| Literature DB >> 18459889 |
Soner Sahin1, Aimen F Shaaban, Bermans J Iskandar.
Abstract
To the best of the authors' knowledge, this report represents the first description of a ventriculoperitoneal (VP) shunt that migrated into the chest cavity where it caused recurrent pneumonias. This 15-year-old boy with a history of hydrocephalus treated with VP shunt therapy as an infant presented with a 2-year history of chronic coughing and recurrent pneumonia. A high-resolution chest computed tomography scan revealed a right lower lobe infiltration and evidence of migration of the peritoneal shunt tubing through the diaphragm into the lung parenchyma. The catheter was pulled back into the peritoneal cavity via a simple abdominal incision. The patient's long-term outcome was excellent, and there was complete cessation of the pneumonia.Entities:
Mesh:
Year: 2007 PMID: 18459889 DOI: 10.3171/PED-07/08/156
Source DB: PubMed Journal: J Neurosurg ISSN: 0022-3085 Impact factor: 5.115