KaydedilenlerDerginizi ekleyin

Dergiler / Pediatric Urology Case Reports / 2020 / Cilt: 7 - Sayı: 2

Cloacal dysgenesis sequence with bilateral renal agenesis, bladder agenesis, pulmonary hypoplasia and left choanal atresia: A case report

Esra OZCAKİR
Sefer Tolga OKAY
İpek GÜNEY VARAL
Mete KAYA
Sayfa
56–59
DOI
—
🏛️Bu makalenin bibliyografik verileri ve tam metin bağlantısı DergiPark üzerinden sağlanmıştır.
DergiPark Kaydı ↗
✨

Yapay Zeka Hızlı Bakış & Çıkarımlar

AI Insight
⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

On the other hand, incomplete valve ablation may contribute to the recurrence of the fistula.

📌 3 Maddede Bu Makale

🎯
Amaç & Hipotez:A case of posterior urethral valve is described with multiple urethroperineal fistulas.
📊
Temel Bulgular & Veri:This association is extremely rare.
💡
Sonuç & Katkı:On the other hand, incomplete valve ablation may contribute to the recurrence of the fistula.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Alan Parametreleri

Özet

A case of posterior urethral valve is described with multiple urethroperineal fistulas. This association is extremely rare. The crucial point in the diagnosis is to distinguish these fistulas from the urethral duplications that actually guide the treatment. The presence of these fistulas in patients with posterior urethral valve may have a beneficial effect on renal function as it reduces the pressure on the bladder. On the other hand, incomplete valve ablation may contribute to the recurrence of the fistula.

🔖

Bu Makaleye Atıf Yap

OZCAKİR, E., OKAY, S. T., VARAL, İ. G., KAYA, M. (2020). Cloacal dysgenesis sequence with bilateral renal agenesis, bladder agenesis, pulmonary hypoplasia and left choanal atresia: A case report. Pediatric Urology Case Reports, Cilt: 7 - Sayı: 2, 56–59. https://ajindex.com/articles/285541

📄 Tam Metin PDF Okuyucu

📄

PDF görüntüleyici hazırlanıyor...

Kaynakça (16)

  1. Bargaje A, Yerger JF, Khouzami A, et al. Cloacal dysgenesis sequence. Ann Diagn Pathol. 2008
  2. 12(1):62–66. [2]Escobar LF, Weaver DD, Bixler D, et al. Urorectal septum malformation sequence: report of six cases and embryological analysis. Am J Dis Child. 1987
  3. 141(9):1021 - 24. [3]Sahinoglu Z, Mulayim B, Ozden S, et al. The prenatal diagnosis of cloacal dysgenesis sequence in six cases: can thetermination of pregnancy always be the first choice? Prenat Diagn. 2004
  4. 24(1):10–16. [4]Jegadeesh S, Mahajan JK. Cloacal dysgenesis sequence with bilateral renal agenesis and normal pulmonary development in twin pregnancy. BMJ Case Rep. 2016
  5. bcr2015214130. [5]Pauli RM. Lower mesodermal defects: a common cause of fetal and early neonatal death. Am J Med Genet. 1994
  6. 50(2):154– 72. [6]Phelan JP, Smith CV, Broussard P, et al. Amniotic fluid volume assessment with the four-quadrant technique at 36–42 weeks’ gestation. J Reprod Med. 1987
  7. 32(7):540– 42. [7]McFadden DE, Pantzar JT. Genital system. In Developmental Pathology of The Embryo and Fetus, Dimmick JE, Kalousek DK (eds). J.B. Lippincott: Philadelphia
  8. pp. 605–624. [8]Qureshi F, Jacques SM, Yaron Y et al. Prenatal diagnosis of cloacal dysgenesis sequence: differential diagnosis from other forms of fetal obstructive uropathy. Fetal Diagn Ther. 1998
  9. 13(2):69–74. [9]Yanai T, Urita Y, Amagai T, et al. Longterm survival with cloacal dysgenesis sequence. Pediatr Surg Int. 2012
  10. 28(1):107–10. [10]Kanamori Y, Iwanaka T, Nakahara S et al. Survival in a neonate with complete urorectal septum malformation sequence after fetal vesico-amniotic shunting for a prominently dilated cloaca. Fetal Diagn Ther. 2008
  11. 24(4):458–61. [11]Kramer RL, Johnson MP, Qureshi F. Concordance for cloacal dysgenesis. Fetal Diagn Ther. 1997
  12. 12(5):279 - 82. [12]Kaya M, Sancar S, Ozcakir E, et al. Omphalocele, exstrophy of cloaca, imperforate anus and spinal defect (OEIS Complex): A case report. Pediatr Urol Case Rep. 2015
  13. 2(4):17-24. [13]Chaubal N, Dighe M, Shah M, et al. Calcified meconium: an important sign in the prenatal sonographic diagnosis of cloacal malformation. J Ultrasound Med. 2003
  14. 22(7):727-30. [14]Dannull K, Sung J. Cloacal dysgenesis diagnosis by prenatal ultrasound and MRI. Pediatr Radiol. 2014
  15. 44(2):230–33. [15]Patil SJ, Phadke SR. Urorectal septum malformation sequence: ultrasound correlation with fetal examination. Indian J Pediatr. 2006
  16. 73(4):287–93. [16]Mukhtar RA, Baskin LS, Stock PG et al. Long-term survival