|
| |
 |
|
| ORIGINAL ARTICLE |
|
| Year : 2022 | Volume
: 10
| Issue : 4 | Page : 154-158 |
|
Types and frequency of neural elements in mature ovarian teratomas: An 11-year study from Rural India
Raj Kumar1, Seema Dayal2, Mani Krishna2
1 Department of Neurosurgery, Uttar Pradesh University of Medical Sciences, Etawah, Uttar Pradesh, India
2 Department of Pathology, Uttar Pradesh University of Medical Sciences, Etawah, Uttar Pradesh, India
| Date of Submission | 18-Sep-2020 |
| Date of Decision | 05-Sep-2021 |
| Date of Acceptance | 07-Sep-2021 |
| Date of Web Publication | 09-Dec-2022 |
Correspondence Address:
Dr. Seema Dayal
Department of Pathology, Uttar Pradesh University of Medical Sciences, Saifai, Etawah, Uttar Pradesh
India
 Source of Support: None, Conflict of Interest: None
DOI: 10.4103/jmau.jmau_94_20
Introduction: Teratomas are those tumors which are derived from the totipotent cells. They may manifest at any site. Ovary is the most common site for teratomas. Ovarian teratomas may be immature and mature depending on the elements they harbor. Mature ovarian teratomas may contain ectoderm, endoderm, and mesoderm. Ectoderm mainly comprises the skin and its adnexa, followed by neural tissue, whereas mesodermal elements are blood vessels, adipose tissue, cartilage, and hematopoietic tissue, similarly, endoderm consists of respiratory tissue, thyroid gland, and gastrointestinal tissue. Materials and Methods: This study was conducted in the histopathology section from January 2008 to April 2019 and included 54 cases of mature ovarian teratomas. The slides of ovarian tumors were evaluated, and the relationship between clinical and pathological findings was studied with emphasis predominantly on neural elements. Results: The most common age group among the women with ovarian teratoma was 21–30 (31.48%) years, the youngest patients been 8 years, and oldest of 60 years. The chief complaints were pain in 37 (68.51%), followed by mass per abdomen 25 (46.29%). On gross examination, most of the tumors were unilateral 53 (98.14%), having tufts of hairs with sebaceous material 34 (61.81%). Microscopic examination confirmed the presence of squamous epithelium and its adnexal structure 52 (94.54%). Neural elements were seen in 14 (25.45%) cases. In every case with neural elements, skin, its adnexa, and adipose tissue were also seen. Conclusion: Teratomas have diversity in the age of presentation, gross findings, and microscopy features. Neural elements are commonly found in 25.45% of ovarian teratoma which is mostly found in association with skin and adipose tissue. The combination of neural elements with adipose tissue signifies an association between them because both arise from different dermal elements.
Keywords: Histopathology, mature ovarian teratoma, neural elements
How to cite this article:
Kumar R, Dayal S, Krishna M. Types and frequency of neural elements in mature ovarian teratomas: An 11-year study from Rural India. J Microsc Ultrastruct 2022;10:154-8 |
How to cite this URL:
Kumar R, Dayal S, Krishna M. Types and frequency of neural elements in mature ovarian teratomas: An 11-year study from Rural India. J Microsc Ultrastruct [serial online] 2022 [cited 2023 Mar 20];10:154-8. Available from: https://www.jmau.org/text.asp?2022/10/4/154/362509 |
| Introduction | |  |
Teratoma is a special type of mixed germ cell tumor which consists of mature and immature elements arising from one or more of the three primordial germ layers. The word teratoma is derived from the Greek word “teras” meaning monster or deformed and “oma” means tumor. Virchow coined the term teratoma in his book on tumors published in 1863.[1] They occur in gonads and in extragonadial sites, that is., in ovary, testis, lung, mesentery, and omentum. Ovary is the most common site of teratoma. It is further divided into mature and immature depending on the contents they have. Teratomas may occur at any age group, but it is frequent in the young age group, that is., 20–40 years of age. Mature cystic teratomas constitute 10%–20% of all ovarian tumors and also the most frequent germ cell tumor of the ovary.[2] The presence of ectodermal tissue is common in mature teratomas, and majority of them have skin and adnexa so that some author still prefer the old term dermoid cyst although nomenclature is inaccurate, because, in addition to that, ectodermal, endodermal, and mesodermal tissue are also seen.[3] The WHO classification of ovarian tumor has separated epidermoid cyst from dermoid cyst[4] this is because the epidermoid cyst is considered to arise from squamous metaplasia of epithelium elements without evidence of mesodermal or endodermal tissue. Glial tissue is reported to be a common neural component of mature teratoma,[5] and the presence of well-organized cerebellum and choroid plexus is also reported. A few number of case reports have been published on neural elements in mature teratoma, but as per the literature search, no original article had been seen depicting this. Thus, this study was conducted with plan to access the correlation of clinical findings with histopathology of mature ovarian tumors with more emphasis on neural elements, the types of neural elements, and its coexistence if any.
| Materials and Methods | | |
This is a retrospective study conducted in the Department of Pathology, Uttar Pradesh University of Medical Sciences, Saifai, Etawah (UP), from January 2008 to April 2019 and included 54 cases of mature ovarian teratomas. All the cases were studied with reference to age, size, clinical profile, gross, and microscopy, that is., histopathology and immunohistochemistry as per need. Surgically excised ovarian masses were sent in 10% formal saline to be fixed, grossed, and processed, multiple sections were made at 3–4 μ and stained with H and E, whenever required immunohistochemistry was applied. Slides were screened and reviewed. Ethical clearance on histopathological evaluation of hystrectomies was taken, permission from head of institution was also taken before conducting this study.
| Results | | |
A total of 54 cases were studied. The most common age group affected with ovarian teratoma was 21–30 (31.48%) years [Table 1], the youngest being 8 years, and oldest 60 years. The common complaint documented was abdominal pain 37 (68.51%), followed by mass per abdomen in 25 (46.29%) [Table 2]. The smallest tumor size was 1.2 cm × 0.8 cm × 0.6 cm, whereas the largest was 16 cm × 14 cm × 5 cm with an average size of 6 cm. For gross evaluation, the details were noted from histopathology records duly maintained in the departmental archive. On gross examination, most of the tumors were unilateral 53 (98.14%) mostly these have hairs tufts with sebaceous material seen in 34 (61.81%), followed by putty-like material 32 (58.18%), bony elements with teeth and cartilage 5 (9.09%) [Table 3]. Microscopic examination confirmed the presence of squamous epithelium and its adnexal structure 52 (94.54%) [Table 4]. Neural elements were seen in 14 (25.45%) cases which comprised glial tissue, ganglion cells, melanotic cells, choroid plexus, and cerebellum [Table 5]. In all the cases of mature teratoma with neural tissue, adipose tissue was also found. The other pathologies seen were struma ovarii (11%), yolk sac tumor (1.8%), fibroma (1.8%), and thecoma (1.8%). Microscopically, struma ovarii was diagnosed in six cases of mature teratoma whereas one case was having struma ovarii and neural elements together. | Table 4: Neural elements with other tissue and pathologies in mature ovarian teratoma
Click here to view |
| Discussion | | |
Mature ovarian teratomas are germ cell tumors which show differentiation along with embryonic rather than extra embryonic pathways. Willis described teratomas as composed of multiple tissues foreign to the parts, and they may arise in both benign and malignant forms. There are some theories regarding histogenesis, first one is being “gastrulation theory” which states that the teratomas arise from remnants of the primitive streak or primitive node, whereas second theory called “missed theory” which suggest that teratomas originate from totipotent primordial germ cells. These cells develop among the endodermal cells of the yolk sac near the origin of the allantois and migrate to the gonadal ridge during 4 and 5 weeks of gestation. A few number of cells miss their target destination and produce teratoma. This theory explains the origin of gonadal teratomas. The third theory is called “incomplete twinning.”[6]
The site of teratoma presentations is gonads which include ovary, testis, and extragonadal tissue including lung, mesentery, mediastinum, retroperitoneal, nasopharyngeal omentum, and brain. In ovary, there are about 10%–20% ovarian tumors and is the most frequent germ cell tumor of the ovary.[7] They often occur in individuals of reproductive age group, between the age range of 20–40 years[8] similar to findings in the present study. Unilateral ovarian teratoma is frequently seen, whereas only 10%–15% of ovarian teratomas are bilateral.[1] Here, we found unilateral ovarian teratomas in 53 (98.14%) cases. For unknown reasons, they are found more in the right side[9],[10] as is noted by us in the present study.
Abdominal pain may arise because of torsion, hemorrhage, infection, and pressure effects.[11] Abdominal pain was the most frequent clinical complaint (68.51%), which might happened due to pressure effects of ovarian masses owing to their size and cystic components. The presence of fertility and infertility is difficult to access in ovarian mature teratoma but infertility may result because of recurrent endometriosis.[12] In the current study, a young female was also diagnosed with mature teratoma ovary during her pregnancy.
Gross examination of mature ovarian teratoma characteristically reveals a thin wall cyst lined with an opaque, gray-white wrinkled apparent epidermis, and from wall hair shafts protrudes along with greasy content which is made up of keratin, sebum, and hair. Teeth and sometimes human body-like structures are seen in mature ovarian teratomas called homunculus.[3],[13] In this study, abovementioned contents are seen.
Histopathology is used as confirmatory diagnostic tool for the diagnosis of mature cystic ovarian teratoma. With the help of histopathology, we can access the ectodermal, mesodermal, and endodermal components. Blackwell and Dockerty found ectodermal derivatives in 100% of the teratomas, mesoderm structures in 93%, and endodermal in 71%.[14] Skin appendages and neural elements, particularly glial tissue, are extremely common, followed by cartilage, respiratory tissue, and gastrointestinal tract tissue [Figure 1]. In the current study on histopathology examination, skin and adnexa were frequent findings (94.54%), and similarly, neural element was also found common (25.45%). In every case, neural elements were found associated with skin and its adnexa, followed by adipose tissue. In teratoma, different types of neural components are found. Neural elements may be seen in ovarian teratoma as neurogenic cyst which is a monodermal teratoma and predominantly comprises neural tissue.[15] The other neural elements seen in relationship with ovarian teratoma are gliomatosis peritonei and different neural elements admixed with tissue other than neural such as glial tissue, ganglion, choroid plexus, cerebellum, nerves, and melanotic cells. Gliomatosis peritoni is a rare disease characterized by peritoneal and omental implant with ovarian teratoma found in the majority with immature teratoma.[3] The Marcial Rojas and Medina reported 22%–47% peripheral nerves, 25%–41% brain tissue, 19%–25% ependymal cells, and 19%–22% ganglionic cells.[16] We have found neural elements in 14 (25.45%) cases of mature ovarian teratomas out of which glial tissue was also found in (78.57%) cases, choroid plexus in cases (21.42%), ganglion (21.42%), melanotic cells (21.42%), nerve fibers (14.28%), and cerebellum (7.1%) [Figure 2]. GFAP is an intermediate filament protein which is expressed in various cell types of central nervous system (CNS). It is highly expressed in the glial tissue of mature teratoma thus suggesting that the GFAP expression is a indicator of teratoma maturation.[17] Its expression was also seen in our study [Figure 3]. The another common immunomarker for neural tissue is S100, which was first isolated from the CNS. Its immunoreactivity is seen in glial tissue, that is., astrocytes, oligodendrocytes, ependymal cells, Schwann cells, and melanocytes.[18] Similar results were found in our study [Figure 4]. The other pathologies seen in our study along with teratomas were yolk sac tumor, fibroma, and thecoma, respectively. Struma ovarii was seen in six cases (11%) and in one case found along with neural elements. Mature cystic teratoma may exist with fibroma and thecoma.[19],[20] This was also seen in current research. Yolk sac tumor with ovarian teratoma is rare finding that we found in our research. Struma ovarii is the variant of monodermal teratoma which shows the expression of the dominant growth of thyroid tissue in teratoma. This was first described in 1889. It comprises <3% of ovarian teratomas.[21] In the present study, we have found six cases of struma ovarii (11%) among them one case of struma ovarii was also having neural elements. The presence of struma ovarii with neural elements is a rare, but it is also reported in the literature.[22] | Figure 1: H- and E-stained section of mature cystic teratoma showing adipose tissue, glands, and neural elements
Click here to view |
 | Figure 2: H- and E-stained section of mature cystic teratoma showing choroid plexus with other neural elements
Click here to view |
 | Figure 3: Focal immunopositivity of GFAP in mature cystic teratoma signifying neural tissue
Click here to view |
 | Figure 4: Strong immunopositivity of S-100 in mature cystic teratoma also signifying neural tissue
Click here to view |
| Conclusion | | |
Mature ovarian teratoma is the common variant of ovarian tumor. Histopathology examination of ovarian masses is a gold standard diagnostic test and mandatory to diagnose teratomas. Ovarian teratoma contains tissues from different germ layers. Ectodermal components such as skin and its adnexa are commonly seen. The neural elements in teratoma are also found and it was frequent to found neural elements with adipose tissue although both arises from different dermal tissue. Further studies must be carried out with large numbers of cases to fully investigate the significance of neural elements in mature teratomas.
Financial support and sponsorship
Nil.
Conflicts of interest
There are no conflicts of interest.
| References | | |
| 1. | Srikanth S, Anandam G. Bilateral dermoid cyst of ovary. Med J DY Patil Univ 2014;7:492-3.  [Full text] |
| 2. | Ayhan A, Bukulmez O, Genc C, Karamursel BS, Ayhan A. Mature cystic teratomas of the ovary: Case series from one institution over 34 years. Eur J Obstet Gynecol Reprod Biol 2000;88:153-7. |
| 3. | Rosai J. Ovary. In: Rosai J, editor. Text book Surgical Pathology. 9 th ed. St Louis, Missouri: Mosby Elsevier; 2004. p. 1686-90. |
| 4. | Nogales F, Talerman A, Kabuk Huch RA, Tavassoli FA, Devouassoux Shisheboran M. Germ cell tumors. In: Tavssoli FA, Devilee P, editors. World Health Organisation Classification of Tumours. Pathology and Genetics Tumors of the Breast and Female Genital Organs. 4 th ed. Lyon: IARC Press; 2003. p. 163-75. |
| 5. | Akbulut M, Kelten EC, Ege CB. Mature cystic teratoma with predominantly neurogenic elements – Case report. Aegean Pathol J 2006;3:18-20. |
| 6. | Keene DJ, Craigie RJ, Shabani A, Batra G, Hennayake S. Bipartite anterior extra peritoneal teratoma. Evidence for the embroyogical origins of teratomas? Case Rep Med 2011;2011:208940. |
| 7. | Cakmak B, Nacar M, Ozsoy Z, Aliyev N, Koseoglu D. Mature cystic teratomas: Relationship between histopathological contents and clinical features. Niger J Clin Pract 2015;18:236-9. [ PUBMED] [Full text] |
| 8. | Chiang AJ, La V, Peng J, Yu KJ, Teng NN. Squamous cell carcinoma arising from mature cystic teratoma of the ovary. Int J Gynecol Cancer 2011;21:466-74. |
| 9. | Varma AV, Malpani G, Agrawal P, Malukani K, Dosi S. Clinicopathological spectrum of teratomas: An 8-year retrospective study from a tertiary care institute. Indian J Cancer 2017;54:576-9. [ PUBMED] [Full text] |
| 10. | Ismail SR. An evaluation of the incidence of right sided ovarian cystic teratoma visualized on sonograms. J Dign Med Sonography 2005;21:336-42. |
| 11. | Nagamuthu EA, Mudavath P, Kishore N, Fatima SS, Samudrala S. Original research article on cystic ovarian lesions diagnosed as teratomas – a 2 year study in a tertiary care hospital. Int J Res Med Sci 2016;4:4136-42. |
| 12. | Kurt S, Avşar HA, Doğan ÖE, Saatli HB, Saygılı U. Effects of mature cystic teratoma on reproductive health and malignant transformation: A retrospective analysis of 80 cases J Turk Ger Gynecol Assoc 2019;20:84-8. |
| 13. | Mohan H. The Female Genital Tract. Textbook of Pathology. 6 th ed. New Delhi, India: Jaypee; 2010. p. 745-7. |
| 14. | Blackwell WJ, Dockerty MB. Dermoid cysts of the ovary: Their clinical and pathologic significance. Am J Obstet Gynecol 1946;51:151-72. |
| 15. | Sah SP, Verma K, Rani S. Neurogenic cyst of ovary: An unusual massive monodermal teratoma. J Obstet Gynaecol Res 2001;27:21-5. |
| 16. | Marcial-Rojas RA, Medina R. Cystic teratomas of the ovary; a clinical and pathological analysis of two hundred sixty-eight tumors. AMA Arch Pathol 1958;66:577-89. |
| 17. | Gu S, Wu YM, Hong L, Zhang ZD, Yin MZ. Glial fibrillary acidic protein expression is an indicator of teratoma maturation in children. World J Pediatr 2011;7:262-5. |
| 18. | Mc Nutt NS. The S100 family of multipurpose calcium binding protein. J Cutan Pathol 1998;25:521-9. |
| 19. | Tan GC, Chandramaya SF, Nordin A, S. Tap PY. Collision tumor of the ovary: Fibroma and mature cystic teratoma. Indian J Pathol Microbiol 2021;64:171-3. [ PUBMED] [Full text] |
| 20. | Kim JH. Torsion of collision tumor: Dermoid cyst and fibrothecoma with postmenopausal bleeding. J Menopausal Med 2016;22:114-7. |
| 21. | Yoo SC, Chang KH, Lyu MO, Chang SJ, Ryu HS, Kim HS. Clinical characteristics of struma ovarii. J Gynecol Oncol 2008;19:135-8. |
| 22. | Dayal S. Mature cystic teratoma with neurogenic components and struma ovarii: A rare case report and review of the literature. Kasr Al Ainy Med J 2017;23:154-5. [Full text] |
[Figure 1], [Figure 2], [Figure 3], [Figure 4]
[Table 1], [Table 2], [Table 3], [Table 4], [Table 5]
|
Search Pubmed for