Collision Tumors in Ovary: Case Series and Literature Review
A B S T R A C T
Histologically distinct tumors that coexist in an organ without any histological admixture at their interface are denominated collision tumors. We report 3 cases of colliding mature cystic teratoma with mucinous cystadenoma and a case of mature cystic teratoma colliding with benign Brenner tumor in the ovary. We also provide a literature review based on 35 previously published ovarian collision cases. Ovarian tumors from all classes, benign, borderline and malignant lesions may collide. Both our case series and the literature review indicate that ovarian tumor collisions tend to be clinically and ultrasonographically/radiologically unrecognized. The awareness among surgeons, radiologists and pathologists of this rare phenomenon and histological recognition are crucial in order to offer adequate treatment to patients. There is a need to identify novel and more specific imaging clues pointing towards collision tumors in the ovary.
Keywords
Brenner tumor, collision tumors, mucinous cystadenoma, ovarian lesion imaging, ovarian neoplasm, teratoma
Introduction
Collision tumors are histologically distinct neoplasms that coexist in the same organ without any histological intermixing [1]. Although very rare, they have been found to affect a range of organs, including skin, esophagus, stomach, colon, as well as the ovary [1-5]. We report and discuss the tumors colliding in the ovary that we witnessed in 4 patients and, also, provide a review based on 35 other cases identified by PubMed search for original articles electronically listed until October 2018 and by checking their respective references.
Presentation of the Cases
Case 1
A 37-year-old nulliparous woman, with regular menstrual cycles, no hormonal contraception use and medical history of psoriasis (medicated with methotrexate and glicocorticoids), presented with complaints of progressive abdominal-pelvic discomfort over six months, associated with the development of a low abdominal lump. She denied any other symptoms. The patient was in a good general condition. Furthermore, on physical examination, the abdomen was soft while palpation revealed a mobile, elastic and tender mass in the right iliac fossa, approximately measuring 15 cm. With the exception of a vaginal discharge compatible with candidiasis, no other significant changes were noted. Namely, there were no signs of ascites or lymphadenopathies.
Abdominal and transvaginal ultrasonography revealed a cystic multilocular formation (2 locules), apparently originating from the right ovary and measuring 141 x 126 x 130 mm, with regular external and internal borders, “ground glass” content and Color Doppler score 1, i.e. no vascularization with Color Doppler (Figure 1A-C). The International Ovarian Tumor Analysis (IOTA) diagnostic prediction model ADNEX classified the lesion as a benign formation (Figure 1D). Tumor markers were negative (CEA = 1,80 ng/mL, CA19.9 = 12 U/mL and CA125 24,6 U/mL). Abdominal-pelvic magnetic resonance imaging (MRI) identified a cystic multiloculated tumor of the right ovary (170 x 113 x 137 mm), morphologically compatible with mucinous cystadenoma (Figure 1E and 1F). Signs of malignant disease were not observed. A laparotomic right salpingo-oophorectomy was performed. Histopathological examination established the diagnosis of colliding ovarian mature cystic teratoma and mucinous cystadenoma. The patient had a favorable postoperative evolution, without complications.
Case 2
A 35-year-old nulliparous women, with regular menstrual cycles, no current hormonal contraceptive use, in good general condition and asymptomatic, underwent a routine gynecological check-up visit and transvaginal ultrasound which identified bilateral ovarian formations. A level II transvaginal ultrasound subsequently detected unilocular, mixed-content and non-vascularized formation of 79 x 53 x 53 mm in the left ovary (Figure 2A and 2B). In parallel, another unilocular, mixed-content and non-vascularized formation of 32 x 31 x 31 mm was evidenced within the right ovary. There was no free fluid in pouch of Douglas. Tumor markers were negative (CEA = 3.90 ng/mL, CA19.9 = 32.5 U/mL and CA125 15.10 U/mL). The abdominal-pelvic MRI revealed an heterogenous nodular formation with a thin capsule, measuring 66 x 45 x 84 mm and containing a solid nodular component (45 x 36 x 51 mm) in the left ovary, and an heterogeneous nodular formation of 38 x 32 x 46 mm, with thin capsule and hypointense content in the right ovary, both lacking of enhancement. Morphologically these formations appeared compatible with bilateral teratomas. A laparoscopic bilateral salpingo-oophorectomy was performed. Histopathological examination established the diagnosis of colliding ovarian mature cystic teratoma and mucinous cystadenoma of the left ovary and ovarian mature cystic teratoma in the right ovary. The patient had a favorable postoperative evolution, without complications.
Case 3
A 44-year-old multiparous woman, with regular menstrual cycles under combined oral contraception, and with medical history of hypothyroidism and surgical history of benign ovarian cyst removal a decade ago, was referenced to our Unit due to persistence of a left ovarian formation, which was diagnosed by an abdominal ultrasound during her last pregnancy. Transvaginal ultrasonography revealed a cystic multilocular formation (2 locules), apparently originating from the left ovary and measuring 80 x 39 x 50 mm, with regular external and internal borders, acoustic shadow and a Color Doppler score 2 (Figure 2C). Tumor markers were negative (CEA = 1.50 ng / ml, CA19.9 = 8.4 U / ml, HE4 62.9 pm / l and CA125 19.25 U / ml). The IOTA diagnostic prediction model ADNEX classified the lesion as a benign formation. A laparoscopic removal of right ovary cyst was performed. Histopathological examination established the diagnosis of colliding ovarian mature cystic teratoma and mucinous cystadenoma. The patient presented an uneventful postoperative evolution.
Case 4
A 42-year-old nulliparous, on the course of her gynecological follow-up due to uterine fibromas, performed a transvaginal ultrasound, which identified a cystic multilocular formation (4 locules), apparently originating from the parenchyma of the right ovary and measuring 54 x 54 x 52 mm, with regular external and internal borders, mixed content and Color Doppler score 1 (Figure 3). The IOTA diagnostic prediction model ADNEX classified the lesion as a benign formation. Tumor marker CA125 was negative (25,2 U/ml).
A laparotomic right salpingo-oophorectomy was performed. Histopathological examination established the diagnosis of colliding ovarian mature cystic teratoma (5 cm) and benign Brenner tumor (5 mm). This is the first reported case of a collision tumor of the ovary associated to a Brenner tumor, which was only postoperatively recognized. The patient had uneventful postoperative recovery.
Literature Review and Discussion
The concept of collision tumors implies the absence of histological admixture at the interface of two or more coexisting tumors in an organ [6]. As such, we witnessed 4 benign ovarian collisions and identified 35 previously published cases (Table 1), being both benign tumors in 19 patients (54.3%) and benign-malignant collisions in 16 cases (45.7%; including a patient with benign-borderline tumor collision). Mature teratoma appears in all our patients as well as the most frequently collision component in previous publications (21/35 cases, 60%), although the ovarian tumors from all classes, i.e. epithelial, germ cell and sex-cord/stromal neoplasms may collide. While others have reported that the combination teratoma-mucinous tumor is the most common, which is indeed supported by our series, our literature review have found that mature teratoma-cystadenoma (serous in 5/21 and mucinous in 4/21 cases) and mature teratoma-carcinoma (serous in 6/21 and mucinous in 2/21 cases) predominate [7]. Thus, mature teratoma-serous epithelial lesion, whether benign or malignant, is actually the most frequent of all published combinations, including our cases. Furthermore, collision tumors tend to be a unilateral phenomenon (26/35 cases, 21 affecting right ovary). We identified in literature only one true bilateral case and 8 collisions accompanied by sole tumor in the contralateral ovary. Collision tumor pathogenesis is unknown, being the simplest theory the accidental development of two different tumors [6, 8]. Alternative hypotheses include:
1. common origin from pluripotent stem cell.
2. simultaneous proliferation of two different cell lines.
3. common carcinogenic agent interacting with different tissues and inducing different tumors, and
4. tumor growth promotion by microenvironmental changes induced by primary lesion such as oncogenic growth factor productions, neoangiogenesis and inflammation [6].
Collision tumors affect both pre- and postmenopausal women (median age: 50, range 18 to 83 years); however, the patients with benign lesions are younger (median age: 44, range 18 to 77 years) than patients bearing a malignant disease (median age 52, range 40 to 83 years). Their clinical manifestations include abdominal swelling (12/35 cases), palpable mass (12/35), abdominal pain (10/35), pelvic pain (7/35) and abnormal uterine bleeding (7/35) while less frequently they represent an accidental finding. The utility of tumor markers to predict benign vs. malignant lesion nature is limited as in single ovarian tumors. For instance, CA-125 levels have been found increased in 8/9 collisions including malignant lesion, but also in 2/8 benign collisions.
Generally, collision tumors are diagnosed postoperatively, by histopathological examination. Not expecting a collision, in our and most other cases, the imaging techniques usually to describe collision as a unique lesion. When mature cystic teratoma is present, classic ultrasound presentation, i.e. mixed content unilocular ovarian formation is commonly observed. However, it has been previously reported that the collisions with mature teratoma may have radiologic clues pointing towards the presence of two different tumors, such as the presence of non-fatty fluid in the cyst and a large solid component in the ovarian mass [6, 9].
Since most ovary collision tumors are not recognized by ultrasound or MRI, appropriate frozen section analysis and the surgeon and histopathologist awareness of the existence of collision tumors are fundamental to guide the type and extent of surgery. Importantly, collision tumors have to be histologically distinguished from mixed tumors, another type of composite ovarian tumor characterized by the intermingling of different components in one neoplastic mass (e.g. malignant mixed müllerian tumor) [6, 10]. In our 4 cases, benign tumors collided; thus, the curative treatment consisted on the excision of the affected ovary. In general, regarding both management strategy and prognosis establishment, the main factors to be considered are the types of colliding components, most aggressive component and the stage of malignant tumor.
Table 1: Collision tumor of the ovary (summary of previously published cases).
Conclusion
As far as our knowledge goes, this is the most complete revision of collision tumor in the ovary, which aims to alert clinicians, radiologists and histopathologists about the phenomenon. Its rarity makes it difficult to plan the research in order to understand the etiopathogenesis of collisions. Since collision tumors tend to be clinically and ultrasonographically/radiologically indistinguishable from single lesions, histological recognition of such neoplasms is important, allowing appropriate treatment to be offered to patients according to the individual biological characteristic of each of the components. Careful revision of the images, whenever histology confirms the coexistence of ovarian tumors without intermixing, may contribute to the identification of novel and probably more specific imaging clues pointing toward the collision tumors.
Acknowledgment
The authors declare no prior presentation/publication.
The patients gave their informed consent to the publication of this case series. Institutional Review Board ruled that approval was not required for this study.
Conflicts of interest
None.
Funding
None.
Article Info
Article Type
Case Report & Literature ReviewPublication history
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© 2023 Dusan Djokovic. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Hosting by Science Repository.
DOI: 10.31487/j.JSO.2019.03.06
Author Info
Fanni D
Loddo A
Martins A
Peiretti M
Borges A
Dusan Djokovic
Corresponding Author
Dusan DjokovicDepartment of Obstetrics & Gynecology, Hospital S. Francisco Xavier, Centro Hospitalar Lisboa Ocidental, Lisbon, Portugal
Table 1: Collision tumor of the ovary (summary of previously published cases).
- Bige O, Demir A, Koyuncuoglu M, Secil M, Ulukus C et al. (2009) Collision tumor: serous cystadenocarcinoma and dermoid cyst in the same ovary. Arch Gynecol Obstet 279: 767-770. [Crossref]
- Bolte C, Cullen R, Sazunic I (2017) Collision tumor between trichofolliculoma and melanocytic nevus. Int J Trichology 9: 181-183. [Crossref]
- Yazici O, Aksoy S, Ozhamam EU, Zengin N (2015) Squamous cell and neuroendocrine carcinoma of esophagus: Collision versus composite tumor: A case report and review of literature. Indian J cancer 52: 603-604. [Crossref]
- Kitagawa H, Kaneko M, Kano M, Ibuki Y, Amatya VJ et al. (2018) Coexistence of gastrointestinal stromal tumor and leiomyosarcoma of the stomach presenting as a collision tumor: A case report and review of literature. Pathol Int 68: 313-317. [Crossref]
- Kim VM, Goicochea L, Fang SH (2016) Case Report: Collision Tumour of Colon Leiomyosarcoma and Adenocarcinoma. J Clin Diagn Res 10: PD03-PD04. [Crossref]
- Singh AK, Singh M (2014) Collision tumours of ovary: a very rare case series. J Clin Diagn Res 8: FD14-FD16. [Crossref]
- Kim SH, Kim YJ, Park BK, Cho JY, Kim BH et al. (1999) Collision Tumors of the Ovary Associated with Teratoma: Clues to the Correct Preoperative Diagnosis. J Comput Assist Tomogr 23: 929-933. [Crossref]
- Brandwein-Gensler M, Urken M, Wang B (2004) Collision tumor of the thyroid: a case report of metastatic liposarcoma plus papillary thyroid carcinoma. Head Neck 26: 637-641. [Crossref]
- Patterson DM, Murugaesu N, Holden L, Seckl MJ, Rustin GJ (2008) A review of the close surveillance policy for stage I female germ cell tumors of the ovary and other sites. Int J Gynecol Cancer 18: 43-50. [Crossref]
- Lewin K (1987) Carcinoid tumors and the mixed (composite) glandular-endocrine cell carcinomas. Am J Surg Pathol 11: 71-86. [Crossref]
- Choudhary S, Adisesha S (2012) Collision tumors of ovary: A rare phenomenon. Int J Case Rep Image 3: 68-70.
- Pal S, Lobo F, Nayak S, Rao A, Bansal D (2014) Collision Tumors of Ovary: A Rare Entity. Int J Innovative Res Develop 3: 424-427.
- Hemalatha A, Ashok K, Anoosha K, Amita K, Raghuveer C (2015) A Morphologically Distinct Yet Seldom Seen Entity-Ovarian Collision Tumor. NJLM 24: 25-27.
- Papaziogas B, Souparis A, Grigoriou M, Tsiaousis P, Kogia E et al. (2007) A Rare Triple Coexistence of a Collision Tumor, A Benign Mature Cystic Teratoma And a Hemorrhagic Follicular Cyst of The Ovaries. Int J Surg 14.
- Sofoudis C (2018) Collision Tumor of the Ovary. Adjunction Cystic Teratoma and Serous Cystic Adenofi broma. Presentation of a Rare Case. J Surg Surg Res 2018: 7-9.
- GalloVallejo JL, González Paredes A, Navarro M, de la Ossa RM, José Rubí M (2007) Tumores de colisión ováricos asociados con teratoma. Progresos de Obstetricia y Ginecología 50: 316-319.
- Bostanci MS (2015) Collision Tumor: Dermoid Cysts and Mucinous Cystadenoma in the Same Ovary and a Review of the Literature. Obstetr Gynaecol Cases Rev 2.
- Kajo K, Machalekova K (2007) Collision of invasive serous adenocarcinoma and mature cystic teratoma in the ovary. Letter to the editor. APMIS 115: 769-771. [Crossref]
- Bhagat P, Dey P (2015) Bilateral Serous Adenocarcinoma of Ovary Coexisting with Mature Cystic Teratoma: Case Report and Review of Literature. APALM 2.
- Karki D, Karki S, Adhikari P, Dahal M, Adhikari M et al. (2018) Collision tumor of ovary: A rare entity. Asian J Med Sci 9: 61.
- Kocak C, Nalbant M (2015) Collision Tumor of Ovary: Invasive Serous Papillary Cystadenocarcinoma and Mature Cystic Teratoma. Sch J Med Case Rep 3: 1026-1031.
- Gauri Q, Verma S, Bairwa N, Ajay B, Dharmendra, Gauri L (2016) Collision tumour: bilateral mucinous adenocarcinoma coexisting with dermoid cyst in an ovary: an extreamly rare case. IJARR 1: 14-19.
- Naim M, Haider N, John VT, Hakim S (2011) Mature embryoid teratoma in the wall of a mucinous cyst adenoma of ovary in multiparous female. BMJ Case Rep 2011.
- Shi M, Al-Delfi F, Al Shaarani M, Knowles K, Cotelingam J (2017) Ovarian Adenomatoid Tumor Coexisting with Mature Cystic Teratoma: A Rare Case Report. Case Rep Obstet Gynecol 2017: 3702682. [Crossref]
- Kim JH (2016) Torsion of Collision Tumor: Dermoid Cyst and Fibrothecoma with Postmenopausal Bleeding. J Menopausal Med 22: 114-117. [Crossref]
- Dgani R, Rozenman D, Lifschitz-Mercer B (1993) Granulosa cell tumor arising in an ovary with mature cystic teratoma. Int J Gynaecol Obstet 41: 287-289. [Crossref]
- Chandanwale SS, Pal SS, Kumar HB, Sammi AB (2015) Serous Cystadenoma and Fibrothecoma: A Rare Combination in Collision Tumor of Ovary with Pseudo-Meigs Syndrome. J Pathol Transl Med 49: 163-166. [Crossref]
- Mishra A, Shamsunder S, Malik S, Zaheer S (2017) Collision tumour of ovary: a rare combination of fibrothecoma with serous cystadenoma. Int J Repro Contrac Obstet Gynecol 6: 1643.
- Prat J, Scully RE (1979) Sarcomas in ovarian mucinous tumors: a report of two cases. Cancer 44: 1327-1331. [Crossref]
- Doussis-Anagnostopoulou IA, Remadi S, Czernobilsky B (1996) Mucinous elements in Sertoli-Leydig and granulosa cell tumours: a revaluation. Histopathology 28: 372-375. [Crossref]
- Shahid M, Siddiqi A (2017) Primary well differentiated neuroendocrine tumor of ovary collides with Mucinous borderline tumor in a postmenopausal female: a report of case and review of literature. Pathologica 109: 375-378. [Crossref]
- Nirenberg A, Östör AG, Quinn MA (1992) Collision tumor: serous adenocarcinoma and steroid cell tumor of the ovary. Pathology 24: 60-62. [Crossref]
- Sengupta S, Pal S, Biswas BK, Chakrabarti S, Bose K et al. (2014) Collision tumor of ovary: a rare combination of dysgerminoma and serous cystadenocarcinoma. Bangladesh J Med Sci 13.
- Bichel P (1985) Simultaneous occurrence of a granulosa cell tumour and a serous papillary cystadenocarcinoma in the same ovary. A case report. Acta Pathol Microbiol Immunol Scand A 93: 175-181. [Crossref]
- Ozbey C, Erdogan G, Pestereli HE, Simsek T, Karaveli S (2005) Serous papillary adenocarcinoma and adult granulosa cell tumor in the same ovary. An unusual case. APMIS 113: 713-715. [Crossref]
- Heo JH, Lee YH, Kim GI, Kim TH, Kang H et al. (2011) A Case of Ovarian Microinvasive Mucinous Carcinoma and Co-existent Angiosarcoma. Korean J Pathol 45: 96.
- Schoolmeester JK, Keeney GL (2012) Collision tumor of the ovary: adult granulosa cell tumor and endometrioid carcinoma. Int J Gynecol Pathol 31: 538-540. [Crossref]
- Triratanachat S NS, Trivijitsilp P (2004) Granulosa cell tumor and ovarian hepatoid carcinoma as a collision tumor. Chula Med J 48: 101-109.
- McGregor SM, Schoolmeester JK, Lastra RR (2017) Collision Signet-Ring Stromal Tumor and Steroid Cell Tumor of the Ovary: Report of the First Case. Int J Gynecol Pathol 36: 261-264. [Crossref]