Pediatric surgery international
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Pediatr. Surg. Int. · Oct 2008
Case ReportsIncarcerated femoral hernia with ovary and fallopian tube torsion in an infant: a rare occurrence.
Incarcerated femoral hernia with ovary and fallopian tube torsion is very rare in children. We herein report a case of incarcerated femoral hernia with ovary and fallopian tube torsion in a 7-month-old female who was diagnosed on the basis of operative findings. We released the torsion of the left fallopian tube. ⋯ Left salpingo-oophorectomy and McVay repair for femoral hernia were performed. She has experienced no recurrence of femoral hernia for 3 years. We must consider incarcerated femoral hernia in the differential diagnosis for infants with groin redness and swelling.
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Pediatr. Surg. Int. · Oct 2008
Gender assignment and hormonal treatment for disorders of sexual differentiation.
To study the gender assignment and hormonal treatment advocated for disorders of sexual differentiation (DSD). ⋯ The patients included male pseudohermaphrodite (MPH) 169; congenital adrenal hyperplasia (CAH) 91; mixed gonadal dysgenesis (MGD) 29; true hermaphrodite (TH) 25; pure gonadal dysgenesis (PGD) 2; persistent mullerian duct syndrome (PMDS) 2 and others (micropenis, severe hypospadias with cryptorchidism, 46XX male) 39. Out of 91 cases of CAH, 70 (76.9%) were on steroids (prednisolone, hydrocortisone) and/or mineralocorticoids (fluoricortisone) for adrenal suppression. Out of 146 cases of male pseudohermaphrodite and 21 cases of true hermaphrodite and 3 cases of mixed gonadal dysgenesis reared as males, testosterone was given for local application for phallic growth in 101 and/or as systemic injection for mental makeup after puberty in 41 cases. Systemic testosterone injection was also given for 7 cases of CAH reared as males. Out of 26, 15 cases with mixed gonadal dysgenesis and one out of 2 cases of pure gonadal dysgenesis that attained puberty after being reared as females, after female genitoplasty, were given conjugated oestrogen (Premarin) supplemented with progesterone, as the uterus was preserved. For 12 post-pubertal cases of complete androgen insensitivity syndrome (AIS), only premarin was given as there was no uterus. Growth hormone and Gn RH analogue was given in 2 patients with CAH to tide over the early bone maturation induced by hormones with equivocal results. Thus judicious hormonal supplementation based upon type of DSD and gender assigned can provide a psychological and cosmetic benefit to patients with DSD.