検索結果 722 件
| タイトル（別表記） | A case of duodenal diverticulitis in a patient receiving tocilizumab for rheumatoid arthritis |
|---|---|
| 著者 | 岩室 雅也| 馬場 雄己| 河原 祥朗| 岡田 裕之| |
| 抄録 | A Japanese woman was diagnosed with rheumatoid arthritis at the age of 41. At the age of 56, her rheumatoid arthritis worsened and a subcutaneous injection of tocilizumab and oral prednisolone was administered, which led to an improvement of arthritis. At the age of 57, right lower abdominal pain and vomiting suddenly appeared. Abdominal computed tomography showed a parapapillary diverticulum in the descending duodenum. The diverticulum was filled with residue, and an inflammation of the surrounding adipose tissue was observed; no free air was found. The patient was diagnosed with duodenal diverticulitis and treated with antibiotics, which resulted in an uneventful recovery. The maximum value of CRP was 1.88㎎/dL on the third day of hospitalization. Esophagogastroduodenoscopy performed on the 8th day of hospitalization revealed a parapapillary diverticulum with adhesion of pus and redness of the mucosa at the opening of the diverticulum, consistent with diverticulitis. This case highlights that diverticulitis in infrequent areas such as the duodenum may occur in patients who are treated with tocilizumab. In addition, inflammation of diverticulitis may be underestimated because abnormal laboratory values such as those induced by inflammatory reactions are less likely to occur during tocilizumab treatment. |
| キーワード | トシリズマブ（tocilizumab） 十二指腸憩室（duodenal diverticulum） 憩室炎（diverticulitis） |
| 出版物タイトル | 岡山医学会雑誌 |
| 発行日 | 2022-12-01 |
| 巻 | 134巻 |
| 号 | 3号 |
| 開始ページ | 166 |
| 終了ページ | 170 |
| ISSN | 0030-1558 |
| 関連URL | isVersionOf https://doi.org/10.4044/joma.134.166 |
| 言語 | 日本語 |
| 著作権者 | Copyright (c) 2022 岡山医学会 |
| 論文のバージョン | publisher |
| DOI | 10.4044/joma.134.166 |
| JaLCDOI | 10.18926/AMO/65155 |
|---|---|
| フルテキストURL | 77_2_227.pdf |
| 著者 | Obayashi, Atsuto| Aoki, Kazuma| Wada, Tadayoshi| Furuie, Hiromi | Kuraoka, Kazuya| Hamamoto, Takao| Tatsukawa, Takaharu| |
| 抄録 | We describe the use of the tyrosine kinase inhibitor lenvatinib in a patient with brain tumor metastases from anaplastic thyroid carcinoma (ATC). A 52-year-old Japanese male presented with consciousness loss. Imaging revealed a thyroid tumor and multiple brain lesions. After the brain tumor’s resection, pathology results provided the diagnosis of ATC. Total thyroidectomy was performed, followed by whole-brain irradiation. Additional brain lesions later developed, and lenvatinib therapy was initiated with no remarkable complications. However, the treatment effects were limited, and the patient died 2 months after starting lenvatinib, 202 days after the initial brain surgery. Relevant literature is discussed. |
| キーワード | anaplastic thyroid carcinoma brain metastasis lenvatinib |
| Amo Type | Case Report |
| 出版物タイトル | Acta Medica Okayama |
| 発行日 | 2023-04 |
| 巻 | 77巻 |
| 号 | 2号 |
| 出版者 | Okayama University Medical School |
| 開始ページ | 227 |
| 終了ページ | 232 |
| ISSN | 0386-300X |
| NCID | AA00508441 |
| 資料タイプ | 学術雑誌論文 |
| 言語 | 英語 |
| 著作権者 | Copyright Ⓒ 2023 by Okayama University Medical School |
| 論文のバージョン | publisher |
| 査読 | 有り |
| PubMed ID | 37094963 |
| Web of Science KeyUT | 000982563800006 |
| JaLCDOI | 10.18926/AMO/65154 |
|---|---|
| フルテキストURL | 77_2_221.pdf |
| 著者 | Iriyoshi, Hiroki| Sada, Ken-ei| Miyauchi, Atsushi| Yamamoto, Hirotaka| Hashimoto, Daisuke| Nojima, Shigeru| Yamanaka, Shingo| Kawamura, Masafumi| Oka, Satoshi| |
| 抄録 | Several previous case reports have shown that patients with immunoglobulin D (IgD) multiple myeloma (MM) can be withdrawn from hemodialysis, however, the characteristics that can predict withdrawal in these patients have not yet been elucidated. A 57-year-old Japanese woman required hemodialysis because of renal dysfunction due to IgD-λ and Bence Jones protein-λ MM. Bortezomib-based chemotherapy nine days after admission led to her withdrawal from hemodialysis on Day 50. In our case-based review, younger age and early initiation of bortezomib-based chemotherapy emerged as possible predictors of successful hemodialysis withdrawal. |
| キーワード | IgD-type multiple myeloma acute renal dysfunction urinary protein hemodialysis bortezomib |
| Amo Type | Case Report |
| 出版物タイトル | Acta Medica Okayama |
| 発行日 | 2023-04 |
| 巻 | 77巻 |
| 号 | 2号 |
| 出版者 | Okayama University Medical School |
| 開始ページ | 221 |
| 終了ページ | 225 |
| ISSN | 0386-300X |
| NCID | AA00508441 |
| 資料タイプ | 学術雑誌論文 |
| 言語 | 英語 |
| 著作権者 | Copyright Ⓒ 2023 by Okayama University Medical School |
| 論文のバージョン | publisher |
| 査読 | 有り |
| PubMed ID | 37094962 |
| Web of Science KeyUT | 000982563800005 |
| JaLCDOI | 10.18926/AMO/65153 |
|---|---|
| フルテキストURL | 77_2_215.pdf |
| 著者 | Washio, Kana| Tamefusa, Kosuke| Ochi, Motoharu| Kanamitsu, Kiichiro| Ishida, Hisashi| Fujiwara, Kaori| Nishida, Kenji| Tamai, Kei| Washio, Yosuke| Yoshimoto, Junko| Noda, Takuo| Tsukahara, Hirokazu| |
| 抄録 | Among patients with transient abnormal myelopoiesis (TAM) associated with Down syndrome, approximately 20% die within 6 months from multiorgan failure, especially liver fibrosis. We experienced three children with TAM who had low white blood cell counts but increased bilirubin levels. Here, we discuss the detailed clinical courses of these patients, including the pathological findings of liver biopsies. Our cases, together with previous literature, suggest that liver biopsy can be performed safely and provides useful information, especially regarding disease activities, and that low-dose cytarabine is a reasonable option to prevent early death in TAM patients with liver dysfunction. |
| キーワード | liver biopsy transient abnormal myelopoiesis Down syndrome low-dose cytarabine |
| Amo Type | Case Report |
| 出版物タイトル | Acta Medica Okayama |
| 発行日 | 2023-04 |
| 巻 | 77巻 |
| 号 | 2号 |
| 出版者 | Okayama University Medical School |
| 開始ページ | 215 |
| 終了ページ | 220 |
| ISSN | 0386-300X |
| NCID | AA00508441 |
| 資料タイプ | 学術雑誌論文 |
| 言語 | 英語 |
| 著作権者 | Copyright Ⓒ 2023 by Okayama University Medical School |
| 論文のバージョン | publisher |
| 査読 | 有り |
| PubMed ID | 37094961 |
| Web of Science KeyUT | 000982563800004 |
| JaLCDOI | 10.18926/AMO/65152 |
|---|---|
| フルテキストURL | 77_2_209.pdf |
| 著者 | Sakamoto, Masaki| Teraishi, Fuminori| Shigeyasu Kunitoshi| Kagawa, Shunsuke| Fujiwara, Toshiyoshi| |
| 抄録 | A 70-year-old male with anal pain and fever was diagnosed with rectal cancer perforation and abscess in the right gluteus maximus (GM) muscle. He underwent a transverse colon colostomy followed by preoperative capecitabine+oxaliplatin. Some local control was achieved but a residual abscess was observed in the right GM muscle. To secure circumferential resection margin by tumor reduction, he received chemoradiotherapy as total neoadjuvant therapy (TNT) and underwent laparoscopic abdominoperineal resection, D3 lymph node dissection, combined coccyx resection, and partial resection of the right GM muscle. The skin defect and pelvic dead space were filled with a right lateral vastus lateral great muscle flap. Histopathologically, the resected specimen showed no tumor cells in the primary tumor or lymph nodes, indicating a pathological complete response (pCR). This case suggests that TNT might improve the R0 resection and pCR rates and overall survival. |
| キーワード | locally advanced rectal cancer total neoadjuvant therapy lateral vastus lateral great muscle flap |
| Amo Type | Case Report |
| 出版物タイトル | Acta Medica Okayama |
| 発行日 | 2023-04 |
| 巻 | 77巻 |
| 号 | 2号 |
| 出版者 | Okayama University Medical School |
| 開始ページ | 209 |
| 終了ページ | 213 |
| ISSN | 0386-300X |
| NCID | AA00508441 |
| 資料タイプ | 学術雑誌論文 |
| 言語 | 英語 |
| 著作権者 | Copyright Ⓒ 2023 by Okayama University Medical School |
| 論文のバージョン | publisher |
| 査読 | 有り |
| PubMed ID | 37094960 |
| Web of Science KeyUT | 000982563800003 |
| JaLCDOI | 10.18926/AMO/65151 |
|---|---|
| フルテキストURL | 77_2_203.pdf |
| 著者 | Fukushima, Shinnosuke| Hagiya, Hideharu| Iio, Koji| Honda, Hiroyuki| Ishida, Tomoharu| Nagaoka, Hirokazu| Hasegawa, Kou| Otsuka, Fumio| |
| 抄録 | Granulicatella species are rare, nutritionally variant streptococci that cause infective endocarditis. Their clinical and microbiological characteristics remain unknown. We reviewed five years of Granulicatella cases in our hospital database (Jan 2017-Jun 2022), finding 6 Granulicatella adiacens cases and 1 Granulicatella elegans case. Clinical backgrounds and bacteremia sources were diverse; 3 cases developed polymicrobial bacteremia. Antimicrobial testing showed non-susceptibility to penicillin G in 4 of 7 cases (57.1%), and high susceptibility to carbapenems and vancomycin in all cases. Determining optimal antibiotic therapy for Granulicatella infections is vital in this era of antimicrobial resistance. |
| キーワード | antimicrobial resistance bacteremia Granulicatella species nutritionally variant streptococci |
| Amo Type | Case Report |
| 出版物タイトル | Acta Medica Okayama |
| 発行日 | 2023-04 |
| 巻 | 77巻 |
| 号 | 2号 |
| 出版者 | Okayama University Medical School |
| 開始ページ | 203 |
| 終了ページ | 207 |
| ISSN | 0386-300X |
| NCID | AA00508441 |
| 資料タイプ | 学術雑誌論文 |
| 言語 | 英語 |
| 著作権者 | Copyright Ⓒ 2023 by Okayama University Medical School |
| 論文のバージョン | publisher |
| 査読 | 有り |
| PubMed ID | 37094959 |
| Web of Science KeyUT | 000982563800002 |
| JaLCDOI | 10.18926/AMO/65150 |
|---|---|
| フルテキストURL | 77_2_199.pdf |
| 著者 | Nagano, Tomohiro| Hosokawa, Shinobu| Miyahara, Hideaki| Yamada, Kotaro| Umeno, Takayuki| Kano, Hirohisa| Kayatani, Hiroe| Sakugawa, Makoto| Takehisa, Yasushi| Takenaka, Tadasu| Takeuchi, Makoto| Bessho, Akihiro| |
| 抄録 | Meningitis-retention syndrome (MRS) is the combination of aseptic meningitis and acute urinary retention that occurs in the absence of other neurological diseases. The cause(s) of MRS remain unclear. A 57-year-old Japanese woman was referred to our hospital for the evaluation of persistent fever and headache. The fever’s cause was initially unclear, but the presence of urinary retention raised concern about possible aseptic meningitis despite no physical indications of meningeal irritation. Only typical cases of MRS have been reported thus far to our knowledge, and it is important that clinicians are aware of MRS when it presents in this atypical form. |
| キーワード | meningitis-retention syndrome aseptic meningitis acute urinary retention |
| Amo Type | Case Report |
| 出版物タイトル | Acta Medica Okayama |
| 発行日 | 2023-04 |
| 巻 | 77巻 |
| 号 | 2号 |
| 出版者 | Okayama University Medical School |
| 開始ページ | 199 |
| 終了ページ | 201 |
| ISSN | 0386-300X |
| NCID | AA00508441 |
| 資料タイプ | 学術雑誌論文 |
| 言語 | 英語 |
| 著作権者 | Copyright Ⓒ 2023 by Okayama University Medical School |
| 論文のバージョン | publisher |
| 査読 | 有り |
| PubMed ID | 37094958 |
| Web of Science KeyUT | 000982503800010 |
| JaLCDOI | 10.18926/AMO/65147 |
|---|---|
| フルテキストURL | 77_2_179.pdf |
| 著者 | Kondo, Hidenori| Saito, Taichi| Nakahara, Ryuichi| Nakamichi, Ryo| Shimamura, Yasunori| Harada, Ryozo| Imatani, Junya| Ozaki, Toshifumi| |
| 抄録 | Rupture of the extensor pollicis longus (EPL) tendon is a known complication after undisplaced distal radius fracture (DRF). However, no report has revealed the relationship between EPL tendon rupture and the fracture pattern. Thus, this study aimed to investigate the characteristics of fractures at risk of EPL tendon rupture using fracture line mapping of undisplaced DRFs. This study used computed tomography imaging data of undisplaced DRFs with (n=18) and without EPL tendon rupture (n=52). Fracture lines obtained from 3D reconstruction data were drawn manually after matching with a 2D template wrist model. Fracture maps represented the fracture line distribution by superimposing the fracture lines of all 70 patients. Heat maps showed the relative frequency of the fracture lines as a gradual color change. Fracture lines of cases with EPL tendon rupture were concentrated in the proximal border of Lister’s tubercle. By contrast, fracture lines of cases without EPL tendon rupture were relatively dispersed. |
| キーワード | distal radius fracture rupture of extensor pollicis longus tendon fracture mapping |
| Amo Type | Original Article |
| 出版物タイトル | Acta Medica Okayama |
| 発行日 | 2023-04 |
| 巻 | 77巻 |
| 号 | 2号 |
| 出版者 | Okayama University Medical School |
| 開始ページ | 179 |
| 終了ページ | 184 |
| ISSN | 0386-300X |
| NCID | AA00508441 |
| 資料タイプ | 学術雑誌論文 |
| 言語 | 英語 |
| 著作権者 | Copyright Ⓒ 2023 by Okayama University Medical School |
| 論文のバージョン | publisher |
| 査読 | 有り |
| PubMed ID | 37094955 |
| Web of Science KeyUT | 000982503800007 |
| フルテキストURL | fulltext20230317-1.pdf |
|---|---|
| 著者 | Tominaga, Yusuke| Fujii, Masanori| Sadahira, Takuya| Katayama, Satoshi| Iwata, Takehiro| Nishimura, Shingo| Bekku, Kensuke| Edamura, Kohei| Kobayashi, Tomoko| Kobayashi, Yasuyuki| Kiura, Katsuyuki| Maeda, Yoshinobu| Wada, Koichiro| Araki, Motoo| |
| キーワード | bladder tuberculosis bacillus Calmette-Guerin bladder cancer ureteral stricture voiding dysfunction |
| 発行日 | 2022-12-20 |
| 出版物タイトル | Molecular and Clinical Oncology |
| 巻 | 18巻 |
| 号 | 2号 |
| 出版者 | Spandidos Publications |
| 開始ページ | 7 |
| ISSN | 2049-9450 |
| 資料タイプ | 学術雑誌論文 |
| 言語 | 英語 |
| OAI-PMH Set | 岡山大学 |
| 著作権者 | © Tominaga et al. |
| 論文のバージョン | publisher |
| PubMed ID | 36761388 |
| DOI | 10.3892/mco.2022.2603 |
| Web of Science KeyUT | 000928771000001 |
| 関連URL | isVersionOf https://doi.org/10.3892/mco.2022.2603 |
| フルテキストURL | fulltext.pdf |
|---|---|
| 著者 | Kojima, Nana| Kuroda, Kosuke| Tani, Makiko| Kanazawa, Tomoyuki| Shimizu, Kazuyoshi| Maki, Jota| Masuyama, Hisashi| Morimatsu, Hiroshi| |
| キーワード | HELLP syndrome Postpartum Plasma exchange therapy Thrombotic microangiopathy |
| 発行日 | 2023-02-20 |
| 出版物タイトル | JA Clinical Reports |
| 巻 | 9巻 |
| 号 | 1号 |
| 出版者 | Springer |
| 開始ページ | 9 |
| ISSN | 2363-9024 |
| 資料タイプ | 学術雑誌論文 |
| 言語 | 英語 |
| OAI-PMH Set | 岡山大学 |
| 著作権者 | © The Author(s) 2023. |
| 論文のバージョン | publisher |
| PubMed ID | 36805852 |
| DOI | 10.1186/s40981-023-00602-2 |
| Web of Science KeyUT | 000934508200002 |
| 関連URL | isVersionOf https://doi.org/10.1186/s40981-023-00602-2 |
| フルテキストURL | fulltext.pdf |
|---|---|
| 著者 | Kikuchi, Tatsuya| Tanaka, Yoshinori| Ichimura, Kouichi| Okada, Hiroyuki| Okamoto, Ryoichi| |
| キーワード | Hodgkin lymphoma Hemophagocytic syndrome TAFRO syndrome |
| 発行日 | 2023-02-21 |
| 出版物タイトル | Journal of Medical Case Reports |
| 巻 | 17巻 |
| 号 | 1号 |
| 出版者 | BMC |
| 開始ページ | 61 |
| ISSN | 1752-1947 |
| 資料タイプ | 学術雑誌論文 |
| 言語 | 英語 |
| OAI-PMH Set | 岡山大学 |
| 著作権者 | © The Author(s) 2023. |
| 論文のバージョン | publisher |
| PubMed ID | 36805700 |
| DOI | 10.1186/s13256-023-03776-6 |
| Web of Science KeyUT | 000934595500003 |
| 関連URL | isVersionOf https://doi.org/10.1186/s13256-023-03776-6 |
| フルテキストURL | fulltext.pdf |
|---|---|
| 著者 | Tanimoto, Terutaka| Noda, Takuo| Nouso, Hiroshi| Miyata, Yukinori| |
| キーワード | Esophageal atresia with tracheoesophageal fistula Right-sided aortic arch Right ductus arteriosus |
| 発行日 | 2022-01-03 |
| 出版物タイトル | Journal of Pediatric Surgery Case Reports |
| 巻 | 77巻 |
| 出版者 | Elsevier |
| 開始ページ | 102167 |
| ISSN | 22135766 |
| 資料タイプ | 学術雑誌論文 |
| 言語 | 英語 |
| OAI-PMH Set | 岡山大学 |
| 著作権者 | © 2022 The Authors. |
| 論文のバージョン | publisher |
| DOI | 10.1016/j.epsc.2021.102167 |
| Web of Science KeyUT | 000788534800003 |
| 関連URL | isVersionOf https://doi.org/10.1016/j.epsc.2021.102167 |
| フルテキストURL | fulltext.pdf |
|---|---|
| 著者 | Fukushima, Shinnosuke| Ocho, Kazuki| Fujita, Koji| Hagiya, Hideharu| Otsuka, Fumio| |
| キーワード | basal meningitis cerebral infarction miliary tuberculosis tuberculous meningitis |
| 発行日 | 2023-01-16 |
| 出版物タイトル | Clinical Case Reports |
| 巻 | 11巻 |
| 号 | 1号 |
| 出版者 | Wiley |
| 開始ページ | e06865 |
| ISSN | 2050-0904 |
| 資料タイプ | 学術雑誌論文 |
| 言語 | 英語 |
| OAI-PMH Set | 岡山大学 |
| 著作権者 | © 2023 The Authors. |
| 論文のバージョン | publisher |
| PubMed ID | 36694639 |
| DOI | 10.1002/ccr3.6865 |
| Web of Science KeyUT | 000921577100058 |
| 関連URL | isVersionOf https://doi.org/10.1002/ccr3.6865 |
| フルテキストURL | fulltext.pdf |
|---|---|
| 著者 | Hiyoshi, Toshiharu| Shimizu, Kazuyoshi| Kimura, Satoshi| Naritani, Toshiki| Morimatsu, Hiroshi| |
| キーワード | Osler-Weber-Rendu syndrome Arteriovenous malformations General anesthesia Neuraxial anesthesia |
| 発行日 | 2023-02-08 |
| 出版物タイトル | JA Clinical Reports |
| 巻 | 9巻 |
| 号 | 1号 |
| 出版者 | Springer |
| 開始ページ | 6 |
| ISSN | 2363-9024 |
| 資料タイプ | 学術雑誌論文 |
| 言語 | 英語 |
| OAI-PMH Set | 岡山大学 |
| 著作権者 | © The Author(s) 2023. |
| 論文のバージョン | publisher |
| PubMed ID | 36750473 |
| DOI | 10.1186/s40981-023-00600-4 |
| Web of Science KeyUT | 000928586100001 |
| 関連URL | isVersionOf https://doi.org/10.1186/s40981-023-00600-4 |
| JaLCDOI | 10.18926/AMO/64372 |
|---|---|
| フルテキストURL | 77_1_117.pdf |
| 著者 | Obara, Takafumi| Yumoto, Tetsuya| Aoshima, Kenji| Tsukahara, Kohei| Naito, Hiromichi| Nakao, Atsunori| |
| 抄録 | A 38-year-old primipara Japanese woman suffered cardiac arrest due to a pulmonary thromboembolism 1 day after undergoing a cesarean section. Extracorporeal cardiopulmonary resuscitation was initiated and extracorporeal membrane oxygenation support was needed for 24 h. Despite intensive care, the patient was diagnosed with brain death on day 6. With the family’s consent, comprehensive end-of-life care including organ donation was discussed based on our hospital’s policy. The family decided to donate her organs. Specific training and education are required for emergency physicians to optimize the process of incorporating organ donation into end-of-life care while respecting the patient’s and family’s wishes. |
| キーワード | brain death end-of-life extracorporeal cardiopulmonary resuscitation organ donation potential organ donor |
| Amo Type | Case Report |
| 出版物タイトル | Acta Medica Okayama |
| 発行日 | 2023-02 |
| 巻 | 77巻 |
| 号 | 1号 |
| 出版者 | Okayama University Medical School |
| 開始ページ | 117 |
| 終了ページ | 120 |
| ISSN | 0386-300X |
| NCID | AA00508441 |
| 資料タイプ | 学術雑誌論文 |
| 言語 | 英語 |
| 著作権者 | Copyright Ⓒ 2023 by Okayama University Medical School |
| 論文のバージョン | publisher |
| 査読 | 有り |
| PubMed ID | 36849156 |
| Web of Science KeyUT | 000953005500003 |
| JaLCDOI | 10.18926/AMO/64371 |
|---|---|
| フルテキストURL | 77_1_111.pdf |
| 著者 | Amano, Katsuhiko| Sugauchi, Akinari| Yamada, Chiaki| Kogo, Mikihiko| Iida, Seiji| |
| 抄録 | Medication-related osteonecrosis of the jaw (MRONJ) is a side effect in patients taking bone-modifying agents (BMAs), which are highly beneficial for treating osteoporosis and cancer. Bisphosphonates are prescribed to treat secondary osteoporosis in patients with rheumatoid arthritis (RA). We recently encountered two unusual cases of intraoral ONJ in RA patients who had not been treated with a BMA and did not have features of methotrexate- associated lymphoproliferative disorder. Their ONJ stage II bone exposures were treated by conservative therapy, providing good prognoses. These cases indicate that ONJ can occur in RA patients not treated with bisphosphonates. Several risk factors are discussed. |
| キーワード | osteonecrosis of the jaw rheumatoid arthritis risk factor bisphosphonate |
| Amo Type | Case Report |
| 出版物タイトル | Acta Medica Okayama |
| 発行日 | 2023-02 |
| 巻 | 77巻 |
| 号 | 1号 |
| 出版者 | Okayama University Medical School |
| 開始ページ | 111 |
| 終了ページ | 116 |
| ISSN | 0386-300X |
| NCID | AA00508441 |
| 資料タイプ | 学術雑誌論文 |
| 言語 | 英語 |
| 著作権者 | Copyright Ⓒ 2023 by Okayama University Medical School |
| 論文のバージョン | publisher |
| 査読 | 有り |
| PubMed ID | 36849155 |
| Web of Science KeyUT | 000953005500002 |
| JaLCDOI | 10.18926/AMO/64370 |
|---|---|
| フルテキストURL | 77_1_105.pdf |
| 著者 | Iwasaki, Yoshiaki| Higuchi, Chigusa| |
| 抄録 | The inactivated coronavirus disease 2019 vaccine CoronaVac has not been approved in Japan. Little information is available on cases in Japan in which an approved mRNA vaccine was administered as the initial (first or second) dose after two doses of CoronaVac. Furthermore, the safety and efficacy of this combination are not established. We here evaluated the safety and efficacy in a patient who showed an antibody response to an approved vaccine, mRNA-1273, after a previous vaccination with CoronaVac. The adverse events consisted of only mild local and systemic common reactions and were transient. In addition, a strong and persistent antibody response was observed. |
| キーワード | coronavirus disease 2019 severe acute respiratory syndrome coronavirus 2 vaccine adverse events antibody response |
| Amo Type | Case Report |
| 出版物タイトル | Acta Medica Okayama |
| 発行日 | 2023-02 |
| 巻 | 77巻 |
| 号 | 1号 |
| 出版者 | Okayama University Medical School |
| 開始ページ | 105 |
| 終了ページ | 109 |
| ISSN | 0386-300X |
| NCID | AA00508441 |
| 資料タイプ | 学術雑誌論文 |
| 言語 | 英語 |
| 著作権者 | Copyright Ⓒ 2023 by Okayama University Medical School |
| 論文のバージョン | publisher |
| 査読 | 有り |
| PubMed ID | 36849154 |
| Web of Science KeyUT | 000953005500001 |
| JaLCDOI | 10.18926/AMO/64369 |
|---|---|
| フルテキストURL | 77_1_97.pdf |
| 著者 | Hoshijima, Mitsuhiro| Oka, Naoki| Matsumura, Tatsushi| Iida, Seiji| Kamioka, Hiroshi| |
| 抄録 | Appropriate operations in severe anterior open bite (AOB) cases are extremely complicated to perform because of the multiple surgical procedures involved, the difficulty of predicting posttreatment aesthetics, and the high relapse rate. We herein report a 16-year-old girl with skeletal Class II, severe AOB malocclusion, and crowding with short roots, and aesthetic and functional problems. Four-piece segmental Le Fort I osteotomy with horseshoe osteotomy was performed for maxillary intrusion, and bilateral sagittal split ramus osteotomy (SSRO) and genioplasty were performed for mandibular advancement. The malocclusion and skeletal deformity were significantly improved by the surgical orthodontic treatment. Functional and aesthetic occlusion with an improved facial profile was established, and no further root shortening was observed. Acceptable occlusion and dentition were maintained after a two-year retention period. This strategy of surgical orthodontic treatment with a complicated operative procedure might be effective for correcting certain severe AOB malocclusion cases. |
| キーワード | anterior open bite short roots severe crowding four-piece segmental horseshoe Le Fort I osteotomy |
| Amo Type | Case Report |
| 出版物タイトル | Acta Medica Okayama |
| 発行日 | 2023-02 |
| 巻 | 77巻 |
| 号 | 1号 |
| 出版者 | Okayama University Medical School |
| 開始ページ | 97 |
| 終了ページ | 104 |
| ISSN | 0386-300X |
| NCID | AA00508441 |
| 資料タイプ | 学術雑誌論文 |
| 言語 | 英語 |
| 著作権者 | Copyright Ⓒ 2023 by Okayama University Medical School |
| 論文のバージョン | publisher |
| 査読 | 有り |
| PubMed ID | 36849153 |
| Web of Science KeyUT | 000952978000003 |
| JaLCDOI | 10.18926/AMO/64368 |
|---|---|
| フルテキストURL | 77_1_91.pdf |
| 著者 | Takahashi, Toshiaki| Kakiuchi, Yoshihiko| Kikuch, Satoru| Kuroda, Shinji| Takeda, Sho| Shigeyasu, Kunitoshi| Kondo, Yoshitaka| Teraishi, Fuminori| Kagawa, Shunsuke| Fujiwara, Toshiyoshi| |
| 抄録 | An annular pancreas is a rare anomaly of the pancreas, defined as pancreatic tissue that totally or partly encircles the duodenum, usually the descending portion. A 76-year-old man who was diagnosed with gastric cancer cT3N0M0 Stage IIB underwent laparoscopic distal gastrectomy with D2 lymph node dissection. Intraoperatively, the dorsal half of the duodenal bulb was seen to be half surrounded by the pancreas, and a non-typical annular pancreas was diagnosed. Because of the risk to the pancreas, it was considered impossible to perform anastomosis by a linear stapler as in the usual laparoscopic procedure. Therefore, we performed laparoscopically assisted distal gastrectomy and Billroth-I reconstruction using a circular stapler, and the surgery was completed without difficulties. His postoperative course was good despite the development of a pancreatic fistula, which was an International Study Group for Pancreas Fistula biochemical leak. Some APs can be diagnosed preoperatively, but the rarer subtypes such as ours are more difficult to visualize on imaging. In gastrectomy, it is both oncologically important and technically challenging to perform lymph node dissection around the pancreas. In this case with an especially proximal pancreas, a circular stapler was considered better suited for gastroduodenal anastomosis and required a broader field than that afforded by laparoscopy. A case of non-typical annular pancreas diagnosed during laparoscopic gastric surgery is described. |
| キーワード | annular pancreas gastric cancer laparoscopic distal gastrectomye |
| Amo Type | Case Report |
| 出版物タイトル | Acta Medica Okayama |
| 発行日 | 2023-02 |
| 巻 | 77巻 |
| 号 | 1号 |
| 出版者 | Okayama University Medical School |
| 開始ページ | 91 |
| 終了ページ | 95 |
| ISSN | 0386-300X |
| NCID | AA00508441 |
| 資料タイプ | 学術雑誌論文 |
| 言語 | 英語 |
| 著作権者 | Copyright Ⓒ 2023 by Okayama University Medical School |
| 論文のバージョン | publisher |
| 査読 | 有り |
| PubMed ID | 36849152 |
| Web of Science KeyUT | 000952978000002 |
| JaLCDOI | 10.18926/AMO/64367 |
|---|---|
| フルテキストURL | 77_1_85.pdf |
| 著者 | Matsuda, Yuki| Otani, Yoshihiro| Yasuhara, Takao| Ando, Mizuo| Higaki, Takaya| Makino, Takuma| Matsumoto, Hiroshi| Oyama, Tadashi| Nishimori, Hisakazu| Date, Isao| |
| 抄録 | A 35-year-old female presented with headache, photophobia and developed sudden loss of vision after having undergone right-side ophthalmectomy and radiochemotherapy for retinoblastoma in infancy. A neoplastic lesion was found in the left middle cranial fossa and was surgically removed. The diagnosis was radiation-induced osteosarcoma with RB1 gene alteration. Although she received chemotherapy for the residual tumor, it progressed 17 months later. Maximal surgical resection with craniofacial reconstruction was required. We utilized two three-dimensional models for surgical planning. She was discharged without neurological deficits other than loss of light perception subsequent to left ophthalmectomy. In cases where retinoblastoma is treated with radiotherapy, long-term follow-up is necessary to monitor for radiation-induced tumor development. |
| キーワード | bone model skull base surgery radiation-induced osteosarcoma RB1 gene alteration |
| Amo Type | Case Report |
| 出版物タイトル | Acta Medica Okayama |
| 発行日 | 2023-02 |
| 巻 | 77巻 |
| 号 | 1号 |
| 出版者 | Okayama University Medical School |
| 開始ページ | 85 |
| 終了ページ | 90 |
| ISSN | 0386-300X |
| NCID | AA00508441 |
| 資料タイプ | 学術雑誌論文 |
| 言語 | 英語 |
| 著作権者 | Copyright Ⓒ 2023 by Okayama University Medical School |
| 論文のバージョン | publisher |
| 査読 | 有り |
| PubMed ID | 36849151 |
| Web of Science KeyUT | 000952978000001 |