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3 Results
- Rapid Communication
Neurocutaneous melanosis associated with Hirschsprung's disease in a male neonate
Journal of Pediatric SurgeryVol. 40Issue 8e11–e13Published in issue: August, 2005- Toshihisa Iwabuchi
- Takashi Shimotake
- Taizo Furukawa
- Tomoki Tsuda
- Shigeyoshi Aoi
- Naomi Iwai
Cited in Scopus: 9Hirschsprung'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. - Rapid Communication
Respiratory insufficiency in a newborn with mesenchymal hamartoma of the chest wall occupying the thoracic cavity
Journal of Pediatric SurgeryVol. 40Issue 4E13–E16Published in issue: April, 2005- Takashi Shimotake
- Shigehisa Fumino
- Shigeyoshi Aoi
- Tomoki Tsuda
- Naomi Iwai
Cited in Scopus: 16The 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. - Rapid Communication
Mucoepidermal carcinoma of the lung detected by positron emission tomography in a 5-year-old girl
Journal of Pediatric SurgeryVol. 40Issue 4E1–E3Published in issue: April, 2005- Hiromi Kinoshita
- Takashi Shimotake
- Taizo Furukawa
- Eiichi Deguchi
- Naomi Iwai
Cited in Scopus: 14The 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.