V. Rajshekhar et Mj. Chandy, VALIDATION OF DIAGNOSTIC-CRITERIA FOR SOLITARY CEREBRAL CYSTICERCUS GRANULOMA INPATIENTS PRESENTING WITH SEIZURES, Acta neurologica Scandinavica, 96(2), 1997, pp. 76-81
Objective - To evaluate a set of clinical and computed tomographic (CT
) criteria (previously described by us) to predict the diagnosis of a
solitary cerebral cysticercus granuloma (SCCG) at initial presentation
, in patients presenting with seizures. Material and methods - The dia
gnostic criteria were applied prospectively to patients presenting wit
h seizures and solitary lesion on the CT scan. The clinical diagnostic
criteria were as follows: seizures should be the presenting complaint
there should be no evidence of persistent raised intracranial pressur
e, progressive neurological deficit or an active systemic disease. The
CT diagnostic criteria were: evidence of a solitary contrast enhancin
g lesion measuring 20 mm or less in its maximal dimension without a sh
ift of the midline structures due to the surrounding oedema. A diagnos
is of SCCG was made only when all the clinical and CT criteria were fu
lfilled. Over a period of 36 months. we managed 401 patients presentin
g with seizures and a solitary mass on the CT scan; 215 met the criter
ia for the diagnosis of an SCCG. Results - Of the 215 patients initial
ly diagnosed to have an SCCG, 197 were ultimately determined to have t
hat diagnosis (true positive diagnosis) while 16 were excluded because
of lack of follow-up CT assessment. Two of the 215 patients with the
initial diagnosis of an SCCG subsequently had histological diagnosis o
f a secondary metastasis and a pyogenic abscess (false positive diagno
sis). Our set of diagnostic criteria for SCCG had a sensitivity of 99.
5%; specificity of 98.9%; a positive predictive value of 99%; and a ne
gative predictive value of 99.5%. The likelihood ratios for the positi
ve and negative tests were 92.99 and 0.005 respectively. Conclusions -
Our diagnostic criteria help in not only accurately identifying an SC
CG but also in differentiating if: from a solitary tuberculoma and oth
er brain masses. However, confirmation of the diagnosis of an SCCG is
only obtained at follow-up evaluation and therefore careful clinical a
nd CT re-evaluation is essential in all patients Initially diagnosed t
o have an SCCG.