• 제목/요약/키워드: Shunts, portosystemic

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Transcolonic scintigraphy for diagnosis of canine portosystemic shunts

  • Lee, Young-won
    • 대한수의학회지
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    • 제39권2호
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    • pp.390-393
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    • 1999
  • Transcolonic scintigraphy using $^{99m}Technetium$ pertechnetate ($^{99m}TcO_{4}$) was performed in 5 dogs with portosystemic shunts. In all dogs, the activity in the heart was seen before liver activity. Also time activity curve was revered. The mean shunt index in 5 dogs was 82.3% (range 79.6~87.1%). Transcolonic scintigraphy is quick, simple and useful diagnostic method for canine portosysternic shunts.

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Endovascular Closure Resolves Trimethylaminuria Caused by Congenital Portosystemic Shunts

  • Ponce-Dorrego, Mar?a Dolores;Garzon-Moll, Gonzalo
    • Pediatric Gastroenterology, Hepatology & Nutrition
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    • 제22권6호
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    • pp.588-593
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    • 2019
  • This study aimed to report three new cases of an association between two rare conditions, congenital portosystemic shunts (CPSS) and trimethylaminuria (TMAU), and the efficacy of endovascular closure of the CPSS for resolving TMAU. Between November 2014 and April 2017, 15 patients with CPSS were enrolled in this prospective study to assess the efficacy of percutaneous endovascular shunt closure. Three patients presented with clinical symptoms of TMAU that were confirmed by urine analysis of trimethylamine (TMA) and TMA n-oxide. One year after endovascular closure of the congenital portosystemic shunt, the same parameters were evaluated were obtained and the values were compared to the pretreatment values. The results indicated the disappearance of clinical symptoms of TMAU and normalization of the urine test parameters in two patients and no changes in one patient, who developed new portosystemic communications.

산전 초음파로 발견되고 출생 후 4회의 코일 색전술과 심 교정술로 치료된 심실 중격 결손을 동반한 선천성 간내 문맥전신성 단락 1례 (A Case of Congenital Intrahepatic Portosystemic Shunt Associated with VSD Detected by Antenatal Sonography and Treated with Four Coil Embolizations and Open Heart Surgery after Birth)

  • 나지윤;김은선;김상덕;김이경;김한석;최중환;천정은;정진욱
    • Neonatal Medicine
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    • 제15권2호
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    • pp.176-182
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    • 2008
  • 드문 선천성 문맥전신성 단락에 대한 표준화된 치료는 없으나 저자들은 출생 직후부터 심부전 증상을 보인 환아에서 심실 중격 결손증을 동반한 선천성 문맥전신성단락을 4회의 코일 색전술 및 심 교정술로 치료한 증례를 경험하였기에 문헌고찰과 함께 보고하는 바이다.

Endovascular Treatment of Congenital Portosystemic Shunt: A Single-Center Prospective Study

  • Ponce-Dorrego, Maria-Dolores;Hernandez-Cabrero, Teresa;Garzon-Moll, Gonzalo
    • Pediatric Gastroenterology, Hepatology & Nutrition
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    • 제25권2호
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    • pp.147-162
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    • 2022
  • Purpose: To design a prospective study on endovascular closure of congenital portosystemic shunts. The primary endpoint was to assess the safety of endovascular closure. The secondary endpoint was to evaluate the clinical, analytical and imaging outcomes of treatment. Methods: Fifteen patients (age range: 2 days to 21 years; 10 male) were referred to our center due to congenital portosystemic shunts. The following data were collected prior to treatment: age, sex, medical history, clinical and analytical data, urine trimethylaminuria, abdominal-US, and body-CT. The following data were collected at the time of intervention: anatomical and hemodynamic characteristics of the shunts, device used, and closure success. The following data were collected at various post-intervention time points: during hospital stay (to confirm shunt closure and detect complications) and at one year after (for clinical, analytical, and imaging purposes). Results: The treatment was successful in 12 participants, migration of the device was observed in two, while acute splanchnic thrombosis was observed in one. Off-label devices were used in attempting to close the side-to-side shunts, and success was achieved using Amplatzer™ Ductus-Occluder and Amplatzer™ Muscular-Vascular-Septal-Defect-Occluder. The main changes were: increased prothrombin activity (p=0.043); decreased AST, ALT, GGT, and bilirubin (p=0.007, p=0.056, p=0.036, p=0.013); thrombocytopenia resolution (p=0.131); expansion of portal veins (p=0.005); normalization of Doppler portal flow (100%); regression of liver nodules (p=0.001); ammonia normalization (p=0.003); and disappearance of trimethylaminuria (p=0.285). Conclusion: Endovascular closure is effective. Our results support the indication of endovascular closure for side-to-side shunts and for cases of congenital absence of portal vein.

개의 다발성 간외성 간문맥전신단락증의 진단 2예 (Diagnosis of Multiple Extrahepatic Portosystemic Shunt in Two Dogs)

  • 김주형;한성영;전혜영;김태훈;강지훈;한태성;나기정;양만표;김근형;강상철;김재훈;장동우
    • 한국임상수의학회지
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    • 제24권2호
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    • pp.269-275
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    • 2007
  • Two dogs referred to Veterinary Medical Center, Chungbuk National University diagnosed as multiple extrahepatic portosystemic shunt were reported. The first dog was a 20-month-old, 8 kg, male Cocker spaniel with history of peritoneal effusion, diarrhea, anorexia and stunted growth. The second dog was a 3-year-old, 13.4 kg, male Jindo with a history of severe depression. Hematologic examination of first dog revealed mild microcytosis and nonregenerative anemia. All of 2 cases, serum chemical values showed increase of serum ammonia, ALP, r-GTP and glucose. In survey radiography, microhepatia was apparent. In the color Doppler ultrasonographic examination, the first dog revealed a dilated tortuous vein communicating with caudal vena cava was observed near the left kidney and the second dog revealed numerous shunting vessels ventral to L5 and L6. Transcolonic portal scintigraphy of the first dog confirmed the presence of portosystemic shunt. In intraoperative jejunoportography, the first dog showed single congenital extrahepatic portosystemic shunt and multiple acquired extrahepatic portosystemic shunts. The second dog showed multiple acquired extrahepatic portosystemic shunts. In these dogs, the presence of congenital and acquried portosystemic shunts and histopathologic findings were considered to represent a combination of multiple extrahepatic portosystemic shunts and noncirrhotic portal hypertension or portal vein hypoplasia.

신생아기에 진단된 선천성 간내 문맥 전신성 단락의 임상적 고찰과 치료 (A Clinical Study of Congenital Intrahepatic Portosystemic Shunt Diagnosed in Neonatal Period)

  • 김지영;김경아;이연경;고선영;신손문;한병희
    • Neonatal Medicine
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    • 제18권1호
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    • pp.117-123
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    • 2011
  • 목적: 선천성 문맥 전신성 단락은 매우 희귀한 질환으로, 대부분은 증상이 없어 우연히 시행된 영상 검사를 통해서 발견되고, 심각한 합병증을 일으킬 수 있어 진단과 치료에 신중을 기해야 하는 질환이나, 재태 상태 또는 신생아기에 단락의 진단을 위한 표준화된 방법이 제시되고 있지 않은 실정이다. 이에 선천성 간내 문맥 전신성 단락이 신생아기에 복부 초음파로 확인된 8예의 임상 양상과 치료 및 예후에 대해 알아보았다. 방법: 2006년 1월부터 2010년 12월까지 관동대학교 의과대학 제일병원에서 출생한 환아 36,572명 중 산전에 단락이 진단된 신생아 6예와, 출생 후 간내 문맥 전신성 단락이 진단된 신생아 2예를 대상으로 의무 기록 정보를 후향적으로 분석하였다. 결과: 선천성 간내 문맥 전신성 단락은 해당 기간의 출생아중 8명에서 발생하였으며, 이 중 6예는 산전검사에서 진단되었으며, 2예는 출생 후 복부 초음파 검사를 시행하여 진단되었다. 산전의 진단된 6예 중 3예는 자궁 내 성장 지연을 보였으며, 2예는 미숙아였다. 1예에서 암모니아의 상승을 보여, 코일 색전술을 시행하였으며, 4예에서 생후 11개월 내에 단락의 자연 소실을 확인하였다. 출생 후 단락이 확인된 경우는 2예로 모두 자궁 내성장 지연을 보였으며, 단락은 생후 4개월과 6개월에 자연 소실된 것을 확인하였다. 고찰: 선천성 간내 문맥 전신성 단락은 생후 2년 내에 자연 소실되는 것으로 알려져 있으나, 소실 시까지 경과 관찰을 요한다. 단락은 4,500명의 출생아 중 1명에서 발생하였으며, 자궁 내 성장지연을 보인 5예를 포함한 8예에서 경험하였다. 뚜렷한 원인이 동반되지 않은 자궁 내 성장 지연을 보이는 경우, 반드시 선천성 문맥 전신성 단락을 의심하여야 하며, 산전 초음파를 시행하여 검증하여야 한다. 산전 초음파 결과 단락이 의심될 경우, 태아의 상태를 지속적으로 관찰해야 하며, 생후에도 단락의 자연 소실까지 주기적인 감시가 필요하다.

Acquired Portosystemic Shunts Secondary to Hepatic Microvascular Dysplasia in a Young Dog

  • Hwang, Taesung;An, Soyon;Kim, Ahreum;Han, Changhee;Huh, Chan;Lee, Hee Chun
    • 한국임상수의학회지
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    • 제37권2호
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    • pp.88-90
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    • 2020
  • A one year old spayed female Bichon Frise dog presented with gait abnormalities and seizure. Serum biochemical results showed elevated levels of alkaline phosphatase, alanine aminotransferase, and ammonia. Serum bile acid level was also increased to be over 30 μmol/L on preprandial. Urinalysis identified the presence of ammonium urate crystal. Abdominal ultrasonography and CT revealed aberrant, tortuous, and multiple small vessels connected to the caudal vena cava between left kidney and caudal vena cava. Macroscopic specific findings associated with extrahepatic congenital portosystemic shunts (PSS) or other liver diseases were not identified. Liver biopsy was performed. Histopathologic evaluation revealed hepatic lobular hypoplasia with portal arterial duplication and vascular shunts. Based on these finding, this case was diagnosed as multiple acquired PSS secondary to hepatic microvascular dysplasia (HMD) and hepatic encephalopathy. A liver biopsy is recommended to differentiate HMD from other liver diseases and to confirm HMD when a young dog has multiple acquired PSS.

Outcomes of Portosystemic Shunts in Children with and without Liver Transplantation

  • Hamza Hassan Khan;Stuart S. Kaufman;Nada A. Yazigi;Khalid M. Khan
    • Pediatric Gastroenterology, Hepatology & Nutrition
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    • 제27권1호
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    • pp.37-42
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    • 2024
  • Purpose: Limited data exist regarding outcome and morbidity associated with portosystemic shunts in the pediatric transplant population. Our study assesses the outcomes of pediatric patients who underwent a portosystemic shunt procedure, both with and without liver transplantation (LT). Methods: This study retrospectively reviewed the medical records of pediatric patients aged 0-19 years who underwent shunt placement between 2003 and 2017 at a tertiary care center. The analysis included cases of shunt placement with or without LT. Results: A total of 13 pediatric patients were included in the study with median age of 8.8 years. Among the cases, 11 out of 13 (84.6%) underwent splenorenal shunt, 1 (7.7%) underwent a mesocaval shunt, and another 1 (7.7%) underwent a Modified Rex (mesoportal) shunt. Additionally, 5 out of 13 (38.5%) patients had LT, with 4 out of 5 (80.0%) receiving the transplant before shunt placement, and 1 out of 5 (20.0%) receiving it after shunt placement. Gastrointestinal bleeding resulting from portal hypertension was the indication in all cases. A total of 10 complications were reported in 5 patients; the most common complication was anemia in 3 (23.1%) patients. At the most recent follow-up visit, the shunts were functional without encephalopathy, and no deaths were reported. Conclusion: Shunt placement plays a crucial role in the management of patients with portal hypertension. Our study demonstrates favorable long-term outcomes in pediatric patients who underwent shunt placement. Long term shunt outcomes were similar and unremarkable in patients with LT and without LT.

개 문맥전신순환단락의 진단영상 43례 (Diagnostic imaging of portosystemic shunts in 43 dogs)

  • 최지혜;김현욱;장재영;김준영;윤정희
    • 대한수의학회지
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    • 제48권2호
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    • pp.227-233
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    • 2008
  • Portosystemic shunt (PSS) was diagnosed in 43 dogs by mesenteric portogram from January, 2002 to June 2007 in Haemaru referral animal hospital. PSS was found in various breeds including Maltese, Miniature Schnauzer and Yorkshire Terrier and there was no predisposition in gender. In laboratory parameters, mean cell volume was lower than normal value in single shunt and alanine aminotransferase was higher than normal range in multiple shunts with clinical significance. Cystic calculi were found in over 50% dogs with PSS and even in 70.8% dogs with single shunt. In 81% dogs with PSS, extrahepatic single shunt such as portocarval type and portoazygous type was identified. Extrahepatic multiple shunt and intrahepatic single shunt were observed in 4 dogs, respectively. Gradual attenuation using ameroid constrictor was applied to 35 dogs with extrahepatic single shunt and the prognosis of these dogs were good except two dogs, which showed poor prognosis because of acquired multiple PSS and renal disease unrelated with PSS, respectively.

개의 간내성 문맥-전신성 단락의 초음파적 고찰 (Ultrasonographic Examination for Intrahepatic Porto-systemic Shunts in Dogs)

  • 최지혜;안용주;이희천;황국진;이영원;엄기동;윤화영;최민철;권오경
    • 한국임상수의학회지
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    • 제16권2호
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    • pp.514-518
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    • 1999
  • Portosystemic shunts in 3 Dogs with respiratory sign of cough and with dementia signs characterized by hypersensitivity, salivation, and seizure were diagnosed at veterinary teaching hospital of Seoul National University. In radiographs, microhepatica was observed. In abdominal ultrasonography, abnormal intrahepatic connections between the portal vein and the systemic vessels and tortuous vascularity were found. There was no complication such as ammonium urate urolith in kidney or urinary bladder, These dogs were treated with medicine and protein-restricted diet.

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