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Dr. Mamta Gupta,
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Aug 2018




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Thanking you
With sincere regards
Dr. Rajendra Kumar Ghritlaharey, M.S., M. Ch., FAIS
Associate Professor,
Department of Paediatric Surgery, Gandhi Medical College & Associated
Kamla Nehru & Hamidia Hospitals Bhopal, Madhya Pradesh 462 001 (India)
E-mail: drrajendrak1@rediffmail.com
On May 11,2011




Dr. Shankar P.R.

"On looking back through my Gmail archives after being requested by the journal to write a short editorial about my experiences of publishing with the Journal of Clinical and Diagnostic Research (JCDR), I came across an e-mail from Dr. Hemant Jain, Editor, in March 2007, which introduced the new electronic journal. The main features of the journal which were outlined in the e-mail were extensive author support, cash rewards, the peer review process, and other salient features of the journal.
Over a span of over four years, we (I and my colleagues) have published around 25 articles in the journal. In this editorial, I plan to briefly discuss my experiences of publishing with JCDR and the strengths of the journal and to finally address the areas for improvement.
My experiences of publishing with JCDR: Overall, my experiences of publishing withJCDR have been positive. The best point about the journal is that it responds to queries from the author. This may seem to be simple and not too much to ask for, but unfortunately, many journals in the subcontinent and from many developing countries do not respond or they respond with a long delay to the queries from the authors 1. The reasons could be many, including lack of optimal secretarial and other support. Another problem with many journals is the slowness of the review process. Editorial processing and peer review can take anywhere between a year to two years with some journals. Also, some journals do not keep the contributors informed about the progress of the review process. Due to the long review process, the articles can lose their relevance and topicality. A major benefit with JCDR is the timeliness and promptness of its response. In Dr Jain's e-mail which was sent to me in 2007, before the introduction of the Pre-publishing system, he had stated that he had received my submission and that he would get back to me within seven days and he did!
Most of the manuscripts are published within 3 to 4 months of their submission if they are found to be suitable after the review process. JCDR is published bimonthly and the accepted articles were usually published in the next issue. Recently, due to the increased volume of the submissions, the review process has become slower and it ?? Section can take from 4 to 6 months for the articles to be reviewed. The journal has an extensive author support system and it has recently introduced a paid expedited review process. The journal also mentions the average time for processing the manuscript under different submission systems - regular submission and expedited review.
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Dr. P. Ravi Shankar
KIST Medical College, P.O. Box 14142, Kathmandu, Nepal.
E-mail: ravi.dr.shankar@gmail.com
On April 2011
Anuradha

Dear team JCDR, I would like to thank you for the very professional and polite service provided by everyone at JCDR. While i have been in the field of writing and editing for sometime, this has been my first attempt in publishing a scientific paper.Thank you for hand-holding me through the process.


Dr. Anuradha
E-mail: anuradha2nittur@gmail.com
On Jan 2020

Important Notice

Original article / research
Year : 2021 | Month : August | Volume : 15 | Issue : 8 | Page : EC16 - EC20 Full Version

Role of Squash Cytology in Intraoperative Diagnosis of Meningioma


Published: August 1, 2021 | DOI: https://doi.org/10.7860/JCDR/2021/47878.15260
Gowri Prakasam, K Karkuzhali, Veeraraghavan Gurusamy

1. Assistant Professor, Department of Pathology, Government Kilpauk Medical College, Chennai, Tamil Nadu, India. 2. Assistant Professor, Department of Pathology, Thanjavur Medical College, Thanjavur, Tamil Nadu, India. 3. Assistant Professor, Department of Pathology, Government Kilpauk Medical College, Chennai, Tamil Nadu, India.

Correspondence Address :
Dr. Gowri Prakasam,
31, Chinna Mudali Street, Pudhupet, Gudiyatham, Vellore-632602, Tamil Nadu, India.
E-mail: gowriprakasam18@gmail.com

Abstract

Introduction: Primary Central Nervous System (CNS) tumours constitute less than 2% of overall cancers in adults and are the second most frequently encountered tumours in children. Meningiomas form 24-30% of primary intracranial tumours. Most intrinsic brain tumours are soft and gelatinous in consistency, smear preparation can readily made which gives excellent cytological details when compared to frozen section as the latter produces ice crystal artifacts.

Aim: To assess the diagnostic utility of squash cytological evaluation of meningiomas and its comparison with final histopathological diagnosis.

Materials and Methods: The cross-sectional study was done at Thanjavur Medical College, Thanjavur, Tamil Nadu, India for period of three years from January 2015 to December 2017. Total of 54 clinically diagnosed and radiologically suspected case of meningiomas were selected. Smears were prepared from the biopsy samples sent in normal saline and stained by Haematoxylin and Eosin (H&E) method. The cytological features were noted and matched with biopsy findings. Descriptive statistics were used to analyse the results.

Results: Total of 54 squash smears with male to female ratio was 1:1.5. Maximum number of cases were seen between 41-50 years followed by 51-60 years. Complete concordance was obtained in 51 cases (94.44%) and partial concordance was noted in a case due to underestimation of malignancy grade in squash cytology. Out of 54 cases, two cases were found to be discordant with final histopathological diagnosis.

Conclusion: Intraoperative squash cytology is easy, rapid, reliable and cost-effective technique for neurosurgical consultation with fairly high accuracy in diagnosing meningiomas.

Keywords

Central nervous system tumours, Cytological-histological comparison, Cytomorphological features, Squash smear cytology

Primary Central Nervous System (CNS) tumours constitute less than 2% of overall cancers in adults and are the second most frequently encountered tumours in children (1). It is estimated that annual incidence of CNS tumours ranges from 10-17 per 1,00,000 persons for intra-cranial tumours and 1-2 per 1,00,000 persons for intraspinal tumours (1). Meningiomas form 24-30% of primary intracranial tumours (2).

Most intrinsic brain tumours are soft and gelatinous in consistency, smear preparation can readily made which gives excellent cytological details when compared to frozen section as the latter produces ice crystal artifacts (3). Intraoperative squash cytology preparation was first introduced by Eisenhardt and Cushing in early 1930 and by Badt in 1937 (4),(5),(6),(7). This technique was furthered and documented by Russell et al., in 1937 (5). Recently, the role of intraoperative smear preparation technique has gained importance because of advent of Computed Tomography (CT) and Magnetic Resonance Imaging (MRI) guided stereotactic biopsies (5),(6).

The advantages of squash smear technology are: (1) simple and rapid technique; (2) no technical expertise is required for preparation of smear; (3) provides both cytological and architectural features of CNS tumours; (4) background matrix and necrosis are easy to appreciate; (5) rapid diagnosis aids the neurosurgeon to plan the extent of surgery (8).

Objectives

• To assess the utility of intraoperative squash smear cytology in diagnosing meningioma and its limitations.
• To study about cytomorphological features of different types of meningioma in squash preparation.

Material and Methods

This cross-sectional study was done in Thanjavur Medical College and Hospital, Thanjavur, Tamil Nadu, India, for a period of three years from January 2015 to December 2017. The study was conducted after obtaining approval from Institutional Ethical Committee, Thanjavur (IEC NO. 117/dated/10.04.2015). A total of 54 clinically diagnosed and radiologically suspected cases of meningiomas were included and other CNS tumours were excluded from the study.

Study Procedure

For all the 54 cases, unfixed fresh biopsy material sent in normal saline from operation theatre was obtained. Initially, gross examination of specimen was done to evaluate the nature of spread. Care was taken not to allow the tissue to dry out. To prepare squash smears, small pin head sized or 2-3 mm tissue was taken and placed on one end of the slide. Flat surface of another slide placed at right angle on the top of the specimen and advanced with uniform motion without exerting undue pressure on the tissue. Minimum of 4-6 smears were made depending on the amount and sample of the tissue received. All the smears were fixed in 99.9% isopropyl alcohol and stained with Harris haematoxylin and eosin stain and examined.

Remaining tissue was fixed in 10% neutral buffered formalin for histopathological examination. Intraoperative squash smear cytological diagnosis was then compared with histopathological findings. Histopathological diagnosis was considered as final gold standard diagnosis to estimate the accuracy of squash smear cytology. The diagnosis was made, based on World Health Organisation (WHO) 2007 classification of CNS neoplasm and graded accordingly (2). In all cases, relevant clinical data and radiological findings were obtained.

Cytology results were classified into the following categories (9):

Complete agreement- Cases with same diagnosis and grade on cytology and histopathology.
Partial agreement- Cases with same diagnosis, but the grade was misdiagnosed on cytology.
Disagreement- Cases where there is difference in the cell of origin.

The overall accuracy rate was calculated by including the cases which show complete concordance with final histopathological diagnosis.

Statistical Analysis

The data obtained were analysed using Statistical Package for the Social Sciences (SPSS) and then the parameters were evaluated and expressed in percentage.

Results

A total of 54 squash smears comprising 38 females and 26 males were included in the study. Male to female ratio was 1:1.5 irrespective of age group with female predilection. The age group ranged from 21 years to 80 years. Maximum number of cases was seen between 41-50 years followed by 51-60 years comprising 21 cases and 14 cases respectively (Table/Fig 1).

Meningiomas were encountered in the following sites like parasagittal region, sphenoid wing region, olfactory groove adjacent to cribriform plate, the tentorium, falx cerebri, free surfaces of cerebral convexities of frontal, temporal, parietal region followed by Cerebellopontine (CP) angle/posterior fossa location Convexities of cerebral hemispheres followed by Cerebellopontine angle. Most common site of presentation for meningiomas in the present study was angle/posterior fossa location (Table/Fig 2).

Out of 54 cases, 51 cases showed complete concordance with final histopathological findings and partial concordance was obtained in a case due to underestimation of grading of malignancy in squash cytology. Two cases were found to be discordant with final histopathological diagnosis. The overall diagnostic accuracy of squash cytology in diagnosing meningioma was 94.44% (Table/Fig 3), (Table/Fig 4).

Total of 44 cases of meningothelial and transitional meningioma showed plump to ovoid meningothelial cells arranged in syncytial pattern with characteristic whorled configuration and were unrelated to blood vessels as shown in (Table/Fig 5), (Table/Fig 6). Occasional concentric calcification termed as psammoma bodies which appear as round dark blue formations was noted in few cases as shown in (Table/Fig 7). Histopathological examination revealed lobules of meningothelial cells with indistinct cell borders having syncytial cytoplasm as shown in (Table/Fig 8). Nuclei are pale round to oval with marginated chromatin.

Four cases of psammomatous meningioma showed numerous psammoma bodies occupying more than half of the slide with very few tumour cells as shown in (Table/Fig 9).

Two cases of angiomatoid and a case of metaplastic meningioma were really very difficult to make smear and it showed occasional clusters of meningothelial cells in syncytial pattern, reported as grade I meningioma in smear cytology. Nuclei in maximum cases were round to ovoid with delicate nuclear chromatin and scant cytoplasm. Intranuclear inclusions were noted in few cases in the present study (Table/Fig 10).

Histopathological examination of angiomatoid meningioma revealed numerous small to large vascular spaces lined by flattened endothelial cells with thickened hyalinised vessel walls, and surrounding nests of meningothelial cells having syncytial cytoplasm as shown in (Table/Fig 11). Metaplastic meningioma showed syncytial nests of meningothelial cells admixed with lobules of mature adipocytes with eccentrically placed nuclei as shown in (Table/Fig 12).

A case of schwannoma in posterior fossa location was reported as fibrous meningioma, which lacks characteristic whorls in squash smear cytology (Table/Fig 13). As a result of non representative sampling, a case of anaplastic meningioma downgraded as grade I meningioma, and a case of anaplastic meningioma on squash cytology turned out to be glioblastoma (WHO Grade IV) on HPE.

Discussion

Meningiomas are benign slow growing neoplasm arising from meningothelial cells of arachnoid layer (10). It is the most frequently reported brain tumour accounting for 36% of all brain tumours (10). About 20-25% and 1-6% of meningiomas are WHO grade II and III, respectively (10). High water and fat content and innate fragility of brain tissue may give rise to freezing artifacts on frozen section studies (13). Neurosurgeons often depend upon rapid intraoperative diagnosis for immediate surgical management in Central Nervous System (CNS) lesions (6). Squash smear technique is frequently offered by neurosurgeons for rapid and reliable diagnosis and also helps to plan the extent of surgery intraoperatively and modify the treatment accordingly (6).

The current study was to assess the diagnostic accuracy of intraoperative squash smear cytology of meningiomas and to compare it with the final histopathological diagnosis. The overall diagnostic accuracy in the present study was 94.44%. Following studies have also reported higher degree of accuracy rate in diagnosing meningiomas on squash smear cytology Karanjekar SR and Parate SN, Gopal R and Lalitha, Rao S et al., Dumitrescu G et al., Shukla K et al., Roessler K et al., and Acharya S and Azad S, (11),(12),(13),(14),(15),(16),(17).

Clinically, most of the patients presented with headache, seizures and other pressure symptoms due to compression of underlying brain parenchyma. Radiological finding in most of the cases were, uniformly contrast enhancing circumscribed dural mass with well-defined brain tumour interface (Table/Fig 14). Higher diagnostic accuracy rate in squash smear cytology is achieved by correlating cytological features with clinical and radiological findings (16).

Out of 54 cases, 33 cases were reported as meningothelial meningioma, 11 cases of transitional meningioma, followed by four cases of psammomatous meningioma, two cases of angiomatous meningioma and one case of metaplastic meningioma. The tumours were classified and graded according to the World Health Organisation (WHO) classification of CNS neoplasms 2007. Characteristic type of each meningioma was finally confirmed in histopathological diagnosis mainly for transitional, metaplastic and angiomatous meningioma. Jha B et al., also stated that, it was not possible to provide clear cut differentiation between types of meningioma on cytology as in the present study (3).

Most of the cases of meningothelial and transitional meningioma showed the characteristic whorling pattern of meningothelial cells as stated by Karanjekar SR and Parate SN (11).

Krishna Prasad HV et al., stated that psammomatous meningiomas are invariably occurs in spinal canal, but in the present study most of the cases located in the supratentorial region as extradural space occupying lesion (4). Basically, meningiomas are easy to spread but in psammomatous meningioma and transitional type with high fibrous component were difficult to make a uniform smear (2),(18).

Exact subtyping of angiomatoid and metaplastic meningioma was found to be difficult due to loss of specific features in the tissue submitted for squash preparation (17). Each meningioma shows variable cellularity found to be high in meningothelial and transitional meningioma, low in fibrous meningioma (4). Metaplastic changes include xanthomatous, cartilaginous, osseous, myxoid changes (19),(20). Foci of meningothelial cells give a clue to the diagnosis.

Schwannoma and meningioma, particularly the fibrous type resist smearing (19),(20),(21),(22),(23),(24),(25),(26). Features such as whorling, psammoma bodies and plump to ovoid cells with syncytial cytoplasm are more in favour of meningioma.

Possible reasons for the discordance in a case of anaplastic meningioma diagnosed as glioblastoma were, one of the reasons was the exact tumour’s anatomic relationship with dura and brain was obscured on imaging. Another reason was found to be sampling error as the smear shows only varying amount of oval to spindle shaped cells with necrotic debris in the background. Hence, in a radiologically high grade tumour it is wise to get more representative sample, if needed multiple samples from various sites before coming to a definitive diagnosis. This needs proper communication with the neurosurgeon.

Due to the non representative sampling, a case of atypical meningioma was diagnosed as grade I meningioma in squash smear cytology. This situation signifies the importance of radiological finding and representative sampling in diagnosing CNS tumours using smear cytology (10),(15),(24).

Limitation(s)

Major limitation encountered was non representative sampling, in which necrotic areas misleads the final diagnosis in the present study. This could overcome by representative sampling.

Conclusion

This study shows a higher degree of cytological-histological matching in diagnosing meningiomas. It needs adequate clinical history, neuroimaging details and intraoperative impression of neurosurgeon in aiding the pathologists to improve the diagnostic accuracy. Squash smear cytology is fairly accurate, relatively safe, rapid, and simple tool to diagnose meningioma intraoperatively and helps the neurosurgeon to plan about the extent of surgery.

References

1.
Frosch MP, Anthony DC, De Girolami U. The Central Nervous System. In: Kumar AA, editor. Robbins and Cotran Pathologic Basis of Disease. 9th ed. Philadelphia: Elseiver; 2014. p.1306.
2.
Louis DN, Ohgaki H, Weistler OD, Canvenee WK, editors. WHO Classification of Tumours of the Central Nervous System. 4th ed. Lyon, France: IARC Press; 2007.
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Jha B, Patel V, Patel K, Aggarwal A. Role of squash smear technique in intraoperative diagnosis of CNS tumors. Int J Med Sci Public Health. 2013;2:889-92. [crossref]
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Krishna Prasad HV, Fernandes H, Nayak TM. Role of crush cytology in the intraoperative diagnosis of meningioma. Int J Recent Trends Sci Technol. 2015;14:559-62.
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Pawar N, Deshpande K, Surase S, D’costa G, Balgi S, Goel S. Evaluation of the squash smear technique in the rapid diagnosis of central nervous system tumours: A cytomorphological study. Internet J Pathol. 2009;11. [crossref]
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Deshpande K, Surase S, Shedge R, D’costa G, Bharambe B. Accuracy and diagnostic yield of intraoperative squash smear technique in the rapid diagnosis of CNS lesions. Bombay Hosp J. 2010;52:153-60.
7.
Eisenhardt L, Cushing H. Diagnosis of intracranial tumours by supravital technique. Am J Pathol. 1930;6(5):541-52.
8.
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DOI and Others

10.7860/JCDR/2021/47878.15260

Date of Submission: Nov 24, 2020
Date of Peer Review: Feb 03, 2021
Date of Acceptance: Jun 25, 2021
Date of Publishing: Aug 01, 2021

AUTHOR DECLARATION:
• Financial or Other Competing Interests: None
• Was Ethics Committee Approval obtained for this study? Yes
• Was informed consent obtained from the subjects involved in the study? Yes
• For any images presented appropriate consent has been obtained from the subjects. Yes

PLAGIARISM CHECKING METHODS:
• Plagiarism X-checker: Dec 02, 2020
• Manual Googling: Jun 11, 2021
• iThenticate Software: Jul 23, 2021 (17%)

ETYMOLOGY: Author Origin

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