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2008 | 3 | 4 | 517-520
Tytuł artykułu

Intracranial meningioma in a patient with osteogenesis imperfecta

Treść / Zawartość
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
Osteogenesis imperfecta (OI) is a heritable disorder characterized mainly by connective tissue manifestations. In dinstinct cases, several neurological features have also been described. A 46-year-old male with a known family history of OI type I presented with progressive gait disturbances and diminished muscle strength. Brain MRI scans revealed an infiltrative intracranial mass occupying both frontoparietal lobes. The patient underwent surgical intervention. The histological diagnosis was an atypical (Grade II) meningioma. The bony parts demonstrated a mixture of osseous defects due to OI and infiltration by the tumor. At one-year follow up the patient′s muscle power partially returned while repeat MRI scans were negative for tumor recurrence.
Wydawca
Czasopismo
Rocznik
Tom
3
Numer
4
Strony
517-520
Opis fizyczny
Daty
wydano
2008-12-01
online
2008-10-22
Twórcy
  • Department of Neurosurgery, Hippokratio General Hospital, Aristotle University Medical School, 54642, Thessaloniki, Greece , par_tsits@yahoo.gr
  • Department of Neurosurgery, Hippokratio General Hospital, Aristotle University Medical School, 54642, Thessaloniki, Greece
  • Department of Neurosurgery, Hippokratio General Hospital, Aristotle University Medical School, 54642, Thessaloniki, Greece
  • Department of Pathology, Hippokratio General Hospital, 54642, Thessaloniki, Greece
  • Department of Neurosurgery, Hippokratio General Hospital, Aristotle University Medical School, 54642, Thessaloniki, Greece
Bibliografia
  • [1] Rausch F., Glorieux F.H., Osteogenesis imperfecta, Lancet, 2004, 363, 1377–1385 http://dx.doi.org/10.1016/S0140-6736(04)16051-0[Crossref]
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  • [5] Charmas L.R., Marini JC., Neurologic profile in osteogenesis imperfecta, Connect. Tissue Res., 1995, 31(4), S23–26 http://dx.doi.org/10.3109/03008209509116828[Crossref]
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  • [7] Korkko J., Ala-Kokko L., De Paepe A., Nuytinck L., Earley J., Prockop D.J., Analysis of the COLIA1 and COLIA2 genes by PCR amplification and scanning by conformation-sensitive gel electrophoresis identifies only COLIA1 mutation in 15 patients with osteogenesis imperfecta type I: identification of common sequences of null allele-mutations, Am. J. Hum. Genet., 1998, 62, 98–110 http://dx.doi.org/10.1086/301689
  • [8] Byers P.H., Osteogenesis imperfecta: perspectives and opportunities, Curr. Opin. Pediatr., 2000, 12, 603–609 http://dx.doi.org/10.1097/00008480-200012000-00016[Crossref]
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  • [10] Burgeson R.E., Nimni M.E., Collagen types. Molecular structure and tissue distribution, Clin. Orthop., 1992, 282, 250–272
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  • [12] Frank E., Berger T., Tew J.M., Basilar impression and platybasia in osteogenesis imperfecta tarda, Surg. Neurol., 1981, 17, 116–119 http://dx.doi.org/10.1016/S0090-3019(82)80033-5[Crossref]
  • [13] Pozo J., Crockard H., Ransford A.O., Basilar impression in ostegenesis imperfecta: a report of three cases in one family, J. Bone Joint Surg. [Br], 1984, 66, 233–238
  • [14] Simon M., Boström J.P., Hartman C., Molecular genetics of meningiomas: From basic research to potential clinical application, Neurosurgery, 2007, 60, 787–798 http://dx.doi.org/10.1227/01.NEU.0000255421.78431.AE[WoS][Crossref]
  • [15] Reeder J., Orwoll E., Adults with osteogenesis imperfecta, NEJM, 2006, 355, 26 http://dx.doi.org/10.1056/NEJMicm062996[Crossref]
Typ dokumentu
Bibliografia
Identyfikatory
Identyfikator YADDA
bwmeta1.element.-psjd-doi-10_2478_s11536-008-0053-7
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