Literature DB >> 7077470

Reoperation in the treatment of biliary atresia.

K Suruga, T Miyano, K Kimura, T Arai, Y Kojima.   

Abstract

Rehepatic-portoenterostomy and curettage were performed as reoperative procedures for treatment of biliary atresia. In cases of rehepatic-portoenterostomy, microsurgical technique is an important factor in order to obtain satisfactory operative results. The indication for rehepatic-portoenterostomy, the age of the patient, the size of the intrahepatic bile ducts at the porta hepatis area, the degree of liver fibrosis and liver cell change are closely related to the prognosis of rehepatic-portoenterostomy cases. Since 1977, all seven cases who underwent rehepatic-portoenterostomy showed bile excretion and at present, 3 out of 7 have no jaundice. Curettage is an effective treatment for cessation of bile flow in cases which underwent hepatic portoenterostomy and showed bile excretion for a certain period postoperatively. The timing of curettage is closely related to the results of the curettage. In 9 out of 17 cases which received curettage, we were able to obtain fairly good bile flow and at present, 4 out of 9 show no jaundice.

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Year:  1982        PMID: 7077470     DOI: 10.1016/s0022-3468(82)80315-1

Source DB:  PubMed          Journal:  J Pediatr Surg        ISSN: 0022-3468            Impact factor:   2.545


  8 in total

1.  Mechanical obstruction of a Roux-Y limb : A rare cause of recurrent jaundice after apparently succesfuul surgery for biliary atresia.

Authors:  S Watanatittan
Journal:  Pediatr Surg Int       Date:  2013-09-21       Impact factor: 1.827

2.  Indication for redo hepatic portoenterostomy for insufficient bile drainage in biliary atresia: re-evaluation in the era of liver transplantation.

Authors:  T Hasegawa; T Kimura; T Sasaki; A Okada; S Mushiake
Journal:  Pediatr Surg Int       Date:  2003-04-03       Impact factor: 1.827

Review 3.  Surgical modifications, additions, and alternatives to Kasai hepato-portoenterostomy to improve the outcome in biliary atresia.

Authors:  Shilpa Sharma; Devendra K Gupta
Journal:  Pediatr Surg Int       Date:  2017-10-04       Impact factor: 1.827

4.  Effect of microscopy-assisted portoenterostomy (MAPE) for biliary atresia.

Authors:  Takehisa Ueno; Tasuku Kodama; Yuki Noguchi; Motonari Nomura; Ryuta Saka; Yuichi Takama; Yuko Tazuke; Kazuhiko Bessho; Hiroomi Okuyama
Journal:  Pediatr Surg Int       Date:  2021-01-02       Impact factor: 1.827

Review 5.  Prenatal diagnosis of congenital anomalies. What can and should be done?

Authors:  J C Langer
Journal:  Can Fam Physician       Date:  1993-03       Impact factor: 3.275

6.  Progress in the treatment of biliary atresia.

Authors:  R Ohi; M Hanamatsu; I Mochizuki; T Chiba; M Kasai
Journal:  World J Surg       Date:  1985-04       Impact factor: 3.352

7.  A long-term experience with biliary atresia. Reassessment of prognostic factors.

Authors:  D U Tagge; E P Tagge; R A Drongowski; K T Oldham; A G Coran
Journal:  Ann Surg       Date:  1991-11       Impact factor: 12.969

Review 8.  Review of redo-Kasai portoenterostomy for biliary atresia in the transition to the liver transplantation era.

Authors:  Wataru Sumida; Hiroo Uchida; Yujiro Tanaka; Takahisa Tainaka; Chiyoe Shirota; Naruhiko Murase; Kazuo Oshima; Ryo Shirotsuki; Kousuke Chiba
Journal:  Nagoya J Med Sci       Date:  2017-08       Impact factor: 1.131

  8 in total

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