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Journal of Pediatric Surgery
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    • Online Exclusives
    • Iwai, NaomiRemove Iwai, Naomi filter
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    Article Type

    • Rapid Communication5
    • Research Article1

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    Author

    • Fumino, Shigehisa3
    • Ono, Shigeru3
    • Shimotake, Takashi3
    • Aoi, Shigeyoshi2
    • Deguchi, Eiichi2
    • Furukawa, Taizo2
    • Iwabuchi, Toshihisa2
    • Kinoshita, Hiromi2
    • Tsuda, Tomoki2
    • Chiba, Fumiko1
    • Furukawa, Taizow1
    • Kimura, Osamu1
    • Nishimura, Tohru1
    • Sakai, Kohei1
    • Shimadera, Shinichi1

    Journal

    • Journal of Pediatric Surgery6

    Keyword

    • Choledochal cyst2
    • Anomalous arrangement of the pancreaticobiliary duct1
    • Bile duct cancer1
    • Bile peritonitis1
    • Biliary pseudocyst1
    • Chest wall tumor1
    • Children1
    • Cholangiocarcinoma1
    • Chylous ascites1
    • Congenital hydrocephalus1
    • FDG-PET1
    • Hirschsprung's disease1
    • Lung1
    • Lymphangioma1
    • Lymphatic malformation1
    • Mesenchymoma1
    • Mucoepidermal carcinoma1
    • Neural crest1
    • Neurocutaneous melanosis1
    • OK-432 therapy1
    • Pancreaticobiliary maljunction1
    • Pleural effusion1
    • Pulmonary hypoplasia1
    • Rupture1

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    • Rapid Communication

      OK-432 therapy for chylous pleural effusion or ascites associated with lymphatic malformations

      Journal of Pediatric Surgery
      Vol. 45Issue 9e7–e10Published in issue: September, 2010
      • Shigeru Ono
      • Naomi Iwai
      • Fumiko Chiba
      • Taizow Furukawa
      • Shigehisa Fumino
      Cited in Scopus: 14
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        OK-432 therapy is effective for the treatment of macrocystic lymphatic malformations (LMs), but the optimal management of patients with microcystic LMs associated with large chylous pleural effusions or chylous ascites is not resolved. We performed thoracoscopic- or laparoscopic-guided injection of OK-432 for 2 patients with diffuse microcystic LMs accompanied by refractory chylous pleural effusion or chylous ascites. Both cases responded well to OK-432 therapy with improvement/resolution of fluid collections and associated symptoms.
        OK-432 therapy for chylous pleural effusion or ascites associated with lymphatic malformations
      • Research Article

        Development of bile duct cancer in a 26-year-old man after resection of infantile choledochal cyst

        Journal of Pediatric Surgery
        Vol. 43Issue 6e17–e19Published in issue: June, 2008
        • Shigeru Ono
        • Kohei Sakai
        • Osamu Kimura
        • Naomi Iwai
        Cited in Scopus: 30
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          Anomalous arrangement of the pancreaticobiliary duct is considered to be a high-risk factor for biliary tract malignancy. We report a case of intrahepatic cholangiocarcinoma in a 26-year-old man after total resection of choledochal cyst with anomalous arrangement of the pancreaticobiliary duct at the age of 5 months. He had been doing well after total resection of the choledochal cyst; however, he suddenly presented with a spiky fever and abdominal pain in the right upper quadrant at the age of 26 years.
          Development of bile duct cancer in a 26-year-old man after resection of infantile choledochal cyst
        • Rapid Communication

          Spontaneous rupture of choledochal cyst with pseudocyst formation—report on 2 cases and literature review

          Journal of Pediatric Surgery
          Vol. 41Issue 6e19–e21Published in issue: June, 2006
          • Shigehisa Fumino
          • Naomi Iwai
          • Eiichi Deguchi
          • Shigeru Ono
          • Shinichi Shimadera
          • Toshihisa Iwabuchi
          • and others
          Cited in Scopus: 34
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            Spontaneous rupture and subsequent bile peritonitis are rare complications of choledochal cysts. Of these complications, the formation of a biliary pseudocyst is an unusual form, and its preoperative diagnosis is difficult. In this report, we describe 2 cases showing spontaneous rupture with biliary pseudocyst formation. Inflammatory tissue surrounded those pseudocysts, one of which was adjacent to the perforation and the other formed in the transverse mesocolon apart from the biliary tract. These pseudocysts were removed by careful dissection, and single-stage cyst excision with biliary reconstruction was successfully performed in both cases.
            Spontaneous rupture of choledochal cyst with pseudocyst formation—report on 2 cases and literature review
          • Rapid Communication

            Neurocutaneous melanosis associated with Hirschsprung's disease in a male neonate

            Journal of Pediatric Surgery
            Vol. 40Issue 8e11–e13Published in issue: August, 2005
            • Toshihisa Iwabuchi
            • Takashi Shimotake
            • Taizo Furukawa
            • Tomoki Tsuda
            • Shigeyoshi Aoi
            • Naomi Iwai
            Cited in Scopus: 9
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              Hirschsprung's disease is an inherited disorder characterized by the absence of ganglion cells in the distal bowel. Neurocutaneous melanosis is a rare congenital syndrome characterized by proliferation of melanin-producing cells in the skin and leptomeninges. The authors described a newborn patient with neurocutaneous melanosis associated with Hirschsprung's disease. This male baby had congenital hydrocephalus, large and multiple pigmented skin nevi, and severe abdominal distension. He showed marked hydrocephalus at birth and underwent a ventriculo-peritoneal shunt at the age of 5 days.
              Neurocutaneous melanosis associated with Hirschsprung's disease in a male neonate
            • Rapid Communication

              Respiratory insufficiency in a newborn with mesenchymal hamartoma of the chest wall occupying the thoracic cavity

              Journal of Pediatric Surgery
              Vol. 40Issue 4E13–E16Published in issue: April, 2005
              • Takashi Shimotake
              • Shigehisa Fumino
              • Shigeyoshi Aoi
              • Tomoki Tsuda
              • Naomi Iwai
              Cited in Scopus: 16
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                The authors describe a newborn patient with mesenchymal hamartoma of the chest wall associated with pulmonary hypoplasia. A massive thoracic tumor was diagnosed by prenatal ultrasonography and magnetic resonance imaging at the 28th week of gestation. She was delivered through cesarean delivery at the 36th gestational week. Respiratory distress because of pulmonary hypoplasia necessitated neonatal intensive care. The tumor extensively involved the left hemithorax including all 12 ribs and the first 10 thoracic vertebrae, resulting in marked deformity of the thorax.
                Respiratory insufficiency in a newborn with mesenchymal hamartoma of the chest wall occupying the thoracic cavity
              • Rapid Communication

                Mucoepidermal carcinoma of the lung detected by positron emission tomography in a 5-year-old girl

                Journal of Pediatric Surgery
                Vol. 40Issue 4E1–E3Published in issue: April, 2005
                • Hiromi Kinoshita
                • Takashi Shimotake
                • Taizo Furukawa
                • Eiichi Deguchi
                • Naomi Iwai
                Cited in Scopus: 14
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                  The authors describe a rare case of mucoepidermal carcinoma of the lung incidentally identified in preoperative assessments for inguinal hernia repair in a 5-year-old girl. This patient was referred for right external inguinal hernia, and a 3.0-cm round-shaped lesion was found in the right lower lung field of a chest x-ray film. She had no respiratory tract complaints, but her serum carcinoembryonic antigen concentration was markedly elevated (21.2 ng/mL). Chest and abdominal computed tomography/magnetic resonance images could not determine the nature of the lesion, but 2-[18F]fluoro-2-deoxy-d-glucose positron emission tomography (FDG-PET) indicated a malignant tumor pattern.
                  Mucoepidermal carcinoma of the lung detected by positron emission tomography in a 5-year-old girl
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                • Home
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