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Table 1 Baseline data of patients who were prenatally diagnosed with CC at various ages

From: The timing of minimally invasive surgery for prenatally diagnosed choledochal cysts

Age at surgery

≤ 1 month(n = 15)

1–2 months (n = 27)

2–3 months (n = 14)

> 3 months (n = 17)

P

Gestational age < 37 weeks(Yes/No, n)

1/14

2/25

0/14

0/17

0.599

Sex(Male/Female, n)

7/8

7/20

2/12

1/16

0.045

Birth weight (kg, M[P25,P75])

3.20[3.00, 3.50]

3.25[3.05, 3.40]

3.33[3.10, 3.40]

3.50[3.28, 3.73]

0.057

aClinical symptoms(Yes/No, n)

8/7

7/20

3/11

3/14

0.146

bCC size (mm, M[P25,P75])

35.67[28.33, 46.67]

37.66[28.67,49.67]

29.0[19.0,35.25]

31.33[23.74, 66.25]

0.169

  1. a: Clinical symptoms were identified in 21 patients, including 19 with cholestasis, 1 with clay-colored stool and 1 with a rapid increase in CC size. In 19 patients with cholestasis, 2 had clay-colored stool, 2 had vomiting, and 1 had a rapid increase in CC size. b: CC size in patients with clinical symptoms was significantly greater than that in patients without clinical symptoms (44.33 [35.50, 63.75] vs. 30.34 [22.47, 42.88] mm, p = 0.001); however, no difference in CC size was detected among CC patients of various ages. M means median