| Literature DB >> 30287249 |
Abdul Badran1, Matthew J Shepard2, Alexander Ksendzovsky2, Roger Murayi3, Christina Hayes3, DeeDee Smart3, Prashant Chittiboina4.
Abstract
Low-pressure hydrocephalus (LPH) is a rare clinical diagnosis, characterized by neurologic decline and ventriculomegaly that persists despite normal to low intracranial pressure. LPH is typically managed by negative-pressure drainage via ventriculostomy, followed by low-resistance shunt insertion. We present the case of a middle-aged man with a history of hemangioblastomatosis who had spontaneous subarachnoid hemorrhage. He was treated with a ventriculoperitoneal shunt and then underwent resection of a Meckel's cave hemangioblastoma and whole brain irradiation. One month later, he presented to us with worsening symptoms and hydrocephalus despite shunt interrogations and revisions revealing no malfunction. Ventriculostomy drainage at negative-pressure was required for resolution of symptoms and ventriculomegaly, leading us to a diagnosis of LPH. This was successfully treated using an improvised ultra-low pressure valveless ventriculoperitoneal shunt, with maintained resolution of LPH for over one year. The system was created by ligating the distal slit valve end of a peritoneal catheter to prevent reflux and allow sub-zero pressure drainage by siphoning. Published by Elsevier Ltd.Entities:
Keywords: CSF drainage; Hemangioblastoma; Low-pressure hydrocephalus; Negative-pressure hydrocephalus
Mesh:
Year: 2018 PMID: 30287249 PMCID: PMC7265979 DOI: 10.1016/j.jocn.2018.08.028
Source DB: PubMed Journal: J Clin Neurosci ISSN: 0967-5868 Impact factor: 1.961