WHO [2007] GRADING OF MENINGIOMA

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SAS Journal of Surgery ISSN 2454-5104 SAS J. Surg., Volume-3; Issue-1 (Jan, 2017); p-25-29 Available online at http://sassociety.com/sasjs/ Original Research Article Histopathological analysis of meningiomas- A retrospective study Dr. Vijaya Gattu 1, Dr. Suhela Rachakonda 2 1,2 Consultant Pathologist, Yashoda Hospital, Malakpet, Hyderabad, India *Corresponding author Dr. Vijaya Gattu Email: vijjupatho@gmail.com Abstract: Meningioma, so named by Harvey Cushing in 1922, is a group of heterogeneous tumors that arise from meningothelial cells. Meningiomas are predominantly benign tumors usually attached to the duramater that arise from the meningothelial cells of the arachnoids. Meningioma may be found along any of the external surface of the brain as well as within the ventricular system, where they arise from the stromal arachnoid cells of the choroid plexus. The objective is to evaluate the incidence of various histopathological variants of meningioma its, frequency in various parts of the brain, and its age and sex distribution. This is a retrospective study of 38 cases conducted in Yashoda Hospital, Malakpet for the period of 2 years from August 2013 to July 2015. A total of 38 cases of meningioma were studied. Most common variant is meningothelial meningioma, 16 cases (42%), grade I consisting of 36 (94.7%) cases and the most common site is intracranial. Female predominance is seen in meningioma. Keywords: Brain Tumors, Diagnosis, Grading, Classification. INTRODUCTION Meningiomas account for approximately 13 19% of all primary intracranial tumors and their prognosis is generally favorable. The incidence increases with increasing age, peak during 6 th and 7 th decades of life; these tumors are very rare in children. The incidence in women is approximately twice that in men. The vast majority of meningiomas are considered histologically benign (90%). Meningiomas may produce seizures, headache, confusion drowsiness, vomiting due to their effects on underlying cerebral cortex. However, meningiomas may also remain asymptomatic and be identified as an incidental finding on imaging.1 Grade II: Defined by one or more of the following 4 criteria. Chordoid or clear cell histologic sub type 4 to 19 mitoses/10hpfs Brain infiltration Three or more of the following five histologic features Small cell change Increased cellularity Prominent nucleoli Sheet like growth Necrosis WHO [2007] GRADING OF MENINGIOMA Grade I: Based on histologic sub type and lack of anaplastic features. Grade III: 20 or more mitosis/10hpfs Table-1: WHO Grades and Histomorphological Variants Benign (Grade I) -90% Meningothelial, Fibrous, Transitional, Psammomatous, Angioblastic Atypical (Grade II)- 7% includes brain invasion. Chordoid, clear cell, atypical Anaplastic / Malignant (Grade III)-2% Papillary, Rhabdoid, anaplastic GRADE RECURRENCE GRADE I 7-25% GRADE II 29-52% GRADE III 50-94% WHO GRADES AND HISTOMORPHOLOGICAL VARIANTS Meningotheliomatous Meningioma: Most common variant of meningioma. Syncytial and epithelial cells, indistinct cell borders and classic whorls, May have sparse Psammoma bodies Transitional meningioma: Coexistence of 25

meningothelial and fibrous psammoma bodies. pattern, associated with To study various Histomorphological variants in meningiomas. Psammomatous meningioma: Found in spinal region. Numerous psammoma bodies (more than 50%) Fibroblastic meningioma: Shows proliferation of spindled meningothelial cells arranged in interlacing bundles, nuclear features are characterstic, Psammoma bodies infrequent. Angiomatous Meningioma: Accounts for 2% of all meningiomas. Vascular component should exceed 50% of total tumor area. meningothelial cells are wrapped around small blood vessels also has large vessels. Do not recur if entirely resected. Atypical Meningioma: Increased cellularity, mitotic activity, high N:C ratio, prominent nucleoli. Papillary Meningiomas: Are rare meningeal tumors Presence of perivascular psuedopapillary pattern, associated with aggressive clinical behavior. The number of grade II meningiomas increased when using the WHO 2007 classification (30%) compared with previous editions, mainly due to the definition of brain infiltrating meningiomas as atypical (grade II). 1 AIMS & OBJECTIVES To study the incidence of Menigiomas. MATERIALS & METHODS This is a retospective study of 38 cases of meningioma, conducted in department of pathology, Yashoda Hospital, malakpet, for the period of 2 years from August 2013 to July 2015. Specimens received in department of Pathology, Yashoda Hospital, Malakpet are immediately fixed in 10%buffered formalin. Specimens less than 2 cm are all embedded. All the specimens are subjected to routine processing. RESULTS The most common affected age group was 41-50 years -12 cases (31.6%) (Table 1). Females 30cases (79%) were most commonly affected compared to males (Table 2). The most common location was intracranial 32 cases (84%) with para sagittal being commonly involved in 12 cases (31.6%) (Table 3). The most common histological type was meningothelial 16 cases (42%) (Table 4). Among the benign meningiomas relatively very rare variant is angiomatous 2 cases (5.3%) grade I meningiomas were 36 cases ( 94.7%). Grade II Meningiomas Were 2 Cases (5.3%). Table-2: Age Distribution Age group (years) No. Of Cases % 1-10 years - - 11-20 years - - 21-30 years 2 5.3 31-40years 6 15.8 41-50years 12 31.6 51-60years 10 26.4 61-70years 4 10.5 71-80years 4 10.5 Total 38 100 Table-2: Gender distribution Gender No.of cases % Females 30 79 Males 8 21 Table-3: Location of meningioma No. Of. Cases Location % 12 Para sagital 31.6 8 Sphenoid 21 6 Spinal 15.8 4 Frontal 10.5 4 Supra sellar 10.5 2 CP Angle 5.3 2 Parietal 5.3 Total = 38 100 26

Table-4: Histomorphological Patterns of Meningioma S. No Variants No. Of Cases Percentage 1 Meningothelial 16 42 2 Psammomatous 10 26.4 3 Transitional 4 10.5 4 Angioblastic 2 5.3 5 Fibroblastic 4 10.5 6 Atypical (Grade II) 2 5.3 7 Papillary( Grade III) - - Total 38 100 Fig-1: Histomorphological Patterns of Meningioma DISCUSSION Meningiomas account for 25-30% of all CNS tumours and are the most common tumours arising from the meninges [1-3]. Most benign meningiomas occur in adult women, but atypical and anaplastic forms seem to be more common in men and the younger age group. Childhood meningiomas are less common [4, 5]. Most meningiomas are intracranial.190% is supratentorial; the anterior cranial fossa is involved far more frequently than the posterior. Most of the intracranial tumors occur in the convexities. Intraspinal Meningiomas constitute 25-46% of all tumors occurring in the spinal cord and are more common in the thoracic region [6, 7]. Extracranial location is rare. Histologically meningiomas are of three grades. Grade I meningiomas comprise 90%, Grade II Atypical meningiomas comprise between 4.7% to 7.2% of meningiomas, whereas Grade III malignant meningiomas comprise between 1.0% to 2.8% [1-3]. Majority are positive for EMA and 100% for Vimentin. High grade types may be negative or weakly reactive for both [1]. Irrespective of the sex of the patient progesterone receptors are expressed by many and lack of its expression is associated with poor outcome [1-3]. Recurrence is not limited to meningiomas with malignant histological features. Benign meningiomas can also recur following incomplete resection, if large and associated with monosomy14 and del (1p36)[8]. The extent of surgical resection depends on the site, size of the tumor and its relation to vital structures. Higher rates of recurrence are seen in younger age, male sex, parasagittal location and an aggressive histologic type. Reported recurrence rates of grade I, II, and III meningiomas are 7-25%, 29-52%, 50-94%, respectively [9, 10]. The treatment in grade I tumors is total resection [3, 9]. Surgery and adjuvant radiotherapy are the treatment of choice in grade II and grade III meningiomas [9-10]. 27

Extent of surgical resection is one of the most important factors in predicting recurrence along with histological grading. Subtotal resections were associated with more recurrence or re growth. The most common age group involved was the 41-50year was similar to studies done by A B Shah et al. [11], Ruberti et al. [12], Intisar SH Patty et al. [13], and J amjoom et al. [14]. The most common location was parasagittal area similar to the various studies. The classical type is the Meningothelial variant cases were 16 (42%) in the present study being the most common histological type seen in all the studies by Sangamithra et al. [15], Nasrin Samadi et al. [16], S Babu et al. [17] and Thomas Backer et al. [10]. The rare variant angiomatous type 2 cases (5.3%) and Angiomatous meningiomas are rare and comprise 2.1% of all the types of meningioma. Meningiomas are graded into Grade I and Grade II with incidence in a ratio of 94.70%:5.3% in this study similar to a studies done by Nasrin Samadi et al. [16] (86.1%: 8%: 5.9%) and Konstantinos Violaris et al. [8] (89.82%:5.82%:4.36%). Grade I meningiomas are benign and rarely recur. Grade II and Grade III meningiomas tend to recur more frequently. In all the reference studies Grade I tumors were more Common. Higher incidence of Grade II tumors was noted in the studies done by S Babu et al. [17], (26%) and Thomas Backer et al. [9] (30.1%). Grade III tumors were less common in all the studies and in our study cases with brain invasion were not reported. Whereas Thomas Backer et al. [9] reported 30% of the meningiomas as atypical, due to the inclusion of 9 cases with brain invasion and with otherwise benign histology. Table-5: Comparative Evaluation of Gradei Histological Variants of the Present Study with Other Study Authors Total cases Meningothelial Transitional Fibroblastic Psammomatous Age of presentation FF Cruz 41 19 3 8 0 40-60 years Sanch et al. [18] Our study 38 16 4 2 10 40-60 years Variants of meningioma Thomas Baker et al. [9] Our study Meningothelial 17.00% 42.00% Transitional 40.00% 10.50% Psammomatous 0.50% 26.40% Fibroblastic 7.00% 10.50% Angiomatous 1.50% 5.30% Total 196 38 Variants Thomas Baker et al. [9] Our study Benign (Grade I) 135 (69.9%) 36 (94.7) Atypical (Grade II) 59 (30%) 2 (5.3) Anaplastic (GradeIII) 2 (1%) 0 Total number of cases 196 38 CONCLUSION In this study the prevalence of tumor location, histologic subtypes and grades as well as age and sex distribution were similar to other studies. From our study, we can conclude that most common histopathological variants of meningioma are meningothelial meningioma followed by psammomatous meningioma, and least common is angiomatous meningioma. Most common WHO grade is grade 1. Benign meningiomas are most common meningioma. Intracranial location is the most common location for meningioma. Most common age group for presentation is 41 50 years. REFERENCES 1. Perry A, Louis DN, Scheithauer BW, Budka H, Von Deimling A. Meningiomas. WHO classification of tumours of the central nervous system. 2007; 4:164-72. 2. Commins DL, Atkinson RD, Burnett ME. Review of meningioma histopathology. 3. Lee JH, editor. Meningiomas: diagnosis, treatment, and outcome. Springer Science & Business Media; 2008 Dec 11. 4. Germano IM, Edwards MS, Davis RL, Schiffer D. Intracranial meningiomas of the first two decades of life. Journal of neurosurgery. 1994 Mar; 80(3):447-53. 5. Mehta N, Bhagwati S, Parulekar G. Meningiomas in children: a study of 18 cases. Journal of pediatric neurosciences. 2009 Jul 1;4(2):61. 6. Yoon SH, Chung CK, Jahng TA. Surgical outcome of spinal canal meningiomas. Journal of Korean Neurosurgical Society. 2007 Oct 1; 42(4):300-4. 7. Gottfried ON, Gluf W, Quinones-Hinojosa A, Kan P, Schmidt MH. Spinal meningiomas: surgical 28

management and outcome. Neurosurgical focus. 2003 Jun; 14(6):1-7. 8. Violaris K, Katsarides V, Sakellariou P. The recurrence rate in meningiomas: analysis of tumor location, histological grading, and extent of resection. Open Journal of Modern Neurosurgery. 2011 Dec 31; 2(01):6. 9. Backer-Grondahl T, Moen BH, Torp SH. The histopathological spectrum of human meningiomas. Int J Clin Exp Pathol. 2012 Jan 1; 5(3):231-42. 10. Soheithuer BW, Perry A, Stafford SL, Lohse CM, Wollan PC. " Malignancy" In Meningiomas: A Clinicopathologic Study Of 116 Patients With Grading Implications. Journal of Neuropathology & Experimental Neurology. 1999 May 1; 58(5):524. 11. Shah AB, Muzumdar GA, Chitale AR. Meningiomas: report of a hospital-based registry. Indian journal of pathology & microbiology. 2005 Oct;48(4):468-71. 12. Ruberti RF. The surgery of Meningiomas: A review of 215 cases. Afr J Neurol Sci. 1995; 14:1. 13. Patty IS. Central Nervous System Tumours- AClinicopathological study. J Dohuk Univ. 2008; 11(1):173-80. 14. Ur-Rahrnan N, Sharneena AR. Intracranial Meningiomas: Analysis Of 53 Consecutive Cases With Special Reference To Their Operability And Surgical Outcome. Annals of Saudi Medicine. 1990; 10(1). 15. Mukherjee S, Ghosh SN, Chatterjee U, Chatterjee S. Detection of progesterone receptor and the correlation with Ki-67 labeling index in meningiomas. Neurology India. 2011 Nov 1; 59(6):817. 16. Samadi N, Ahmadi SA. Meningioma: A clinicopathological evaluation. The Malaysian journal of medical sciences: MJMS. 2007 Jan; 14(1):46. 17. Babu S, Uppin SG, Uppin MS, Panigrahi MK, Saradhi V, Bhattacharjee S, Sahu BP, Purohit AK, Challa S. Meningiomas: correlation of Ki67 with histological grade. Neurology India. 2011 Mar 1; 59(2):204. 18. Miquel R, Rossi ML, Figols J, Palacin A, Cardesa A, Cruz-Sánchez FF. Clinico-pathological correlations in meningiomas, a DNA and immunohistochemical study. Histology and histopathology. 1993. 29