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Acute Severe Colitis after mRNA Coronavirus Disease 2019 Vaccination. 接种 mRNA 冠状病毒疾病 2019 疫苗后出现急性严重结肠炎:病例报告。
IF 1 4区 医学 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-01-15 Epub Date: 2024-11-08 DOI: 10.2169/internalmedicine.4224-24
Akira Nakanishi, Sakuma Takahashi, Tomoki Inaba, Eriko Yasutomi, Hugh Shunsuke Colvin, Koichi Izumikawa, Shigenao Ishikawa, Masaki Wato, Midori Ando, Satoko Nakamura

A 74-year-old woman developed acute severe colitis after receiving her sixth mRNA vaccine against coronavirus disease 2019 (COVID-19). On the day after vaccination, she experienced bloody diarrhea, abdominal pain, and high-grade fever. Laboratory tests revealed leukocytosis and increased C-reactive protein. Contrast-enhanced computed tomography revealed bowel wall thickening with a reduced contrast effect within the colon, in addition to ascites. Sigmoidoscopy revealed extensive sloughing of the mucosa. Her symptoms and laboratory findings improved immediately after the initiation of prednisolone therapy. Pre-discharge total colonoscopy revealed mucosal repair in most of the colon. Clinicians should acknowledge that severe acute colitis can occur after COVID-19 vaccination.

一名 74 岁的妇女在接种了第六针冠状病毒病-2019(COVID-19)mRNA 疫苗后,患上了急性重症结肠炎。接种后第二天,她出现了血性腹泻、腹痛和高烧。实验室检查显示白细胞增多,C反应蛋白升高。造影剂增强计算机断层扫描显示肠壁增厚,结肠内造影剂效果减弱,此外还伴有腹水。乙状结肠镜检查发现黏膜广泛脱落。开始使用泼尼松龙治疗后,她的症状和实验室检查结果立即得到改善。出院前的全结肠镜检查显示大部分结肠粘膜已修复。临床医生应该认识到,接种 COVID-19 疫苗后可能会出现严重的急性结肠炎。
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引用次数: 0
Multimodality Imaging in Detecting Cardiac Masses in Patients with Lymphoma. 多模态成像检测淋巴瘤患者的心脏肿块
IF 1 4区 医学 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-01-15 Epub Date: 2024-06-06 DOI: 10.2169/internalmedicine.3985-24
Yusuf Ziya Sener
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引用次数: 0
Delayed Superior Orbital Fissure Syndrome Arising More than One Month after Herpes Zoster Ophthalmicus and Meningitis. 带状疱疹眼炎和脑膜炎一个多月后出现的延迟性眼眶上裂综合征。
IF 1 4区 医学 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-01-15 Epub Date: 2024-06-06 DOI: 10.2169/internalmedicine.3652-24
Sunao Takahashi, Kotaro Okabayashi, Itsuki Soejima, Ayako Oniki, Shoichiro Ishihara, Hiroyuki Tomimitsu

A 79-year-old woman developed herpes zoster ophthalmicus (HZO) with a vesicular rash on the nasal root, which developed soon after intravenous acyclovir therapy. Although varicella zoster virus DNA was undetectable in the cerebrospinal fluid, she presented with ophthalmoplegia without optic nerve dysfunction 32 days after the onset of HZO. We diagnosed the patient with superior orbital fissure syndrome and administered intravenous immunoglobulin and systemic corticosteroids. Ophthalmoplegia did not immediately respond to these therapies but resolved 4 months later. We should be aware that ophthalmoplegia can occur, even after HZO and meningitis are completely treated.

一名 79 岁的妇女在静脉注射阿昔洛韦治疗后不久,患上了带状疱疹眼炎(HZO),鼻根部出现水泡状皮疹。虽然在脑脊液中检测不到水痘带状疱疹病毒 DNA,但她在 HZO 发病 32 天后出现眼球震颤,且无视神经功能障碍。我们诊断患者患有眶上裂综合征,并静脉注射了免疫球蛋白和全身皮质类固醇激素。眼肌麻痹并没有立即对这些疗法产生反应,但在 4 个月后得到了缓解。我们应该意识到,即使在 HZO 和脑膜炎完全治愈后,眼肌麻痹仍有可能发生。
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引用次数: 0
Extensive but Steroid-sensitive Pulmonary Infiltration by Natural Killer-large Granular Lymphocytic Leukemia. 自然杀伤型大颗粒淋巴细胞白血病广泛但类固醇敏感的肺浸润。
IF 1 4区 医学 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-01-15 DOI: 10.2169/internalmedicine.4714-24
Masahiro Tokunaga, Satoshi Tetsumoto, Hayato Maruoka, Akito Miyazaki, Shinichi Yoshikawa, Tetsuo Maeda

A 51-year-old woman with persistent proliferation of natural killer (NK) cells in her peripheral blood was diagnosed with NK-large granular lymphocytic leukemia (NK-LGLL). During follow-up, computed tomography revealed multiple infiltrative pulmonary lesions. A flow cytometric analysis of bronchoalveolar lavage fluid showed infiltration of NK cells, resulting in a diagnosis of pulmonary infiltration by NK-LGLL. A histological examination of thoracoscopic lung biopsy specimens supported this diagnosis. She was started on 1 mg/kg prednisolone, which resulted in a durable reduction in these lesions. This is the first report of a NK-LGLL patient with pulmonary infiltration who received medication. Furthermore, treatment with prednisolone alone was successful.

51岁女性外周血自然杀伤(NK)细胞持续增殖,诊断为NK-大颗粒淋巴细胞白血病(NK- lgll)。随访期间,计算机断层扫描显示多发浸润性肺病变。支气管肺泡灌洗液流式细胞分析显示NK细胞浸润,诊断为NK- lgll肺浸润。胸腔镜肺活检标本的组织学检查支持这一诊断。她开始使用1mg /kg强的松龙,导致这些病变持久减少。这是首例NK-LGLL患者肺部浸润接受药物治疗的报道。此外,单独使用强的松龙治疗是成功的。
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引用次数: 0
Intravenous Thrombolysis for Pediatric Ischemic Stroke Secondary to Cancer Therapy-related Cardiac Dysfunction. 静脉溶栓治疗癌症治疗相关心功能障碍继发的小儿缺血性中风:病例报告。
IF 1 4区 医学 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-01-15 Epub Date: 2024-05-30 DOI: 10.2169/internalmedicine.3755-24
Futoshi Eto, Tomohisa Nezu, Hideaki Sakahara, Yumiko Yamamoto, Shiro Aoki, Maiko Shimomura, Shuhei Karakawa, Hirofumi Maruyama

An 11-year-old boy developed cardioembolic stroke (CES) and cancer therapy-related cardiac dysfunction (CTRCD). He originally developed Ewing sarcoma and was treated with high-dose chemotherapy including doxorubicin. On admission, he had severe aphasia, and magnetic resonance imaging showed occlusion of the left middle cerebral artery M3 segment. Transthoracic echocardiography revealed severe left ventricular dysfunction and a mobile thrombus at the left ventricular apex. Intravenous thrombolysis was administered, and effective recanalization was achieved. The patient did not exhibit any neurological deficits during discharge. Reperfusion therapy for pediatric patients has not yet been established; however, it may be effective for CES secondary to CTRCD.

一名 11 岁男孩患上了心肌栓塞性中风(CES)和癌症治疗相关心功能不全(CTRCD)。他最初患的是尤文肉瘤,接受了包括多柔比星在内的大剂量化疗。入院时,他出现严重失语,磁共振成像显示左侧大脑中动脉M3段闭塞。经胸超声心动图显示左心室严重功能障碍,左心室心尖有移动血栓。患者接受了静脉溶栓治疗,并获得了有效的再通。患者出院时未出现任何神经功能障碍。针对儿科患者的再灌注疗法尚未确立,但对继发于 CTRCD 的 CES 可能有效。
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引用次数: 0
Acute Hemorrhagic Leukoencephalitis with Concurrent Retinal Vasculitis in an Elderly Japanese Patient. 一名日本老年患者的急性出血性白脑炎并发视网膜血管炎:病例报告。
IF 1 4区 医学 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-01-15 Epub Date: 2024-06-20 DOI: 10.2169/internalmedicine.3518-24
Yoshitaka Yamaguchi, Ryosuke Sawaya, Natsuko Shichinohe, Zen-Ichi Tanei, Maeho Yamasaki, Fumiki Tomeoka, Minoru Ajiki, Tatsuro Takada, Toshiya Shinohara, Katsuyuki Asaoka

A 68-year-old Japanese man developed a fever, headache, hiccups, and altered consciousness. Brain magnetic resonance imaging revealed a hemorrhagic lesion in the right temporal lobe and multiple high-intensity white matter lesions. A brain biopsy showed pathological findings consistent with acute disseminated encephalomyelitis (ADEM), suggesting a diagnosis of acute hemorrhagic leukoencephalitis (AHLE), an aggressive ADEM variant. The patient also developed myodesopsia and was diagnosed with retinal vasculitis, likely due to a hyperimmune state caused by AHLE. Corticosteroids enabled full recovery. Although AHLE is uncommon in elderly individuals, clinicians should be aware of its occurrence in this patient subgroup and recognize potential retinal manifestations associated with AHLE.

一名 68 岁的日本男子出现发烧、头痛、打嗝和意识改变。脑磁共振成像(MRI)显示右侧颞叶有出血性病变和多处高密度白质病变。脑活检显示病理结果与急性播散性脑脊髓炎(ADEM)一致,提示诊断为急性出血性白质脑炎(AHLE),这是ADEM的一种侵袭性变异。患者还出现了肌张力障碍,并被诊断为视网膜血管炎,这很可能是由于急性出血性白脑炎引起的高免疫状态所致。皮质类固醇使患者完全康复。尽管AHLE在老年人中并不常见,但临床医生应该意识到它在这一患者亚群中的发生率,并认识到与AHLE相关的潜在视网膜表现。
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引用次数: 0
A Male Japanese Patient with Temple Syndrome Complicated by Type 2 Diabetes Mellitus. 一名患有坦普尔综合征并发 2 型糖尿病的日本男性患者。
IF 1 4区 医学 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-01-15 Epub Date: 2024-05-16 DOI: 10.2169/internalmedicine.2743-23
Masanori Iwanishi, Tohru Yorifuji, Yukako Yamamoto, Jun Ito-Kobayashi, Akira Shimatsu, Shingo Kikugawa, Masayo Kagami

We herein present the case of a 21-year-old male Japanese diabetic patient with Temple syndrome, caused by maternal uniparental disomy of chromosome 14. The patient was overweight and had type 2 diabetes, dyslipidemia, metabolic dysfunction-associated steatotic liver disease, and microalbuminuria. He had an increased fat mass in the truncal region and a decreased lean mass throughout the body. This may lead to insulin resistance due to the absence of delta-like homolog 1 (DLK1) and retrotransposon gag-like 1 (RTL1). The patient had experienced social withdrawal at home (hikikomori in Japanese), had poorly controlled type 2 diabetes, and was overweight despite receiving diet therapy and oral hypoglycemic agents.

我们在此介绍一例 21 岁的日本男性糖尿病患者,他患有坦普尔综合征(Temple Syndrome),由母体 14 号染色体单亲断裂引起。患者体重超重,患有 2 型糖尿病、血脂异常、代谢功能障碍相关性脂肪肝和微量白蛋白尿。他的躯干部位脂肪量增加,全身瘦肉量减少。由于缺乏δ样同源物1(DLK1)和逆转录病毒gag样1(RTL1),这可能会导致胰岛素抵抗。该患者曾在家中出现社交退缩(日语中的蛰居),2 型糖尿病控制不佳,体重超重,尽管接受了饮食治疗和口服降糖药。
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引用次数: 0
Pseudogout Localized to the Pubic Symphysis. 耻骨联合局部假性痛风
IF 1 4区 医学 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-01-15 Epub Date: 2024-05-23 DOI: 10.2169/internalmedicine.3825-24
Jun Nishinarita, Tomoya Tsuchida, Hirotoshi Fujii, Yoshiyuki Ohira
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引用次数: 0
Clinical Limitations of Vasoreactivity Testing as a Diagnostic Tool in Patients with Vasospastic Angina. 将血管活性测试作为血管痉挛性心绞痛患者诊断工具的临床局限性
IF 1 4区 医学 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-01-15 Epub Date: 2024-05-30 DOI: 10.2169/internalmedicine.3567-24
Shozo Sueda, Yutaka Hayashi

The Japanese Circulation Society guidelines recommend a class I vasoreactivity test to diagnose patients with vasospastic angina (VSA). However, the acetylcholine or ergonovine test has been established as the gold standard for variant angina (VA). The sensitivity and specificity of intracoronary vasoreactivity testing in patients with VA were acceptable. Cardiologists have employed these vasoreactivity tests to conveniently diagnose the presence of coronary spasms in patients with all VSA. The majority of VSAs may have lower disease activity than VA cases. We have summarized the usefulness of spasm provocation tests in patients with VA and VSA. A positive-provoked spasm diagnosed by standard vasoreactivity testing may indicate a disease state similar to that of VA, whereas a negative-provoked spasm after standard vasoreactivity testing may indicate a lower disease state than that of VA. Cardiologists should reconsider the limited usefulness of vasoreactivity testing when diagnosing the presence of coronary spasms in all VSAs, but not VA.

日本循环学会指南建议采用 I 类血管反应试验来诊断血管痉挛性心绞痛(VSA)患者。然而,乙酰胆碱或麦角新碱试验已被确定为变异型心绞痛(VA)的金标准。冠状动脉内血管活性检测对 VA 患者的敏感性和特异性都是可以接受的。心脏病专家利用这些血管反应性测试方便地诊断出所有 VSA 患者是否存在冠状动脉痉挛。大多数 VSA 的疾病活动度可能低于 VA 病例。我们总结了痉挛激发试验对 VA 和 VSA 患者的作用。通过标准血管反应性测试诊断出的阳性诱发痉挛可能表明其疾病状态与 VA 相似,而经过标准血管反应性测试诊断出的阴性诱发痉挛可能表明其疾病状态低于 VA。心脏病专家应重新考虑血管反应性检测在诊断所有 VSA(而非 VA)是否存在冠状动脉痉挛时的有限作用。
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引用次数: 0
Successful Treatment of Bilocular Walled-off Necrosis with Transmural Naso-cyst Continuous Irrigation. 经壁鼻腔-囊肿连续灌洗成功治疗双眼球壁脱落坏死:病例报告
IF 1 4区 医学 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-01-15 Epub Date: 2024-06-06 DOI: 10.2169/internalmedicine.3770-24
Mari Matsuyama, Hisanori Matsuzawa, Kazuya Kimura, Yuki Izumiya, Kae Sugawara, Satoko Tsuda, Tsuyotoshi Tuji, Kunio Nakane, Masafumi Komatsu, Katsunori Iijima

Recently, transmural naso-cyst continuous irrigation (TNCCI) has been reported as an effective and safe treatment for walled-off necrosis (WON). We herein report a case of bilocular WON that was successfully treated with TNCCI. The patient was a 60-year-old man. The patient underwent endoscopic ultrasound-guided cyst drainage of the main cavity and subcavity using a single transluminal gateway transcystic multiple drainage technique, which was ineffective. Subsequently, a lumen-apposing metal stent (LAMS) was placed in the main cavity and TNCCI was successfully performed in the subcavity. TNCCI with LAMS was effective in treating bilocular WON.

最近有报道称,经壁鼻腔-膀胱持续灌注(TNCCI)是一种有效、安全的治疗穿壁坏死(WON)的方法。在此,我们报告了一例使用 TNCCI 成功治疗的双眼 WON 病例。患者是一名 60 岁的男性。患者接受了内镜超声引导下的主腔和腔下囊肿引流术,采用了单腔门径经囊多次引流技术,但效果不佳。随后,在主腔放置了一个腔隙贴壁金属支架(LAMS),并在子腔成功实施了 TNCCI。使用 LAMS 的 TNCCI 能有效治疗双腔 WON。
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引用次数: 0
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Internal Medicine
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