Periventricular Heterotopias: Neuroependymal Abnormalities

被引:0
|
作者
Costanza, Giuseppe [1 ]
Fichera, Valeria [1 ]
Zanghi, Antonio [2 ]
Polizzi, Agata [3 ]
Falsaperla, Raffaele [4 ]
Vecchio, Michele [5 ]
Palmucci, Stefano [6 ]
Belfiore, Giuseppe [7 ]
David, Emanuele [7 ]
Pratico, Andrea D. [8 ]
机构
[1] Univ Catania, Pediat Postgrad Residency Program, Catania, Italy
[2] Univ Catania, Res Ctr Surg Complex Malformat Syndromes Transit, Dept Med & Surg Sci & Adv Technol, Catania, Italy
[3] Univ Catania, Chair Pediat, Dept Educ Sci, Catania, Italy
[4] Univ Hosp Policlin G Rodol San Marco, Neonatol & Neonatal Intens Care Unit, Catania, Italy
[5] Univ Catania, Dept Biomed & Biotechnol Sci, Rehabil Unit, Catania, Italy
[6] Univ Hosp Policlin G Rodol San Marco, Dept Med Surg Sci & Adv Technol, IPTRA Unit, Catania, Italy
[7] Univ Hosp Policlin G Rodolico San Marco, Dept Med Surg Sci & Adv Technol, Radiol Unit 1, Catania, Italy
[8] Kore Univ, Chair Pediat, Dept Med & Surg, Enna, Italy
关键词
epilepsy; malformation of cortical development; periventricular heterotopias; genetics; NODULAR HETEROTOPIA; MENTAL-RETARDATION; PHENOTYPIC SPECTRUM; NATURAL-HISTORY; EPILEPSY; MUTATIONS; DELETION; DISEASE; IMMUNOTHERAPY; MALFORMATIONS;
D O I
10.1055/s-0044-1786772
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Periventricular nodular heterotopia (PVNH) is a group of malformation of cortical development characterized by ectopic neuronal nodules, located along the lateral ventricles. Magnetic resonance imaging can identify gray matter nodules located in wall of ventricles, which appear as island having the same signal of gray matter within white matter. The symptomatological spectrum is various, but the most common clinical presentation is with epileptic seizures, often a drug-resistant type. Features as severity, age of presentation, and associated malformations depend on the underlying etiology. From a genetic point of view, FLNA1 and ERMARD are acknowledged to be the main target of mutations that cause PVNH, although recently many other genes have shown a clear pathogenetic involvement. PVNH may manifest as a solitary discovery in brain imaging or present in conjunction with various other brain or systemic abnormalities. The diagnosis of PVNH is mainly carried out with electroneurophysiological and neuroimaging examinations, while the etiological diagnosis is made with genetic investigations. Treatment consists of use of anticonvulsant drugs, but no significant difference exists among them. In addition, frequently, PVNH-related seizures show poor response to drug, leading to requirement for surgical treatment, performed taking advantages from stereotactic ablative techniques that have a meaningful impact on surgical outcome.
引用
收藏
页码:321 / 331
页数:11
相关论文
共 50 条
  • [21] Periventricular Leukomalacia and Placental Histopathologic Abnormalities
    Maleki, Zahra
    Bailis, Anya J.
    Argani, Cynthia H.
    Askin, Frederic B.
    Graham, Ernest M.
    OBSTETRICS AND GYNECOLOGY, 2009, 114 (05): : 1115 - 1120
  • [22] MARGINAL GLIONEURONAL HETEROTOPIAS IN 9 CASES WITH AND WITHOUT CORTICAL ABNORMALITIES
    DAMBSKA, M
    WISNIEWSKI, KE
    SHER, JH
    JOURNAL OF CHILD NEUROLOGY, 1986, 1 (02) : 149 - 157
  • [23] Periventricular nodular heterotopias is associated with mutation at the FLNA locus-a case history and a literature review
    Lin Yang
    GuangSheng Wu
    HuiMei Yin
    MengLan Pan
    YaFei Zhu
    BMC Pediatrics, 23
  • [24] Bilateral periventricular heterotopias in an X-linked dominant transmission in a family with two affected males
    Gérard-Blanluet, M
    Sheen, V
    Machinis, K
    Neal, J
    Apse, K
    Danan, C
    Sinico, M
    Brugières, P
    Mage, K
    Ratsimbazafy, L
    Elbez, A
    Janaud, JC
    Amselem, S
    Walsh, C
    Encha-Razavi, F
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2006, 140A (10) : 1041 - 1046
  • [25] Periventricular nodular heterotopias is associated with mutation at the FLNA locus-a case history and a literature review
    Yang, Lin
    Wu, GuangSheng
    Yin, HuiMei
    Pan, MengLan
    Zhu, YaFei
    BMC PEDIATRICS, 2023, 23 (01)
  • [26] Novel Nonsense Mutation of FLNA in a 26 year Old Female with Periventricular Nodular Heterotopias and Severe Emphysema
    Kirby, Patricia
    Savage, Erica
    Darbro, Benjamin
    JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 2014, 73 (06): : 621 - 621
  • [27] A FIRST NATIONS CANADIAN FAMILY WITH PERIVENTRICULAR NODULAR HETEROTOPIAS AND CEREBELLAR DYSGENESIS DUE TO A MUTATION IN THE ARX GENE
    Caluseriu, O.
    Leonard, N.
    Radziminsky, N.
    Jacob-Morneau, F.
    Bharghava, R.
    Leonard, H.
    Merchant, S.
    Dzwiniel, T.
    Scott, D.
    Billinghurst, L.
    Blaser, S.
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2019, 179 (04) : 714 - 715
  • [28] Ictal EEG patterns from intracerebral depth electrodes placed within periventricular nodular heterotopias in 3 patients with gray matter heterotopias and refractory complex partial seizures
    Kothare, SV
    VanLandingham, K
    Armon, C
    Friedman, A
    Radtke, R
    NEUROLOGY, 1998, 50 (04) : A25 - A25
  • [29] Myelin abnormalities without oligodendrocyte loss in periventricular leukomalacia
    Billiards, Saraid S.
    Haynes, Robin L.
    Folkerth, Rebecca D.
    Borenstein, Natalia S.
    Trachtenberg, Felicia L.
    Rowitch, David H.
    Ligon, Keith L.
    Volpe, Joseph J.
    Kinney, Hannah C.
    BRAIN PATHOLOGY, 2008, 18 (02) : 153 - 163
  • [30] Placental abnormalities: Insights into pathogenesis of cystic periventricular leukomalacia
    Roland, EH
    Magee, JF
    Rodriguez, E
    Lupton, BA
    Hill, A
    ANNALS OF NEUROLOGY, 1996, 40 (02) : 136 - 136