HIGH RISK OF GESTATIONAL TROPHOBLASTIC
NEOPLASIA DEVELOPMENT IN RECURRENT
HYDATIDIFORM MOLES WITH NLRP7
PATHOGENIC VARIATIONS
Kocabey M.1,a, Gulhan I.2, Koc A.1,b, Cankaya T.1, Karatasli V.2, Ileri A.3
*Corresponding Author: MD Mehmet Kocabey, Address: Güzelburc District Kıbrıs Street No: 81,
31175 Antioch/Hatay, e-mail: mehmet_kocabey@hotmail.com
page: 45
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CONCLUSION
In conclusion, we contribute to the scientific literature
with the clinical course and genetic results of 3 Turkish
FRHM cases caused by NLRP7 variants. We recommend
closer follow-up of RHM cases, since GTN development
is more frequent in these patients. In our opinion, genetic
testing can be proposed to patients whose first pregnancy
resulted in a mole, thus preventing possible delays and
complications. In addition, we suggest that all RHM cases
in our region should be principally investigated for pathogenic
NLRP7 variants, and that genetic counseling involving
a discussion about in vitro fertilization with oocyte
donation should be provided at the earliest opportunity to
families with pathogenic NLRP7 variants.
Acknowledgements.
None.
Conflict of Interest Statement.
The authors report no conflicts of interest.
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