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Journal of Japanese Society of Oral Medicine最新文献

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A Case of Plasmacytosis Successfully Treated with Corticosteroids 皮质类固醇成功治疗浆细胞增多症1例
Pub Date : 1900-01-01 DOI: 10.6014/jjsom.25.51
Kentarou Muramatsu, Keisuke Ohno, H. Katou, Shuzi Yoshida, Akira Watanabe, N. Yamamoto, M. Takano, T. Chujo, K. Matsuzaka, T. Shibahara
Plasmacytosis is a chronic inflammatory disease that occurs in a body opening, such as the oral cavity or vulva, and is accompanied by mucosal redness, erosion, and edematous changes. Histopathological examination has revealed epithelial thinning and plasma cells. Plasmacytosis is a relatively rare disease with infiltration. Herein, we report a case of open-cell plasmacytosis that was successfully treated with corticosteroids despite difficulties in diagnosis and treatment.
浆细胞病是一种慢性炎症性疾病,发生在身体开口,如口腔或外阴,并伴有粘膜红肿、糜烂和水肿变化。组织病理学检查显示上皮变薄和浆细胞。浆细胞病是一种少见的浸润性疾病。在此,我们报告一例开放细胞浆细胞病,成功地与皮质类固醇治疗,尽管在诊断和治疗困难。
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引用次数: 0
A Case of Aggressive Growth of Gingival Metastasis from Lung Adenocarcinoma without Maxillary Bone Invasion 肺腺癌侵袭性牙龈转移生长,未侵犯上颌骨1例
Pub Date : 1900-01-01 DOI: 10.6014/jjsom.27.33
M. Takahashi, Shigehiro Abe, K. Shinoda, Atsushi Mamiya, Toru Takemoto, Souichi Aizawa, H. Kitano
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引用次数: 0
Clinical Statistics of Trigeminal Neuralgia Based on the International Classification of Orofacial Pain (1st Edition) 基于国际口面痛分类(第一版)的三叉神经痛临床统计
Pub Date : 1900-01-01 DOI: 10.6014/jjsom.27.1
Souichirou Tadokoro, N. Noma, Daiki Takanezawa, K. Ozasa, Akiko Okada, T. Shinozaki, Kaede Aono, Y. Imamura
{"title":"Clinical Statistics of Trigeminal Neuralgia Based on the International Classification of Orofacial Pain (1st Edition)","authors":"Souichirou Tadokoro, N. Noma, Daiki Takanezawa, K. Ozasa, Akiko Okada, T. Shinozaki, Kaede Aono, Y. Imamura","doi":"10.6014/jjsom.27.1","DOIUrl":"https://doi.org/10.6014/jjsom.27.1","url":null,"abstract":"","PeriodicalId":124417,"journal":{"name":"Journal of Japanese Society of Oral Medicine","volume":"124 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"127570190","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Clinicopathological Study of 24 Cases of Pemphigoid 类天疱疮24例临床病理分析
Pub Date : 1900-01-01 DOI: 10.6014/jjsom.25.1
Chisato Nakagawa, Fumihiko Tsushima, J. Sakurai, Atsushi Uesugi, Kiyoshi Sato, Seiichiro Oda, H. Harada
: Pemphigoid is an autoimmune bullous disease characterized by a subepithelial blister. We report 24 cases of pemphigoid who visited our department from 2007 through 2017. Twenty-one cases were classified as mucous membrane pemphigoid and 3 cases as bullous pemphigoid. They consisted of 5 males and 19 females, 44 to 91 years of age (median: 65.5 years). Lesions in the oral cavity were most frequently located in the gingiva (19 cases), followed by the buccal mucosa (7 cases) and the palate (6 cases). Eighteen of the 24 cases showed only oral manifestations. Treatment with systemic steroid was given to 12 cases, and topical steroid to 12 cases. In 8 of the 12 cases with topical steroid, we co-administered tetracycline, diaminodiphenyl and / or nicotinamide. The lesions of all patients were improved, and we have continued to treat them with attention to relapse. It is considered that a prompt diagnosis should be made and ap-propriate treatment for pemphigoid, which often shows only oral manifestations, should be provided in cooperation with dermatologists.
类天疱疮是一种以上皮下水疱为特征的自身免疫性大疱性疾病。我们报告了从2007年到2017年到我科就诊的24例类天疱疮患者。其中粘膜类天疱疮21例,大疱性类天疱疮3例。男性5例,女性19例,年龄44 ~ 91岁(中位数:65.5岁)。口腔病变以牙龈(19例)居多,其次为颊黏膜(7例)和上颚(6例)。24例中有18例仅表现为口腔症状。全身性类固醇治疗12例,局部类固醇治疗12例。在12例外用类固醇的病例中,我们联合给药四环素、二氨基二苯基和/或烟酰胺。所有患者的病变都得到了改善,我们继续治疗,并注意复发。我们认为,类天疱疮通常只表现为口腔症状,应与皮肤科医生合作,及时诊断并适当治疗。
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引用次数: 0
A Case of Xanthogranulomatous Sialadenitis of the Sublingual Gland:A Review of Literature 舌下腺黄色肉芽肿性涎腺炎1例:文献复习
Pub Date : 1900-01-01 DOI: 10.6014/jjsom.25.20
N. Kitamura, Seiji Ohno, Tetsuya Yamamoto
: Xanthogranulomatous tissue reaction is an inflammatory change that forms granulomas mainly composed of histiocytes, and xanthogranulomatous sialadenitis is extremely rare. Here we report a case of xanthogranulomatous sialadenitis of the sublingual gland. The patient was a 68-year-old Japanese woman. An elastic slightly hard mass with a diameter of 1 cm was palpated under the oral mucosa on the right side of the oral floor. We suspected a diagnosis of sublingual gland tumor and performed excisional biopsy. The histopathological diagnosis was xanthogranulomatous sialadenitis. Currently, 2.5 years have elapsed since the surgery, without recurrence.
:黄色肉芽肿性组织反应是一种炎性改变,形成肉芽肿,主要由组织细胞组成,黄色肉芽肿性涎腺炎极为罕见。我们在此报告一例舌下腺黄色肉芽肿性涎腺炎。患者为一名68岁的日本妇女。在口腔底右侧的口腔黏膜下触诊到直径约1 cm的弹性微硬肿块。我们怀疑诊断为舌下腺肿瘤,并进行了切除活检。组织病理学诊断为黄色肉芽肿性涎腺炎。目前,手术已经过去了2.5年,没有复发。
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引用次数: 0
Two Cases of Microscopic Polyangiitis Complicated with Multiple Oral Ulcers 镜下多血管炎并发多发性口腔溃疡2例
Pub Date : 1900-01-01 DOI: 10.6014/jjsom.28.32
T. Yakushiji, Eri Hasegawa, Masayasu Shibano
{"title":"Two Cases of Microscopic Polyangiitis Complicated with Multiple Oral Ulcers","authors":"T. Yakushiji, Eri Hasegawa, Masayasu Shibano","doi":"10.6014/jjsom.28.32","DOIUrl":"https://doi.org/10.6014/jjsom.28.32","url":null,"abstract":"","PeriodicalId":124417,"journal":{"name":"Journal of Japanese Society of Oral Medicine","volume":"28 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"125095187","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Oral Symptom Contributes to Diagnosis of Intestinal Behçet’s Disease:A Case Report 口腔症状有助于诊断肠道behaperet病1例
Pub Date : 1900-01-01 DOI: 10.6014/jjsom.25.25
M. Koike, Kazuhiro Ikeura, K. Fujita, H. Shimizu, S. Kato, H. Miyashita, T. Nakagawa, K. Tsunoda
{"title":"Oral Symptom Contributes to Diagnosis of Intestinal Behçet’s Disease:A Case Report","authors":"M. Koike, Kazuhiro Ikeura, K. Fujita, H. Shimizu, S. Kato, H. Miyashita, T. Nakagawa, K. Tsunoda","doi":"10.6014/jjsom.25.25","DOIUrl":"https://doi.org/10.6014/jjsom.25.25","url":null,"abstract":"","PeriodicalId":124417,"journal":{"name":"Journal of Japanese Society of Oral Medicine","volume":"27 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"123034918","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A Case of Buccal Mucosa and Tongue Amyloidosis Associated with Multiple Myeloma 口腔黏膜及舌淀粉样变合并多发性骨髓瘤1例
Pub Date : 1900-01-01 DOI: 10.6014/jjsom.27.26
Mizuki Abe, J. Nomura, Shinnosuke Nakamura, T. Iwamoto, K. Yamaguchi, S. Tamaki
{"title":"A Case of Buccal Mucosa and Tongue Amyloidosis Associated with Multiple Myeloma","authors":"Mizuki Abe, J. Nomura, Shinnosuke Nakamura, T. Iwamoto, K. Yamaguchi, S. Tamaki","doi":"10.6014/jjsom.27.26","DOIUrl":"https://doi.org/10.6014/jjsom.27.26","url":null,"abstract":"","PeriodicalId":124417,"journal":{"name":"Journal of Japanese Society of Oral Medicine","volume":"641 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"123336729","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A Case of Syphilis That Was Diagnosed with Oral Symptoms after a Prolonged Course 梅毒病程延长后被诊断为口腔症状1例
Pub Date : 1900-01-01 DOI: 10.6014/jjsom.26.36
Mikiko Ikehata, Takashi Yasuda, A. Enomoto, Naoki Ikehata, D. Chikazu
: Syphilis is one of the sexually transmitted infections. The incidence of syphilis in Japan has increased rap-idly 1︲3) in recent years, and so medical professionals need to be able to make an accurate diagnosis. We experienced a case of syphilis that had been diagnosed with oral mucosal lesions. The patient was a 40-year-old male who was diagnosed with syphilis based on oropharyngeal mucosal findings such as butterfly signs and serological examinations. He was treated with amoxicillin hydrate and was cured in about 10 weeks.
梅毒是性传播疾病之一。近年来,日本的梅毒发病率迅速上升(︲3),因此医疗专业人员需要能够做出准确的诊断。我们经历了一例梅毒,已被诊断为口腔粘膜病变。患者为40岁男性,经口咽黏膜蝶状征及血清学检查诊断为梅毒。他接受了阿莫西林水合物治疗,大约10周后痊愈。
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引用次数: 0
Clinical Statistics of Iatrogenic Trigeminal Nerve Injury 医源性三叉神经损伤的临床统计
Pub Date : 1900-01-01 DOI: 10.6014/jjsom.27.13
Hiroyoshi Yamamoto, A. Nishiyama, K. Sugiura, Sei Tanaka, Azusa Yamazaki, Takaharu Ariizumi, M. Murayama, Kiyohiro Kasahara, M. Takano, A. Katakura
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引用次数: 0
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Journal of Japanese Society of Oral Medicine
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