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n2:pmcid
PMC0
bibo:doi
10.1007%2Fs00401-007-0243-4
n6:contains
_:vb2516939 _:vb2516931 _:vb2516956 _:vb2516958 _:vb2516950 _:vb2516893 _:vb2516905 _:vb2516908 _:vb2516911 _:vb2516896 _:vb2516899 _:vb2516926 _:vb2516916 _:vb2516919
Subject Item
_:vb2516893
rdf:type
n6:Section
dc:title
angiocentric glioma
n6:contains
_:vb2516894 _:vb2516895
Subject Item
_:vb2516894
rdf:type
n2:Context
rdf:value
A total of 28 cases has been reported from the United States [>>51<<], France [33], and Austria/Germany [41].
n2:mentions
n3:16215459
Subject Item
_:vb2516895
rdf:type
n2:Context
rdf:value
A total of 28 cases has been reported from the United States [51], France [>>33<<], and Austria/Germany [41].
n2:mentions
n3:16389940
Subject Item
_:vb2516896
rdf:type
n6:Section
dc:title
papillary glioneuronal tumour (pgnt)
n6:contains
_:vb2516897 _:vb2516898
Subject Item
_:vb2516897
rdf:type
n2:Context
rdf:value
2) was established as a distinct clinico-pathologic entity by Komori et al. in 1998 [>>28<<]. Histopathologically similar tumours had previously been described as pseudopapillary ganglioglioneurocytoma [29] and pseudopapillary neurocytoma with glial differentiation [23]. PGNT manifests over a wide age range (mean 27 years) and
n2:mentions
n3:9777979
Subject Item
_:vb2516898
rdf:type
n2:Context
rdf:value
Histopathologically similar tumours had previously been described as pseudopapillary ganglioglioneurocytoma [29] and pseudopapillary neurocytoma with glial differentiation [>>23<<]. PGNT manifests over a wide age range (mean 27 years) and is a clinically benign neoplasm that typically corresponds to WHO grade I. Its preferential location is the temporal lobe. On CT and MR images, it appears as a contrast-enhancing,
n2:mentions
n3:9255395
Subject Item
_:vb2516899
rdf:type
n6:Section
dc:title
rosette-forming glioneuronal tumour of the fourth ventricle
n6:contains
_:vb2516904 _:vb2516900 _:vb2516901 _:vb2516902 _:vb2516903
Subject Item
_:vb2516900
rdf:type
n2:Context
rdf:value
This newly included entity, initially described as dysembryoplastic neuroepithelial tumour (DNT) of the cerebellum [>>32<<], was established as distinct disease entity in a report of 11 cases by Komori et al. in 2002 [30].
n2:mentions
n3:7610772
Subject Item
_:vb2516901
rdf:type
n2:Context
rdf:value
This newly included entity, initially described as dysembryoplastic neuroepithelial tumour (DNT) of the cerebellum [32], was established as distinct disease entity in a report of 11 cases by Komori et al. in 2002 [>>30<<]. Since then, a total of 17 cases have been reported.
n2:mentions
n3:11979088
Subject Item
_:vb2516902
rdf:type
n2:Context
rdf:value
Histopathologically, RGNTs are characterized by a biphasic neurocytic and glial architecture [>>18<<, 30, 40]. The neuronal component consists of neurocytes that form neurocytic rosettes with eosinophilic, synaptophysin-positive cores and/or perivascular pseudorosettes. The glial component dominates and typically exhibits features of
n2:mentions
n3:16599951
Subject Item
_:vb2516903
rdf:type
n2:Context
rdf:value
Histopathologically, RGNTs are characterized by a biphasic neurocytic and glial architecture [18, >>30<<, 40]. The neuronal component consists of neurocytes that form neurocytic rosettes with eosinophilic, synaptophysin-positive cores and/or perivascular pseudorosettes. The glial component dominates and typically exhibits features of
n2:mentions
n3:11979088
Subject Item
_:vb2516904
rdf:type
n2:Context
rdf:value
Histopathologically, RGNTs are characterized by a biphasic neurocytic and glial architecture [18, 30, >>40<<]. The neuronal component consists of neurocytes that form neurocytic rosettes with eosinophilic, synaptophysin-positive cores and/or perivascular pseudorosettes. The glial component dominates and typically exhibits features of pilocytic
n2:mentions
n3:12915951
Subject Item
_:vb2516905
rdf:type
n6:Section
dc:title
papillary tumour of the pineal region
n6:contains
_:vb2516906 _:vb2516907
Subject Item
_:vb2516906
rdf:type
n2:Context
rdf:value
In addition to the initial 2003 report of six cases by Jouvet et al. [>>20<<], a total of 38 cases have been published to date.
n2:mentions
n3:12657936
Subject Item
_:vb2516907
rdf:type
n2:Context
rdf:value
Ultrastructural features suggest ependymal differentiation and a possible origin from specialized ependymal cells of the subcommissural organ (SCO) has been suggested [>>20<<]. The biological behaviour of papillary tumour of the pineal region (PTPR) is variable and may correspond to WHO grades II or III, but precise histological grading criteria remain to be defined. The code 9395/3 has been proposed for the
n2:mentions
n3:12657936
Subject Item
_:vb2516908
rdf:type
n6:Section
dc:title
pituicytoma
n6:contains
_:vb2516909 _:vb2516910
Subject Item
_:vb2516909
rdf:type
n2:Context
rdf:value
Histologically, they show a compact architecture consisting of elongate, bipolar spindle cells arranged in interlacing fascicles or assuming a storiform pattern [>>2<<, 48]. Mitotic figures are absent or rare. Pituicytomas are generally positive for vimentin, S-100 protein and, to a variable degree, GFAP. In contrast to spindle cell oncocytoma (see below), oncocytic change is lacking. Due to their slow
n2:mentions
n3:10716149
Subject Item
_:vb2516910
rdf:type
n2:Context
rdf:value
Histologically, they show a compact architecture consisting of elongate, bipolar spindle cells arranged in interlacing fascicles or assuming a storiform pattern [2, >>48<<]. Mitotic figures are absent or rare. Pituicytomas are generally positive for vimentin, S-100 protein and, to a variable degree, GFAP. In contrast to spindle cell oncocytoma (see below), oncocytic change is lacking. Due to their slow
n2:mentions
n3:15028154
Subject Item
_:vb2516911
rdf:type
n6:Section
dc:title
spindle cell oncocytoma of the adenohypophysis
n6:contains
_:vb2516912 _:vb2516913 _:vb2516914 _:vb2516915
Subject Item
_:vb2516912
rdf:type
n2:Context
rdf:value
Since the initial 2002 report of five cases by Roncaroli et al. [>>43<<], five additional cases have been published from three institutions [4, 27, 49].
n2:mentions
n3:12170092
Subject Item
_:vb2516913
rdf:type
n2:Context
rdf:value
Since the initial 2002 report of five cases by Roncaroli et al. [43], five additional cases have been published from three institutions [>>4<<, 27, 49]. The code 8291/0 has been proposed for the fourth edition of ICD-O.Fig.
n2:mentions
n3:15973544
Subject Item
_:vb2516914
rdf:type
n2:Context
rdf:value
Since the initial 2002 report of five cases by Roncaroli et al. [43], five additional cases have been published from three institutions [4, >>27<<, 49]. The code 8291/0 has been proposed for the fourth edition of ICD-O.Fig.
n2:mentions
n3:15644783
Subject Item
_:vb2516915
rdf:type
n2:Context
rdf:value
Since the initial 2002 report of five cases by Roncaroli et al. [43], five additional cases have been published from three institutions [4, 27, >>49<<]. The code 8291/0 has been proposed for the fourth edition of ICD-O.Fig.
n2:mentions
n3:16884858
Subject Item
_:vb2516916
rdf:type
n6:Section
dc:title
pilomyxoid astrocytoma
n6:contains
_:vb2516917 _:vb2516918
Subject Item
_:vb2516917
rdf:type
n2:Context
rdf:value
Originally described by Jänisch et al. in 1985 as ‘diencephalic pilocytic astrocytoma with clinical onset in infancy’ [>>19<<], the term pilomyxoid astrocytoma was introduced in 1999 by Tihan et al. [47] who also defined its characteristic histopathological features.
n2:mentions
n3:3984542
Subject Item
_:vb2516918
rdf:type
n2:Context
rdf:value
Originally described by Jänisch et al. in 1985 as ‘diencephalic pilocytic astrocytoma with clinical onset in infancy’ [19], the term pilomyxoid astrocytoma was introduced in 1999 by Tihan et al. [>>47<<] who also defined its characteristic histopathological features. Pilomyxoid astrocytoma (PMA) (Fig.
n2:mentions
n3:10515229
Subject Item
_:vb2516919
rdf:type
n6:Section
dc:title
small cell glioblastoma
n6:contains
_:vb2516920 _:vb2516921 _:vb2516922 _:vb2516923 _:vb2516924 _:vb2516925
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_:vb2516920
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Although small cells are common in glioblastoma, they are predominant or exclusive in a subset known as small cell glioblastoma [>>38<<]. This glioblastoma subtype displays a monomorphic cell population characterized by small, round to slightly elongated, densely packed cells with mildly hyperchromatic nuclei, high nuclear:
n2:mentions
n3:15470710
Subject Item
_:vb2516921
rdf:type
n2:Context
rdf:value
The small cell glioblastoma phenotype frequently shows EGFR amplification [>>3<<, 16, 38], p16INK4a homozygous deletion [16], PTEN mutations [16] and LOH 10q [38].
n2:mentions
n3:11706939
Subject Item
_:vb2516922
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n2:Context
rdf:value
The small cell glioblastoma phenotype frequently shows EGFR amplification [3, 16, >>38<<], p16INK4a homozygous deletion [16], PTEN mutations [16] and LOH 10q [38].
n2:mentions
n3:15470710
Subject Item
_:vb2516923
rdf:type
n2:Context
rdf:value
The small cell glioblastoma phenotype frequently shows EGFR amplification [3, 16, 38], p16INK4a homozygous deletion [16], PTEN mutations [16] and LOH 10q [>>38<<]. In one study [38], these tumours more commonly expressed the EGFR (83 vs. 35%) and its variant EGFR-vIII (50 vs. 21%) as compared to non-small cell glioblastomas. This glioblastoma type appears to have a poor prognosis [38] although in
n2:mentions
n3:15470710
Subject Item
_:vb2516924
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n2:Context
rdf:value
In one study [>>38<<], these tumours more commonly expressed the EGFR (83 vs. 35%) and its variant EGFR-vIII (50 vs.
n2:mentions
n3:15470710
Subject Item
_:vb2516925
rdf:type
n2:Context
rdf:value
This glioblastoma type appears to have a poor prognosis [>>38<<] although in one population-based study there was no significant overall survival difference when compared to non-small cell glioblastoma [16].
n2:mentions
n3:15470710
Subject Item
_:vb2516926
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n6:Section
dc:title
glioblastoma with oligodendroglioma component
n6:contains
_:vb2516927 _:vb2516928 _:vb2516929 _:vb2516930
Subject Item
_:vb2516927
rdf:type
n2:Context
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Two large studies of malignant gliomas suggest that necrosis is associated with significantly worse prognosis in anaplastic gliomas with both oligodendroglial and astrocytic components [>>36<<, 50]: patients whose tumours showed necrosis had a substantially shorter median overall survival compared to patients whose tumours did not. At the WHO consensus meeting, the designation of these tumours was controversial. Some
n2:mentions
n3:17135643
Subject Item
_:vb2516928
rdf:type
n2:Context
rdf:value
Two large studies of malignant gliomas suggest that necrosis is associated with significantly worse prognosis in anaplastic gliomas with both oligodendroglial and astrocytic components [36, >>50<<]: patients whose tumours showed necrosis had a substantially shorter median overall survival compared to patients whose tumours did not. At the WHO consensus meeting, the designation of these tumours was controversial. Some participants
n2:mentions
n3:16782911
Subject Item
_:vb2516929
rdf:type
n2:Context
rdf:value
In particular, it should be established whether or not these tumours carry a better prognosis than standard glioblastomas [>>13<<, 16, 31]. For the time being, the new WHO Classification recommends classifying such tumours as ‘glioblastoma with oligodendroglioma component’.
n2:mentions
n3:11556543
Subject Item
_:vb2516930
rdf:type
n2:Context
rdf:value
In particular, it should be established whether or not these tumours carry a better prognosis than standard glioblastomas [13, 16, >>31<<]. For the time being, the new WHO Classification recommends classifying such tumours as ‘glioblastoma with oligodendroglioma component’.
n2:mentions
n3:11355302
Subject Item
_:vb2516931
rdf:type
n6:Section
dc:title
glioneuronal tumour with neuropil-like islands
n6:contains
_:vb2516936 _:vb2516937 _:vb2516938 _:vb2516932 _:vb2516933 _:vb2516934 _:vb2516935
Subject Item
_:vb2516932
rdf:type
n2:Context
rdf:value
Reported cases were located supratentorially [>>46<<], with the exception of one example situated in the cervicothoracic spinal cord [12].
n2:mentions
n3:10328080
Subject Item
_:vb2516933
rdf:type
n2:Context
rdf:value
Reported cases were located supratentorially [46], with the exception of one example situated in the cervicothoracic spinal cord [>>12<<]. As a rule, the underlying lesions were astrocytomas WHO grade II or III [39, 46]; one case was associated with ependymoma [10].
n2:mentions
n3:11045681
Subject Item
_:vb2516934
rdf:type
n2:Context
rdf:value
As a rule, the underlying lesions were astrocytomas WHO grade II or III [>>39<<, 46]; one case was associated with ependymoma [10].
n2:mentions
n3:11112223
Subject Item
_:vb2516935
rdf:type
n2:Context
rdf:value
As a rule, the underlying lesions were astrocytomas WHO grade II or III [39, >>46<<]; one case was associated with ependymoma [10].
n2:mentions
n3:10328080
Subject Item
_:vb2516936
rdf:type
n2:Context
rdf:value
As a rule, the underlying lesions were astrocytomas WHO grade II or III [39, 46]; one case was associated with ependymoma [>>10<<].
n2:mentions
n3:15549332
Subject Item
_:vb2516937
rdf:type
n2:Context
rdf:value
Usually [>>46<<], but not always [22], these cells show a lower proliferative activity than the predominant glial component which typically shows a high degree of atypia, and consists mainly of GFAP-positive, fibrillary and gemistocytic elements
n2:mentions
n3:10328080
Subject Item
_:vb2516938
rdf:type
n2:Context
rdf:value
Usually [46], but not always [>>22<<], these cells show a lower proliferative activity than the predominant glial component which typically shows a high degree of atypia, and consists mainly of GFAP-positive, fibrillary and gemistocytic elements identical to those populating
n2:mentions
n3:11484825
Subject Item
_:vb2516939
rdf:type
n6:Section
dc:title
medulloblastoma with myogenic differentiation versus medullomyoblastoma
n6:contains
_:vb2516940 _:vb2516941 _:vb2516942 _:vb2516943 _:vb2516944 _:vb2516945 _:vb2516946 _:vb2516947 _:vb2516948 _:vb2516949
Subject Item
_:vb2516940
rdf:type
n2:Context
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The code remains but since its clinical features and genetic profile are similar to those of other medulloblastomas, this lesion is no longer considered a distinct entity [>>14<<, 34] and it is suggested that the code for medulloblastoma (9470/3) be applied.
n2:mentions
n3:15368333
Subject Item
_:vb2516941
rdf:type
n2:Context
rdf:value
The code remains but since its clinical features and genetic profile are similar to those of other medulloblastomas, this lesion is no longer considered a distinct entity [14, >>34<<] and it is suggested that the code for medulloblastoma (9470/3) be applied.
n2:mentions
n3:11453402
Subject Item
_:vb2516942
rdf:type
n2:Context
rdf:value
containing focal rhabdomyoblastic elements with immunoreactivity to desmin [>>15<<, 44], myoglobin [6, 15, 45], and fast myosin [21], but not smooth muscle α-actin alone [15, 44].
n2:mentions
n3:1662856
Subject Item
_:vb2516943
rdf:type
n2:Context
rdf:value
containing focal rhabdomyoblastic elements with immunoreactivity to desmin [15, >>44<<], myoglobin [6, 15, 45], and fast myosin [21], but not smooth muscle α-actin alone [15, 44].
n2:mentions
n3:1327526
Subject Item
_:vb2516944
rdf:type
n2:Context
rdf:value
containing focal rhabdomyoblastic elements with immunoreactivity to desmin [15, 44], myoglobin [>>6<<, 15, 45], and fast myosin [21], but not smooth muscle α-actin alone [15, 44].
n2:mentions
n3:6355400
Subject Item
_:vb2516945
rdf:type
n2:Context
rdf:value
containing focal rhabdomyoblastic elements with immunoreactivity to desmin [15, 44], myoglobin [6, >>15<<, 45], and fast myosin [21], but not smooth muscle α-actin alone [15, 44].
n2:mentions
n3:1662856
Subject Item
_:vb2516946
rdf:type
n2:Context
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containing focal rhabdomyoblastic elements with immunoreactivity to desmin [15, 44], myoglobin [6, 15, >>45<<], and fast myosin [21], but not smooth muscle α-actin alone [15, 44].
n2:mentions
n3:6202392
Subject Item
_:vb2516947
rdf:type
n2:Context
rdf:value
containing focal rhabdomyoblastic elements with immunoreactivity to desmin [15, 44], myoglobin [6, 15, 45], and fast myosin [>>21<<], but not smooth muscle α-actin alone [15, 44].
n2:mentions
n3:3136447
Subject Item
_:vb2516948
rdf:type
n2:Context
rdf:value
containing focal rhabdomyoblastic elements with immunoreactivity to desmin [15, 44], myoglobin [6, 15, 45], and fast myosin [21], but not smooth muscle α-actin alone [>>15<<, 44].
n2:mentions
n3:1662856
Subject Item
_:vb2516949
rdf:type
n2:Context
rdf:value
containing focal rhabdomyoblastic elements with immunoreactivity to desmin [15, 44], myoglobin [6, 15, 45], and fast myosin [21], but not smooth muscle α-actin alone [15, >>44<<].
n2:mentions
n3:1327526
Subject Item
_:vb2516950
rdf:type
n6:Section
dc:title
medulloblastoma with melanotic differentiation versus melanotic medulloblastoma
n6:contains
_:vb2516952 _:vb2516953 _:vb2516954 _:vb2516955 _:vb2516951
Subject Item
_:vb2516951
rdf:type
n2:Context
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The melanotic tumour cells may appear undifferentiated or epithelial, with formation of tubules or papillae [>>1<<, 7, 9]. They usually express S-100 protein [1, 9]. Since clusters of melanotic tumour cells can occur in any variant of medulloblastoma, such lesions are not regarded as a distinct variant or entity.
n2:mentions
n3:9526628
Subject Item
_:vb2516952
rdf:type
n2:Context
rdf:value
The melanotic tumour cells may appear undifferentiated or epithelial, with formation of tubules or papillae [1, >>7<<, 9]. They usually express S-100 protein [1, 9]. Since clusters of melanotic tumour cells can occur in any variant of medulloblastoma, such lesions are not regarded as a distinct variant or entity.
n2:mentions
n3:3188844
Subject Item
_:vb2516953
rdf:type
n2:Context
rdf:value
The melanotic tumour cells may appear undifferentiated or epithelial, with formation of tubules or papillae [1, 7, >>9<<]. They usually express S-100 protein [1, 9]. Since clusters of melanotic tumour cells can occur in any variant of medulloblastoma, such lesions are not regarded as a distinct variant or entity.
n2:mentions
n3:2203326
Subject Item
_:vb2516954
rdf:type
n2:Context
rdf:value
They usually express S-100 protein [>>1<<, 9]. Since clusters of melanotic tumour cells can occur in any variant of medulloblastoma, such lesions are not regarded as a distinct variant or entity.
n2:mentions
n3:9526628
Subject Item
_:vb2516955
rdf:type
n2:Context
rdf:value
They usually express S-100 protein [1, >>9<<]. Since clusters of melanotic tumour cells can occur in any variant of medulloblastoma, such lesions are not regarded as a distinct variant or entity.
n2:mentions
n3:2203326
Subject Item
_:vb2516956
rdf:type
n6:Section
dc:title
who grading
n6:contains
_:vb2516957
Subject Item
_:vb2516957
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The WHO classification of tumours of the nervous system includes a grading scheme that is a ‘malignancy scale’ ranging across a wide variety of neoplasms rather than a strict histological grading system [>>25<<, 52]. It is widely used, but not a requirement for the application of the WHO classification. The WHO Working Group responsible for the fourth edition included some novel entities (see above); however, since the number of cases of some
n2:mentions
n3:8293185
Subject Item
_:vb2516958
rdf:type
n6:Section
dc:title
grading of astrocytic tumours
n6:contains
_:vb2516959 _:vb2516964 _:vb2516960 _:vb2516961 _:vb2516962 _:vb2516963
Subject Item
_:vb2516959
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These neoplasms are graded in a three-tiered system similar to that of the Ringertz [>>42<<], St Anne-Mayo [5] and the previously published WHO schemes [52].
n2:mentions
n3:15406242
Subject Item
_:vb2516960
rdf:type
n2:Context
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These neoplasms are graded in a three-tiered system similar to that of the Ringertz [42], St Anne-Mayo [>>5<<] and the previously published WHO schemes [52].
n2:mentions
n3:12910070
Subject Item
_:vb2516961
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n2:Context
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This system is similar to the St Anne/Mayo classification [>>5<<], with the only major difference being grade I; in the WHO system, grade I is assigned to the more circumscribed pilocytic astrocytoma, whereas the St Anne/Mayo classification assigns grade 1 to an exceedingly rare diffuse astrocytoma
n2:mentions
n3:12910070
Subject Item
_:vb2516962
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Since the finding of a solitary mitosis in an ample specimen does not confer grade III behaviour, separation of grade II from grade III tumours may be more reliably achieved by determination of MIB-1 labelling indices [>>11<<, 17, 37]. For WHO grade IV, some authors accept only the criterion of endothelial proliferation, i.e. an apparent multi-layering of endothelium. The WHO classification also accepts glomeruloid microvascular proliferations. Necrosis may be
n2:mentions
n3:9848865
Subject Item
_:vb2516963
rdf:type
n2:Context
rdf:value
Since the finding of a solitary mitosis in an ample specimen does not confer grade III behaviour, separation of grade II from grade III tumours may be more reliably achieved by determination of MIB-1 labelling indices [11, >>17<<, 37]. For WHO grade IV, some authors accept only the criterion of endothelial proliferation, i.e. an apparent multi-layering of endothelium. The WHO classification also accepts glomeruloid microvascular proliferations. Necrosis may be of
n2:mentions
n3:3325615
Subject Item
_:vb2516964
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n2:Context
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Since the finding of a solitary mitosis in an ample specimen does not confer grade III behaviour, separation of grade II from grade III tumours may be more reliably achieved by determination of MIB-1 labelling indices [11, 17, >>37<<]. For WHO grade IV, some authors accept only the criterion of endothelial proliferation, i.e. an apparent multi-layering of endothelium. The WHO classification also accepts glomeruloid microvascular proliferations. Necrosis may be of any
n2:mentions
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