Breast ovarian cancer syndrome

Authors

  • Abhirup H. R. Department of General Surgery, KVG Medical College and Hospital, Sullia, Dakshina Kannada, India
  • Priyanka Kenchetty Department of Dermatology, KVG Medical College and Hospital, Sullia, Dakshina Kannada, India
  • Aishwarya K. Chidananda Department of Radio-Diagnosis, KVG Medical College and Hospital, Sullia, Dakshina Kannada, India

DOI:

https://doi.org/10.18203/2349-2902.isj20213144

Keywords:

Carcinoma breast, Ovarian cancer, BRCA1, BRCA2

Abstract

BRCA1 and BRCA2, known as breast and ovarian cancer predisposition genes, were discovered in the 1990s. As part of a normal genetic structure, these genes are intrinsic to all human beings, but they are mutated in some individuals increasing the risk for breast and ovarian cancers development. BRCA1 is not only expressed in endocrine tissues but is also detected in other cells such as the neuroepithelial cells in the early stage of cell development. Like BRCA1, BRCA2 is also expressed in a wide variety of tissues and is observed with higher rates in the breast and thymus and with lower rates in the lung, ovary and spleen. We presented to you a case of 40 year old female admitted in surgical ward with lump in the left breast since 2 months with ipsilateral discrete axillary lymphadenopathy. Bilateral sono-mammography showed BIRADS V lesion in left breasts with satellite nodules. Ultrasonography of abdomen and pelvis showed large left adnexal solid mass lesion and right sided ovarian cyst with retrocaval, preaortic lymphadenopathy. Patient underwent a diagnostic laparoscopy which was converted to a laparotomy. Total abdominal hysterectomy with bilateral salphingo-oophorectomy was done. For the breast lump, patient underwent left sided modified radical mastectomy. Gene testing for revealed BRCA1 positivity. Chemotherapy was given to cover both breast and ovarian carcinoma. Patient came back with abdominal distension after 9 months and was offered palliative care. Patient succumbed for disease after 1 year after diagnosis. We reviewed the literature for the same.

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References

Baretta Z, Mocellin S, Goldin E, Olopade OI, Huo D. Effect of BRCA germline mutations on breast cancer prognosis: a systematic review and meta-analysis. Medicine (Baltimore). 2016;95(40):4975.

Hughes DJ, Ginolhac SM, Coupier I, Corbex M, Bressac-de-Paillerets B, Chompret A, et al. Common BRCA2 variants and modification of breast and ovarian cancer risk in BRCA1 mutation carriers. Cancer Epidemiol Biomarkers Prev 2005;14(1):265-7.

Xu K, Yang S, Zhao Y. Prognostic significance of BRCA mutations in ovarian cancer: an updated systematic review with meta-analysis. Oncotarget. 2017;8(1):285-302.

Nanda R, Schumm LP, Cummings S, Fackenthal JD, Sveen L, Ademuyiwa F, et al. Genetic testing in an ethnically diverse cohort of high-risk women: a comparative analysis of BRCA1 and BRCA2 mutations in American families of European and African ancestry. JAMA. 2005;294(15):1925-33.

Chodosh LA. Expression of BRCA1 and BRCA2 in normal and neoplastic cells. J Mammary Gland Biol Neoplasia. 1998;3(4):389-402.

Lane TF, Deng C, Elson A, Lyu MS, Kozak CA, Leder P. Expression of BRCA1 is associated with terminal differentiation of ectodermally and mesodermally derived tissues in mice. Genes Dev. 1995;9:2712-22.

O’Quinn C, Steele P, Ludman MD, Kieser K. Hereditary breast ovarian cancer syndromes in the Maritimes. J Obstet Gynaecol Can. 2010;32(2):155-9.

Hanna NN, Mentzer RM. Molecular genetics and management strategies in hereditary cancer syndromes. J Ky Med Assoc. 2003;101(3):100-7.

Neri A, Rabinerson D, Kaplan B, Levani H. Hereditary ovarian cancer. Isr J Med Sci. 1995;31(2-3):172-5.

Casey MJ, Synder C, Bewtra C, Narod SA, Watson P, Lynch HT. Intra-abdominal carcinomatosis after prophylactic oophorectomy in women of hereditary breast ovarian cancer syndrome kindreds associated with BRCA1 and BRCA2 mutations. Gynecol Oncol. 2005;97(2):457-67.

Piek JM, vanDiest PJ, Zweemer RP, Jansen JW, Poort-Keesom RJ, Menko FH, et al. Dysplastic changes in prophylactically removed Fallopian tubes of women predisposed to developing ovarian cancer. J Pathol. 2001;195(4):451-6.

Lee YJ, Lee SW, Kim KR, Jung KH, Lee JW, Kim YM. Pathologic findings at risk-reducing salpingo-oophorectomy (RRSO) in germline BRCA mutation carriers with breast cancer: significance of bilateral RRSO at the optimal age in germline BRCA mutation carriers. J Gynecol Oncol. 2017;28(1):3.

Leeper K, Garcia R, Swisher E, Goff B, Greer B, Paley P. Pathologic findings in prophylactic oophorectomy specimens in high-risk women. Gynecol Oncol. 2002;87(1):52-6.

Schlosshauer PW, Cohen CJ, Penault-Llorca F, Miranda CR, Bignon Y, Dauplat J, et al. Prophylactic oophorectomy: a morphologic and immunohistochemical study. Cancer. 2003;98(12):2599-606.

Barakat RR, Federici MG, Saigo PE, Robson ME, Offit K, Boyd J. Absence of premalignant histologic, molecular or cell biologic alterations in prophylactic oophorectomy specimens from BRCA1 heterozygotes. Cancer. 2000;89(2):383-90.

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Published

2021-07-28

How to Cite

R., A. H., Kenchetty, P., & Chidananda, A. K. (2021). Breast ovarian cancer syndrome. International Surgery Journal, 8(8), 2454–2456. https://doi.org/10.18203/2349-2902.isj20213144

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Section

Case Reports