Araştırma Makalesi

Secondary pseudotumor cerebri in the pediatric population: clinical features, treatment, and prognosis

Cilt: 17 Sayı: 2 1 Nisan 2024
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Secondary pseudotumor cerebri in the pediatric population: clinical features, treatment, and prognosis

Öz

Purpose: Pseudotumor cerebri syndrome (PTCS) is characterized by elevated intracranial pressure (ICP) without intracranial mass, hydrocephalus, or abnormalities in cerebrospinal fluid (CSF) composition. In secondary PTCS (sPTCS), there is a reason that increases the CSF pressure. The aim of this study is to evaluate the diagnosis, treatment, and follow-up of pediatric patients diagnosed with sPTCS. Materials and methods: This is a retrospective study conducted in a single-center tertiary pediatric hospital. We included patients aged 1-17 years who were diagnosed with sPTCS in a tertiary hospital between 2018 and 2023 and met the current diagnostic criteria for PTCS. We evaluated the complaints, etiology, ophthalmological evaluations, and treatment results of the cases. Results: Seventeen patients with a diagnosis of PTCS were included in the study. The mean age was 9.82 (±4.6). Of the patients, 9 (56.2%) were male and 8 (43.7%) were female. The most common symptoms were headache in 10 patients (62.5%), nausea/vomiting in 6 patients (37.5%), and double vision in 5 patients (31.2%). All patients had papilledema and 7 (43.7%) patients had sixth nerve palsy. Recurrence was observed in 3 (16%) patients. Optic nerve fenestration was performed in three patients as a second-line treatment. Conclusion: In cases that do not respond to medical treatment, optic nerve sheath fenestration may be a good treatment option.

Anahtar Kelimeler

Destekleyen Kurum

yok

Proje Numarası

yok

Etik Beyan

Etik kurulu onayı alındı.

Teşekkür

.

Kaynakça

  1. 1. Chiu HH, Reginald YA, Moharir M, Wan MJ. Secondary pseudotumour cerebri syndrome in children: clinical characteristics and long-term outcomes. Can J Ophthalmol 2022;57:216-218. https://doi.org/10.1016/j.jcjo.2022.02.021
  2. 2. Kilic K, Korsbæk JJ, Jensen RH, Cvetkovic VVJC. Diagnosis of idiopathic intracranial hypertension-the importance of excluding secondary causes: a systematic review. Cephalalgia 2022;42:524-541. https://doi.org/10.1177/03331024211056580
  3. 3. Paley GL, Sheldon CA, Burrows EK, Chilutti MR, Liu GT, McCormack SE. Overweight and obesity in pediatric secondary pseudotumor cerebri syndrome. Am J Ophthalmol 2015;159:344-352.e1. https://doi.org/10.1016/j.ajo.2014.11.003
  4. 4. Matthews YY, Dean F, Lim MJ, et al. Pseudotumor cerebri syndrome in childhood: incidence, clinical profile and risk factors in a national prospective population-based cohort study. Arch Dis Child 2017;102:715-721. https://doi.org/10.1136/archdischild-2016-312238
  5. 5. Sinclair AJ, Walker EA, Burdon MA, et al. Cerebrospinal fluid corticosteroid levels and cortisol metabolism in patients with idiopathic intracranial hypertension: a link between 11β-HSD1 and intracranial pressure regulation? J Clin Endocrinol Metab 2010;95:5348-5356. https://doi.org/10.1210/jc.2010-0729
  6. 6. Friedman DI, Liu GT, Digre KB. Revised diagnostic criteria for the pseudotumor cerebri syndrome in adults and children. Neurology 2013;81:1159-1165. https://doi.org/10.1212/WNL.0b013e3182a55f17
  7. 7. Kalyvas AV, Hughes M, Koutsarnakis C, et al. Efficacy, complications and cost of surgical interventions for idiopathic intracranial hypertension: a systematic review of the literature. Acta Neurochir 2017;159:33-49. https://doi.org/10.1007/s00701-016-3010-2
  8. 8. Gilbert AL, Chwalisz B, Mallery R, editors. Complications of optic nerve sheath fenestration as a treatment for idiopathic intracranial hypertension. Semin Ophthalmol 2018;33:36-41. https://doi.org/10.1080/08820538.2017.1353810

Ayrıntılar

Birincil Dil

İngilizce

Konular

Göz Hastalıkları ve Göz Ölçümleri (Diğer)

Bölüm

Araştırma Makalesi

Erken Görünüm Tarihi

23 Ocak 2024

Yayımlanma Tarihi

1 Nisan 2024

Gönderilme Tarihi

9 Ekim 2023

Kabul Tarihi

23 Ocak 2024

Yayımlandığı Sayı

Yıl 2024 Cilt: 17 Sayı: 2

Kaynak Göster

APA
Güngör, O., Ün, E., Kıpcak, B., & Parça, O. (2024). Secondary pseudotumor cerebri in the pediatric population: clinical features, treatment, and prognosis. Pamukkale Medical Journal, 17(2), 279-284. https://izlik.org/JA54TP54FN
AMA
1.Güngör O, Ün E, Kıpcak B, Parça O. Secondary pseudotumor cerebri in the pediatric population: clinical features, treatment, and prognosis. Pam Tıp Derg. 2024;17(2):279-284. https://izlik.org/JA54TP54FN
Chicago
Güngör, Olcay, Emine Ün, Beste Kıpcak, ve Osman Parça. 2024. “Secondary pseudotumor cerebri in the pediatric population: clinical features, treatment, and prognosis”. Pamukkale Medical Journal 17 (2): 279-84. https://izlik.org/JA54TP54FN.
EndNote
Güngör O, Ün E, Kıpcak B, Parça O (01 Nisan 2024) Secondary pseudotumor cerebri in the pediatric population: clinical features, treatment, and prognosis. Pamukkale Medical Journal 17 2 279–284.
IEEE
[1]O. Güngör, E. Ün, B. Kıpcak, ve O. Parça, “Secondary pseudotumor cerebri in the pediatric population: clinical features, treatment, and prognosis”, Pam Tıp Derg, c. 17, sy 2, ss. 279–284, Nis. 2024, [çevrimiçi]. Erişim adresi: https://izlik.org/JA54TP54FN
ISNAD
Güngör, Olcay - Ün, Emine - Kıpcak, Beste - Parça, Osman. “Secondary pseudotumor cerebri in the pediatric population: clinical features, treatment, and prognosis”. Pamukkale Medical Journal 17/2 (01 Nisan 2024): 279-284. https://izlik.org/JA54TP54FN.
JAMA
1.Güngör O, Ün E, Kıpcak B, Parça O. Secondary pseudotumor cerebri in the pediatric population: clinical features, treatment, and prognosis. Pam Tıp Derg. 2024;17:279–284.
MLA
Güngör, Olcay, vd. “Secondary pseudotumor cerebri in the pediatric population: clinical features, treatment, and prognosis”. Pamukkale Medical Journal, c. 17, sy 2, Nisan 2024, ss. 279-84, https://izlik.org/JA54TP54FN.
Vancouver
1.Olcay Güngör, Emine Ün, Beste Kıpcak, Osman Parça. Secondary pseudotumor cerebri in the pediatric population: clinical features, treatment, and prognosis. Pam Tıp Derg [Internet]. 01 Nisan 2024;17(2):279-84. Erişim adresi: https://izlik.org/JA54TP54FN
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