Histopathological
analysis of testicular lesions- a three year experience in a tertiary care
center, Telangana
Tekumalla A.1, Ragi S.2,
Thota R.3
1Dr. Aruna Tekumalla, Associate Professor,
Department of Pathology, CAIMS, Karimnagar, 2Dr. Sreedhar Ragi,
Associate Professor, Department of Pharmacology, KIMS, Narketpally, 3Dr.
Ravinder Thota, Professor, Department of Pathology, CAIMS, Karimnagar,
Telangana, India.
Correspondence Address: Dr. Sreedhar Ragi, Associate Professor,
Department of Pharmacology, KIMS, Narketpally, Telangana, India. E-mail: drsreedharkrnr@gmail.com
Abstract
Introduction: Testicular lesions can be of varied
etiologies including non-neoplastic and neoplastic lesions. Non-neoplastic
lesionsare most common compared to neoplastic lesions. Inflammatory lesions,
torsion, atrophy and cryptorchidism are major non-neoplastic conditions. Germ
cell neoplasms, among which seminoma is the most common malignancy. Though
rare, incidence of these neoplasms is on rise for the past 1 or 2 decades in
western countries. Aim and Objectives:
Thisstudy is undertaken to analyse all the testicular lesions reported in
CAIMS, Karimnagar, which is atertiary care center in Telangana and to see the
incidence of testicular neoplasms in this region. Materials and Methods: This is a retrospective study of 3 year
period from July 2015 to June 2018. Total of 80 cases have been studied and
analyzed descriptively. Results: Out
of 80 cases 65 were non-neoplastic and 15 were neoplastic lesions. Non specific
Epididymoorchitis is the most common non-neoplastic lesion followed by
testicular atrophy with maturation arrest. Seminoma is the most common
malignant tumor followed by seminomatous mixed germ cell tumor. Conclusion: Our study is mostly
comparable with the other studies.
Key words: Testicular lesions, Spectrum,
Non-neoplastic and Neoplastic.
Author Corrected: 28th April 2019 Accepted for Publication: 1th May 2019
Introduction
Normal adult testis
is a paired organ that lies within the scrotum suspended by spermatic cord [1].
Testis is affected by variousnon-neoplastic and neoplastic diseases at various
stages of life. Cryptorchidism, otherwise known as undescended testes is one of
the congenital malformations seen approximately in 1% of one year old boys [2].
Other
non-neoplastic lesions include inflammatory lesions like acute and chronic
Epididymoorchitis, vascular lesions like torsion of testis, atrophy with
maturation arrest of spermatogenesis. Neoplastic lesions of testis are rare
tumors accounting for approximately 1% of all male cancers [3]. They present in
a younger age group between 15-35 years and it shows inverse relationship to
the age of occurrence [4-7].
There is a great
geographical variation in the incidence of testicular cancers [5]. Incidence of
testicular cancers is rising in western countries for the past 50 years [5, 8].
Clinically patients
present with scrotal swelling with or without pain, fever and empty scrotum.
Testicular cancers usually present with painless unilateral scrotal swelling.
Despite the all the modalities of diagnosis histopathology plays an important
role in accurate diagnosis and help in accurate treatment of the patient. Hence
this is an attempt to analyse all the orchidectomy specimens encountered in
CAIMS, Karimnagar and to categorize intonon-neoplastic and neoplastic lesions
of testis Surgical removal of testes also known an orchidectomy. Indications for orchidectomy include
non-neoplastic and neoplastic conditions of testis. Also bilateral orchidectomy
is done to know any spread of malignancy from adjacent organs like from
prostate or penis. Cryptorchidism is one of the major risk factors for
development of testicular cancer.
Aims
& Objectives
1. To analyse all orchidectomy specimens and
categories into non-neoplastic and neoplastic lesions.
2. To see the spectrum of all testicular
lesions.
3. To see the age wise distribution of lesions
and laterality of the testis affected.
4. To see the relative incidence of various
testicular neoplasms.
5. To compare with other studies.
Materials
&Method
Place & Type of
Study: It is a
retrospective study carried out in Department of Pathology- Chalmeda Anand Rao
Institute of Medical Science, Karimnagar, Telangana from July 2015 to June
2018.
Sampling Method: Clinical data was taken from the requisition
forms and the specimens were fixed in 10% buffered formalin.
Sample Collection: Gross examination of the specimens was
carried out, appropriate tissue bits were taken and processed by automated
tissue processor. After paraffin embedding tissue blocks were prepared and were
cut into 3-4micron thin sections by rotary microtome. These tissue sections
were submitted for routine H&E staining.
Inclusion criteria: All orchidectomy specimens received at
histopathology department, CAIMS, Karimnagar were included in the study.
Exclusion criteria: Small testicular biopsies which were sent for
infertility evaluation were excluded from the study.
Statistical Method: Data were collected from requisition forms
and specimens, entered and prepared master chart for further statistical
analysis, data is shown by using proportions in various tables and analysis was
done using Microsoft Excel 2010 and SPSS V.25
Ethical Consideration & Permission: The necessary approval to conduct this study
was obtained from the Institutional Ethics Committee (IEC) of the college
before starting the study. In the present study scoring system or any surgical
procedure were not used.
Results
All orchidectomy
specimens were analyzedand categorized into non-neoplastic and neoplastic
lesions. Age wise distribution of all cases were studied. Various
non-neoplastic lesions and neoplastic lesions observed in this region was
noted. Total of 80 cases studied over a period of 3 yrs. Out of 80 cases 65
were non-neoplastic and 15cases were neoplastic accounting for 81.25%
&18.75% respectively. Acute and chronic non-specific Epididy moorchitisis
the most common non-neoplasticlesion together 25 cases accounting for 38.5%
followed by testicular atrophy with maturation arrest of spermatogenesis, 15
cases accounting for 23.08%. Testicular Torsion with hemorrhagic infarction
constituted 12.3% with 8 cases. Next followed by cryptorchidism only 3cases
accounting for 4.6%. Another major category included are cases with normal
study. Total 14 cases with 21.5% (Table:1)
Table-1: Relative
frequency of non-neoplastic lesions with percentage
Histologic type |
Number of cases |
Percentage |
1) Nonspecific Epididymoorchitis |
25 |
38.5% |
2) Atrophy with maturation arrest |
15 |
23.1% |
3) Hemorrhagic infarction |
8 |
12.3% |
4) Cryptorchidism |
3 |
4.6% |
5) Normal study |
14 |
21.5% |
Total |
65 |
100 |
Among neoplastic lesions germ cell tumors
were more common compared to non-germ cell tumors, 14 out of 15 cases
constituting 93.33%. Others were 1 case of non-Hodgkin’s lymphoma. Among all
tumors seminoma was most common 6 cases out of 15 cases 40.5%, followed by
mixed GCT seminomatous 3cases with 20%, non seminomatous mixed GCT 2cases
constituted 13.33% of all tumors. Mature Teratoma 2 cases with 13.33%, Yolk sac
tumor 6.66% & NHL 6.66 %.( table: 2)
Table-2: Spectrum of
neoplastic lesions
Spectrum of Neoplastic lesions |
No. of cases |
Percentage |
1 seminoma |
6 |
40% |
2) mixed GCT (seminomatous) |
3 |
20% |
3) mixed GCT (non-seminomatous) |
2 |
13.33% |
4) mature Teratoma |
2 |
13.33% |
5) yolk sac tumor |
1 |
6.66% |
6) NHL |
1 |
6.66% |
Total
|
15 |
100% |
Majority of patients presented with
unilateral scrotal swelling, 70 out of 80 cases, accounting for 87.5%. Pain is
the second most common symptom noted in 50 out of 80 cases constituting 62.5%,
followed by fever in 30 cases accounting for 37.5%. Majority of cases presented with right sided
involvement, 41 out of 80 cases constituting 51.25%. Left sided involvement was
in 25 out of 80 cases accounting for 31.25%. Remaining cases 14 out of 80
presented with bilateral orchidectomy accounting for 17.5 % (Table:3)
Table-3: Laterality of
the specimens
Laterality of Specimens |
Number |
Percentage |
Right sided |
41 |
51.25% |
Left sided |
25 |
31.25% |
Bilateral |
14 |
17.50% |
Total |
80 |
100% |
Age distribution of non-neoplastic lesions
showed highest incidence of Epididymoorchitis presented in 7th
decade with 8 cases out of 25, corresponding to 32%, followed by 6th decade
with 6 cases out of 25 corresponding to 24%. Testicular Atrophy with maturation
arrest majority of cases presented in 7th decade, 5 out of 15 cases
with 33.3%, followed by equal incidence in 2nd, 4th, 5th,
6th, decades, 2 cases in each with13.3%. Hemorrhagic infarction
majority presented in 2nd decade, 3 out of 8 cases with 37.5%,
followed by equal incidence in 3rd& 5th decades, 2
cases in each with 25%. Cryptorchidism 3
cases with equal incidence 1 case each in 2nd, 5th& 6th
decades corresponding to 33.3% each. Normal study majority of cases presented
in 7th decade, 7 cases out of 14cases, corresponding to 50% followed
by 6th decade 3 out of 7 cases with 21.4%(table:4).
Table-4: Age range of
non-neoplastic lesions
Non- Neoplastic Lesions |
0-10 |
11-20 |
21-30 |
31-40 |
41-50 |
51-60 |
61-70 |
71-80 |
1) NonspecificEpididymoorchitis |
0 |
0 |
0 |
4 |
5 |
6 |
8 |
2 |
2) Atrophy
|
0 |
2 |
1 |
2 |
2 |
2 |
5 |
1 |
3) Hemorrhagic infarction |
0 |
3 |
2 |
1 |
2 |
0 |
0 |
0 |
4) Cryptorchidism |
0 |
1 |
0 |
0 |
1 |
1 |
0 |
0 |
5) Normal study |
0 |
2 |
0 |
0 |
0 |
3 |
7 |
2 |
Total |
0 |
8 |
3 |
7 |
10 |
12 |
20 |
5 |
Age distribution of neoplastic lesions mostly
presented in 3rd decade,5 out of 15 cases with 33.33%. Most common
neoplastic lesion seminoma presented with a wide age range between 18-73 years,
predominantly in 2nd decade. Seminomatous mixed germ cell tumor, 2
out of 3 cases presented in 3rd decade. Non seminomatous mixed GCT,
2 cases presented each in 3rd & 5th decade. One case
of yolk sac tumor presented in 20year old patient another case of NHL presented
in 80 years old. 2 cases of mature Teratoma presented each in 3rd&
4th decade (Table: 5).
Table-5: Age range of
neoplastic lesions
Age |
Seminoma |
S-MGCT |
Non S-MGCT |
Mature teratoma |
Yolk sac tumor |
NHL |
0-10 |
0 |
0 |
0 |
0 |
0 |
0 |
11-20 |
2 |
- |
- |
- |
1 |
|
21-30 |
1 |
2 |
1 |
1 |
- |
- |
31-40 |
1 |
- |
- |
1 |
- |
- |
41-50 |
- |
1 |
1 |
- |
- |
- |
51-60 |
- |
- |
- |
- |
- |
- |
61-70 |
1 |
- |
- |
- |
- |
- |
71-80 |
- |
- |
- |
- |
- |
1 |
Total |
6 |
3 |
2 |
2 |
1 |
1 |
Discussion
Testis is affected
by both non-neoplastic and neoplastic lesions. Our study comprised of total of
80 cases studied over a period of 3yrs.Majority are non-neoplastic lesions
compared to neoplastic lesions. This is in concordance with Mansi Sharma et al,
Mahesh B Patel et al, Hemavathi Reddy et al, Sundari Devi et al(table:6).
Table-6: Comparison of
non-neoplastic and neoplastic lesions with other studies.
Table |
Non-neoplastic lesions |
Neoplastic lesions. |
Mansi S et al [7] |
93% |
7% |
Mahesh B Patel [3] |
80% |
20% |
Hemavathi R et al [4] |
86% |
14% |
Sundari Devi et al [9] |
94.20% |
5.80% |
Present study |
81.25% |
18.75% |
Commonest mode of clinical presentation is
unilateral scrotal swelling which is similar in our study, followed by
pain [3,4]. In our study right sided
involvement is more common similar to Mahesh B et al and Mansi S et al in
contrast to left sided involvement which is seen in Reddy H et al [3,4,7]. Among
non-neoplastic lesions most common histologic type is non- specific Epididymoorchitis
constituting 38.5% followed by testicular atrophy with maturation arrest
accounting for 23.08%.
Table-7: Comparison of various non-neoplastic testicular lesions with
other studies.
Histologic type with % |
Mansi etaI |
Mahesh et al |
Hemavathi et al |
Sundari Devi et al |
Present study |
1) Nonspecificepididymo
orchitis |
15.1 |
9.41 |
3.5 |
39.28 |
38.5 |
2) Atrophy with
maturation arrest |
16.96 |
- |
19.8 |
14.28 |
23.08 |
3) Hemorrhagic infarction |
18.86 |
55.29 |
22.1 |
17.85 |
12.03 |
4) Cryptorchidism |
39.62 |
8.24 |
14 |
- |
4.6 |
5) Normal study |
- |
- |
- |
22.3 |
21.5 |
There is varying incidence of different non-neoplastic lesions form
study to study in different regions. Our study is mostly in concordance with
Sundari Devi et al [9](table:7)
Figure-1: Microscopic picture of chronic nonspecific Epididymoorchitis
Acute and chronic non-specific epididymoorchitis is most common (n=25)
in this region, presenting with a wide age range (35 to 75 years). Peak
incidence is seen 7th and 6th decades. This is similar to
Mahesh B Patel and Kaveret al [3,16]. Spread from adjacent urinary tract
infection caused by E.Coli is the most common cause of Epididymoorchitis. Older
age of presentation may be attributed to partial obstruction of urethra by
prostate enlargement or stricture of urethra.
Chronicnon-specificEpididymoorchitis histopathology showed chronic inflammatory
cell infiltration of testis and epididymis with fibrous scarring. Leydig cells
are spared (Fig 1)
Figure-2: Microscopic picture of atrophy with maturation arrest
Acute pyogenic Epididymoorchitis
histopathology presented with acute supportive inflammation of testis and
epididymis with dense infiltration by neutrophils.
Testicular Atrophy
with maturation arrest 15cases were studied presented with a wide age range (18
to 71 years).This may be due to cryptorchidism or due to end stage chronic
non-specific inflammation. Grossly smaller size of the testis with histopathology
showing hyalinized tubules with maturation arrest of spermatogenesis at various
levels, starting from spematogonia to spermatids (Fig. 2)
Figure-3:
Microscopic picture of torsion with hemorrhagic infarction
Testicular Torsion
with hemorrhagic infarction 8 cases studied, presented in a younger age group
(12to 50 years). Grossly slightly enlarged testis, soft and hemorrhagic,
histopathology showing intense congestion, extravasation of blood into
interstitial tissue and hemorrhagic infarction (Fig. 3).
Cryptorchidism, 3
cases showed grossly normal to atrophied testis with maturation arrest (Fig 4)
Figure-4: Microscopic Picture of Cryptorchidism
Normal study of
testis was observed in bilateral testes which were removed to see if there is
any spread from adjacent cancers like adenocarcinoma of prostate or rarely for
squamous cell carcinoma of penis and papillary urothelial carcinoma of penile
urethra.
Cancer of testis is
one of rare malignancies accounting for 0.5 to 1.5 % of all male cancers.
Highest incidence is seen in European countries compared to Asian and African
countries. It is the most common malignancy occurring in young men between
15-34 years [5].
Among neoplastic
lesions most common lesion is seminoma constituting 40% followed by
seminomatous mixed germ cell tumor 20% and non seminomatous mixed GCT 13.33%.
Table- 8: Comparison of histological types of neoplastic testicular
lesions with other studies
Histologic type with % |
Mansi et al |
Gupta A et al [10] |
Sanjay M et al [11] |
Hemavathi et al |
Mahesh B et al |
Present study |
|
Seminoma |
25% |
48% |
38.90% |
42.90% |
40% |
40% |
|
Mixed GCT seminomatous
and non seminomatous |
25% |
16% |
33.33% |
43% |
- |
33.30% |
|
Teratoma |
25% |
12% |
11.11% |
- |
33.30% |
13.33% |
|
Yolk sac tumor |
25% |
4% |
5.50% |
- |
6.60% |
6.66% |
|
Others |
- |
4% |
11.11% |
7.20% |
20% |
6.66% |
Figure-5: Gross picture of Seminoma
Our study is mostly
in concordance with Sanjay M et al(table:8). Variations may occur from region
to region due to various predisposing factors. Seminoma presented with a wide
age range 18-73 yrs. Maximum number presented in 2nd decade. All
cases were from right sided involvement. Grossly seminoma presented with
uniformly enlarged testis. Cut section was showing solid, homogenous gray white
without any involvement of tunica albugenia, epididymis or spermatic cord (Fig.
5).
Figure-6: Microscopic Picture of Seminoma
Histopathology
showed sheets of uniform large round to polygonal cells with central nucleus
and clear cytoplasm, divided into lobules by fibrous septae which are
infiltrated by lymphocytes. (Fig. 6)One case showed microscopic extension of
tumor tissue into spermatic cord.
All mixed germ cell
neoplasms grossly presented with irregularly enlarged testis, cut section showing variegated appearance with areas of
necrosis and hemorrhages.
Seminomatous mixed germ cell tumors age range
is between 21-41 yrs. Maximum cases seen in 3rd decade with left
sided involvement. Seminoma component along with mature Teratoma was seen in
one case and with embryonic carcinoma in another case. In later case there was
also microscopic extension into tunica vaginalis and metastatic tumor deposits
in 2/2 adjacent lymph nodes.
Figure-7: Gross picture of Non Seminomatous Mixed Germ Cell Tumor
Non seminomatous
mixed GCT presented in 3rd& 5th decades with equal
incidence in right and left sides. One case presented with components of yolk
sac tumor, embryonal carcinoma and Teratoma (Fig. 7)
Other case presented with only embryonal
carcinoma with Teratoma. Mature Teratoma 2 cases studied, presented with
enlarged testis with cut section showing mature cartilage and gray white areas (Fig.
8)
Figure-8:
Gross Picture of Mature Figure 9: Microscopic picture of mature
Teratoma
Teratoma
Histopathology
showed mature cartilage, many keratin horn cysts and glandular structures (Fig
9)
1 case of yolk sac tumor presented in 2nd
decade with left sided involvement. Grossly presented with enlarged testis. Cut
section showing gray white, yellow brown with gelatinous and cystic areas.
Histopathology showed lace like arrangement of medium sized cuboidal cells with
vacuolated cytoplasm. (Fig. 10) Areas of papillary structures and endodermal
sinus like structures (Schiller Duval bodies) were observed. (Fig. 11)
Figure-10, 11: Microscopic picture of
Yolk Sac Tumour
1 case of Non
Hodgkins lymphoma was encountered which presented in 7th decade with
right sided involvement. Grossly testis was reduced in size and tan white on
cut section. Histopathology showed as small lymphocytic lymphoma.
Vast majority of
previous series showed germ cell tumors are most frequent malignancy ranging
from 76 to 95% [13, 14]. Present study also correlates well by showing 93.33%
of germ cell tumors. In the present study maximum number of neoplastic lesions
seen in 3rd decade with 33.33% cases. Similar results were found in
Mustaq S et al[5], Gill MS et al [13], Deotra A et al [14] and Stewart BW et
al[15]. Majority of tumors were presenting with right sided involvement. This
is also in concordance with Preethi Rihal Chakrabarti et al [12].
Conclusion
Our study is mostly
comparable with the other studies with respect to relative frequency, age
distribution and other clinical features of all non-neoplastic and neoplastic
testicular lesions. Though testicular neoplasms are rare, constitute only 1% of
all male cancers it is important for the accurate diagnosis and proper
management of the patients.
Contribution by
different authors- For this manuscript, study was done by Dr.
ArunaTekumalla, Statistics and manuscript prepared by Dr. Sreedhar Ragi with
the help of Dr. Ravinder Thota.
What this study
adds to existing knowledge?This study enables us to know the
relative frequency of testicular lesions and incidence testicular neoplasms.
Histopathology is the mainstay of diagnosis in the testicular neoplasms and
helps in accurate management of the patients by further submitting for
immunohistochemistry.
Acknowledgement: Nil
Conflict of Interest: Nil
Funding: Nil
References
How to cite this article?
Tekumalla A, Ragi S, Thota R. Histopathological analysis of testicular lesions- a three year experience in a tertiary care center, Telangana.Trop J Path Micro 2019;5(5):260-268.doi:10.17511/jopm.2019.i5.02.