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The purpose of this study was to provide preliminary data on morphological patterns of intracranial space occupying lesions (ICSOL) in central Punjab province. This is a cross-sectional
prospective study on 100 consecutive cases of intra-cranial space occupying lesions admitted to
both the neurosurgery units of Lahore General Hospital, Lahore, Pakistan. The biopsy materials
were examined histologically using paraffin sections. Eighty nine (89) patients had neoplasms,
while eleven (11) had non-neoplastic lesions. Neuroepithelial tumours comprised 41% of all the
neoplasms, followed by meningiomas being 23%, schwannomas 11% and metastatic tumours
6%. Males were affected slightly more than females (1.17:1). Tuberculomas constituted 3% of the
lesions. It was concluded that age and sex distribution were generally comparable to the other
published literature. Similarly neuroepithehal tumours formed majority of the lesions. However
meningiomas had a higher frequency as compared to the western literature; moreover
tuberculomas should also be considered in the differential diagnosis of such lesions in this part
of the world.
INTRODUCTION
The term Intra-cranial space occupying lesion is
defined as any neoplasm, benign or malignant, primary or secondary, as well as any inflammatory or
parasitic mass lying within the cranial cavity1. The
list also includes haematomas,2 different types of
cysts,3,4 and vascular malformations5,1,6. Space
occupying primary tumours of the central nervous
system and its coverings account for about 9% of
all the primary neoplasms of the human body.
Among the intracranial space occupying tumours,
those of central neurogenic origin claim priority in
number and complexity. These are the tumours
derived from parenchymatous neuroepithelial elements of central nervous system excluding the
microglia; and they are widely credited to account
for 40-50% of all the intra-cranial space occupying
tumours7,8. Systemic study of tumours of the central nervous system began when Baily and Cushing started their studies in the early 1920s. Over
the past three decades, many reports suggested
that both incidence and pattern of intracranial
neoplasia are subject to considerable geographic
and racial variations. Knowledge of the regional
peculiarities of these lesions, may, therefore, help
in identifications of possible risk factors and also
in establishing measures for an improved
diagnosis, treatment and outcome. No accurate
32
RESULTS
Sex
Total
Male
Female
48
41
89
11
54
46
100
Sex
Total
(%)
15
41
(41%)
16
23
(23%)
11
(11%)
(2%)
5. Vascular
Tumours
(1%)
6. Arterio-venous
malformation
(1%)
7. Extension from
regional Tumours
(2%)
8. Metastatic
Tumours
(6%)
9. Germ cell
Tumours
(1%)
Types of Tumor
Male
Female
26
2. Meningiomas
3. Nerve sheet
tumours (Schwannomas)
4. Primary
adenomas
1. Neuro-epithelial
Tumours
10. Lymphomas
Sex*
Total
Male
Female
1.
09
2.
10 19
13
3.
20 29
14
14
28
4.
30 39
13
5.
40 49
14
6.
50 59
13
20
7.
60 69
14
46
100
Total
(1%)
48
41
89
(89%)
Sex
Total
(%)
19
(46.3%)
(21.9%)
(14.6%)
Male
Female
1. Benign
Astrocytomas
15
2. Anaplastic
Astrocytomas
3. Glioblastomas
Multiforme
4. Ependymomas
(4.8%)
5. Oligodendrogliomas
(4.8%)
6. Medulloblastomas
(2.4%)
7. Choroid plexus
papilloma
(2.4%)
8. Mixed Tumour
(2.4%)
26
15
41
(100%)
Total
In a total 41 cases, 19 were benign astrocytomas and 15 cases were malignant astrocytomas.
These astrocytomas collectivity accounted for
82.8% of the total neuroepithelial tumours. M/F
ratio was 1.17:1. Meningiomas constituted 23% of
33
Oligodendroglioma
4.8%
Medulloblastoma
2.4%
Choroid plexus
papilloma 2.4%
Ependymoma 4.8%
Glioblastoma
Multiforme 14.8%
Benign
Astrocytomas
46.3%
Anaplastic
Astrocytomas
21.9%
Types of Lesion
Total
(%)
(3%)
(2%)
(2%)
(2%)
5. Cholesteatoma
(1%)
6. Chronic infection
(1%)
11
(11%)
Male
Female
1. Tuberculoma
2. Fungal Infection
3. Cysts
4. Haemorrhages
Total
Chrohic
Chronic
infection
9%
Cholesteatoma 9%
Tuberculomas 27%
Haemorrhages 18%
Cysts 18%
Fungal
Infection
18%
Fig. 1: Distribution of
41 cases of Neuroepithelial tumors
DISCUSSION
Despite some limiting factors in this study, the
analysis shows that these 100 cases of ICSOLs
share several features common with other
published series. Both age and sex distribution lie
within the estimated ranges in the other reports.
In this study, brain tumours occurred mostly
during the third and sixth decades of life. In comparison to that most series reported from Asian
countries,14,3,15,5,1,16,17 brain tumours occurred mostly during fourth decade of life, in Western countries during the fifth and sixth decades of life18,19,20.
This could be due to the differrrent age characteristics of the populations as well as different case
ascertainment in the two country groups, with a
higher rate of autopsies in the latter.
The percentage of pediatric brain tumours, occurring below the age of twenty years, in the present series was18% as compared with13% in Saudi
Arabia1, 10.0% in United States,21 16.8% in India22,
18.6% in China,5 28.4% in Thailand23. This figure
seems to be related to the size of the pediatric
population in each country. The most common
tumours in pediatric group were astrocy-tomas,
followed by medulloblastomas, in line with other
published reports24,25. The male to female ratio of
1.17:1 in the present 100 cases corresponds to an
overall male / female ratio ranging from 1:1 to
1:626,27,28,29,30,31,32. i. e. more males that females
develop brain tumours.
As in all other series tumours of the neuroepithelial origin were also in the present study, the
most frequent type of intracranial neoplasms
except in a study reported from Nigeria,33 where
Biomedica Vol. 21 (Jan. Jun., 2005)
34
Number
of cases
Range
Mean SD
Neuroepithelial Tumours
41 (41%)
9-60
29.34
14.10
Non-Neuroepithelial tumours
48 (48%)
1-65
*38.26
15.89
Lesion
The relative incidence of malformative tumours in this series was markedly below the rates reported from Japan, Thailand and China but within
the comparable ranges given by most Western
series.
The ratio of secondary brain tumours in the
present series is near the limits estimated in the
other series. Unexpectedly, the incidence of cerebral tuberculomas in the present series is less than
the rates reported from India and Saudi
Arabia14,15,1 and more than the other series from
Kuwait, Germany and France38,39,40. Thus in
conclusion, this study has highlighted the relative
frequency of different intracranial space occupying
lesions in the central Punjab Province.
REFERENCES
1.
2.
3.
4.
5.
6.
Jamjoom ZAB. Pattern of intra-cranial space occupying lesions: experience at King Khalid University
Hospital. Ann Saudi Med, 1989;9:3-10.
Duncan G, Caird F. Review of 18 years experience of
a diagnostic geriatricneurology referral service.
Scot-Med-J 1991; 36: 139-42.
Darrel F, Weinman. Incidence and Behaviour Pattern of intra-cranial Tumours in Ceylon. International Sur-gery 1973; 58: 548-54.
Conley FK. Epidermiod and dermiod tumours:
Clinical features and surgical management. In
Wilkins R.H. and Rengachary S.S. (eds), Neurosurgery Vol. No. 1. 2nd Ed. New York: McGraw-Hill
1996; 971-6.
Wen-Qing QQ, Shi-Jow, Qing-sheng T, et al. Statistical analysis of central nervous system tumours in
China. J. Neurosurg 1982; 56 (4): 555-64.
Lombardi D, Scheithauer B.W., Piepgras D, Meyer
FB., and Forbes G.S. Angioglioma and the arteriovenous malformation-glioma association. Journal
of Neurosurgery 1991; 75: 589-96.
7.
8.
9.
10.
11.
12.
13.
14.
15.
16.
17.
18.
19.
20.
21.
22.
23.
24.
35
25. Cho KT, Wang KC, Kim SK, Shin SH, Chi JG, Cho
BK. Pediatric brain tumours; statistics of SNUH
Korea (1959-2000). Childs Nerve Syst. 2002 Feb;
18 (1-2): 30-7. Epub 2002 Jan 25.
26. Cohen, A. and Modan, B. Some epidemiological aspects of neoplastic diseases in Israeli immigrant
population III. Brain tumours. Cancer 1968; 22:
1323-8.
27. Kurland, L.T., Schoenberg, B.S., Annegers, J.F.,
Okazaki, H. and Molgaad, C.A. The incidence of primary intracranial neoplasms in Rochester, Minnesota 1935-1977. Annals of New York Academy of
Sciences 1982; 381: 6-16.
28. Sant, M., Crosignani, P., Bordo, B.M., Nicola, G.N.,
Bianchi, M. and Berrino, F. Incidence and survival
of brain tumours; a population based study.
Tumori 1988; 74: 243-52.
29. Preston-Martin S., Thomas, D.C., Wright, W.E and
Henderson, B.E. Noise trauma in the etiology of
acoustic neuromas in men in Los Angeles county,
1978-1985. British Journal of Cancer 1989; 69: 7836.
30. Kallio, M. The incidence, survival, and prognostic
fac-tors of patients with intra-cranial glioma and
meningioma in Finland from 1953-1987. Academy
of Dissertation, University of Helskinki, Finland
1993.
31. Preston-Martin S., Staples, M., Farrugia, H. and
Giles, G. Primary tumours of the brain, cranial
nerves and cranial meninges in Victoria, Australia,
1982-1990: pattern of incidence and survival. Neuroepidemiology 1993; 12:270-9.
32. Olasode BJ, Shokunbi MT, Aghadiuno PU, Intracranial Neoplasms in Ibadan, Nigeria, East Afr Med J.
2000 Jan; 77 (1): 4-8.
33. Olasode BJ. A pathological review of intra-cranial
tumours seen at the University College Hospital,
Ibadan between 1980 and 1990. Nigeria Post grad
Med J. 2002 Mar; 9 (1): 23-8.
34. Sundaram C, Naidu MR, Reddy JJ. Pleomorphic
xanthoastrocytoma - a clinicopathological study.
Indian J Pathol Microbiol. 2000 Jul; 43 (3): 357-61.
35. Chowdhary UM, Ibrahim AW, Sohaibani M, Boehme DH. Experience with brain tumours in Eastern
Province of Saudi Arabia (letter to the editor). Ann
Saudi Med 1987; 7 (2): 166.
36. Siqueira E. Neurosurgical diseases at King Faisal
specialist Hospital and Research centre, 1982 to
1986 (letter to the editor). Ann Saudi Med 1988; 8
(2): 152-3.
37. Irfan A, Qureshi A. Intra-cranial space occupying
lesions; review of 386 cases. JPMA 1995; 45 (12):
319-20.
38. Abdul-Ghaffar NU, El-Sonbaty MR, Rahman NA.
Intracranial tuberculoma in Kuwait. Int J tuberc
Lung Dis. 1998 May; 2 (5): 413-8.
39. Pagnou C, Genereau T, Lafitte F, Congy F, Chiras J,
Herson S. Brain Tuberculomas; Ann Med Interne
(Paris). 2000 Oct; 151 (6): 448-55.
40. Giese A, Kucinski T, Hagel C, Lohmann F. Intracranial tuberculomas mimicking a malignant disease in an immuncompetent patient. Acta Neurochir
(Wien). 2003 Jun; 145 (6): 513-7.
Biomedica Vol. 21 (Jan. Jun., 2005)