Abstract
Congenital perineal grove (CPG) is a rare anorectal anomaly; only 65 cases have been reported in literature. Two cases who were referred for evaluation of a lesion in the perineum are reported here. The patients were diagnosed clinically as CPG in neonatal period and were initially managed conservatively. Surgery was required in one case as the lesion was persistent and symptomatic. A high index of suspicion is required for diagnosis of CPG to avoid parental anxiety and unnecessary diagnostic workup and surgery. Surgery is required only in cases where the lesion persists or there is infection, pain, and ulceration.
Original language | English |
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Pages (from-to) | 1311-1313 |
Number of pages | 3 |
Journal | Journal of the Pakistan Medical Association |
Volume | 73 |
Issue number | 6 |
DOIs | |
Publication status | Published - Jun 2023 |
Externally published | Yes |
Keywords
- Anorectal malformations
- Perineal cleft
- Perineal grove