“…Duplication cysts can occur in the context of other congenital abnormalities, such as those of the vertebral bodies and genitourinary tract, though they most often are seen in patients without other developmental malformations [2–4]. The lesions are typically present in the first year of life (70% of cases) or early childhood, though they more rarely have been reported in older patients [5–7]. Initial symptomatology is dictated by the size and location of the lesion and most commonly includes obstruction, with or without vomiting, abdominal distension, dysphagia, palpable mass, or, more infrequently, urinary symptoms [4, 5, 8].…”