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Revista Mexicana de Cirugía Endoscópica

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2018, Number 2

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Rev Mex Cir Endoscop 2018; 19 (2)

Testicular torsion in the inguinal canal with recurrent hernia, in a patient with complete androgenic insensitivity syndrome («feminizing testicle»)

Baca PJE, Leuchter IJ, Domínguez CLG, Mayagoitia GJC
Full text How to cite this article

Language: Spanish
References: 13
Page: 82-86
PDF size: 309.56 Kb.


Key words:

Androgenic insensitivity syndrome, feminizing testis, inguinal hernia, inguinal hernia repair, testicular torsion, orchiectomy.

ABSTRACT

Introduction: The finding of a testicle with acute torsion at the level of the deep inguinal ring is uncommon during a hernia repair. The androgen insensitivity syndrome or «feminizing testicle» is a recessive genetic disorder linked to chromosome X; it is characterized by the resistance of the target tissues to the action of male hormones, preventing normal male genitalia development of genetically male individuals (46, XY). We present the case of a recurrent inguinal hernia with testicular torsion in the inguinal canal. Case report: This is a phenotypically female patient of 36 years. Primary amenorrhea. A clinical history of surgery at two months of age due to a tumor in the left upper lip and right inguinal hernia repair three years ago. Seen at the emergency room for inguinal and right lower quadrant throbbing pain, progressive and increasing in intensity, accompanied by nausea and vomiting. Physical examination: Pain with pressure on the right lower quadrant and inguinal region with negative McBurney and Blumberg, a palpable mass of 3.5 × 2.5 cm on right inguinal region, extremely painful with pressure, fixed and not reducible, external genitalia without abnormalities, leukocytes count reported of 12,000. Abdominal tomography showing: Absence of uterus, ovaries and other female annexes, and a 3.5 × 2.5 cm mass in the right inguinal canal. With a diagnosis of strangulated recurrent right inguinal hernia. Then a diagnostic laparoscopic surgery was performed, finding a hematoma in the internal ring of the inguinal canal and torsion of the right testicle inside the internal ring. Orchiectomy and a TAPP hernia repair with heavy polypropylene mesh were performed. In the postoperative period, karyotype and chromatin were requested with a 46, XY and absence of Barr corpuscles results.


REFERENCES

  1. Morris JM, Mahesh VB. Further observations on the syndrome “testicular feminization”. Am J Obstet Gynecol. 1963; 87: 731-748.

  2. Morris JM. The syndrome of testicular feminization in male pseudohermaphrodites. Am J Obstet Gynecol. 1953; 65: 1192-1211.

  3. Brown CJ, Goss SJ, Lubahn DB, Joseph DR, Wilson EM, French FS et al. Androgen receptor locus on the human X chromosome: Regional localization to Xq11-12 and description of a DNA polymorphism. Am J Hum Genet. 1989; 44: 264-269.

  4. Ahmed SF, Cheng A, Dovey L, Hawkins JR, Martin H, Rowland J et al. Phenotypic features, androgen receptor binding, and mutational analysis in 278 clinical cases reported as androgen insensitivity syndrome. J Clin Endocrinol Metab. 2000; 85: 658-665.

  5. Maki Kusumi, Makiko Mitsunami, Hiroki Onoue, Momo Noma, Fumiko Matsumura, Chisa Tabata, et al. Complete androgen insensitivity syndrome and anti-Müllerian hormone levels before and after laparoscopic gonadectomy. Gynecology and Minimally Invasive Therapy. 2017; 6: 126-128.

  6. Solari A, Groisman B, Bidondo MP, Cinca C, Alba L. Síndrome de insensibilidad completa a los andrógenos: Diagnóstico y características clínicas. Arch Argent Pediatr. 2008; 106: 265-268.

  7. Cohen-Kettenis PT. Psychosocial and psychosexual aspects of disorders of sex development. Best Pract Res Clin Endocrinol Metab. 2010; 24: 325-334.

  8. Cochs B, Costa L, Martí L, Guitart M, Cos R, Abad C y cols. Síndrome de insensibilidad a los andrógenos como causa de amenorrea. Prog Obstet Ginecol. 2011; 54: 592-595.

  9. Oakes BM, Eyvazzadeh AD, Quint E, Smith YR. Complete androgen insensitivity syndrome-- a review. J Pediatr Adolesc Gynecol. 2008; 21: 305-310.

  10. Bianca S, Cataliotti A, Bartoloni G, Torrente I, Barrano B, Boemi G et al. Prenatal diagnosis of androgen insensitivity syndrome. Fetal Diagn Ther. 2009; 26: 167-169.

  11. Larios GC, Bautista DN. Orquidectomía bilateral por laparoscopia en síndrome de insensibilidad androgénica completa. Urol Colomb. 2016; 25: 261-263.

  12. Alvarez NR, Lee TM, Solorzano CC. Complete androgen insensitivity syndrome: the role of the endocrine surgeon. Am Surg. 2005; 71: 241-243.

  13. Patel V, Kastl CR, Gómez LV. Timing of gonadectomy in patients with complete androgen insensitivity syndrome-current recommendations and future directions. J Ped Adolsc Ginecol. 2016; 29: 320-325.




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Rev Mex Cir Endoscop. 2018;19