Evidence map›Paper›PMID 41036045›Full record

ArticleSurgical neurology international2025

A radiological finding suggesting Blake's pouch cyst: A rare pediatric anomaly associated with hydrocephalus - A case report.

Feda Anisah Makkiyah, Enrico Yusuf, Rendy Badri

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In one paragraph

Article in Surgical neurology international, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Feda Anisah MakkiyahDepartment of Neurosurgery, Faculty of Medicine Universitas Pembangunan Nasional (UPN), Veteran Jakarta, Indonesia.
Enrico YusufDepartment of Surgery, Bachelor of Medicine Program, Faculty of Medicine, Universitas Pembangunan Nasional, Veteran Jakarta, Indonesia.
Rendy BadriDepartment of Neurosurgery, Cileungsi District Hospital, Jawa Barat, Indonesia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Blake's pouch cyst (BPC) is a rare congenital anomaly resulting from the failure of the embryonic Blake's pouch to perforate during early fetal development. This condition leads to hydrocephalus, which may lead to increased intracranial pressure and a range of symptoms. According to authors, Indonesia faces infrastructure shortages in performing endoscopic third ventriculostomy or cyst fenestration; not many neurosurgeons are equipped to perform this procedure. The patient was treated with a ventriculoperitoneal (VP) shunt, resulting in good outcomes. Case Description: A 6-month-old female infant was brought to the emergency department, presenting with signs of elevated intracranial pressure, including vomiting and irritability. Computed tomography (CT) scans confirmed the presence of hydrocephalus. Due to limited hospital resources and the high cost associated with endoscopic third ventriculostomy, which requires specialized equipment and expertise not readily available in our setting, a VP shunt procedure was chosen as a more economically feasible treatment option. The procedure significantly improved the patient's condition, resulting in substantial neurological recovery without complications. Conclusion: A CT scan diagnosis and placement of a VP shunt effectively improved the patient's outcome, highlighting the differences in treatment in developed countries.

Indexed as

Blake’s pouch cystCerebrospinal fluidGood outcomeHydrocephalusVentriculoperitoneal shunt

Identifiers

PMID41036045
PMCPMC12482707

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