Ovotesticular disorder of sex development (OT-DSD) is a condition in which, both testicular tissue and ovarian tissue are co-existent in the same gonad (ovotestis) or independently in separate gonads characterizing the anatomical form of lateral ovotestis. Here, in this study, we report a case of lateral ovotestis associated with a chimera, Chi 46,XX/46,XY. He presented for fertility assessment and karyotyping because of DSD characterized by gynecomastia associated with hypospadias; Karyotyping of peripheral blood revealed a 46,XX/46,XY chimeric condition confirmed by SNP array analysis. After surgical exploration, an hemi-uterus with its tube and gonad was found and remove. Histology revealed ovarian tissue with follicules at different stage while semen analysis revealed a severe oligoastheno teratozoospermia. A gonad was palpable on the right hemiscrotum and ultrasound showed a testis structure. The patient clamed conservation of its testicle and requested bilateral mastectomy. A multidisciplinary approach was warranted to establish this rare entity’s diagnosis and its management. In the case of gonad preservation, the risk of gonadoblastom is to be discussed and follow up recommended.
References
[1]
Diamond, D.A. and Yu, R.N. (2012) Sexual Differentiation: Normal and Abnormal. In: Wein, A.J., Kavoussi, L.R., Novick, A.C., Partin, A.W. and Peters, C.A., Eds., Campbell-Walsh Urology (10th Edition), Saunders Elsevier, 3613-3614.
[2]
van Bever, Y., Wolffenbuttel, K.P., Brüggenwirth, H.T., Blom, E., de Klein, A., Eussen, B.H.J., et al. (2017) Multiparameter Investigation of a 46,XX/46,XY Tetragametic Chimeric Phenotypical Male Patient with Bilateral Scrotal Ovotestes and Ovulatory Activity. SexualDevelopment, 12, 145-154. https://doi.org/10.1159/000479946
[3]
Özdemir, M., Kavak, R.P., Yalcinkaya, I. and Guresci, K. (2019) Ovotesticular Disorder of Sex Development: An Unusual Presentation. JournalofClinicalImagingScience, 9, 34. https://doi.org/10.25259/jcis_45_2019
[4]
Syryn, H., Van De Vijver, K. and Cools, M. (2021) Ovotesticular Difference of Sex Development: Genetic Background, Histological Features, and Clinical Management. HormoneResearchinPaediatrics, 96, 180-189. https://doi.org/10.1159/000519323
[5]
Wiersma, R. and Ramdial, P.K. (2009) The Gonads of 111 South African Patients with Ovotesticular Disorder of Sex Differentiation. JournalofPediatricSurgery, 44, 556-560. https://doi.org/10.1016/j.jpedsurg.2008.08.013
[6]
Ganie, Y., Aldous, C., Balakrishna, Y. and Wiersma, R. (2017) Disorders of Sex Development in Children in Kwazulu-Natal Durban South Africa: 20-Year Experience in a Tertiary Centre. JournalofPediatricEndocrinologyandMetabolism, 30, 11-18. https://doi.org/10.1515/jpem-2016-0152
[7]
Madan, K. (2020) Natural Human Chimeras: A Review. EuropeanJournalofMedicalGenetics, 63, Article ID: 103971. https://doi.org/10.1016/j.ejmg.2020.103971
[8]
Berger-Zaslav, A., Mehta, L., Jacob, J., Mercado, T., Gadi, I., Tepperberg, J.H., et al. (2009) Ovotesticular Disorder of Sexual Development (True Hermaphroditism). Urology, 73, 293-296. https://doi.org/10.1016/j.urology.2008.08.428
[9]
World Health Organization (2021) WHO Laboratory Manual for the Examination and Processing of Human Semen. 6th Edition, WHO Press. https://www.who.int/publications/i/item/9789240030787
[10]
Lee, P.A., Houk, C.P., Ahmed, S.F. and Hughes, I.A. (2006) Consensus Statement on Management of Intersex Disorders. Pediatrics, 118, e488-e500. https://doi.org/10.1542/peds.2006-0738
[11]
Wettasinghe, K.T., Sirisena, N.D., Andraweera, P.H., Jayasekara, R.W. and Dissanayake, V.H.W. (2012) A Case Series of Five Sri Lankan Patients with Ovotesticular Disorder of Sex Development. ClinicalPediatricEndocrinology, 21, 69-73. https://doi.org/10.1297/cpe.21.69
[12]
Matsui, F., Shimada, K., Matsumoto, F., Itesako, T., Nara, K., Ida, S., et al. (2011) Long-Term Outcome of Ovotesticular Disorder of Sex Development: A Single Center Experience. InternationalJournalofUrology, 18, 231-236. https://doi.org/10.1111/j.1442-2042.2010.02700.x
[13]
Scarpa, M., Lesma, A., Di Grazia, M. and Rigamonti, W. (2019) Ovotesticular Differences of Sex Development: Male or Female? Case Series. ItalianJournalofPediatrics, 45, Article No. 66. https://doi.org/10.1186/s13052-019-0660-8
[14]
Baetens, D., Stoop, H., Peelman, F., Todeschini, A., Rosseel, T., Coppieters, F., et al. (2017) NR5A1 Is a Novel Disease Gene for 46,XX Testicular and Ovotesticular Disorders of Sex Development. GeneticsinMedicine, 19, 367-376. https://doi.org/10.1038/gim.2016.118
[15]
Bashamboo, A., Donohoue, P.A., Vilain, E., Rojo, S., Calvel, P., Seneviratne, S.N., et al. (2016) A Recurrent p.Arg92Trp Variant in Steroidogenic Factor-1 (NR5A1) Can Act as a Molecular Switch in Human Sex Development. HumanMolecularGenetics, 25, 3446-3453. https://doi.org/10.1093/hmg/ddw186
[16]
Kawamura, R., Kato, T., Miyai, S., Suzuki, F., Naru, Y., Kato, M., et al. (2020) A Case of a Parthenogenetic 46,XX/46,XY Chimera Presenting Ambiguous Genitalia. JournalofHumanGenetics, 65, 705-709. https://doi.org/10.1038/s10038-020-0748-4
[17]
Ramsay, M., Pfaffenzeller, W., Kotze, E., Bhengu, L., Essop, F. and De Ravel, T. (2008) Chimerism in Black Southern African Patients with True Hermaphroditism 46,XX/47XY, +21 and 46,XX/46,XY. AnnalsoftheNewYorkAcademyofSciences, 1151, 68-76. https://doi.org/10.1111/j.1749-6632.2008.03570.x
[18]
Cho, S., Lee, H.Y., Kim, M., Lyoo, S. and Lee, S.D. (2020) A Case of 46,XX/46,XX Chimerism in a Phenotypically Normal Woman. InternationalJournalofLegalMedicine, 134, 2045-2051. https://doi.org/10.1007/s00414-020-02296-y
[19]
Schoenle, E., Schmid, W., Schinzel, A., Mahler, M., Ritter, M., Schenker, T., et al. (1983) 46,XX/46,XY Chimerism in a Phenotypically Normal Man. HumanGenetics, 64, 86-89. https://doi.org/10.1007/bf00289485
[20]
Verp, M.S., Harrison, H.H., Ober, C., Oliveri, D., Amarose, A.P., Lindgren, V., et al. (1992) Chimerism as the Etiology of a 46,XX/46,XY Fertile True Hermaphrodite. FertilityandSterility, 57, 346-349. https://doi.org/10.1016/s0015-0282(16)54843-2
[21]
Bottega, R., Cappellani, S., Fabretto, A., Spinelli, A.M., Severini, G.M., Aloisio, M., et al. (2019) Could a Chimeric Condition Be Responsible for Unexpected Genetic Syndromes? The Role of the Single Nucleotide Polymorphism-Array Analysis. MolecularGenetics&GenomicMedicine, 7, e546. https://doi.org/10.1002/mgg3.546
[22]
Green, A.J., Barton, D.E., Jenks, P., Pearson, J. and Yates, J.R. (1994) Chimaerism Shown by Cytogenetics and DNA Polymorphism Analysis. JournalofMedicalGenetics, 31, 816-817. https://doi.org/10.1136/jmg.31.10.816
[23]
Conlin, L.K., Thiel, B.D., Bonnemann, C.G., Medne, L., Ernst, L.M., Zackai, E.H., et al. (2010) Mechanisms of Mosaicism, Chimerism and Uniparental Disomy Identified by Single Nucleotide Polymorphism Array Analysis. HumanMolecularGenetics, 19, 1263-1275. https://doi.org/10.1093/hmg/ddq003
[24]
Sheets, K.M., Baird, M.L., Heinig, J., Davis, D., Sabatini, M. and Starr, D.B. (2017) A Case of Chimerism-Induced Paternity Confusion: What ART Practitioners Can Do to Prevent Future Calamity for Families. JournalofAssistedReproductionandGenetics, 35, 345-352. https://doi.org/10.1007/s10815-017-1064-6
[25]
Yu, N., Kruskall, M.S., Yunis, J.J., Knoll, J.H.M., Uhl, L., Alosco, S., et al. (2002) Disputed Maternity Leading to Identification of Tetragametic Chimerism. NewEnglandJournalofMedicine, 346, 1545-1552. https://doi.org/10.1056/nejmoa013452
[26]
Li, Z., Liu, J., Peng, Y., Chen, R., Ge, P. and Wang, J. (2020) 46,XX Ovotesticular Disorder of Sex Development (True Hermaphroditism) with Seminoma: A Case Report. Medicine, 99, e22530. https://doi.org/10.1097/md.0000000000022530
[27]
Ulbright, T.M. and Young, R.H. (2014) Gonadoblastoma and Selected Other Aspects of Gonadal Pathology in Young Patients with Disorders of Sex Development. SeminarsinDiagnosticPathology, 31, 427-440. https://doi.org/10.1053/j.semdp.2014.07.001
[28]
Hercent, A., Amar, E., Valent, A., Belloc, S., Ferraretto, X., Hermieu, J., et al. (2019) Various Genital and Reproductive Phenotypes in 46,XX/46,XY Chimeras. SexualDevelopment, 13, 271-277. https://doi.org/10.1159/000510532
[29]
Charalsawadi, C., Jaruratanasirikul, S., Hnoonual, A., Chantarapong, A., Sangmanee, P., Trongnit, S., et al. (2022) Case Report: Molecular Analysis of a 47,XY, +21/46,XX Chimera Using SNP Microarray and Review of Literature. FrontiersinGenetics, 13, Article 802362. https://doi.org/10.3389/fgene.2022.802362
[30]
He, Y., Yan, Y., Lv, Y. and Zeng, J. (2024) Molecular Analysis of Parthenogenetic Chimerism in a 46,XX/46,XY Patient with Idiopathic Oligoasthenoteratozoospermia. CytogeneticandGenomeResearch, 164, 16-22. https://doi.org/10.1159/000538396
[31]
Chen, L., Wang, L., Zeng, Y., Yin, D., Tang, F., Xie, D., et al. (2024) A Prenatal Case Misunderstood as Specimen Confusion: 46,XY/46,XY Chimerism. BMCPregnancyandChildbirth, 24, Article No. 126. https://doi.org/10.1186/s12884-024-06321-5