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Journal of Pediatric Surgery
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    Article Type

    • Rapid Communication2
    • Research Article1

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    Author

    • Baba, Kazunor1
    • Hashimoto, Daijo1
    • Hoshino, Takanobu1
    • Hosoi, Hajime1
    • Iehara, T1
    • Inokuma, Shigehisa1
    • Ishida, Hideyuki1
    • Iwai, N1
    • Kawashima, Hiroshi1
    • Koizumi, M1
    • Liu, Hongxu1
    • Liu, Tieqin1
    • Misawa, A1
    • Miyaji, M1
    • Nishimura, T1
    • Odaka, Akio1
    • Satomi, Akira1
    • Sugimoto, T1
    • Sun, Changbo1
    • Takahashi, Shigeki1
    • Tamura, Masanori1
    • Tanimizu, Takemaru1
    • Tokiwa, K1
    • Tsuchiya, K1
    • Xu, Shun1

    Journal

    • Journal of Pediatric Surgery3

    Keyword

    • Brachial plexus1
    • Carinatum1
    • Complications1
    • Injury1
    • Malignant rhabdoid tumor1
    • Mesenchymal hamartoma1
    • Pectus excavatum1
    • Pleural effusion1
    • Pleuroamniotic shunt1
    • Prenatal diagnosis1
    • Relapse1
    • Remission1
    • Surgery1

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    • Research Article

      Brachial plexus palsy, a rare delayed complication of the Nuss procedure for pectus excavatum: a case report

      Journal of Pediatric Surgery
      Vol. 47Issue 11e19–e20Published in issue: November, 2012
      • Tieqin Liu
      • Hongxu Liu
      • Chunlu Yang
      • Shun Xu
      • Changbo Sun
      Cited in Scopus: 3
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        We report a rare complication after the Nuss procedure for the correction of pectus excavatum in a 15-year-old adolescent boy. He began to have delayed right brachial plexus injury on the 15th postoperative day. Careful physical check-up revealed a painful and enlarged subaxillary lymph node. He was successfully treated using anti-inflammatory medications and physical therapy.
      • Rapid Communication

        Continuous remission in an infant with chest wall malignant rhabdoid tumor after relapse

        Journal of Pediatric Surgery
        Vol. 42Issue 10e9–e12Published in issue: October, 2007
        • Hajime Hosoi
        • T. Iehara
        • K. Tsuchiya
        • A. Misawa
        • M. Miyaji
        • S. Yagyu
        • and others
        Cited in Scopus: 8
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          Malignant rhabdoid tumor (MRT) is a highly aggressive tumor that occurs in infancy or childhood. The prognosis, especially in infants, is very poor. Here we report the long-term survival of a 5-month-old boy with MRT that arose from the chest wall. After total resection of the tumor, the patient was given 4 cycles of doxorubicin, vincristine, and cyclophosphamide, alternating with ifosfamide and etoposide. After 18 months off therapy, he had a local recurrence at the same site. After a second total resection, he was given additional chemotherapy with 30.6-Gy local irradiation.
          Continuous remission in an infant with chest wall malignant rhabdoid tumor after relapse
        • Rapid Communication

          Chest wall mesenchymal hamartoma associated with a massive fetal pleural effusion: a case report

          Journal of Pediatric Surgery
          Vol. 40Issue 5e5–e7Published in issue: May, 2005
          • Akio Odaka
          • Shigeki Takahashi
          • Takemaru Tanimizu
          • Hiroshi Kawashima
          • Shigehisa Inokuma
          • Hideyuki Ishida
          • and others
          Cited in Scopus: 14
          Online Only
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            We report on an extremely rare chest wall mesenchymal hamartoma associated with a massive fetal pleural effusion. Prenatal ultrasound examination demonstrated a heterogeneous mass in the right thorax associated with a massive pleural effusion and right lung compression at 29 weeks of gestation. The patient underwent pleuroamniotic shunting at 30 weeks and was delivered at 33 weeks by cesarean delivery secondary to fetal distress. After management of the respiratory distress and evaluation of the mass, surgery was performed at day of life 8.
            Chest wall mesenchymal hamartoma associated with a massive fetal pleural effusion: a case report
          Page 1 of 1

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