Endoscopic Management for Recurrent Hydrocephalus Associated with Neurosarcoidosis.


Journal

World neurosurgery
ISSN: 1878-8769
Titre abrégé: World Neurosurg
Pays: United States
ID NLM: 101528275

Informations de publication

Date de publication:
12 2020
Historique:
received: 28 06 2020
accepted: 25 08 2020
pubmed: 6 9 2020
medline: 18 5 2021
entrez: 5 9 2020
Statut: ppublish

Résumé

Recurrent hydrocephalus may occur as a complication of neurosarcoidosis with chronic inflammation. We present a case that required a combination of multistage endoscopic diversion of the cerebrospinal fluid pathway and shunt surgery. A 34-year-old man presented with progressive nausea and vomiting. Magnetic resonance imaging revealed hydrocephalus with leptomeningeal enhancement along the base of the fourth ventricle and the bilateral foramina of Luschka. Concurrent endoscopic third ventriculostomy and biopsy were performed. The diagnosis was neurosarcoidosis. Immediately after the procedure, the endoscopic third ventriculostomy stoma was occluded, and a right ventriculoperitoneal shunt was urgently performed. However, left unilateral hydrocephalus developed during the late phase of immunosuppressive therapy for neurosarcoidosis. Endoscopic septostomy with repositioning of the ventricular catheter was indicated. Intraoperative findings included a white pasty tissue with nodules that covered the ventricular wall close to the foramen of Monro and sealed the side holes of the catheter. Chemotherapy with a tumor necrosis factor-α inhibitor was initiated after the surgical procedure. The patient had an uneventful course without recurrence of hydrocephalus for >6 months. Endoscopic diversion of the cerebrospinal fluid pathway should be actively considered for treating hydrocephalus without a shunt and performing biopsy simultaneously. Even if a subsequent shunt is needed, complex hydrocephalus can be avoided with a combination of endoscopic techniques.

Sections du résumé

BACKGROUND
Recurrent hydrocephalus may occur as a complication of neurosarcoidosis with chronic inflammation. We present a case that required a combination of multistage endoscopic diversion of the cerebrospinal fluid pathway and shunt surgery.
CASE DESCRIPTION
A 34-year-old man presented with progressive nausea and vomiting. Magnetic resonance imaging revealed hydrocephalus with leptomeningeal enhancement along the base of the fourth ventricle and the bilateral foramina of Luschka. Concurrent endoscopic third ventriculostomy and biopsy were performed. The diagnosis was neurosarcoidosis. Immediately after the procedure, the endoscopic third ventriculostomy stoma was occluded, and a right ventriculoperitoneal shunt was urgently performed. However, left unilateral hydrocephalus developed during the late phase of immunosuppressive therapy for neurosarcoidosis. Endoscopic septostomy with repositioning of the ventricular catheter was indicated. Intraoperative findings included a white pasty tissue with nodules that covered the ventricular wall close to the foramen of Monro and sealed the side holes of the catheter. Chemotherapy with a tumor necrosis factor-α inhibitor was initiated after the surgical procedure. The patient had an uneventful course without recurrence of hydrocephalus for >6 months.
CONCLUSIONS
Endoscopic diversion of the cerebrospinal fluid pathway should be actively considered for treating hydrocephalus without a shunt and performing biopsy simultaneously. Even if a subsequent shunt is needed, complex hydrocephalus can be avoided with a combination of endoscopic techniques.

Identifiants

pubmed: 32890842
pii: S1878-8750(20)31946-X
doi: 10.1016/j.wneu.2020.08.177
pii:
doi:

Types de publication

Case Reports

Langues

eng

Sous-ensembles de citation

IM

Pagination

121-124

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

Auteurs

Shuntaro Togashi (S)

Department of Neurosurgery, Akita Red Cross Hospital, Akita, Japan; Department of Neurosurgery, Akita University Graduate School of Medicine, Akita, Japan. Electronic address: togashi@med.akita-u.ac.jp.

Jun Maruya (J)

Department of Neurosurgery, Akita Red Cross Hospital, Akita, Japan.

Hideaki Abe (H)

Department of Neurosurgery, Akita Red Cross Hospital, Akita, Japan.

Keiichi Nishimaki (K)

Department of Neurosurgery, Akita Red Cross Hospital, Akita, Japan.

Haruka Ouchi (H)

Department of Neurology, Akita Red Cross Hospital, Akita, Japan.

Kenju Hara (K)

Department of Neurology, Akita Red Cross Hospital, Akita, Japan.

Takuo Tokairin (T)

Department of Pathology, Akita Red Cross Hospital, Akita, Japan.

Kenichi Nishiyama (K)

Department of Neurosurgery, Niigata Medical Center, Niigata, Japan.

Hiroaki Shimizu (H)

Department of Neurosurgery, Akita University Graduate School of Medicine, Akita, Japan.

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Classifications MeSH