5 results on '"Sanabe, Naoya"'
Search Results
2. A Case of Intrathoracic Gastric Duplication Cyst Detected on Prenatal Ultrasound Examination
- Author
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Yagi, Hisako, Kinjyo, Yoshino, Chinen, Yukiko, Nitta, Hayase, Kinjo, Tadatsugu, Mekaru, Keiko, Masamoto, Hitoshi, Goya, Hideki, Yoshida, Tomohide, Sanabe, Naoya, and Aoki, Yoichi
- Subjects
Article Subject - Abstract
A 37-year-old (G4P3) woman was referred to our hospital at 32 weeks of gestation for the evaluation of a fetus with an intrathoracic cystic lesion. Ultrasonography and magnetic resonance imaging revealed that a fetal cystic lesion without a mucosal layer was located in the posterior mediastinum. These findings were consistent with a bronchogenic cyst. At 38 3/7 weeks of gestation, an elective cesarean section was performed because of her previous cesarean section. A female neonate without any external anomalies, weighing 2,442 g, with Apgar scores of 8 and 9, and requiring no resuscitation was born. Four weeks after delivery, the neonate was admitted because of respiratory distress due to mass effect. At right lateral thoracotomy, a 105 × 65 mm of solitary smooth-walled cyst containing serosanguineous fluid was found in the posterior mediastinum, which was excised completely. Histologic examination revealed the diagnosis of the mediastinal gastric duplication cyst. The neonate made an uneventful recovery. Accurate diagnosis is not necessary, but detection and continuous observation are logical. Although gastric duplication, particularly intrathoracic, is a rare pathology, it should be considered in the differential diagnosis of any intrathoracic cyst.
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- 2018
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3. Early parenteral nutrition in neonates with congenital diaphragmatic hernia.
- Author
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Yoshida, Tomohide, Goya, Hideki, Iida, Nobuhiro, Arakaki, Mayumi, Sanabe, Naoya, and Nakanishi, Koichi
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GENETIC disorder treatment ,AMINO acids ,BODY weight ,DIAPHRAGMATIC hernia ,LIPIDS ,LIVER diseases ,NEONATAL intensive care ,PARENTERAL feeding ,PATIENT safety ,PULMONARY hypertension ,WEIGHT gain ,EARLY intervention (Education) ,NEONATAL intensive care units ,RETROSPECTIVE studies ,DESCRIPTIVE statistics ,DISEASE risk factors ,CHILDREN - Abstract
Background: The ideal nutritive strategy for a neonate with congenital diaphragmatic hernia (CDH) has not been elucidated. The purpose of this study was to investigate the efficacy of early parenteral nutrition (PN) in CDH neonates. Methods: Thirty‐five CDH neonates admitted to a single hospital from January 2005 to December 2014 were retrospectively reviewed. For the first 4 years of the study period, neonates received non‐early PN (n‐EPN) (2005–2008, amino acids [AA] <1.0 g/kg/day, no lipids administered). After the transitional period (TP) (2009–2011, AA 1.0–2.5 g/kg/day, lipid 1.0 g/kg/day), early PN (EPN) (2011–2014, AA ≥3.0 g/kg/day, lipid 1.0 g/kg/day) was performed. We investigated the clinical effect of PN for growth‐associated clinical variables and the outcomes. Results: The first day of AA administration was late in the n‐EPN period (6.0 ± 4.6, 0.0 ± 0.8, 0.1 ± 0.3 ; n‐EPN, TP, EPN: in order). The final day of PN (11.0 ± 3.7, 9.2 ± 4.0, 12.4 ± 3.9) and the first day of enteral feeding (4.5 ± 1.9, 4.3 ± 1.4, 4.5 ± 3.2), the first day of full milk feeding (100 mL/kg/day) (10.8 ± 5.4, 9.2 ± 2.3, 11.5 ± 3.5) were statistically equal in every period. The date and body weight at discharge showed no significant differences among the three groups, but the weight‐gain rate from birth to discharge was higher in the EPN group than in the n‐EPN group (P = 0.023). The rate of inhaled nitric oxide (NO) gas administration and the duration of ventilation showed no significant differences among the three groups. Severe PN‐associated liver disease was not noted during the observation period. Conclusions: Early PN for CDH neonates promotes weight gain in the neonatal intensive‐care unit. The long‐term efficacy and safety of EPN for CDH neonates should be elucidated by additional studies. [ABSTRACT FROM AUTHOR]
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- 2020
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4. [症例報告]A large nonparasitic liver cyst requiring surgical intervention : A case report
- Author
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Sanabe, Naoya, Nomura, Hironori, Hiroyasu, Shungo, Shiraishi, Masayuki, and Muto, Yoshihiro
- Subjects
recurrence after aspiration ,surgical intervention (unroofing) ,liver ,nonparasitic cyst - Abstract
The case of a large nonparasitic liver cyst with a 9-year history of cyst recurrence after undergoing aspiration therapy in a 78-year-old woman is herein reported. Nine years prior to this admission, she underwent an operation for a hernia of the lumbar intervertebral disc. At operation, a large liver cyst was incidentally detected, and the cyst was aspirated at that time to relieve her abdominal pain. Five years after the initial therapy, she developed abdominal distension and pain. The patient again underwent cyst aspiration. Thereafter, she experienced a 4-year symptom-free period after the second cyst aspiration. On admission, an abdominal CT scan revealed a large simple cyst measuring 17×12×17 cm in size which occupied most of the right liver lobe extending down to the right lower quadrant. At laparotomy, a large cyst showed entensive fibrous adhesions to the adjacent viscera. Following lysis of adhesions and the evacuation of the cyst fluid, the cyst, which was bulging into the abdominal cavity, was almost totally excised (unroofing). She remained asymptomatic 5 months after discharge. The standard treatment for nonparasitic liver cysts currently consists of cyst aspiration and alcohol sclerotherapy. However, the long-term follow-up of cysts after aspiration is unknown. Therefore, at present, cyst recurrence after aspiration may require either cyst unroofing or a partial excision., 論文
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- 1999
5. Fetal Thoracoamniotic Shunting in a Case of Congenital Pulmonary Airway Malformations with Hydrops Fetalis.
- Author
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Nitta H, Taira Y, Kinjo T, Chinen Y, Masamoto H, Sanabe N, Goya H, Yoshida T, Sugibayashi R, Sumie M, Wada S, Sago H, and Aoki Y
- Abstract
Aim We report a case of congenital pulmonary airway malformation (CPAM) with hydrops in which the fetus underwent thoracoamniotic shunting. Case Report A 40-year-old (G1P1) woman was diagnosed with a macrocystic CPAM. Thoracoamniotic shunting was performed at 19 weeks of gestation but not well drained and was successfully performed again at 23 weeks. However, the CPAM volume ratio, abdominal circumference, and amniotic fluid index started increasing from 28 weeks and hydrops worsened. The insufficient shunting and the fetal cardiac failure had to be considered. At 32 weeks, a male infant with general edema and massive ascites was born weighing 3,362 g (+4.79 SD) with Apgar scores of 2 and 4. The infant was intubated and high-frequency oscillation and nitric oxide therapies were instituted. The resection of CPAM was performed on day 2. Nasal continuous positive airway pressure was instituted on day 16. The infant was discharged and prescribed with home oxygen therapy (HOT) on day 65. The infant was able to leave the HOT at 30 months and is currently 34 months of age in good condition. Conclusion Fetal thoracoamniotic shunting may be life-saving in CPAM complicated by hydrops and that this treatment might be sufficient to cure the child.
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- 2017
- Full Text
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