2023, Number 2
<< Back Next >>
Bol Clin Hosp Infant Edo Son 2023; 40 (2)
Rectal migration of the distal catheter of the ventriculoperitoneal shunt valve. Case report
Balvanera RÉA, Soto VMN, Leyva CDM
Language: Spanish
References: 15
Page: 49-52
PDF size: 185.03 Kb.
ABSTRACT
Complications of ventricular shunt in pediatrics are reported
in 24 to 47% of cases. Distal catheter migration
through the rectum is a very rare complication, with
a great impact on the patient's morbidity and mortality.
This clinical case present a female infant aged 1
year 7 months, with a history of communicating hydrocephalus
at birth, requiring placement of a ventricular
peritoneal shunt valve at 20 days of life. He went to the
emergency department for presenting exteriorization
of the distal catheter of the ventriculoperitoneal valve
through the rectum. His vital signs were normal. The
physical examination revealed no neurological alterations,
no evidence of peritoneal irritation, and an 8-cm
exit from the distal catheter through the anal orifice.
A radiographic series was carried out confirming the
diagnosis, for which the neurosurgery service was
consulted, transferring the patient to the operating
room urgently. The distal catheter was removed and a
broad-spectrum antibiotic scheme was started. Subsequently,
placement of a new shunt valve was scheduled,
which was performed without complications.
Migration of the distal ventriculoperitoneal shunt catheter
through the rectum is a rare complication in
pediatrics. Due to its low frequency, there is no established
management, various recommendations have
been proposed, however, management should always
be individualized, always opting for the most effective
but least invasive procedure.
REFERENCES
Moreno M, Núñez N. Hidrocefalia en Pediatría [Internet].Protoc diagn ter pediatr. 2022; 1: 145-150.Disponible en: https://www.aeped.es/sites/default/files/documentos/15.pdf
Holwerda JC, Van Lindert EJ, Buis DR, Hoving EW.Dutch Pediatric Neurosurgery Study Group. Surgicalintervention for hydrocephalus in infancy; etiology,age and treatment data in a Dutch cohort.Childs Nerv Syst. 2020; 36: 577-82.
Kahle KT, Kulkarni AV, Limbrick DD Jr, Warf BC. Hydrocephalusin children. Lancet. 2016; 387: 788-99.
Téllez R, Mosquera G. Complicaciones de la derivaciónventriculoperitoneal en pacientes pediátricos.Revisión del tema [Internet]. Gaceta MédicaEspirituana. 2021; 23(2): 123-139. Disponible en:http://scielo.sld.cu/pdf/gme/v23n2/1608-8921-gme-23-02-123.pdf
Vinchon M, Rekate H, Kulkami AV. Pediatric hydrocephalusoutcomes: a review. Fluids Barriers CNS.2012; 9(1): 2-10.
Huerta F. Acosta M, Martell M, Flores M. Migraciónde catéter distal a nivel del recto como complicaciónde derivación ventriculoperitoneal [Internet].Revista de la Facultad de Medicina de la UNAM.2023 Enero-Febrero; 66(1). Disponible en: http://doi.org/10.22201/fm.24484865e.2023.66.1.04
Rivero M, Barbeito J, Morcillo J, Marquez J. Malfunciónvalvular intermitente por migración del catéterperitoneal a escroto [Internet]. Arch Argent Pediatr.2013; 111(1): e14-e16. Disponible en: http://www.scielo.org.ar/pdf/aap/v111n1/v111n1a15.pdf
8. Urparela R, Manrique K, Ferreira C. Migracióndel catéter de derivación ventriculoperitoneal conprotrusión por cavidad oral [Internet]. Neurocienciasen Colombia. 2017; 24(2). Disponible en: https://neurocienciasjournal.com/index.php/neurocienciasjournal/article/view/15/13
Cuevas J, Gonzalez O, Torche E, Labra M. Migraciónintracraneal de derivativa ventrículoperitonealen paciente con hidranencefalia: reporte deun caso [Internet]. Rev Chil Neurocirugía. 2014; 40:119-121. Disponible en: https://www.neurocirugiachile.org/pdfrevista/v40_n2_2014/cuevas_p119_v40n2_2014.pdf
Sánchez Y, Dominguez J, Lazo E. et al. Migraciónintratorácica de catéter de derivación ventriculoperitoneal:a propósito de un caso [Internet]. Neurocirugía.2015; 26(5): 256–259. Disponible en: https://www.sciencedirect.com/science/article/abs/pii/S1130147314001547
Quintana C, Clavel P, Trias M, Calderón M, RodríguezR. Migración escrotal de derivación ventriculoperitoneal[Internet]. Acta Medica. 2010; 73(4): 219-21.Disponible en: https://www.medigraphic.com/pdfs/facmed/un-2023/un231d.pdf
Cerqueira L, Catanim, Reis F, Galdino F, Perez- BoscolloA. Anal extrusion of the ventriculoperitoneal derivationcatheter: case report [Internet]. ResidenciaPediátrica. 2022; 12(1): 1-4. Disponible en: https://cdn.publisher.gn1.link/residenciapediatrica.com.br/pdf/en_v12n1aop270.pdf
Kumar-Ghritlaharey R. Review of the Managementof Peroral Extrusion of Ventriculoperitoneal ShuntCatheter [Internet]. J Clin Diagn Res. 2016; 10(11):PE01–PE06. Disponible en: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5198397/
Shariflan A, Abdollahi A, Ghodratollah M, FakhryalsadatA, Alvandipour M, Abbasi M. et al. Spontaneoustransanal protrusion of ventriculoperitoneal catheter:A case report [Internet]. Acta Médica Iránica.2013; 51(2). Disponible en: https://pubmed.ncbi.nlm.nih.gov/23585322/
Sandoval M, Granados R, Sandoval L, Olivares J,Santos J. Complicación de derivación ventrículoperitoneal: perforación intestinal y migración del catéterdistal a nivel del recto. Reporte de tres casos[Internet]. Acta Médica Grupo Ángeles. 2019; 17(1):409-412 Disponible en: https://www.scielo.org.mx/pdf/amga/v17n4/1870-7203-amga-17-04-409.pdf.