• 제목/요약/키워드: Atresia ani

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송아지 항문폐쇄증의 수술 부위 결정을 위한 방사선 진단 (Radiographic Diagnosis for Determination of Operation Site in Calves with Congenital Atresia Ani)

  • 김남수;최인혁
    • 한국임상수의학회지
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    • 제16권2호
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    • pp.486-491
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    • 1999
  • One day to one week-old 3 female Korean native calves were referred to the Veterinary Teaching Hospital, Chonbuk National University, with atresia ani. The authors performed radiographic and ultrasonographic diagnosis with physical examination, general hematology and blood chemical examination as investigation. The atresia ani were type I, II, III in each 3 calves. In abdominal radiography and ultrasonography, there were ventral displacement of descending colon(gas and feces filled) and typical enlargement of the blind end of colon in all cases. Operation site was determined by radiographic and ultrasonographic findings in these cases. Surgical treatment, two cases were translocation of the colon to the body wall exiting as a colostomy and one case was corrected by making a circumcision through the skin covering the site of the anus.

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Surgical Repair of Atresia Ani with Rectovaginal Fistula in an African Buffalo (Syncerus caffer)

  • Ryu, Jisook;Kang, Shin Geun;Yun, Jungsang;Yeo, Yonggu
    • 한국임상수의학회지
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    • 제35권3호
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    • pp.111-113
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    • 2018
  • A three-month-old female African buffalo born at Seoul Zoo showed signs of abdominal distension, bulging of the perineal skin, and small stool volume compared to feed intake. Upon physical examination, atresia ani with rectovaginal fistula was diagnosed. This case was subjected to surgery under inhalation anesthesia after injecting a sedative. Surgery was performed in two steps: anal reconstruction and closing the rectovaginal fistula. First, a circular skin incision was made at the end of the rectal pouch to create an anus, and then the skin of the anus and the mucous membrane of the rectum were brought into apposition by simple interrupted sutures. Second, the rectovaginal fistula was ligated on both vulval and anal side. Antibiotics were administered on every alternate day and the sutures were removed at ten days surgery under sedation. The rectovaginal communication was closed and the calf was able to urinate and defecate normally. The animal grew to become a normal adult without any complications. This is the first case report of atresia ani with rectovaginal fistula in an African buffalo, that was successfully treated by surgical intervention.

고양이의 직장질루가 병발한 Type III 선천성 항문무형성증의 수술적 교정 (Surgical Correction of Congenital Type III Atresia ani with Rectovaginal Fistula in a Cat)

  • 김민경;황용현;최우;이재훈
    • 한국임상수의학회지
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    • 제30권5호
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    • pp.376-379
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    • 2013
  • 4주령의 0.6 kg 암컷 스콧티쉬 폴드 고양이가 예방 접종을 위해 내원하였다. 신체 검사에서 수양성 분변이 질에서 나오는 것이 확인 되었고 항문은 폐쇄되어 있었다. 방사선 양성 조영 검사에서 직장질루, 확장된 결장이 확인 되었다. 영상 검사에 기초하여 Type III 의 항문 무형성과 직장 질루가 병발한 것으로 최종 진단 하였다. 수술적인 직장 질루의 폐쇄와 항문의 재건이 실시되었다. 수술 후 소화능력을 향상시키기 위해서 락툴로즈와 식이요법을 실시 하였고, 고양이는 수술 후 2주에 배변 조절이 가능해졌으며, 8개월 후 추적조사에서 합병증 없이 배변조절 상태가 유지 되었다.

Renal and Ureteral Fusion in a Calf with Atresia Ani

  • Jeong, Won-Il;Lee, Cha-Soo;Kim, Seok-Jae;Kim, Jin-Hyun;Jeong, Kyu-Shik
    • 한국수의병리학회:학술대회논문집
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    • 한국수의병리학회 2002년도 추계학술대회초록집
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    • pp.138-138
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    • 2002
  • A 10-day old male calf exhibited multiple congenital anomalies of the urinary and gastrointestinal tracts, including renal fusion (horseshoe kidney), ureteral fusion, rectovesicular fistula, and atresia ani. The single kidney was fused at the caudal poles. The left kidney and cranial half of right kidney were shrunken, while the remaining lobules were hypertrophic. Ureters were fused cranially and bifurcated caudally. The terminal rectum was narrowed and connected with the bladder. The anus was imperforate. The cause of these anomalies could not be determined. This is the first report of this constellation of congenital anomalies in a calf.

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Rectovaginal Fistula and Atresia Ani in a Kitten: A Case Report

  • Choi, Chun-Ki;Jung, Hye-Jin;Jeong, Soon-Wuk
    • 한국임상수의학회지
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    • 제39권1호
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    • pp.32-37
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    • 2022
  • A 2-month-old intact female domestic short hair presented with physical abnormalities, including discharge of watery feces from the vagina, depression, and dehydration. The rectovaginal fistula and atresia ani type 3 were diagnosed on the vaginogram. During the anoplasty, the fistula could not be identified because the patient was too small. Instead of colotomy, feces were flushed out using a feeding tube. To prevent complications, a 1-cc syringe tip was sutured at the surgical site after the anoplasty. At the 3-month telephone follow-up after surgery, the cat was reported to have no further clinical signs.

개의 선천성 제4형 항문폐쇄증과 요도직장루의 외과 교정술 (Surgical Correction of Congenital Type IV Atresia Ani with a URethrorectal Fistula in a Dog)

  • 김종민;이재영;조기래;한태성;김소섭;한규보;김근형;최석화
    • 한국임상수의학회지
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    • 제22권4호
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    • pp.404-407
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    • 2005
  • A 4-week-old 0.5 kg male Shih Tzu with history of congenital abnormality, abnormality, was referred to Veterinary Teaching Hospital, Chungbuk National University for further evaluation and treatment. During physical examination, the dog revealed mild depression and dyschezia. In plain radiographs, a digital thermometer put in the anus and grasped blind end of the rectum. In contrast radiographs, a urethrorectal fistula was confirmed. Urine specimens were collected with cystocentesis. Bacteria of the urine were detected using an auto microorganism analyzer. According to history taking, physical examination, radiographic signs and urinalysis, it was diagnosed as type IV atresia ani with a urethrorectal fistula. The dog was treated by fistulectomy and anoplasty, and discharged with instruction. Three days after operation, mild dehiscence was appeared. Wound was left to heal by second intention. During the follow-up of eight weeks, wound showed it to be healed and defecation was normal.

한우송아지에서 선천적 항문 무형성증의 외과적 교정례 (Congenital Anal Atresia in a Korean Native Calf)

  • 이상묵;김정은;장광호
    • 한국임상수의학회지
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    • 제23권3호
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    • pp.380-382
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    • 2006
  • A 6-day-old male Korean native calf was referred to Veterinary Teaching Hospital, College of Veterinary Medicine Kyungpook National University because of dyschezia with atresia me. Clinical signs included anorexia, dyschezia, abdominal distention and depression. In radiographic examination, the intestinal loops are filled with gas and there is a fistula connecting the large intestine to the urethra. Colostomy was performed immediately and atresia am was healed on 28 day after colostomy without Buy other complication.

한우 송아지의 이두이안체 (Derodidymus in Korean-Native Calf)

  • 강문일;박영석;한동운
    • 한국가축번식학회지
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    • 제23권1호
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    • pp.69-73
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    • 1999
  • 머리와 목이 두 개인 이두이경체인 한우 송아지를 해부학적으로 관찰하였다. 이 한우 기형 송아지의 외형적 특정은 2 개의 완전한 머리와 목이 형성되어 있었으며 두 개의 경부는 흉강에서 유합되어 한 개의 몸통을 이루고 있었다. 두 개의 두부는 우측의 두부가 좌측의 두부에 비해 크기가 작고 상악과 하악의 비틀림이 심하게 나타나는 편측성 하악골 형성부전을 보였다. 두 개의 경부는 비슷한 길이로 흉부에서 유합되어 있었으며 2 개의 두부와 경부 외에 흉근 내부에 유착되어져 있는 흉골이 1 쌍으로 존재하고 있었다. 전지골격은 외부에 노출된 1 쌍의 완전한 골격과 매몰되어 있는 비교적 완전한 l 쌍의 전지골격외에 견갑부가 소실되고 상완골이 불완전한 l 쌍의 불완전한 전지 골격구조가 흉근과 늑골 사이에서 발견되었다. 그러나 기형적 전지와는 달리 후지는 정상적인 1 쌍의 다리만 보이었다. 경추의 부분적인 유합과 흉추 전반부가 심한 유합으로 척추가 뒤틀려져 있었다. 두개골은 정상적으로 2개의 눈과 귀, 비공과 1개의 업을 가지고 있었으며, 좌측이 우측 두부에 비해 크기가 작았고 하악도 더 심히 뒤틀려져 있었다. 뇌실은 위축되어 대뇌가 작았다. 기관과 식도는 흉강에서 유합되어 1개의 폐와 위로 이어지고 있었다. 흉강내 장기와 복강내 장기는 대부분 정상적인 구조를 유지하고 있었으나 대장의 직장 부분은 항문으로부터 5cm 떨어진 부분에 협착되어 있었으며 항문은 보이지 않았다.

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Fetal bladder outlet obstruction in a stillborn bovine fetus

  • Jeong, Won-Il;Lee, Cha-Soo;Chung, Jae-Yong;Jeong, Da-Hee;Do, Sun-Hee;Noh, Dong-Hyung;Oh, Won-Seok;Jeong, Kyu-Shik
    • 한국수의병리학회:학술대회논문집
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    • 한국수의병리학회 2002년도 추계학술대회초록집
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    • pp.134-134
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    • 2002
  • A stillborn bovine male fetus with abdominal distention, arthrogryposis and atresia ani was presented for diagnostic evaluation. At necropsy, this fetus had a large amount of ascites, urachal obstruction and marked bladder distention. The ventral surface of the bladder had ruptured and attached to the abdominal wall by fibrinous adhesions. There was bilateral hydronephrosis with moderate pelvic dilatation and cortical attenuation. The rectum was filled with meconium but the anus was imperforate. The right forelimb was contracted. The cause(s) of these abnormalities could not be determined; however, we believe that developmental abnormalities during embryogenesis may be the result of chromosomal abnormalities. This report is the first to report congenital urachal obstruction in this species.

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