The nature and fate of punctate (Type IV) cavernous malformations

被引:12
作者
Clatterbuck, RE [1 ]
Elmaci, I [1 ]
Rigamonti, D [1 ]
机构
[1] Johns Hopkins Hosp, Dept Neurosurg, Baltimore, MD 21287 USA
关键词
capillary telangiectasia; cavernous malformation;
D O I
10.1097/00006123-200107000-00004
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
OBJECTIVE: Four types of cavernous malformations (Types I-IV) have been described on the basis of their magnetic resonance imaging (MRI) appearance. The nature of the Type IV cavernous malformation is unclear. It has been suggested that these small lesions, which are well observed only on gradient echo MRI scans, are capillary telangiectasias. We sought to understand the relationship of Type IV cavernous malformations to the other cavernous malformation subtypes. METHODS: We examined serial MRI scans obtained between 1987 and 2000 from 68 patients with more than 228 cavernous malformations. Sixteen patients harbored Type IV cavernous malformations (total, > 114 Type IV lesions). Spin echo T1-weighted, T2-weighted, proton density, and (when available) gradient echo MRI scans were reviewed. Cavernous malformations that met the Zabramski criteria for Type IV (poorly observed on T1- and T2-weighted images) were reviewed in serial scans from individual patients to characterize their radiographic behavior over time. RESULTS: Type IV cavernous malformations were best observed on gradient echo images and have an MRI appearance distinct from capillary telangiectasias. Proton density images demonstrate more Type IV lesions than T1- and T2-weighted images, but far fewer Type IV lesions than gradient echo images. When observed on T1- and T2-weighted images, Type IV cavernous malformations are generally punctate and hypointense. These lesions rarely enhance with gadolinium. Four of the Type IV cavernous malformations observed serially evolved into Type I and Type II cavernous malformations, for an approximate rate of progression of 0.05 per patient year. CONCLUSION: Although most Type IV cavernous malformations remain stable over time, a small subset of these lesions progress into Types I and II cavernous malformations.
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页码:26 / 30
页数:5
相关论文
共 11 条
  • [1] Familial form of intracranial cavernous angioma: MR imaging findings in 51 families
    Brunereau, L
    Labauge, P
    Tournier-Lasserve, E
    Laberge, S
    Levy, C
    Houtteville, JP
    [J]. RADIOLOGY, 2000, 214 (01) : 209 - 216
  • [2] Dynamic nature of cavernous malformations: a prospective magnetic resonance imaging study with volumetric analysis
    Clatterbuck, RE
    Moriarity, JL
    Elmaci, I
    Lee, RR
    Breiter, SN
    Rigamonti, D
    [J]. JOURNAL OF NEUROSURGERY, 2000, 93 (06) : 981 - 986
  • [3] KRIT1 is mutated in hyperkeratotic cutaneous capillary-venous malformation associated with cerebral capillary malformation
    Eerola, I
    Plate, KH
    Spiegel, R
    Boon, LM
    Mulliken, JB
    Vikkula, M
    [J]. HUMAN MOLECULAR GENETICS, 2000, 9 (09) : 1351 - 1355
  • [4] Truncating mutations in CCM1, encoding KRIT1, cause hereditary cavernous angiomas
    Laberge-le Couteulx, S
    Jung, HH
    Labauge, P
    Houtteville, JP
    Lescoat, C
    Cecillon, M
    Marechal, E
    Joutel, A
    Bach, JF
    Tournier-Lasserve, E
    [J]. NATURE GENETICS, 1999, 23 (02) : 189 - 193
  • [5] Brain capillary telangiectasia: MR imaging appearance and clinicohistopathologic findings
    Lee, RR
    Becher, MW
    Benson, ML
    Rigamonti, D
    [J]. RADIOLOGY, 1997, 205 (03) : 797 - 805
  • [6] The natural history of cavernous malformations: A prospective study of 68 patients
    Moriarity, JL
    Wetzel, M
    Clatterbuck, RE
    Javedan, S
    Sheppard, JM
    Hoenig-Rigamonti, K
    Crone, NE
    Breiter, SN
    Lee, RR
    Rigamonti, D
    [J]. NEUROSURGERY, 1999, 44 (06) : 1166 - 1171
  • [7] THE MRI APPEARANCE OF CAVERNOUS MALFORMATIONS (ANGIOMAS)
    RIGAMONTI, D
    DRAYER, BP
    JOHNSON, PC
    HADLEY, MN
    ZABRAMSKI, J
    SPETZLER, RF
    [J]. JOURNAL OF NEUROSURGERY, 1987, 67 (04) : 518 - 524
  • [8] CAVERNOUS MALFORMATIONS AND CAPILLARY TELANGIECTASIA - A SPECTRUM WITHIN A SINGLE PATHOLOGICAL ENTITY
    RIGAMONTI, D
    JOHNSON, PC
    SPETZLER, RF
    HADLEY, MN
    DRAYER, BP
    [J]. NEUROSURGERY, 1991, 28 (01) : 60 - 64
  • [9] Mutations in the gene encoding KRIT1, a Krev-1/rap1a binding protein, cause cerebral cavernous malformations (CCM1)
    Sahoo, T
    Johnson, EW
    Thomas, JW
    Kuehl, PM
    Jones, TL
    Dokken, CG
    Touchman, JW
    Gallione, CJ
    Lee-Lin, SQ
    Kosofsky, B
    Kurth, JH
    Louis, DN
    Mettler, G
    Morrison, L
    Gil-Nagel, A
    Rich, SS
    Zabramski, JM
    Boguski, MS
    Green, ED
    Marchuk, DA
    [J]. HUMAN MOLECULAR GENETICS, 1999, 8 (12) : 2325 - 2333
  • [10] THE NATURAL-HISTORY OF FAMILIAL CAVERNOUS MALFORMATIONS - RESULTS OF AN ONGOING STUDY
    ZABRAMSKI, JM
    WASCHER, TM
    SPETZLER, RF
    JOHNSON, B
    GOLFINOS, J
    DRAYER, BP
    BROWN, B
    RIGAMONTI, D
    BROWN, G
    [J]. JOURNAL OF NEUROSURGERY, 1994, 80 (03) : 422 - 432