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PELVIC OSTEOTOMY IN CLOACAL EXSTROPHY: A CHANGING PERSPECTIVE
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Read the article on jpedsurg.org ↗Article · Jul 2022 · 1 min read
In brief
In brief
Reviews evolving surgical approaches to pelvic osteotomy in cloacal exstrophy, the most severe form of exstrophy-epispadias complex. Addresses challenges of managing severe pelvic diastasis (>6 cm) and associated skeletal abnormalities that complicate abdominal wall and bladder closure in this rare congenital condition.
Written by the GCMD Library team from the article.
Cloacal exstrophy (CE) is a severe congenital malformation with various anomalies involving the bladder, genitals, hindgut, limbs, and spinal cord [1]. The bony pelvis of CE patients involves both rotational and dimensional abnormalities which results in a waddling gait, increased distance between the hips, and outward rotation of the lower limbs [1, 2]. CE is the most severe on the spectrum of the exstrophy-epispadias complex (EEC) with diastasis widths greater than 6 cm, making surgical closure of the abdominal wall, bladder, and bony pelvis challenging [1, 3].
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