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Evidencia Médica e Investigación en Salud

ISSN 2007-6053 (Print)
Órgano oficial de difusión de los Hospitales Regionales de Alta Especialidad (HRAE)
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2014, Number 2

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Evid Med Invest Salud 2014; 7 (2)

Feminizing genitoplasty a case report

Lazo CÓA, Vanzzini GMA, Maldonado VR, Manzo PG
Full text How to cite this article

Language: Spanish
References: 10
Page: 84-88
PDF size: 342.27 Kb.


Key words:

Congenital adrenal hyperplasia, genitoplasty feminizing, vaginoplasty.

ABSTRACT

Introduction: Disorders of sexual differentiation formerly called hermaphroditism, has been documented since ancient times; this term refers to the presence of ambiguous genitalia ie without clear evidence of the assignable sex. The most common cause of female pseudohermaphroditism is congenital adrenal hyperplasia, an inherited disorder of adrenal steroidogenesis. Objective: The aim of this paper is to present a patient under three years of age with this diagnosis, who after being comprehensively evaluated by a multidisciplinary team of Regional Specialty Hospital del Bajio, surgical treatment was performed genitoplasty feminizing type (clitoroplasty and vaginoplasty) to give favorable results. Material and methods: Review of medical records and updated literature search. Results: Two months after surgery, patient has good general condition, with female external genitalia, normal anatomic appearance. Conclusions: All patients with disorders of sexual differentiation, must undergo a comprehensive evaluation by a committee of professionals in this area, clitoroplasty must be made early and if possible also vaginoplasty should be completed in one surgical time that during the procedure respects the neurovascular bundle, thereby retaining the sensitivity and vascularity of the clitoral glans.


REFERENCES

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  2. Sharma S, Gupta DK. Gender assignment and hormonal treatment for disorders of sexual differentiation. Pediatr Surg Int. 2008; 24: 1131-1135.

  3. Escala AJM, Cadena Y, José LP, Ángel LG, Retamal MG, Letelier N. Genitoplastía feminizante en hiperplasia suprarrenal congénita: ¿una o dos etapas quirúrgicas? Arch Esp Urol. 2009; 62 (9): 724-730.

  4. Rink RC, Adams MC. Feminizing genitoplasty: state of the art. World J Urol. 1998; 16: 212-218.

  5. Gupta DK, Shilpa S, Amini AC, Gupta M, Aggarwal G, Deepika G et al. Congenital adrenal hyperplasia: long-term evaluation of feminizing genitoplasty and psychosocial aspects. Pediatr Surg Int. 2006; 22: 905-909.

  6. Núñez S, Laiseca N, Sorando E, López A, Martínez G. Reconstrucción genital integral en la hiperplasia suprarrenal congénita: sensibilidad, estética y función. Cir Plast Iberolatinoam. 2010; 36 (1): 79-86.

  7. Cardosa MIR, Sotelo CN. Hiperplasia suprarrenal congénita: diagnóstico y tratamiento en 20 casos. Revista Mexicana de Pediatría. 2007; 74 (6): 251-256.

  8. Islas DLP, Jiménez JJR, Verduzco GM. Pseudohermafroditismo femenino por hiperplasia suprarrenal congénita. Reporte de un caso. Rev Mex Pediatr. 2005; 72 (2): 74-77.

  9. Puri P, Hollwarth T. Pediatric surgery. 2nd edition. Germany: Springer; 2006.

  10. Ashcraft K, Holder T. Ashcraft Pediatric Surgery. 5th ed. Philadelphia: Elsevier; 2010.




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Evid Med Invest Salud. 2014;7