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Treatment of a Large Hemorrhagic Midbrain Cavernoma Within the Silvian Aqueduct in a Five-Year-Old Girl—A Case Report

Bibliographic Data

ID15716904
AuthorsMatthias Krause (0000-0002-3200-3199, Leipzig University, corresponding author), Armin‐Johannes Michel (0000-0002-4071-1961, Paracelsus Medical University), Johannes Koch (0000-0001-6910-5247, Paracelsus Medical University), Johann Gradl (0000-0001-7942-9122, Paracelsus Medical University), Johannes Pfaff (0000-0003-0672-5718, Paracelsus Medical University), Christoph J Griessenauer (0000-0002-2952-3812, Paracelsus Medical University), Lorenz Auer‐Hackenberg (0000-0002-5634-5791, Paracelsus Medical University)
Year2025
Volume12
Issue5
Pages564-564
Publication date2025-04-26
Open AccessYes
TypeARTICLE
VenueChildren (JOURNAL)
Journal identifiersISSN: 2227-9067 • E-ISSN: 2227-9067
PublisherMultidisciplinary Digital Publishing Institute (PUBLISHER • CH)
DOI10.3390/children12050564
PMID40426743
OpenAlexW4410007919
LanguageEN
References cited12

Brain stem cavernomas are exceedingly rare in pediatric populations, with limited literature addressing their natural history, treatment guidelines, and counseling. We report the case of a 5-year-old girl presenting with acute neurological symptoms, including diplopia, gait ataxia, headache, and altered consciousness. Initial imaging revealed obstructive hydrocephalus caused by a hemorrhagic lesion near the pineal region. After emergency external ventricular drainage (EVD), most symptoms resolved except for diplopia. A subsequent MRI suggested a space-occupying hemorrhagic cyst in the tectal lamina, leading to endoscopic third ventriculostomy (ETV). During ETV, a large hemorrhagic mass at the aqueduct entrance was identified but not removed due to its fragility. Following ETV, the patient improved rapidly and was discharged. However, she was readmitted with recurrent symptoms and altered consciousness. An emergency MRI indicated a progressive hemorrhagic mass lesion compressing the midbrain, necessitating surgical intervention. The patient underwent suboccipital craniotomy using a telovelar approach. The intraoperative findings included cavernoma-like tissue within the aqueduct, which was successfully resected. Histopathology confirmed hemorrhagic and angiomatous tissue, excluding a primary brain tumor. Postoperatively, the patient showed significant, progressive neurological improvement, with mild internuclear strabism, trunk ataxia, and fatigue at the last follow-up. Six months later, a follow-up MRI and cerebral angiography showed no cavernoma remnants but identified a midbrain deep venous anomaly. This case underscores the feasibility of the microsurgical resection of midbrain cavernomas in symptomatic pediatric patients, highlighting the importance of the thorough assessment of atypical hemorrhagic midbrain lesions to exclude rare vascular malformations from differential diagnoses

Diplopia · Hydrocephalus · Midbrain · Radiology · Cerebrospinal fluid and hydrocephalus · Intracerebral and Subarachnoid Hemorrhage Research · Medicine · Vascular Malformations Diagnosis and Treatment · Surgery

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