Dergiler / Acta Medica / 2019 / Cilt: 50 - Sayı: 4

Biliary Atresia Splenic Malformation Syndrome: A Single Center Experience

Sayfa
36–41
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)

Further research is recommended for CMV infections role in BASM pathogenesis.

📌 3 Maddede Bu Makale

🎯
Amaç & Hipotez:Objective: Biliary atresia splenic malformation (BASM) syndrome which is a subgroup of BA is associated with situs inversus, intestinal malrotation, polysplenia, preduodenal portal vein, interrupted vena cava, congenital portocaval shunts and cardiac anomalies.
📊
Temel Bulgular & Veri:Materials and Methods: The data were collected retrospectively from medical records of patients treated in Cukurova University between 2005-2017.
💡
Sonuç & Katkı:Further research is recommended for CMV infections role in BASM pathogenesis.
🔬Tür:Araştırma Makalesi
📍Kapsam:2005-2017 Verileri
⚙️Değişkenler:Alan Parametreleri

Özet

Objective: Biliary atresia splenic malformation (BASM) syndrome which is a subgroup of BA is associated with situs inversus, intestinal malrotation, polysplenia, preduodenal portal vein, interrupted vena cava, congenital portocaval shunts and cardiac anomalies. We aimed to report our experiences in BASM management and association of CMV infection. Materials and Methods: The data were collected retrospectively from medical records of patients treated in Cukurova University between 2005-2017. Sex, age, liver function tests, serological test results, BA types, surgical findings, and mortality were noted. Results: Fifty-nine BA patients were diagnosed in the study period. Seven of them were classified as BASM. The median age was 60 days (45-90 days) with a female/male ratio of 3/4. The main complaint of all patients was jaundice. The jaundice of 6 patients began since birth and one began at 20 daysage. Median total/direct blood bilirubin levels were 9.6/5.4 mg/dL. Median values of liver function tests; ALT, AST, and GGT were 77 IU/L, 201 IU/L and 607 IU/L respectively. Five of the patients showed positive results for anti-CMV Ig M. All patients had positive anti-CMV Ig G. One patient had type 2 BA and all others had type 3 BA. Associated anomalies were polysplenia (n=4), asplenia (n=1), preduodenal portal vein (n=5), midgut malrotation (n=7), inferior vena cava interruption (n=1) and hepatic artery originating from superior mesenteric artery (SMA) (n=1). Patients had Ladd procedure (n=7), duodenoduodenostomy (n=5) along with Kasai portoenterostomy. The median follow-up time was 4 years (1-5 years). All patients are alive and one had liver transplantation. Conclusion: Patients with BASM represent a distinct subgroup of BA which may have additional gastrointestinal anomalies such as midgut malrotation and preduodenal portal vein. Thus additional procedures such as duodenoduodenostomy and Ladd procedure may be added to Kasai portoenterostomy. Further research is recommended for CMV infections role in BASM pathogenesis.

🔖

Bu Makaleye Atıf Yap

ÖZDEN, Ö., KILIÇ, Ş. S., ALKAN, M., TÜMGÖR, G., TUNCER, R. (2019). Biliary Atresia Splenic Malformation Syndrome: A Single Center Experience. Acta Medica, Cilt: 50 - Sayı: 4, 36–41. https://ajindex.com/articles/142573

📄 Tam Metin PDF Okuyucu

📄

PDF görüntüleyici hazırlanıyor...

Kaynakça (15)

  1. Nio M, Ohi R, Miyano T, et al. Five- and 10-year survival rates after surgery for biliary atresia: a report from the Japanese Biliary Atresia Registry. Journal of pediatric surgery 2003; 38(7): 997-00
  2. Nio M, Wada M, Sasaki H, et al. Long-term outcomes of biliary atresia with splenic malformation. J Pediatr Surg 2015; 50(12): 2124-21
  3. Zhan J, Feng J, Chen Y, et al. Incidence of biliary atresia associated congenital malformations: A retrospective multicenter study in China. Asian J Surg 2016
  4. Davenport M, Tizzard SA, Underhill J, et al. The biliary atresia splenic malformation syndrome: a 28-year single-center retrospective study. J Pediatr 2006; 149(3): 393-00
  5. Guttman OR, Roberts EA, Schreiber RA, et al. Biliary atresia with associated structural malformations in Canadian infants. Liver Int 2011; 31(10): 1485-93
  6. Davenport M. Biliary atresia: clinical aspects. Semin Pediatr Surg 2012; 21(3): 175-84
  7. Tanano H, Hasegawa T, Kawahara H, et al. Biliary atresia associated with congenital structural anomalies. J Pediatr Surg 1999; 34(11): 1687-90
  8. Davenport M, Savage M, Mowat AP, et al. Biliary atresia splenic malformation syndrome: an etiologic and prognostic subgroup. Surgery 1993; 113(6): 662-68
  9. Silveira TR, Salzano FM, Howard ER, et al. Congenital structural abnormalities in biliary atresia: evidence for etiopathogenic heterogeneity and therapeutic implications. Acta Paediatr Scand 1991; 80(12): 1192-99
  10. Makin E, Quaglia A, Kvist N, et al. Congenital biliary atresia: liver injury begins at birth. J Pediatr Surg 2009; 44(3): 630-33
  11. Lorent K, Gong W, Koo KA, et al. Identification of a plant isoflavonoid that causes biliary atresia. Science translational medicine 2015; 7(286):286ra267
  12. Waisbourd-Zinman O, Koh H, Tsai S, et al. The toxin biliatresone causes mouse extrahepatic cholangiocyte damage and fibrosis through decreased glutathione and SOX17. Hepatology 2016; 64(3): 880-93
  13. Landing BH. Considerations of the pathogenesis of neonatal hepatitis, biliary atresia and choledochal cyst--the concept of infantile obstructive cholangiopathy. Prog Pediatr Surg 1974; 6:113-39
  14. Tyler KL, Sokol RJ, Oberhaus SM, et al. Detection of reovirus RNA in hepatobiliary tissues from patients with extrahepatic biliary atresia and choledochal cysts. Hepatology 1998; 27(6): 1475-82
  15. Riepenhoff-Talty M, Gouvea V, Evans MJ, et al. Detection of group C rotavirus in infants with extrahepatic biliary atresia. J Infect