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 Table of Contents 
CASE REPORT
Year : 2018  |  Volume : 9  |  Issue : 4  |  Page : 210-211  

Malignant mixed mullerian tumor secondary to tamoxifen for Ca breast: Shadow of the past!


1 Department of Obstetrics and Gynaecology, S. P. Medical College, Bikaner, Rajasthan, India
2 Department of Obstetrics and Gynaecology, SMS Medical College, Jaipur, Rajasthan, India

Date of Web Publication31-Dec-2018

Correspondence Address:
Vinu Choudhary
Department of Obstetrics and Gynaecology, SMS Medical College, Jaipur, Rajasthan
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/jmh.JMH_79_18

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   Abstract 


Tamoxifen is used in the treatment of hormone-responsive breast cancer because of its antiestrogenic effect. However, it also has an estrogenic effect on the uterus, thereby increasing the risk of endometrial hyperplasia, endometrial polyp, and malignant mixed Mullerian tumor (MMMT). This case describes the pathogenesis and risk of MMMT due to long-term tamoxifen intake in hormone-responsive breast cancer.

Keywords: Antioestrogenic effect, malignant mixed mullerian tumor, tamoxifen


How to cite this article:
Bisu S, Choudhary V. Malignant mixed mullerian tumor secondary to tamoxifen for Ca breast: Shadow of the past!. J Mid-life Health 2018;9:210-1

How to cite this URL:
Bisu S, Choudhary V. Malignant mixed mullerian tumor secondary to tamoxifen for Ca breast: Shadow of the past!. J Mid-life Health [serial online] 2018 [cited 2019 Jan 22];9:210-1. Available from: http://www.jmidlifehealth.org/text.asp?2018/9/4/210/249153




   Introduction Top


A malignant mixed Müllerian tumor (MMMT), also known as malignant mixed mesodermal tumor, MMMT[1] is a malignant neoplasm found in the uterus, the ovaries, the  Fallopian tube More Detailss and other parts of the body that contains both carcinomatous and sarcomatous components. MMMT account for between 2% and 5%[1],[2] of all tumors derived from the body of the uterus and are found predominantly in postmenopausal women with an average age of 66 years. Risk factors are similar to those of adenocarcinomas and include obesity, exogenous estrogen therapies, nulliparity, and tamoxifen therapy. There is evidence that some tumors are better explained by the composition theory, due to the aggressive nature of the epithelial cells involved which tend to metastasize much more readily than the sarcomal component. Three predominant theories are proposed for its origin:

  1. The collision theory
  2. The combination theory
  3. In conversion theory.


Tamoxifen also has a weak estrogenic effect on the endometrium, thereby increasing the risk of endometrial polyp, endometrial hyperplasia, endometrial adenocarcinoma, and sarcoma of the uterus. We report a case of uterine MMMT occurring with tamoxifen therapy in a patient with a history of breast cancer.[3]


   Case Report Top


A 58-year-old woman presented with bleeding per vaginum, generalized weakness, decreased urine output, and abdominal distension. Imaging revealed a large polypoid mass within the endometrial cavity, and endometrial biopsy was suggestive of MMMT. The patient underwent a total abdominal hysterectomy, bilateral salpingo-oophorectomy, omentectomy, and bilateral pelvic and para-aortic lymphadenectomy. Histopathological examination confirmed the diagnosis of MMMT infiltrating less than half of the myometrium. Cervix, bilateral adnexae, omentum, and all lymph nodes were free of tumor. The patient had a history of estrogen receptor (ER)-positive breast cancer, diagnosed 3 years back and was on tamoxifen 20 mg OD daily dose.

At present, the patient is on adjuvant radiation therapy and chemotherapy comprising of paclitaxel at 175 mg/m2 followed by carboplatin for a total of 6 cycles every 21 days. As shown in [Figure 1] Specimen included uterus with bilateral ovaries and [Figure 2] Shows HPR depicting malignant stromal component with spindle cell showing marked nuclear pleo morphism and nuclear hyper chromasia.
Figure 1: Gross cut section of uterus

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Figure 2: Malignant stromal component with spindle cells displaying marked nuclear pleomorphism and nuclear hyperchromasia, ×40

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   Discussion Top


MMMTs, although very rare, with an incidence of <2/100 000 women in a year, are aggressive tumors of the uterus resulting in >15% of deaths. Tamoxifen intake for hormone-responsive breast cancer is one of the factors that has been associated with the development of MMMT. Depending on the target organs, tamoxifen exerts both an estrogenic and an antiestrogenic effect. The variability of response to tamoxifen depends on the differences in tissue distribution of ER subtypes (ERα and ERβ are two subtypes of ERs),[3],[4] various transcriptional activating factors and function of co-regulator proteins. Due to its antiestrogenic effect, it is used in the treatment of ER-positive breast cancer in adjuvant and metastatic settings.

The outcome of MMMTs is determined primarily by the depth of invasion and stage. As with endometrial carcinomas, the prognosis is influenced by the grade and type of the adenocarcinoma, being poorest with serous differentiation.

Points to be remembered

  • Although tamoxifen is used in the treatment of hormone-responsive breast cancer due to its antiestrogenic effect, it has an estrogenic effect on the uterus, thus it increases the risk of MMMT and other neoplasms
  • Variability of response to tamoxifen depends on the differences in tissue distribution of ERs, function of coregulatory proteins.[4],[5]



   Conclusion Top


Uterine carcinosarcoma is a rare, highly aggressive, rapidly progressing neoplasm associated with a poor prognosis that has not significantly improved in the past 30 years despite advances in imaging and adjuvant therapies. The optimal management modality remains controversial, with discrepancies regarding patient outcome to lymphadenectomy and radiation therapy. To maximize the probability of cure, prospective multicentric, multi-institutional collaborative randomized trials of treatment protocols have to be performed.

Declaration of patient consent

The authors certify that they have obtained all appropriate patient consent forms. In the form the patient(s) has/have given his/her/their consent for his/her/their images and other clinical information to be reported in the journal. The patients understand that their names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.



 
   References Top

1.
Lorusso D, Martinelli F, Mancini M, Sarno I, Ditto A, Raspagliesi F, et al. Carboplatin-paclitaxel versus cisplatin-ifosfamide in the treatment of uterine carcinosarcoma: A retrospective cohort study. Int J Gynecol Cancer 2014;24:1256-61.  Back to cited text no. 1
    
2.
Moy B, Lee RJ, Smith M. Natural products in cancer chemotherapy. In: Brunton LL, Chabner BA, Knollmann BC, editors. Goodman & Gilman's The Pharmacological Basis of Therapeutics. New York: McGraw Hill; 2011. p. 1757.  Back to cited text no. 2
    
3.
Wells M, Oliva E, Palacios J. Mixed epithelial and mesenchymal tumors. In: Kurman RJ, Carcangiu ML, Herrington S, editors. World Health Organisation Classification of Tumours of Female Reproductive Organs. Lyon: International Agency for Research on Cancer; 2014. p. 150-1.  Back to cited text no. 3
    
4.
Akhavan A, Akhavan Tafti M, Aghili F, Navabii H. Uterine adenosarcoma in a patient with history of breast cancer and long-term tamoxifen consumption. BMJ Case Rep 2012;2012. pii: bcr2012006590.  Back to cited text no. 4
    
5.
El-Nashar SA, Mariani A. Uterine carcinosarcoma. Clin Obstet Gynecol 2011;54:292-304.  Back to cited text no. 5
    


    Figures

  [Figure 1], [Figure 2]



 

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