Authors:
Sebnem Alanya Tosun1, Alptekin Tosun2* and Enis Ozkaya3
Affiliation(s):
1Department of Obstetrics & Gynecology, Bulancak Hospital, Giresun
2Department of Radiology, Giresun University Hospital, Giresun
3Department of Obstetrics & Gynecology, Zeynep Kamil Hospital, Istanbul
Dates:
Received: 05 March, 2015; Accepted: 28 April, 2015; Published: 30 April, 2015
*Corresponding author:
Alptekin Tosun, Department of Radiology, Giresun University Hospital, Giresun, Email: @
Citation:
Tosun SA, Tosun A, Ozkaya E (2015) Premature Ovarian Failure in a Patient with Robertsonian Translocation Rob (14;15): Is it only a Coincidence? Int J Radiol Radiat Oncol 1(1): 002-003.
Copyright:
© 2015 Tosun SA, et al. 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.

Women have fixed ovarian follicles after birth and the number of the follicles declines with age. The decrease can be regulated by genetic, hormonal and/or therapy procedures. Radiation exposure can lead to premature ovarian failure (POF). POF is defined as interruption of the ovarian function in an adolescent woman. Genetic disorders including translocations and damage on the ovarian tissue may result POF. The essential diagnostic criteria is an adolescent woman younger than 40 years of age. The diagnosis depends on at least 4 months of amenorrhea and increased FSH levels (≥40 mIU/ml) in 2 blood samples at an interval of 1 month.

Introduction

Premature ovarian failure (POF) is defined as interruption of the ovarian function in an adolescent woman before 40 years of age. Functional failure in the normal ovary leads to disturbance in the blood hormone levels which in turn leads to oligo- or amenorrhea. Low estrogen levels and increased gonadotrophins result as primary or secondary amenorrhea, and patients experience recurrence abortions [11. Laml T, Preyer O, Umek W, Hengstschlager M, Hanzal E (2002) Genetic disorders in premature ovarian failure. Hum Reprod Update 8:483-491. ]. The essential diagnostic criteria is an adolescent woman younger than 40 years of age. The diagnosis depends on at least 4 months of amenorrhea and increased FSH levels (≥40 mIU/ml) in 2 blood samples over a 1 month period [22. Anasti JN (1998) Premature ovarian failure: an update. Fertil Steril 70: 1-15.]. The histopathology of the ovarian tissue obtained by mini-laparoscopic surgery can confirm the diagnosis. Bilaterally full thickness ovarian biopsy differentiates POF from resistant ovary syndrome [33. Pellicano M, Zullo F, Cappiello F, Di Carlo C, Cirillo D, (2000) Minilaparoscopic ovarian biopsy performed under conscious sedation in women with premature ovarian failure. J Reprod Med 45: 817-822.].

Genetic disorders and damage on the ovarian tissue by surgery, radio- or chemotherapy may result POF. Rare causes including galactosaemia will usually diagnosed in early ages. The analysis of the family history will show variable prevalence of familiar POF up to 31%. [11. Laml T, Preyer O, Umek W, Hengstschlager M, Hanzal E (2002) Genetic disorders in premature ovarian failure. Hum Reprod Update 8:483-491. ,44. van Kasteren YM, Schoemaker J (1999) Premature ovarian failure. A systematic review on therapeutic interventions to restore ovarian function and achieve pregnancy. Hum Reprod Update 5: 483-492. ]. X monosomy as in Turner's syndrome, X deletions and translocations may cause POF. The mutations on the phosphomannomutase 2 gene, the FSH receptor gene, the galactose-1-phosphate uridyltransferase gene, the blepharophimosis gene with chromosome 3q and the autoimmune regulator gene are the autosomal abnormalities seen in POF [11. Laml T, Preyer O, Umek W, Hengstschlager M, Hanzal E (2002) Genetic disorders in premature ovarian failure. Hum Reprod Update 8:483-491. ].

Case Report

A 28-year-old single nulliparous woman presented with a history of oligomenorrhea. Patient had a history of oral contraceptive use which was of inadequate dosage. Physical examination was in normal limits. Body measures were as follows: waist: 86 cm, buttocks: 100 cm. Phenotypic appearance was obese. She has 85 kg weight and 160 cm height. Her body-mass-index (BMI) was increased (33.2). Analysis of her hormone levels revealed high FSH and low E2 levels. Anti-TPO and anti-TG levels were in normal limits. In the lights of these findings, she was diagnosed as having POF. Hormone replacement therapy was prescribed to the patient. Peripheral blood sample received to research chromosomal abnormality. 20 metaphase period were analyzed with Giemsa-trypsin (GTG) banding method (300-400 bandwidth) and high resolution banding (HRB) method (550-850 bandwidth). Chromosomal analysis revealed an abnormality with 45, XX, rob (14,15) (q10; q10) chromosomal sequence. Karyotype displayed 45 chromosomes. Chromosomes of 14 and 15 were not existing to the sequence. Instead of this condition, an additional strange chromosome were obtained in the karyotype. The banding pattern of the short and long arms of the strange chromosome was showing similarity to the chromosome 14 and 15. The findings were shining lights on the presence of a nonhomologous Robertsonian translocation (RT); therefore 45, XX, rob (14,15) (q10:q10) was diagnosed.

Discussion

The average age of menarche has decreased in the recent years. Despite of decreased age of menarche, the mean age of menopause shows no change. The mean age of menopause is around the 50 years. The loss of functional follicles determines under the age of 40 years is defined as having primary ovarian failure (POF) [55. Burton KA, Van Ee CC, Purcell K, Winship I, Shelling AN (2000) Autosomal translocation associated with premature ovarian failure. J Med Genet 37: E2.]. The incidence of POF in the woman population is approximately 1-2% [66. Coulam CB, Adamson SC, Annegers JF (1986) Incidence of premature ovarian failure. Obstet Gynecol 67: 604-606.]. Most common presenting symptom is amenorrhea. Decreased levels of estrogen and increased levels of FSH and LH demonstrate on hormone sampling. Iatrogenic interventions such as radio- and/or chemotherapy, surgery may reduce the number of the follicles. Chromosomal abnormalities are also responsible. X chromosome is usually affected. XO Turner's syndrome, 47, XXX, X chromosome mosaics (45,XO/46,XX, 46 XX/47,XXX, 45,XO/46,XX/47,XXX), X chromosome deletions and inversions and X;autosome balanced translocations [55. Burton KA, Van Ee CC, Purcell K, Winship I, Shelling AN (2000) Autosomal translocation associated with premature ovarian failure. J Med Genet 37: E2.]. Patients with Robertsonian Translocation usually present with history of recurrent abortions and hence POF may be seen in a teenage woman as well.

Chromosomal analysis is essential in both men and woman. The defect on the chromosomes have a significant effect on the fertilization. Chromosomal abnormalities have high incidence in the female gender than males [77. Venkateshwari A, Srilekha A, Tella S, Nallari P, Jyothy A (2010) A Robertsonian translocation rob (14;15) (q10:q10) in a patient with recurrent abortions: a case report. J Reprod Infertil 11: 197-200.]. RT may occur by mutation or separation in the chromosomes. The individual has normal phenotype appearance, hence has a potential for unbalanced gametes and offspring [88. Venkateshwari A, Srimanjari K, Srilekha A, Begum A, Sujatha M, et al. (2012) Mosaic triple X syndrome in a female with primary amenorrhea. Indian J Hum Genet 18: 246-249.,99. Kummer N, Benadiva C, Feinn R, Mann J, Nulsen J, et al. (2011) Factors that predict the probability of a successful clinical outcome after induction of oocyte maturation with a gonadotropin-releasing hormone agonist. Fertil Steril 96: 63-68.].

Cytogenetic analyses of teenage woman with POF has an importance to research the probable existance of chromosomal abnormalities. In cases less than 40 years of age, POF appears infrequently. After analysis of adequate genetic research, patients can get prompt diagnosis and also avoid unnecessary therapies. This approach leads to inform patient for the future reproductive decision.


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