Ra. Prayson et al., Interobserver reproducibility among neuropathologists and surgical pathologists in fibrillary astrocytoma grading, J NEUR SCI, 175(1), 2000, pp. 33-39
Many of the problems associated with the current grading approaches for fib
rillary astrocytomas center around the lack of consistency in grading. This
study compares the diagnoses of five neuropathologists with five experienc
ed surgical pathologists with regard to assigning astrocytoma grade. Thirty
neoplastic and non-neoplastic lesions were sent to each of five neuropatho
logists and five surgical pathologists for placement into one of three grad
es as outlined by modified Ringertz schema. Grading criteria (Burger et al.
, 1985. Cancer 56:1106-1111) were distributed to all participants, who have
been practicing for at least 5 years. An additional category for non-neopl
astic or normal tissue was also provided. The diagnoses, based on the major
ity opinion of the neuropathologist group, included six low grade astrocyto
mas, ii anaplastic astrocytomas, seven glioblastoma multiforme, and six nor
mal/reactive lesions. Agreement by all neuropathologists was reached in 12
cases (40%). A discrepant diagnosis was obtained in one of five neuropathol
ogists in 14 additional cases (46.7%). In the remaining four cases, two neu
ropathologists deviated from the majority opinion; in each of these cases,
the diagnostic problem involved differentiating tumor from reactive gliosis
. All five surgical pathologists agreed in six cases (20%). One discrepant
diagnosis among the surgical pathologist group was seen in seven cases (23.
3%). In the remaining 17 cases, two or more discrepant diagnoses were obtai
ned (56.7%); discrepancies in these cases included differences in assignmen
t of tumor grade and in distinguishing low grade astrocytoma from gliosis.
In conclusion: (1) it is likely that experience with grading accounts for t
he better level of agreement among the neuropathologist group (kappa statis
tic 0.63) versus the surgical pathologist group (kappa statistic 0.36); (2)
in most cases, the neuropathologists all agreed or had one discrepant diag
nosis (86.7%) versus the surgical pathologist group (43.3%); (3) the discre
pancies in diagnosis among both groups is likely related, in good part, to
the limitations of the grading schema in fully enumerating the spectrum of
such grading parameters as cytologic atypia and vascular proliferation. (C)
2000 Elsevier Science B.V. All rights reserved.