial shunt is a good and proven alternative for the LP shunt malfunction.
Figure 1: (a) Case of Arnold–Chiari malformation type I, (b) pseudomeningocele from suboccipital decompression in the Arnold–Chiari type I malformation

Click here to view
Figure 2: Proximal catheter of lumboperitoneal shunt disconnection

Click here to view
Figure 3: Closing of the proximal fibrous tract by tobacco-bag suture

Click here to view
Figure 4: Collagen fibers, fat tissue, and small vessels observed in that fibrous tract

Click here to view
Figure 5: Lumboperitoneal shunt revision

Click here to view



  Discussion Top


Use of silastic catheters for the use in medicine was in the era of 1950s.[7] The material silicon elastomer has high flexibility, chemical stability, and nontoxic properties which made them the preferred choice for the use in the shunt system. The main problem with this shunt is lipophilicity which causes gradual degradation and deterioration of the shunt system. Shunt revision is the choice for a symptomatic patient with shunt malfunction; however, if the patient is asymptomatic with arrested hydrocephalus, then it is a challenging task. As a policy for the management of arrested hydrocephalus we need to keep the patient in supervision without revision of the shunt but sometimes it becomes catastrophic. There are two possible, but not definitive, explanations for normal ICP in the shunt malfunction; patient one can be the arrested hydrocephalus with a nonfunctional shunt, and the second can be explained with a functional subcutaneous fibrous tract. The development of pericatheter subcutaneous reaction and fibrosis around the silicon shunt catheters has been documented histologically in two patients.[8] Fibrosis and tethering to the skin can cause discomfort to the patients. The term “tract fibrosis” denotes for the findings of inflammatory tissue that results from scarring and/or calcinosis surrounding the catheter. These fibrotic tissues usually take a tubular shape, mirroring that of the catheter's tube structure, so the term is coined tract fibrosis.[9] Clyde and Albright mentioned evidence for the patent fibrous tract in fractured, outgrown, or disconnected ventriculoperitoneal (VP) shunts and they mentioned two case reports of this patent fibrous tract.[5] Langmoen et al. noticed delayed hydrocephalus in one patient who had been asymptomatic after the removal of the fractured distal shunt catheter in the follow-up period.[10] Rekate et al. mentioned two patients with Arnold–Chiari malformation who had a cardiac and or respiratory arrest in 9 months and 5 years after shunt removal or ligation of the disconnected or the outgrown shunt.[6] Kazan et al. discussed the four cases which have a patent subcutaneous fibrous tract in children with VP shunt.[11] Nakano et al. reported a fibrous tract formed around the peritoneal catheter which communicated with the lactiferous duct.[12] Many spina bifida patients have surveillance scoliosis radiographs which may identify an incidental withdrawn peritoneal catheter. Clyde and Albright estimated that arrested hydrocephalus occurred in approximately 5% of patients with meningomyelocele with shunts. Our findings supported the theory that opening ICP might be normal with the existence of a patent fibrous tract; however, when we removed the nonfunctioning LP shunt and the fibrous tissue, the patient became symptomatic and we had to place shunt again.


  Conclusion Top


Even though the shuntography cannot be performed, the clinical course can be strongly indicated that the fibrous tract remained patent after the shunt tube disconnection. LP shunt is a popular treatment for hydrocephalus treatment and the proximal catheter disconnection is not so frequently found. A shuntography can identify functioning of shunt and guide management; we should perform shuntography before removal the shunt even though the shunt is disconnected.

Declaration of patient consent

The authors certify that they have obtained all appropriate patient consent forms. In the form the patient(s) has/have given his/her/their consent for his/her/their images and other clinical information to be reported in the journal. The patients understand that their names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.



 
  References Top

1.
Amacher AL, Wellington J. Infantile hydrocephalus: Long-term results of surgical therapy. Childs Brain 1984;11:217-29.  Back to cited text no. 1
    
2.
Feletti A, Avella D, Wikkels C, Klinge P, Hellström P. Ventriculoperitoneal Shunt Complications in the European Idiopathic Normal Pressure Hydrocephalus Multicenter Study. Oper Neurosurg 2018;1-6.  Back to cited text no. 2
    
3.
Davidson RI. Peritoneal bypass in the treatment of hydrocephalus: Historical review and abdominal complications. J Neurol Neurosurg Psychiatry 1976;39:640-6.  Back to cited text no. 3
    
4.
Chumas PD, Kulkarni AV, Drake JM, Hoffman HJ, Humphreys RP, Rutka JT. Lumboperitoneal shunting: A retrospective study in the pediatric population. Neurosurgery 1993;32:376-83.  Back to cited text no. 4
    
5.
Clyde BL, Albright AL. Evidence for a patent fibrous tract in fractured, outgrown, or disconnected ventriculoperitoneal shunts. Pediatr Neurosurg 1995;23:20-5.  Back to cited text no. 5
    
6.
Rekate HL, Nulsen FE, Mack HL, Morrison G. Establishing the diagnosis of shunt independence. Monogr Neural Sci 1982;8:223-6.  Back to cited text no. 6
    
7.
Keucher TR, Mealey J Jr. Long-term results after ventriculoatrial and ventriculoperitoneal shunting for infantile hydrocephalus. J Neurosurg 1979;50:179-86.  Back to cited text no. 7
    
8.
Sugar O, Bailey OT. Subcutaneous reaction to silicone in ventriculoperitoneal shunts. Long-term results. J Neurosurg 1974;41:367-71.  Back to cited text no. 8
    
9.
Lester L, Sharon L, David L, Lee PN, Colum N, Wan TS. Late pediatric ventriculoperitoneal shunt failures: A Singapore tertiary institutions experience. Neurosurg Focus 2016;41:7.  Back to cited text no. 9
    
10.
Langmoen IA, Lundar T, Vatne K, Hovind KH. Occurrence and management of fractured peripheral catheters in CSF shunts. Childs Nerv Syst 1992;8:222-5.  Back to cited text no. 10
    
11.
Kazan S, Açikbaş C, Rahat O, Tuncer R. Proof of the patent subcutaneous fibrous tract in children with V-P shunt malfunction. Childs Nerv Syst 2000;16:351-6.  Back to cited text no. 11
    
12.
Nakano A, Tani E, Sato M, Shimizu Y. Cerebrospinal fluid leakage from the nipple after ventriculoperitoneal shunt: Case report. Surg Neurol 1994;42:224-6.  Back to cited text no. 12
    


    Figures

  [Figure 1], [Figure 2], [Figure 3], [Figure 4], [Figure 5]



 

Top
 
 
  Search
 
<
Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
 Related articles
Access Statistics
Email Alert *
Add to My List *
* Registration required (free)  

 
  In this article
   Abstract
  Introduction
  Case Report
  Discussion
  Conclusion
   References
   Article Figures

 Article Access Statistics
    Viewed220    
    Printed11    
    Emailed0    
    PDF Downloaded26    
    Comments [Add]    

Recommend this journal