Biliary atresia-splenic malformation (BASM) syndrome: a case report
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Tarih
2024
Dergi Başlığı
Dergi ISSN
Cilt Başlığı
Yayıncı
Elsevier Ltd
Erişim Hakkı
info:eu-repo/semantics/openAccess
Özet
Introduction and importance: Biliary atresia (BA) is characterized by the presence of persistent cholestatic jaundice during the neonatal period. This group of patients is at higher risk for liver disease and/or portal hypertension compared with other chronic liver diseases. Case presentation: We present a newborn patient who had biliary stools early postnatally, but her gallbladder was not seen on radiological examination and was referred to our clinic. On examination, polysplenia was seen, and the inferior vena cava was not seen. The patient's stool color changed to a creamy stool without bile three weeks postnatally. The neonate was diagnosed with biliary atresia and splenic malformation (BASM) syndrome. The patient underwent a Kasai portoenterostomy in the 3rd week of age and was preoperatively diagnosed with malrotation and treated with a Ladd procedure at the same time. The patient had a postoperative stool with bile and decreased bilirubinemia with a normal defecation period. Clinical discussion: BASM syndrome, clinically has different causes and a worse prognosis than isolated BA. The syndrome can lead to end-stage cirrhosis and liver failure if left untreated. Although timely Kasai surgery is the standard treatment for BA, the age of the patient at the time of the surgery is different depending on BA groups. Conclusion: The most important prognostic factors for BASM syndrome are early diagnosis and treatment. Despite this, the patients need careful follow-up. Postoperative adjuvant steroid therapy may have a good impact on the outcomes.
Açıklama
Article number: 109937
Anahtar Kelimeler
BASM, Biliary atresia, Case report, Kasai portoenterostomy, Neonatal cholestatic jaundice
Kaynak
International Journal of Surgery Case Reports
WoS Q Değeri
N/A
Scopus Q Değeri
Q3
Cilt
121
Sayı
Künye
Alhashmi, H., Chawshly, E., Çelebi, S. (2024). Biliary atresia-splenic malformation (BASM) syndrome: a case report. International Journal of Surgery Case Reports, 121. 10.1016/j.ijscr.2024.109937
