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Dive into the research topics where Noriomi Suzuki is active.

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Featured researches published by Noriomi Suzuki.


Auris Nasus Larynx | 2014

Transoral closure of pharyngeal perforation caused by gastrointestinal endoscopy

Koichiro Wasano; Sayuri Hashiguchi; Noriomi Suzuki; Taiji Kawasaki; Ichirota Nameki; Hideo Nameki

OBJECTIVE We present a case of pharyngeal perforation caused by gastrointestinal endoscopy that was successfully repaired with transoral mucosal sutures. This is the first report of a transoral surgical closure of a perforation caused by an endoscope. We describe the repair procedure, the necessary equipment, and the effectiveness of suturing pharyngeal perforations. PATIENT An 87-year-old woman brought to our emergency department by ambulance because of hematemesis and endoscopic hemostasis was successfully performed. But after hemostasis, CT scan showed emphysema extending from the right lower jaw to the superior mediastinum and pharyngeal perforation was observed by laryngeal fiberscope. INTERVENTION Even though she had received conservative treatment, exacerbation of inflammation was observed and therefore we performed transoral surgery for closing the pharyngeal perforation. MAIN OUTCOME MEASURE We followed up with CT scans, blood test and vital signs. RESULTS The pharyngeal perforation smoothly closed and exacerbation of inflammation was not observed, even after oral ingestion began. CONCLUSION Transoral closure of a pharyngeal perforation is less invasive and performing this procedure at an early stage can lead to a favorable outcome.


Neuroreport | 2016

Expression pattern of wolframin, the WFS1 (Wolfram syndrome-1 gene) product, in common marmoset (Callithrix jacchus) cochlea.

Noriomi Suzuki; Makoto Hosoya; Naoki Oishi; Hideyuki Okano; Masato Fujioka; Kaoru Ogawa

Wolfram syndrome is an autosomal recessive disorder of the neuroendocrine system, known as DIDMOAD (Diabetes Insipidus, Diabetes Mellitus, Optic Atrophy and Deafness) syndrome, and considered an endoplasmic reticulum disease. Patients show mutations in WFS1, which encodes the 890 amino acid protein wolframin. Although Wfs1 knockout mice develop diabetes, their hearing level is completely normal. In this study, we examined the expression of wolframin in the cochlea of a nonhuman primate common marmoset (Callithrix jacchus) to elucidate the discrepancy in the phenotype between species and the pathophysiology of Wolfram syndrome-associated deafness. The marmoset cochlea showed wolframin immunoreactivity not only in the spiral ligament type I fibrocytes, spiral ganglion neurons, outer hair cells, and supporting cells, but in the stria vascularis basal cells, where wolframin expression was not observed in the previous mouse study. Considering the absence of the deafness phenotype in Wfs1 knockout mice, the expression of wolframin in the basal cells of primates may play an essential role in the maintenance of hearing. Elucidating the function of wolframin protein in the basal cells of primates would be essential for understanding the pathogenesis of hearing loss in patients with Wolfram syndrome, which may lead to the discovery of new therapeutics.


Auris Nasus Larynx | 2017

Successful continual intratympanic steroid injection therapy in a patient with refractory sensorineural hearing loss accompanied by relapsing polychondritis

Koichiro Wasano; Shuta Tomisato; Sayuri Yamamoto; Noriomi Suzuki; Taiji Kawasaki; Kaoru Ogawa

OBJECTIVE To report the treatment efficacy of continual intratympanic steroid injection (ITSI) therapy in a patient with refractory sensorineural hearing loss accompanied by relapsing polychondritis. PATIENT A 49-year-old female diagnosed with relapsing polychondritis at the age of 45 years and who had been treated with corticosteroids and immunosuppressants developed sensorineural hearing loss in the left ear. INTERVENTION Her unilateral hearing loss did not recover despite receiving one cyclophosphamide pulse treatment, one methylprednisolone pulse treatment, and weekly leukapheresis. Thus, we decided to initiate weekly ITSI therapy. MAIN OUTCOME MEASURE Pure tone audiometry. RESULTS A week after the first ITSI treatment, the patients hearing improved. We continued ITSI therapy and attempted to extend the interval between treatments, but her hearing worsened when ITSI therapy was delivered at 2- to 3-week intervals. Thus, we returned ITSI therapy to once per week for 21 months (total of 71 treatments). She experienced no adverse events, like tympanic perforation, and 1 year after terminating the therapy, her hearing remained stable and did not worsen. CONCLUSIONS Continual, weekly ITSI therapy was effective in treating sensorineural hearing loss accompanied by relapsing polychondritis. ITSI therapy may be a promising treatment option for sensorineural hearing loss caused by autoimmune disease.


Auris Nasus Larynx | 2015

Closure of tracheoesophageal puncture with pedicled fascia flap of the sternocleidomastoid muscle

Koichiro Wasano; Noriomi Suzuki; Taiji Kawasaki; Sayuri Yamamoto; Shujiro Minami; Taku Yamashita; Kaoru Ogawa

OBJECTIVE Closure of a tracheoesophageal puncture (TEP) formed during voice prosthesis implantation may sometimes be required. We report a new method of closure that we have termed the RESET method. METHODS We used the RESET method for four patients. An initial incision was made at the mucocutaneous junction of the tracheostoma, and the trachea and esophagus were separated. The TEP was sectioned, and the tracheal and esophageal sides were sutured into separate layers. A pedicled fascia flap lifted from the sternocleidomastoid muscle was sandwiched between the trachea and the esophagus, and subsequently secured. RESULTS The TEP was closed in all patients, and no complications were observed. CONCLUSION The RESET method, using a pedicled fascia flap with stable perfusion, is a simple, reliable method of TEP closure.


Journal of Japan Society for Head and Neck Surgery | 2014

Clinical study on prognostic factors of recurrence in thyroid carcinoma

Noriomi Suzuki; Koichiro Wasano; Taiji Kawasaki; Hideo Nameki

We treated 137 patients with well-differentiated thyroid carcinoma at our hospital from 2002 to 2012. This paper clarifies the high-risk group based on prognostic factors of recurrence. The 5-year survival rate for patients with thyroid carcinoma was 94.9%. Recurrence occurred in 25 cases (18.2%). The factors of patient’s age and sex were not related to recurrence. The factors of disease, vein invasion, extracapsular spread and lymph node metastasis for D2 area made significant independent contributions. We must determine the course of treatment of patients with prognostic factors of recurrence carefully. We also need to follow the patients carefully, such as a CT scan every six months and ultrasound every three months.


Practica oto-rhino-laryngologica | 2013

A case of nasopharyngeal carcinoma ex pleomorphic adenoma

Koichiro Wasano; Yuichi Ikari; Sayuri Hashiguchi; Noriomi Suzuki; Taiji Kawasaki; Hiroyuki Ozawa


Audiology Japan | 2017

Change over the years in the incidence rate of otitis media with effusion in children with a cleft palate

Azusa Maegawa; Naoki Oishi; Kazumi Asano; Noriomi Suzuki; Takashi Kojima; Hideyuki Saito; Minako Sato; Kaoru Ogawa


Nippon Jibiinkoka Gakkai Kaiho | 2016

Usefulness and limitation of thyroglobulin measurement in fine needle aspirates(FNA-Tg) for diagnosis of neck lymph node metastasis from thyroid carcinoma

Koji Sakamoto; Yorihisa Imanishi; Toshiki Tomita; Hiroyuki Ozawa; Yoichiro Sato; Yozo Inagaki; Hiroyuki Yamada; Fumihiro Ito; Noriomi Suzuki; Takeyuki Kono; Shin Saito; Masaru Noguchi; Takanori nishiyama; Shintaro Nakamura; Hiroko Fujita; Takahisa Watabe; Seiichi Shinden; Kaoru Ogawa


Journal of Laryngology and Otology | 2016

A case of presigmoid retrolabyrinthine approach to vestibular schwannoma by use of continuous direct neurophysiological monitoring of facial nerve and cochlear nerve

Naoki Oishi; Hidemi Miyazaki; Noriomi Suzuki; Kaoru Ogawa


Journal of Laryngology and Otology | 2016

Canal wall down tympanoplasty with soft posterior meatal wall reconstruction in cases of recurrent cholesteatoma

Saeko Matsuzaki; Naoki Oishi; Masato Fujioka; Sho Kanzaki; Yoshihiko Hiraga; Noriomi Suzuki; Makoto Hosoya; Kaoru Ogawa

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