Pseudotumor
cerebri in childhood
Kršek P.1, Petrák B.1, Belšan T.2, Pochop P.3, Tichý M.4, Hořínek D.4, Komárek V.1
1Klinika dětské neurologie UK 2. LF a FN Motol, Praha 2Klinika zobrazovacích technik UK 2. LF a FN Motol, Praha 3Dětská oční klinika UK 2. LF a FN Motol, Praha 4Neurochirurgické oddělení UK 2. LF a FN Motol, Praha |
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Summary:
Background. Diagnostics of idiopathic intracranial hypertension (pseudotumor cerebri, PTC) in childhood
is often difficult because the clinical picture differs from that in the adult population. Considering
the significant variability of the disease course and prognosis, it is difficult to standardize
therapeutic procedures.Our study presents experiences in a relatively large group of pediatric patients
with pseudotumor cerebri. Methods. We have retrospectively analyzed clinical data of children hospitalized
for pseudotumor cerebri in the Pediatric Neurology Clinic, 2nd Medical Faculty, Charles
University and Faculty Hospital Motol in the years 1998–2002. Patients were comprehensively examined
using imaging (CT, MRI), electrophysiological (EEG, VEP) and ophthalmological (ophthalmoscopy,
visual acuity, perimeter, US of papillae, ophthalmoscopic photography) methods, all had lumbar
puncture with CSF pressure measurement. Results. Pseudotumor cerebri was diagnosed in 14 children,
age 4–17. Habitus typical of adult patients with PTC (obese girl) was not found in pre-adolescent
children. Some clinical features were different from the adult population (e.g., the absence of tinnitus
or, in contrast, a frequent occurrence of meningeal syndrome). In three patients, we have not demonstrated
increased CSF pressure, most likely because of its temporal fluctuation. MRI played a central
role in the diagnostics: it excluded or demonstrated cerebral venous thrombosis (found in 2 patients
with clinical presentation of PTC) and it further revealed indirect signs of intracranial hypertension
in 9/15 patients. In 13 out of 16 patients, therapy with p.o. acetazolamide and/or i.v.methylprednisolone
was successful. In the 3 remaining refractory cases, lumboperitoneal shunt and/or decompressive
surgery of optic nerve sheaths was indicated. In two patients, irreversible vision impairment has
developed. Discussion. We propose a diagnostic protocol for patients with suspected PTC, including specialMRI studies focusing on optic nerves. Central role in follow-up is played by careful examination
of visual function with perimetry, VEP, US of papillae and photo documentation of fundus. Finally, we
discuss indication criteria for surgery in patients at risk for vision loss.
Key words:
idiopathic intracranial hypertension, papilloedema, intracranial pressure, cerebral venous
thrombosis, lumboperitoneal shunt, optic nerve sheath decompression
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