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Anesthetic Management of a Rett Syndrome Patient at High Risk for Respiratory Complications
Nobuhito Kamekura DDS, PhD,
 Takayuki Hojo DDS, PhD,
 Yukie Nitta DDS, PhD,
 Yuri Hase DDS, PhD, and
 Toshiaki Fujisawa DDS, PhD
Article Category: Case Report
Volume/Issue: Volume 68: Issue 3
Online Publication Date: Oct 04, 2021
DOI: 10.2344/anpr-68-02-07
Page Range: 163 – 167

patient was a 23-year-old female (height 135 cm; weight 24 kg; body mass index 13.2 kg/m 2 ) who required general anesthesia for treatment of dental caries due to her intellectual disability, as she was generally unable to tolerate dental care otherwise. She was diagnosed with RTT at 2 years of age and had a history of pneumonia requiring hospitalization more than 10 years earlier. The patient also had epilepsy, which was difficult to control despite being maintained on antiepileptic medications. Her seizures, presenting as twitching or jerking limb movements and upward

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Figure.; Preoperative anterior-posterior (AP) chest radiograph. AP chest radiograph illustrating severe scoliosis (Cobb angle ∼55°).
Nobuhito Kamekura,
 Takayuki Hojo,
 Yukie Nitta,
 Yuri Hase, and
 Toshiaki Fujisawa
Figure.
Figure.

Preoperative anterior-posterior (AP) chest radiograph. AP chest radiograph illustrating severe scoliosis (Cobb angle ∼55°).


Yoshiki Shionoya DDS, PhD,
 Hatsuko Kamiga DDS,
 Gentarou Tsujimoto DDS, PhD,
 Eishi Nakamura DDS,
 Kiminari Nakamura DDS, PhD, and
 Katsuhisa Sunada DDS, PhD
Article Category: Case Report
Volume/Issue: Volume 67: Issue 1
Online Publication Date: Jan 01, 2020
Page Range: 28 – 34

arrhythmias associated with myocardial fibrosis. 1 Interstitial pneumonia due to pulmonary fibrosis develops in approximately 80% of patients with SSc, 2 so restrictive lung disease is commonly found in these patients. Currently, the most common cause of death in patients with SSc is pulmonary fibrosis. 3 Seventy percent of patients with SSc also develop microstomia secondary to fibrosis of the facial skin and oral mucosa. These patients can have increased discomfort during dental treatment because of the microstomia, which can necessitate excessive stretching of the

Nobuhito Kamekura DDS, PhD,
 Yukie Nitta DDS, PhD,
 Shigeru Takuma DDS, PhD, and
 Toshiaki Fujisawa DDS, PhD
Article Category: Research Article
Volume/Issue: Volume 63: Issue 2
Online Publication Date: Jan 01, 2016
Page Range: 91 – 94

did not require any food modification. However, he needed total assistance in eating because of involuntary movements of the upper limbs. He was not able to take tablets, but was able to take powdered medicine. Physical examination revealed nystagmus; ataxia with spasticity, especially in the lower limbs; and frequent movements of the upper limbs and upper body. He could not stand straight and walk, but he could operate a wheelchair by himself. As he had no past history of epilepsy, aspiration pneumonia, or swallowing difficulties, it was decided to perform general

Reina Hayashi DDS,
 Shigeru Maeda DDS, PhD,
 Taninishi Hideki MD, PhD,
 Hitoshi Higuchi DDS, PhD, and
 Takuya Miyawaki DDS, PhD
Article Category: Case Report
Volume/Issue: Volume 67: Issue 4
Online Publication Date: Dec 31, 2020
Page Range: 214 – 218
Yuki Chogyoji DDS and
 Seiji Watanabe MD, PhD
Article Category: Research Article
Volume/Issue: Volume 67: Issue 2
Online Publication Date: Jul 06, 2020
Page Range: 79 – 85

Cuffed endotracheal tubes (ETTs) are designed to provide a tracheal seal, permit positive-pressure ventilation, and prevent the passage of fluids and other debris that may be present in the pharynx into the lungs, which could otherwise increase the risk of postoperative pneumonia (POP) following anesthesia. 1 Although the use of a cuffed ETT may not completely prevent the aspiration of fluids that have accumulated in the subglottic space, small volumes of fluids leaking around the cuff and into the lower airways are not usually a serious

Michael D. Turner DDS, MD,
 Vasiliki Karlis DMD, MD, and
 Robert S. Glickman DMD
Article Category: Research Article
Volume/Issue: Volume 54: Issue 3
Online Publication Date: Jan 01, 2007
Page Range: 115 – 117

the mandible. The proposed treatment was closed reduction in the operating room under general anesthesia. Her past medical history was significant for liver transplantation performed 6 months earlier, secondary to fulminant hepatitis caused by hepatitis C. Current medications were prednisone and tacrolimus for immunosuppression and dapsone for P. carinii pneumonia (PCP) prophylaxis. The patient was taken to the operating room and standard monitors were placed by the anesthesiologist. Presurgical vital signs revealed a normal sinus rhythm, blood pressure of

Asako Yasuda DDS, PhD,
 Noriko Miyazawa MD, PhD,
 Emiko Inoue DDS,
 Tomoaki Imai DDS,
 Yoshiki Shionoya DDS, PhD, and
 Kiminari Nakamura DDS, PhD
Article Category: Brief Report
Volume/Issue: Volume 68: Issue 2
Online Publication Date: Jun 29, 2021
Page Range: 117 – 118

Juvenile hyaline fibromatosis (JHF) is a rare genetic disease involving mutations of the ANTXR2 gene causing the accumulation of hyaline substance in various tissues and is characterized by multiple subcutaneous nodules or masses, gingival hyperplasia, and joint contracture. Severity of signs and symptoms occur on a spectrum with more severe cases typically occurring at or shortly after birth. 1 – 3 The patient was a 1-year-9-month-old female (height 76.5 cm; weight 7.2 kg) who was previously hospitalized twice with pneumonia. She was scheduled for

Yuki Gomi DDS,
 Asuka Taguchi DDS, PhD,
 Sahoko Matsunari DDS,
 Taisuke Iwamoto DDS,
 Yui Kawamoto DDS,
 Satoshi Tachikawa DDS, PhD,
 Rikuo Masuda DDS, PhD,
 Kinuko Gotoh DDS, PhD, and
 Takehiko Iijima DDS, DMSc, PhD
Article Category: Brief Report
Volume/Issue: Volume 64: Issue 2
Online Publication Date: Jan 01, 2017
Page Range: 102 – 103

maxillary cyst, later diagnosed as a bronchogenic cyst. The patient was diagnosed with congenital bronchial atresia, on the superior segmental bronchus of the left lung, at the age of 1 year old after experiencing frequent bouts of pneumonia. She had been doing well, although one-fifth of her lung was insufficiently aerated. Pulmonary function testing was within normal limits (% vital capacity [VC] 92.7%, % forced expiratory volume [FEV] 1.0 92.13%). Chest radiograph ( Figure 1 ) revealed an extrahilar mass in the upper lobe of the left lung. Chest computed tomography

Yuzuru Kaneko DDS, PhD
Article Category: Research Article
Volume/Issue: Volume 58: Issue 2
Online Publication Date: Jan 01, 2011
Page Range: 106 – 106

From left to right: Prof J. Weaver, Prof Y. Kubota, Mrs Kubota, and Mrs Weaver at IFDAS 2006 in Yokohama, Japan. From left to right: Prof J. Weaver, Prof Y. Kubota, Mrs Kubota, and Mrs Weaver at IFDAS 2006 in Yokohama, Japan. Yasuya Kubota, Professor Emeritus of Tokyo Medical and Dental University, passed away due to pneumonia in December, 2010. He was born in Mie Prefecture, Japan, in 1928. In 1950, he graduated from the Faculty of Medicine of Tokyo Medical and