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- 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
Online Exclusives
3 Results
- Research Article
Brachial plexus palsy, a rare delayed complication of the Nuss procedure for pectus excavatum: a case report
Journal of Pediatric SurgeryVol. 47Issue 11e19–e20Published in issue: November, 2012- Tieqin Liu
- Hongxu Liu
- Chunlu Yang
- Shun Xu
- Changbo Sun
Cited in Scopus: 3We 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 SurgeryVol. 42Issue 10e9–e12Published in issue: October, 2007- Hajime Hosoi
- T. Iehara
- K. Tsuchiya
- A. Misawa
- M. Miyaji
- S. Yagyu
- and others
Cited in Scopus: 8Malignant 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. - Rapid Communication
Chest wall mesenchymal hamartoma associated with a massive fetal pleural effusion: a case report
Journal of Pediatric SurgeryVol. 40Issue 5e5–e7Published in issue: May, 2005- Akio Odaka
- Shigeki Takahashi
- Takemaru Tanimizu
- Hiroshi Kawashima
- Shigehisa Inokuma
- Hideyuki Ishida
- and others
Cited in Scopus: 14We 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.