First case of MELAS syndrome presenting with local brain edema requiring decompressive craniectomy

dc.authorid0000-0003-1513-6149
dc.contributor.authorYeşilbaş, Osman
dc.contributor.authorŞengenç, Esma
dc.contributor.authorErsoy Olbak, Melike
dc.contributor.authorBako, Derya
dc.contributor.authorNizam, Öznur Gökçe
dc.contributor.authorSeyithanoğlu, Mehmet Hakan
dc.contributor.authorPehlivan, Davut
dc.contributor.authorCeylaner, Serdar
dc.contributor.authorİçağasıoğlu, Dilara
dc.contributor.authorAydın, Kürşad
dc.date.accessioned2022-02-03T10:22:36Z
dc.date.available2022-02-03T10:22:36Z
dc.date.issued2022
dc.departmentİstanbul Medipol Üniversitesi, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Çocuk Sağlığı ve Hastalıkları Ana Bilim Dalı
dc.description.abstractMitochondrial encephalomyopathy, lactic acidosis, and recurrent stroke-like episodes (MELAS) syndrome is a rare but one of the most common maternally inherited multisystem disorder. Although patients with MELAS present a variable clinical profile, stroke like lesions have been detected in 90% of cases, with stroke being the first presenting symptom in 25% of cases. However, cases of local brain edema requiring decompressive craniectomy has not been reported. A 12-year-old male patient was admitted to our pediatric intensive care unit with altered mental status, seizures, and vision loss. The patient was stuporous and presented neck stiffness. Complete blood count, serum electrolytes, biochemistry (including lactate level), acute phase reactants, and repeated blood gas analysis were unremarkable. Brain magnetic resonance imaging (MRI) revealed an edematous stroke-like lesion in the right occipital lobe accompanied by brain swelling. Intravenous ceftriaxone, acyclovir, intravenous immunoglobulin (IVIG), and pulse steroid therapy were started for possible diagnosis of viral/bacterial/autoimmune encephalitis; levetiracetam, phenytoin, and an infusion of sodium thiopental were started for refractory status epilepticus; and a 3% NaCl infusion was started for local brain edema. The results of serum autoimmune encephalitis panel were negative. Further investigations for rheumatic, vascular, and metabolic disorders were unremarkable. Despite these supportive treatments, the patient was clinically decompensated due to brain swelling that progressed to the left midline shift, and he underwent decompressive craniectomy. Histologic examination of brain biopsy specimen revealed non-specific encephalitis findings. A pathogenic variant of the MT-TL1 gene (m.3243A>T), responsible for MELAS, was detected. The patient's condition dramatically improved after specific treatment for MELAS. If the diagnosis and treatment are delayed, MELAS syndrome can cause serious brain edema, which may ultimately require decompressive craniectomy.
dc.identifier.citationYeşilbaş, O., Şengenç, E., Ersoy Olbak, M., Bako, D., Nizam, Ö. G., Seyithanoğlu, M. H. ... Aydın, K. (2022). First case of MELAS syndrome presenting with local brain edema requiring decompressive craniectomy. Turkish Neurosurgery, 32(1), 155-159. https://dx.doi.org/10.5137/1019-5149.JTN.34196-21.4
dc.identifier.doi10.5137/1019-5149.JTN.34196-21.4
dc.identifier.endpage159
dc.identifier.issn1019-5149
dc.identifier.issue1
dc.identifier.scopusqualityQ3
dc.identifier.startpage155
dc.identifier.urihttps://dx.doi.org/10.5137/1019-5149.JTN.34196-21.4
dc.identifier.urihttps://hdl.handle.net/20.500.12511/8957
dc.identifier.volume32
dc.identifier.wosqualityQ4
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherTurkish Neurosurgical Society
dc.relation.ispartofTurkish Neurosurgeryen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectChild
dc.subjectBrain Edema
dc.subjectDecompressive Craniectomy
dc.subjectMELAS Syndrome
dc.titleFirst case of MELAS syndrome presenting with local brain edema requiring decompressive craniectomy
dc.typeArticle

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