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Article type: Index
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Koushi Asabe, Takayuki Shirakusa
Article type: Article
2002 Volume 38 Issue 2 Pages
263-267
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From January 1986 through June 2001, 16 patients under 15 years of age with spontaneous pneumothorax were admitted to our hospital and underwent operations. We performed mid-axillary thoracotomy in 6, and thoracoscopic surgery in the remaining 10 patients. There was no significant difference in the age between the two groups. However, the operating time, the duration of drainage and the postoperative hospital stay were significantly shorter in the thoracoscopic surgery group than in the thoracotomy group. From the cosmetic standpoint, the former was superior to the latter. Therefore, the thoracoscopic surgery is very useful for pediatric patients with spontaneous pneumothorax.
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Yasuhiro Kitayama
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2002 Volume 38 Issue 2 Pages
268-274
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Although respiratory management with highfrequency oscillatory ventilation (HFOV) and inhalated nitric oxide (NO) has generally been used for neonates with congenital diaphragmatic hernia (CDH), the entry criteria for extracorporeal membrane oxygenation (ECMO) based on data from patients who underwent HFOV and NO have not yet been reported. Purpose : The aim of this study is to determine the entry criteria for ECMO in neonates with CDH treated with HFOV and NO. Methods : To establish the entry criteria for ECMO, we retrospectively studied 30 neonates with CDH treated by HFOV between 1986 and 1993, and 43 neonates with CDH treated by NO between 1994 and 2000 in our institutions. From the admission records, preductal and postductal arterial blood gas data, and ventilation conditions for 72 hours after admission were extracted. An oxygenation index (OI) and an alveolar-arterial oxygen gradient (A-aDO_2) time interval combination were calculated. Patients were divided into two groups according to requirement for ECMO : (1) candidates for ECMO, who underwent ECMO or who died without ECMO, and (2) noncandidates, who survived without ECMO. Sensitivity, specificity, positive predictive value, and negative predictive value were calculated, and the entry criteria were determined, when all of these values reached over 80%. Results : The preductal and postductal OI for 4 hours (mean value for 4 hours) >25 were determined useful as entry criteria in CDH patients treated with HFOV. The preductal OI for 4 hours (mean value for 4 hours) >20 and the postductal OI for 4 hours (mean value for 4 hours) >35 were determined reasonable as the entry criteria in CDH patients treated with HFOV and NO in combination.
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Masaki Nio, Tomohiro Ishii, Hideyuki Sasaki, Dai Kimura, Ryoji Ohi
Article type: Article
2002 Volume 38 Issue 2 Pages
275-280
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Purpose and Methods : The choice of treatment for small intestinal bleeding (SIB) associated with portal hypertension after surgery for biliary atresia (BA) is still controversial. Nine patients with BA developing SIB were treated in our institution. To assess the management for SIB, we reviewed clinical courses, methods of treatment and outcomes. Results : The ages at bleeding were between 2 years and 14.9 years old (average, 9.2 years old). Two patients had jaundice and 2 other patients had thrombocytopenia due to hypersplenism at SIB. Two patients eventually died. One died of liver failure and the other died of a complication after liver transplantation. SIB was not the cause of death in either patient. Of 7 survivors, no treatment except blood transfusion was performed in 2 patients who recently developed SIB. SIB recurred in 2 patients who underwent dissection of collateral vessels. Partial splenic embolization (PSE), which was employed in 2 patients with hypersplenism, and ligation of collateral vessels in one were effective to control bleeding. Two patients developed pulmonary vascular abnormalities : hepatopulmonary syndrome and portopulmonary hypertension, respectively. Conclusion : Although the liver transplantation should be considered in progressive liver cirrhosis, patients with good liver function and controllable bleeding could be expected to have a favorable prognosis.
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Yukio Ogura, Minoru Horisawa, Noriji Niinomi, Eiji Nakamura, Takahisa ...
Article type: Article
2002 Volume 38 Issue 2 Pages
281-285
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Today, we experience a lot of patients who need a central venous catheter (CVC) for the purpose of chemotherapy, total parenteral nutrition and so on. But when we implant CVC or care for a patient with an implanted CVC in the long term, we must be careful of many kinds of complications. One of the most severe complications which often threatens a patient's life is a fracture and a division of the CVC. We experienced two cases of CVC division in children who had a CVC implanted through the subclavian vein. We thought the cause of the division was pinch-off syndrome. We described the two cases and the way in which we can prevent and cope with the pinch-off syndrome.
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Masaki Nio, Shintaro Amae, Yutaka Hayashi, Takamichi Kamiyama, Megumi ...
Article type: Article
2002 Volume 38 Issue 2 Pages
286-290
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A 6-year-old boy with recurrent episodes of intussusception due to Meckel's diverticulum underwent laparoscopic surgery. He had multiple episodes of hematochezia and abdominal pain between the ages of 8 months and 4 years. At 5 years and 7 months, he developed intussusception and underwent gastrographin hydrostatic reduction. There were negative findings on ^<99m>Tc pertechnetate scintigraphy and abdominal ultrasonography. Fifteen months later, he developed a recurrence of intussusception. Following successful barium hydrostatic reduction, he underwent laparoscopic examination. Intussusception due to Meckel's diverticulum was diagnosed and laparoscopicassisted diverticulectomy was performed. The postoperative course was uneventful. The laparoscopic approach was thought to be useful for diagnosing and treating patients with recurrent intussusception with a possible pathological cause.
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Masaki Nio, Megumi Nakamura, Yutaka Hayashi, Takamichi Kamiyama, Shige ...
Article type: Article
2002 Volume 38 Issue 2 Pages
291-295
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Congenital cystic adenomatoid malformation (CCAM) is an uncommon congenital anomaly. A 7-month-old boy presented with cough and stridor and repeated the same symptoms. The diagnosis of CCAM was confirmed by chest radiography, CT scan and magnetic resonance imaging (MRI). At the opetation at 9 months of age, the left lung was found to have multiple cystic lesions in its upper lobe and to have no major fissure between lobes. Video-assisted upper lobectomy was performed. Video-assisted surgery combined with lateral thoracotomy using longitudinal small incision was useful in this particular case. Histologic examination showed Stocker type II CCAM.
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Minoru Iwasaki, Shinji Uemoto, Akiko Yokoi, Seisuke Sakamoto, Koichi T ...
Article type: Article
2002 Volume 38 Issue 2 Pages
296-301
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A rare case of aberrant hepatic duct with anomalous-pancreatobiliary ductal union in a 3-year-old girl is reported. This case has right hepatic duct draining into gallbladder. According to Knight's report, the frequency of aberrant hepatic duct draining into gallbladder was about 0.7% of all cholecystectomies performed. Preoperative diagnosis of the aberrant hepatic duct is very difficult, but MRCP and ERCP are more efficient methods for it than any other examinations. Moreover, operative cholangiography should be performed and appropriate operation is required.
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Yuki Ishimaru, Junko Fujino, Hideki Yamamoto, Hiroo Uchida, Hitoshi Ik ...
Article type: Article
2002 Volume 38 Issue 2 Pages
302-307
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Mutations of exon 3 of the β-catenin gene and accumulation of β-catenin in the nuclei are frequently observed in hepatoblastoma and adulthood hepatocellular carcinoma. We report a case of hepatocellular carcinoma with a β-catenin gene mutation and nuclear β-catenin accumulation in a 6-year-old boy. The tumor was refractory to multimodal aggressive treatments and the patient died of tumor progression and liver failure two months after diagnosis. Developing a novel treatment against hepatocellular carcinoma is urgent, and at the same time, the clinical and biological significance of the β-catenin gene abnormalities in childhood hepatocellular carcinoma should be investigated.
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Michio Kaneko, Teruyoshi Amagai, Tetsu Hori, Kennichi Ikebukuro, Haruo ...
Article type: Article
2002 Volume 38 Issue 2 Pages
308-313
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Total gastric transposition for substitution of thoracic and abdominal esophagus was performed in two cases with complicated esophageal atresia with satisfactory functional results. Case 1 : 7-year-old boy with esophageal atresia without tracheoesophageal fistula whose lower esophagus was totally absent. Intrathoracic esophageal reconstruction with free jejunal graft was unsuccessful at age 5. At age 7 total gastric transposition via posterior mediastinal route introduced by Lewis Spitz was performed with success. No postoperative leakage nor stenosis was observed at the cervical esophagogastric anastomosis site. Case 2 : At neonatal period a primary repair for esophageal atresia with distal tracheoesophageal fistula was performed but esophageal intubation after an accidental extubation of the orotracheal tube caused a total rupture of the esophageal anastomosis and pyothorax. Later, congenital esophageal stenosis in distal esophagus was found, which required total esophageal reconstruction. After removing the lower esophagus and creation of cervical esophagostomy, the same procedure as in case 1 was performed successfully at age 15. The procedure released him from long lasting daily bouginage and semi solid food. This procedure is quite simple and relatively easy for salvage of complicated esophageal atresia and stenosis.
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Masaki Nio, Nobuyuki Sano, Yutaka Hayashi, Takamichi Kamiyama, Megumi ...
Article type: Article
2002 Volume 38 Issue 2 Pages
314-318
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We report on a neonate with a paratesticular cyst associated with intra-abdominal testis. A large abdominal cyst was detected by prenatal ultrasonography at 34 weeks of gestation. Preoperative diagnostic imaging demonstrated a cystic lesion 6×4×3 cm in size in the left suprapubic area. Left testis was nonpalpable in the inguino-scrotal region. He underwent operation at the age of 21 days. At operation, a large cyst accompanied by left spermatic vessels and vas deference was confirmed laparoscopically. Laparoscopic-assisted orchiectomy was performed. Histopathological diagnosis was a mesothelial cyst arising from paratesticular tissue. His postoperative course was uneventful.
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2002 Volume 38 Issue 2 Pages
319-324
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[in Japanese], [in Japanese], [in Japanese], [in Japanese]
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2002 Volume 38 Issue 2 Pages
325-
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[in Japanese], [in Japanese], [in Japanese], [in Japanese], [in Japane ...
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2002 Volume 38 Issue 2 Pages
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[in Japanese], [in Japanese]
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2002 Volume 38 Issue 2 Pages
325-
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[in Japanese], [in Japanese], [in Japanese]
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2002 Volume 38 Issue 2 Pages
325-
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