Histomorphologic spectrum of ovarian cystic lesions at a tertiary care centre
Kanasagara A.1, Sarvaiya A.2,
Sakariya D.3
Dr. Anand Kanasagara, Tutor, Dr. Ankur Sarvaiya, Assistant Professor, GMERS Medical College, Himmat Nagar, Dr. Dhaval Sakariya, Pathologist, GMERS Medical College, Himmat Nagar, Surat, Gujrat, Indi
Corresponding Author: Dr.
Ankur Sarvaiya, Assistant Professor,
GMERS Medical College, Himmat Nagar. E-mail: ankur.sarvaiya@gmail.com
Abstract
Introduction:
An ovarian cyst is a liquid or semi-liquid material filled sac in an ovary. Proper management depends
on the histomorphological division of nonneoplastic & benign and malignant neoplastic
lesions. So this study was done to differentiate the lesion
histomorphologically and to know the commonest lesion in each age group. Objectives:
To study age wise incidence, nonneoplastic, benign and malignant spectrum of
ovarian cystic lesions. Methods: A
retrospective histo-pathological study of 100 cases of nonneoplastic and
neoplastic cystic lesions of ovary was conducted. Result: We found that out of 100 cases, 58% were non neoplastic and
42% were neoplastic. Benign cystic teratoma was the most common neoplastic
condition. Follicular cyst was the commonest nonneoplastic condition. Conclusion: Histomorphological
parameters along with advanced newer diagnostic modalities like immunohistochemistry
can help to do early diagnosis and plan the line of treatment & they have
effect on prognostic significance.
Key words: Ovarian cyst, Non neoplastic, Neoplastic, cystic
lesion of ovary, Follicular cyst
Author Corrected: 20th July 2018 Accepted for Publication: 26th July 2018
Introduction
The
ovaries are paired pelvic organs located on the sides of the uterus close to
the lateral pelvic wall, behind the broad ligament and anterior to the rectum [1].
An ovarian cyst is a liquid or semi-liquid material filled sac in an ovary. Ovarian
cyst is a finding of considerable anxiety to women because of the fear of
malignancy, but the vast majority are benign. These cysts can develop in
females at any stage of life, from the neonatal period to post menopause. Generally
speaking, these tumors are rarer in childhood and adolescent age groups as
studies have confirmed that only about 2% of ovarian tumors are seen in children
[2,3]. Most benign lesions of the ovary occur in childbearing age group and are
often cystic, while malignant tumors are more common in the elderly women [4]. Globally,
ovarian malignancy constitutes about 23% of all gynecological tumors and 6th
most common female cancer with the highest fatality rate [5,6,7]. In developing
countries including India, there are low epidemiological statistics of ovarian
cancers because most cases are underreported, in spite of the fact that it
constitutes one of the most common gynecological problems locally and globally.
Ovarian neoplasms are usually detected at a late stage and are large in size,
because of their presentation with mild symptoms [8]. Proper management depends
on the histomorphological division of nonneoplastic, benign and malignant lesion.
So this study was done to differentiate the lesion histomorphologically and to
know the commonest lesion in each age group and compare our study to other
researches worldwide.
Aims & Objectives
1. To obtain age wise
incidence of ovarian cystic lesions.
2. To get incidence
ratio of non neoplastic versus neoplastic ovarian cystic lesions.
3. To get incidence
ratio of benign versus malignant ovarian cystic lesions.
4. To study the
morphological aspects of ovarian cystic lesions.
Materials and Methods
Place of Study: Department of Pathology,
N.H.L.
Municipal Medical College, Vadilal Sarabhai
General Hospital, Ahmedabad.
Type
of Study: A retrospective histo-pathological study of 100
cases of nonneoplastic and neoplastic
cystic lesions of ovary from December 2013 - October 2015.
Sampling methods & sample collection:
Ovarian specimen was obtained from hysterectomy specimen with unilateral or
bilateral adnexa & oophorectomy and/or cystectomy specimens received in the
department. Tissues were fixed and preserved in formalin, then passed through
ascending grades of alcohol and xylene and finally embedded in melted paraffin
wax. Then blocks were prepared, single block was made for each section, thin
sections of 4 to 5 microns thickness were cut, slides were prepared and stained
by hematoxylin & eosin.
Inclusion Criteria:
Only the ovarian specimens having cyst were included in this study.
Exclusion criteria:
Ovarian lesions without cyst were excluded from the study.
Statistical Methods: The
non-neoplastic and neoplastic cystic lesions from representative sections were
studied and classified according to Modified World Health Organisation (WHO) classification
2003 and staging was done according to International Federation of Gynaecology
and Obstetrics (FIGO) staging.
Results and Observation
In
a retrospective study of ovarian cystic lesions, we found that out of 100 cases
,58% were non neoplastic and 42% were neoplastic.
Among
the neoplastic ovarian lesions (42 cases), 36 (86%) cases were benign, 4 (9.5
%) cases were borderline and 2 (4.5 %) were malignant. Out of 36 benign ovarian
neoplasms, most common histology was benign cystic teratoma followed by mucinous
cystadenoma and serous cystadenoma. Total 4 tumours were showing borderline histology,
among them 2 were papillary serous, 1 was mucinous and 1 was clear cell
carcinoma. We found 2 cases showing malignant histology, both of which were
adult granulosa cell tumour type.
Most
of the benign neoplastic tumour were observed in the age group of 20-40yr,
while most of the malignant tumours cases were common in elderly (>40 years)
age group.
Among
the non-neoplastic lesions (58 cases), we found follicular cysts (27 cases),
corpus luteal cysts (26 cases) and endometriotic cysts (5 cases).
There
were total 14 cases in 21-30 years, 17 cases in 31-40yrs, 23 cases in >40
years and 4 cases in <20 years of age group among all cystic non-neoplastic
lesions (58 cases). So, cystic non neoplastic lesions occur commonly between
20-40 years of age.
Table-1: Age wise Incidence
of ovarian cystic lesions
Age (in years) |
Non-neoplastic |
Neoplastic |
Total No. of cases |
0-10 |
2 |
1 |
3 |
11-20 |
2 |
2 |
4 |
21-30 |
14 |
14 |
28 |
31-40 |
17 |
14 |
31 |
41-50 |
21 |
5 |
26 |
51-60 |
2 |
6 |
8 |
61-70 |
0 |
0 |
0 |
71-80 |
0 |
0 |
0 |
Total |
58 |
42 |
100 |
Table-2:
Age wise distribution of neoplastic cystic lesions
Neoplastic Lesions |
|||
Age |
Benign |
Borderline |
Malignant |
0-10 |
1 |
0 |
0 |
11-20 |
2 |
0 |
0 |
21-30 |
14 |
0 |
0 |
31-40 |
12 |
2 |
0 |
41-50 |
4 |
0 |
1 |
51-60 |
3 |
2 |
1 |
>60 Yrs |
0 |
0 |
0 |
Total |
36 |
4 |
2 |
Table-3:
Histopathological diagnosis of ovarian cystic lesions
Lesions |
No. of cases |
Follicular Cyst |
27 |
Corpus Luteal Cyst |
26 |
Endometriotic Cyst |
5 |
Dermoid Cyst |
14 |
Serous Cystadenoma |
10 |
Mucinous Cystadenoma |
12 |
Borderline Tumour |
4 |
Malignant Tumour |
2 |
Total |
100 |
Figure-1: Serous Cystadenoma (Gross)
Figure-2:
Mucinous Cystadenoma- Cyst lined by tall, non-cilliated
columnar cells with basally located nuclei and abundant mucin. (10x, 40x, H & E stain)
Figure-3: Dermoid Cyst [skin adnexa and adipose
tissue(above) glial component(below)] (10 & 40x, H & E stain)
Figure-4: Papillary serous borderline tumour (Gross )
Figure-5: Clear Cell Carcinoma (Tubulo-cystic and papillary
pattern) (10x, H & E stain)
Figure-6: Granulosa Cell Tumour (Neoplastic cells arranged in sheets with prominent
nuclear grooving imparting coffee bean appearance) (40x, H & E stain)
Discussion
Ovarian
cancer is second leading cause of mortality amongst all the cancers of female
genital tracts. Due to similar clinical presentation, it is difficult to
diagnose non-neoplastic and neoplastic cystic lesions of ovary although it is labelled
as cystic lesion on ultrasonography and hence removed prophylactically in
routine oophorectomies and hysterectomies [9].
Ovarian
neoplastic cystic lesions may occur at any age, including infancy and
childhood. Incidence rate however increase with age, with the greatest number
of new cases being diagnosed between 4th and 5th decade.
The
non-neoplastic cystic lesions like follicular and corpus luteum cysts are
commonly encountered conditions. Zaman et al. had studied 498 cases in one
year. The authors encountered 68.87% non-neoplastic lesions and 31.12% neoplastic
lesions [10]. In our study 58% lesions were non-neoplastic and 42% were
neoplastic. Out of all the non-neoplastic cystic lesions 46.55% were
follicular, 44.82% were corpus luteal and 8.63% were endometriotic cysts. Maliheh
et al. found serous cystadenoma (38%) followed by mature cystic teratoma (30%)
& mucinous cystadenoma (22%) [11]. We have 39% mature cystic teratoma, 28% serous
cystadenoma and 33% mucinous cystadenoma in our study. Most common benign tumor
in the studies done by Mondal et al, Iqbal et al. & Yasmin et al. were
serous cystadenoma ( 29.9%, 38.5% and
24% respectively ) followed by mature cystic teratoma ( 15.9%, 30.8% and 18%
respectively ) [12,13,14].
In
present study, 42 neoplastic cystic lesions were diagnosed. Most common were
benign followed by, borderline and malignant. Based on histomorphological
features, incidence of surface epithelial cystic tumours were commonest 26(61.9%)
followed by germ cell tumours 14(33.3 %) & sex cord tumours (4.8%). None of
the neoplastic lesion was metastatic in our study. In Gupta et al. study surface
epithelial tumours were the commonest (48.8%) followed by germ cell tumours
(23.9%), sex cord stromal tumors (8.3%) and metastatic tumours (2.0%)[15]. Gurung et al. had
follicular cyst as 4th commonly encountered lesion as compared to
mature cystic teratoma and endometriotic cyst. Maharjan and Zaman et al. found
corpus luteal cyst as commonest in their study, however the study done by Pudasaini
et al. was comparable to other studies as they had serous cystadenoma commonest
followed by mature cystic teratoma and hemorrhagic corpus luteal cyst [16,17,18].
Laterality
of ovarian neoplastic lesions in various studies in comparison with present
study is illustrated in Table 4. Our study revealed that 94 out of 100 ovarian
specimens were unilateral (94%) and only (6%) were bilateral. Our findings are
in concordance with other studies [19,20,21,22].
Table-4: Laterality of ovarian
neoplastic lesions in various studies in comparison with present study
Authors |
Laterality |
|
Unilateral |
Bilateral |
|
Prabhakar et al |
90.9% |
9.1% |
Misra et al |
95.5% |
4.5% |
Couto F. et al |
91.2% |
8.8% |
Kar et al. |
73.13% |
26.87% |
Present Study |
94% |
6% |
The percentage distribution of patients in various age groups
in comparison with other studies is illustrated in Table 5. The majority of our
patients were in the age group 20-39 years (54% of patients) while those in the
age group 40-59 years were the second largest group of patients (40% of
patients). This is in concordance with the studies of Ramachandran et al (20-39
years -53.0%; 40-59 years -30% of patients) and Pilli et al (20-39 years
-58.0%; 40-59 years-30% of patients) [23,24].
Table-5: Percentage distribution of
cases in various age groups in comparison with present study
Authors |
Age group in years |
|||
0-19 |
20-39 |
40-59 |
≥ 60 |
|
Ramchandran et al |
7.9% |
53% |
30% |
9.1% |
Pilli et al |
7% |
58% |
30% |
5% |
Kar et al |
7.4% |
41.7% |
46.2% |
4.4% |
Present Study |
4% |
54% |
40% |
2% |
Ovarian
cancers are known as “silent killers” as most of the primary ovarian tumours remain
asymptomatic until the advanced stage. However, histomorphological study of
tumour is still a gold standard method today to diagnose and classify them into
neoplastic and non-neoplastic cystic lesions. These observations and results
may provide valuable base line information regarding frequency and pattern of
non neoplastic and neoplastic ovarian cystic lesions in urban settings like our
Vadilal Sarabhai General Hospital, Ahmedabad, India.
Conclusion
All
these histomorphological parameters along with advanced newer diagnostic
modalities like immunohistochemistry can help early diagnosis, plan the line of
treatment and have effect on prognostic significance.
Because
of the geographic location, poverty and illiteracy, patients seek medical
advice late in rural health facility. So, along with proper histomorphological
study, awareness among public and doctors, education of people, passive
surveillance, and community screening facility will also be helpful in early
detection of the ovarian cystic lesions and tumours. This study shows the commonest
benign and nonneoplasic cystic lesions of ovary. This study also shows wide
histomorphologic spectrum of ovarian cystic lesions. This distinction is very
much important clinically to further plan the management accordingly.
What
this study adds to existing knowledge?
Our
distribution of histomorphologic spectrum of ovarian cystic lesions is similar
to most of the other studies worldwide as stated in discussion. However we had
only few cases of malignant lesions as compared to others. Genetic profiling
and Immunohistochemistry in prospective study may provide more details and
elaborate the facts.
Contribution
by authors
Study
Conception and Design: Dr. Anand & Dr. Dhaval, Acquisition
of Data: Dr. Anand & Dr. Dhaval, Analysis and Interpretation of Data:
Dr. Ankur, Dr. Anand & Dr. Dhaval, Drafting of Manuscript: Dr.
Ankur, Dr. Anand, Critical Revision: Dr. Ankur, Dr. Anand
References
1. Rosai J, Rosai and Ackerman's
Surgical Pathology, Rosai, 10thed,
Edinburg:Mosby Elsevier; 2011:1553-1554.
2. Warner BW, Kuhn JC, Bar LL. Conservative management
of large ovarian cysts in children: The value of serial pelvic ultrasonography. Surgery
1992;112:749-55.
3.
Choudry A , Bangash N, Malik A, Choudry H. Adolescent ovarian tumors: a
clinicopathlogical review of 15 cases. J Ayub Med Coll Abbottabad. 2008
Oct-Dec;20(4):18-21.[pubmed]
4.
Pudasaini S , Lakhey M, Hirachand S, et al. A study of ovarian
cyst in a tertiary hospital of Kathmandu valley. Nepal Med Coll J. 2011
Mar;13(1):39-41.[pubmed]
5. Tortolero L, Mitchell FM, Rhodes HE. Epidemiology
and screening of ovarian cancer. Obstet Gyanecol Clin North Am. 1994;21:63-75.[pubmed]
6. Merino MJ , Jaffe G. Age contrast in ovarian pathology. Cancer. 1993 Jan 15;71(2 Suppl):537-44.[pubmed]
7.
Malik IA . A prospective study of clinico-pathological features of
epithelial ovarian cancer in Pakistan. J Pak Med Assoc. 2002
Apr;52(4):155-8.[pubmed]
8.
Bhattacharya M, Shinde SD, Purandare VN A clinicopathological analysis
of 270 ovarian tumours. J Postgrad Med. 1980 Apr;26(2):103-7.[pubmed]
9. Rosai J, Rosai and Ackerman's
Surgical Pathology, Rosai, 10thed, Edinburg: Mosby Elsevier;
2011:1557.
10.
Zaman S , Majid S, Hussain M, et al. A retrospective study of
ovarian tumours and tumour-like lesions. J Ayub Med Coll Abbottabad.
2010 Jan-Mar;22(1):104-8.[pubmed]
11. Maliheh A, et al. Surgical
Histopathology of Benign Ovarian cysts, a multicentre study, Iranian journal of
Pathology 2010; 5(3): 132-6.
12. Mondal SK, Et al. Histologic
pattern, bilaterality and clinical evaluation of 957 ovarian neoplasms:
A10-year study in a tertiary hospital of eastern India. J Can Ras Ther2011 ;
7:433-7 ( serial online ) 2011 ( cited 2014 Jan 3 ) ; 7:433-7.
13. Iqbal J. Et al, Pattern of ovarian
Pathologies. Journal of Rawalpindi Medical College (JRMC) 2013; 17(1):113-5.
14.
Yasmin S, Yasmin A, Asif M. Clinicohistological pattern of ovarian
tumours in Peshawar region. J Ayub Med Coll Abbottabad. 2008
Oct-Dec;20(4):11-3.[pubmed]
15.
Gupta N, Bisht D, Agarwal AK, Sharma VK. Retrospective and prospective
study of ovarian tumours and tumour-like lesions. Indian J Pathol
Microbiol. 2007 Jul;50(3):525-7.[pubmed]
16. Gurung P, Hirachand S, Pradhanang S. Histopathological study
of ovarian cystic lesions in tertiary care hospital of Kathmandu, Nepal.
Journal of Institute of Medicine. 2013; 35(3):44-7.
17. Maharjan S. Clinicomorphological study of ovarian lesions.
Journal of Chitwan Medical College. 2013; 3(6):17-24.
18.
Pudasaini S, Lakhey M, Hirachand S, et al. A study of ovarian cyst in a
tertiary hospital of Kathmandu valley. Nepal Med Coll J. 2011
Mar;13(1):39-41.[pubmed]
19. Prabhakar BR, Maingi K. Ovarian tumours--prevalence in Punjab. Indian J Pathol Microbiol. 1989 Oct;32(4):276-81.[pubmed]
20. Couto F, Nadkarni NS, Rebello MJ. Ovarian tumors in
Goa. A clinicopathological study. J Obstet Gynecol of India. 1993;43(3):408-12.
21. Misra RK, Sharma SP, Gupta U, Gaur R, Misra SD.
Pattern of ovarian neoplasms in eastern UP. J Obstet Gynecol. 1990;41(2):242-6
22. Kar T, Kar A, Mohapatra PC. Intra-operative cytology
of ovarian tumors. J Obstet Gynecol India. 2005;55(4):345-9.
23. Ramachandran
G, Harilal KR, Chinnamma K, Thangavelu H. Ovarian neoplasms -A study of 903
cases. J Obstet Gynecol India. 1972;22:309 -15.
24. Pilli GS , Suneeta KP, Dhaded AV, Yenni VV. Ovarian tumours: a study of 282 cases. J Indian Med Assoc. 2002 Jul;100(7):420, 423-4, 447.[pubmed]
How to cite this article?
Kanasagara A, Sarvaiya A, Sakariya D. Histomorphologic spectrum of ovarian cystic lesions at a tertiary care centre.
Trop J Path Micro 2018;4(3):270-275.doi:10. 17511/jopm.2018.i3.06