先天性単腎の2例
スポンサーリンク
概要
- 論文の詳細を見る
Recently we had 2 cases of congenital solitary kidney. A case of them is twenty-eight years-old female and other thirty-four years-old male. In the first case she had only the press pain fit at the left abdominal region and no other subjective symptom. Ps a re sult of cystoscopic and several rentogenographic examinations she was diagnosed as doubt of left hydronephrosis after the gynecologic operation. We tried an operation on her and found a congenital solitary kidney. In the second case he has been complained of lumbal pain of the right side last eight month but he had neither hematuria nor colic pain. We tried cystoscopic and rentogenographic examination (pnemoretroperitsneum and arteriography) and diagnosed as doubt of congenital solitary kidney and it was proved by the operation. Congenital solitary kidney is relatively rare in the l iteratures. In the case 1 she had bihorn uterus but in the case 2 we could not find other deformity.
- 泌尿器科紀要刊行会の論文
泌尿器科紀要刊行会 | 論文
- MVAC療法後の転移性尿路上皮癌に対するGemcitabine, Docetaxel, Carboplatin併用化学療法の検討
- Grade 3 Ta-1表在性膀胱癌に対する膀胱温存治療
- 腹腔鏡下に摘出した後腹膜神経線維腫の1例
- 移植腎生検による腎内動脈瘤破裂の1例
- Modified M-VAC療法後に残存腫瘍切除を施行した進行尿路上皮癌患者の治療成績