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Congenital cavernous angioma exhibits a progressive decrease in size after birth

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Abstract

Case report

We report a case of congenital intracranial cavernous angioma, which was initially found at a gestational age of 34 weeks in utero as a mass lesion associated with hydrocephalus. After birth, the patient was treated for hydrocephalus first by external drainage and then by ventricular peritoneal shunt. The natural course of the mass lesion was observed until the age of 8 months when the histopathological diagnosis confirmed the cavernous angioma after tissue was obtained by surgery. CT scans repeated monthly during this period demonstrated that the angioma continuously decreased in size. There was no evidence of hemorrhage in the angioma on serial CT scans. The histopathology revealed thrombosis of cavernous vessels with hyaloid changes in the angioma.

Discussion

The mechanisms of the decreasing size of the cavernous angioma have often been discussed in relation to spontaneous hemorrhages and resolution. The present case suggests a mechanism in which the spontaneous formation of a thrombus might be the dominant factor for the decrease in size. Thrombus formation may result from low perfusion due to the large size of the angioma.

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References

  1. Clatterbuck RE, Moriarity JL, Elmaci I, Lee RR, Breiter SN, Rigamonti D (2000) Dynamic nature of cavernous malformations: a prospective magnetic resonance imaging study with volumetric analysis. J Neurosurg 93:981–986

    CAS  PubMed  Google Scholar 

  2. Hashimoto H, Sakaki T, Ishida Y, Shimokawara T (1997) Fetal cavernous angioma—case report. Neurol Med Chir (Tokyo) 37:346–349

    Google Scholar 

  3. Kawagishi J, Suzuki M, Kayama T, Yoshimoto T (1993) Huge multilobular cavernous angioma in an infant: case report. Neurosurgery 32:1028–1031

    CAS  PubMed  Google Scholar 

  4. Kim DS, Park YG, Choi JU, Chung SS, Lee KC (1997) An analysis of the natural history of cerebral cavernous malformations. Surg Neurol 48:9–18

    Article  CAS  PubMed  Google Scholar 

  5. Kondziolka D, Lunsford LD, Kestle JRW (1995) The natural history of cerebral cavernous malformations. J Neurosurg 83:820–824

    CAS  PubMed  Google Scholar 

  6. Lanzi G, Fazzi E, Orcesi S, Cavallini A, Danova S, Uggetti C, Egitto MG (1997) Cerebral cavernous angiomas: an atypical case in infancy. Childs Nerv Syst 13:412–414

    Article  CAS  PubMed  Google Scholar 

  7. Little JR, Awad IA, Jones SC, Ebrahim ZY (1990) Vascular pressure and cortical blood flow in cavernous angioma of the brain. J Neurosurg 73:555–559

    CAS  PubMed  Google Scholar 

  8. Moriarity JL, Wetzel M, Clatterbuck RE, Javedan S, Sheppard JM, Hoenig-Rigamonti K, Crone NE, Breiter SN, Lee RR, Rigamonti D (1999) The natural history of cavernous malformations: a prospective study of 68 patients. Neurosurgery 44:1166–1171

    PubMed  Google Scholar 

  9. Moritake K, Handa H, Nozaki K, Tomiwa K (1985) Tentorial cavernous angioma with calcification in a neonate. Neurosurgery 16:207–211

    CAS  PubMed  Google Scholar 

  10. Robinson JR, Issam AA, Litte JR (1991) Natural history of the cavernous angioma. J Neurosurg 75:709–714

    CAS  PubMed  Google Scholar 

  11. Schemmer DC, Goh RH, Maguire JA (1999) Cavernous angioma: a cryptic CT and MRI presentation. Pediatr Radiol 29:146

    Article  CAS  PubMed  Google Scholar 

  12. Scott RM, Barnes P, Kupsky W, Adelman LS (1992) Cavernous angiomas of the central nervous system in children. J Neurosurg 76:38–46

    CAS  PubMed  Google Scholar 

  13. Tekkok IH, Ventureyra EC (1997) Spontaneous intracranial hemorrhage of structural origin during the first year of life. Childs Nerv Syst 13:154–165

    Article  CAS  PubMed  Google Scholar 

  14. Zabramski JM, Wascher TM, Spetzler RF, Johnson B, Golfinos J, Drayer BP, Brown B, Rigamonti D, BrownG (1994) The natural history of familial cavernous malformations: results of an ongoing study. J Neurosurg 80:422–432

    CAS  PubMed  Google Scholar 

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Acknowledgement

We thank Walter C. Low, Ph.D. at the University of Minnesota for preparation of the manuscript.

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Correspondence to Takeshi Kondoh.

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Hayashi, S., Kondoh, T., Morishita, A. et al. Congenital cavernous angioma exhibits a progressive decrease in size after birth. Childs Nerv Syst 20, 199–203 (2004). https://doi.org/10.1007/s00381-003-0844-8

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  • DOI: https://doi.org/10.1007/s00381-003-0844-8

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