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The great imitator: Tuberculosis with lymphadenopathy and splenomegaly 伟大的模仿者伴有淋巴结病和脾肿大的肺结核
IF 1.5 Q4 INFECTIOUS DISEASES Pub Date : 2024-01-01 DOI: 10.1016/j.idcr.2024.e01968
Ashton D. Hall , Laura Victoria Medina Rodriguez , Jared Vearrier , Kavya Patel , Bryan C. Hambley , Moises A. Huaman

Tuberculosis (TB) is a leading infectious killer worldwide. Over two-thirds of new TB diagnoses in the United States occur among first-generation immigrants, especially within a year of migration. Hodgkin lymphoma (HL) accounts for a minority of lymphoma cases but presents similarly to disseminated or extrapulmonary TB. Clinical overlap between TB and HL increases patient risk of misdiagnosis. Concomitant presentation of both diseases is not uncommon but infrequently reported. We present a case of isoniazid-resistant TB with progressively worsening lymphadenopathy and splenomegaly despite appropriate TB treatment. The patient was diagnosed with HL following PET/CT and axillary lymph node biopsy.

结核病(TB)是全球主要的传染病杀手。在美国,超过三分之二的结核病新诊断病例发生在第一代移民中,尤其是在移民一年之内。霍奇金淋巴瘤(HL)在淋巴瘤病例中占少数,但其表现与播散性或肺外结核类似。肺结核与霍奇金淋巴瘤的临床症状重叠,增加了患者被误诊的风险。两种疾病同时出现的情况并不少见,但鲜有报道。我们报告了一例耐异烟肼肺结核患者,尽管接受了适当的肺结核治疗,但淋巴结病和脾肿大仍不断恶化。经 PET/CT 和腋窝淋巴结活检,患者被确诊为 HL。
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引用次数: 0
Malignant syphilis requiring differentiation from Kaposi's sarcoma 需要与卡波西肉瘤区分的恶性梅毒
IF 1.5 Q4 INFECTIOUS DISEASES Pub Date : 2024-01-01 DOI: 10.1016/j.idcr.2024.e01943
Mieko Tokano , Norihito Tarumoto , Kazuo Imai , Hiroshi Yamaguchi , Masaaki Takeji , Fumito Inayoshi , Keita Okamoto , Nobuhito Okumura , Shigefumi Maesaki

Malignant syphilis (MS) is a rare variant of secondary syphilis. Also known as rupioid syphilis, MS is characterized by the presence of multiple papules, papulopustules, black lamellate crust that may resemble an oyster shell, or nodules with ulceration lacking central clearing. MS is often associated with immunodeficiency and frequently co-occurs with HIV infection. We here report a case of MS in a patient with HIV infection. HIV infection can cause atypical clinical symptoms of syphilis. In this case, unlike previous cases, cutaneous lesions of MS were limited to the face, making the diagnosis challenging based on clinical findings alone. However, his laboratory findings, appearance of the Jarisch-Herxheimer reaction, and a dramatic response to antibiotic therapy are characteristic of MS, making the diagnosis even more certain. Our case suggests the importance of physicians considering the possibility of MS when observing black-crusted lesions.

恶性梅毒(MS)是继发性梅毒的一种罕见变种。恶性梅毒又称覆膜梅毒,其特征是出现多发性丘疹、丘疹性脓疱、黑色片状结痂(可能像牡蛎壳),或伴有溃疡的结节,缺乏中央清扫。多发性硬化症通常与免疫缺陷有关,经常与艾滋病病毒感染并发。我们在此报告一例艾滋病病毒感染者的多发性硬化症病例。艾滋病病毒感染可引起梅毒的非典型临床症状。在本病例中,与以往病例不同的是,多发性硬化症的皮肤病变仅限于面部,因此仅凭临床表现很难做出诊断。然而,他的实验室检查结果、贾里希-赫克海默反应的出现以及对抗生素治疗的显著反应都是多发性硬化症的特征,这使得诊断更加确定。我们的病例提示医生在观察黑痂病变时考虑多发性硬化症可能性的重要性。
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引用次数: 0
Tracheostomy wound myiasis in a patient with hypoxic encephalopathy 一名缺氧性脑病患者的气管造口伤口肌炎
IF 1.5 Q4 INFECTIOUS DISEASES Pub Date : 2024-01-01 DOI: 10.1016/j.idcr.2024.e01969
Kazuhiro Itoh , Atsushi Kuwata , Chiyo Kiriba , Yukari Kuwata , Tooru Enomoto , Yukie Yoshioka , Michie Nakayama , Hiroshi Tsutani , Yasuhiko Mitsuke , Hiromichi Iwasaki
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引用次数: 0
Bacillus Calmette-Guérin (BCG) prostato-epididymitis in a patient treated for a non-invasive urothelial cancer: A case report 一名接受非侵袭性尿路上皮癌治疗的患者出现卡介苗前列腺附睾炎:病例报告
IF 1.5 Q4 INFECTIOUS DISEASES Pub Date : 2024-01-01 DOI: 10.1016/j.idcr.2024.e01967
Ayemane Salif , Ferdinand Bigirimana , Sophie Willems , Gina Reichman , Johanna Noels , Sigi Van Den Wijngaert , Sophie Lecomte , Evelyne Maillart , Philippe Clevenbergh

Introduction

The Bacillus Calmette-Guérin (BCG) used as anti-tuberculous vaccine is also a well-known therapy for superficial urothelial cancer. Local or general side effects can occur, although it is generally well tolerated.

Case

We present the case of a 65 year-old caucasian man consulting for gross hematuria and lower urinary tract symptoms. Magnetic resonance imaging (MRI) demonstrated a non-invasive urothelial carcinoma (NMIBC) and Prostate Imaging–Reporting and Data System (PIRADS) IV lesions. Transurethral resection of the bladder tumor revealed a non-invasive transitional cell carcinoma. Intravesical Bacillus Calmette Guerin (BCG) therapy was provided. After 6 intravesical instillations, the patient presented with prostato-epididymitis. Forthcoming BCG instillations were canceled, and cancer treatment was switched to epirubicine. Treatment with ethambutol, rifampicin and isoniazid was started with rapid resolution of the symptoms. Urinary and semen cultures grew Mycobacterium tuberculosis complex strain BCG. As prostate specific antigen (PSA) rose, prostate’s biopsies were performed showing extensive necrosis boarded by granulomas without signs of malignancy.

Discussion

BCGitis is a rare complication in patients treated for non-invasive urothelial cancer. Several risk factors, local and systemic, should be considered prior to this immunotherapy. BCGitis (local or disseminated) or hypersensitivity reactions to BCG must be included in the differential diagnosis even if therapy was administered several years before the symptoms. Adequate treatment must be started as fast as possible to avoid serious complications.

导言作为抗结核疫苗使用的卡介苗(Bacillus Calmette-Guérin,BCG)也是治疗浅表性尿道癌的著名疗法。尽管卡介苗一般耐受性良好,但也可能出现局部或全身副作用。本病例是一名 65 岁的白种男子,因严重血尿和下尿路症状就诊。磁共振成像(MRI)显示为非侵袭性尿路上皮癌(NMIBC)和前列腺成像报告和数据系统(PIRADS)IV 级病变。经尿道膀胱肿瘤切除术显示为非浸润性过渡细胞癌。患者接受了卡介苗(BCG)膀胱内注射治疗。膀胱内注射卡介苗 6 次后,患者出现了前列腺附睾炎。接下来的卡介苗注射被取消,癌症治疗改用表阿霉素。开始使用乙胺丁醇、利福平和异烟肼治疗后,症状迅速缓解。尿液和精液培养出了结核分枝杆菌复合菌株卡介苗。随着前列腺特异性抗原(PSA)的升高,前列腺活检显示肉芽肿广泛坏死,但无恶变迹象。在采用这种免疫疗法之前,应考虑到局部和全身的几个风险因素。卡介苗炎(局部或播散性)或对卡介苗的超敏反应必须纳入鉴别诊断,即使治疗是在症状出现前几年进行的。必须尽快开始适当的治疗,以避免严重的并发症。
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引用次数: 0
Peritonsillar abscess associated with Helicobacter cinaedi bacteremia: A case report 与丙酸螺旋杆菌菌血症有关的扁桃体周围脓肿:病例报告
IF 1.5 Q4 INFECTIOUS DISEASES Pub Date : 2024-01-01 DOI: 10.1016/j.idcr.2024.e01975
Taku Harada , Toshiyuki Nakanishi , Satoshi Kutsuna , Mori Nakai

Helicobacter cinaedi, a gram-negative spiral bacterium, has historically been associated with infections primarily in immunocompromised patients. Recently, however, its potential to cause infections in immunocompetent individuals has been recognized. We report a unique case of a man in his 20 s who reported having sex with men. He presented with symptoms of fever and throat discomfort and was diagnosed with a peritonsillar abscess. While the rapid antigen test for Group A Streptococcus was positive and antibiotics were administered, a puncture fluid from the peritonsillar abscess taken the day after antibiotic treatment revealed the presence of Group C Streptococcus. By the fifth day, the blood culture taken on the first day detected a gram-negative spirochete, which was subsequently identified H. cinaedi. The patient had engaged in oral sex with his male partner, suggesting a potential transmission route. This is significant as H. cinaedi was initially identified from rectal cultures in men who have sex with men (MSM), raising the possibility of pharyngeal transmission through oral sex. In our patient, although H. cinaedi was not isolated from the aspirate of the peritonsillar abscess, its presence in the blood culture and lack of other potential sources of bacteremia make the abscess a likely primary site of infection. This case highlights the importance of considering H. cinaedi as a potential pathogen in immunocompetent patients, particularly in cases of MSM. The potential for H. cinaedi transmission through oral sex and its role in the development of peritonsillar abscesses, a previously unreported association, requires further investigation.

阴性螺旋杆菌(Helicobacter cinaedi)是一种革兰氏阴性螺旋菌,历来主要与免疫力低下患者的感染有关。但最近,人们认识到它有可能导致免疫功能正常的人感染。我们报告了一例独特的病例,患者是一名 20 多岁的男子,自称有男男性行为。他出现发烧和咽喉不适症状,被诊断为腹腔脓肿。虽然 A 群链球菌快速抗原检测呈阳性,并使用了抗生素,但在抗生素治疗后的第二天,从腹腔脓肿中抽取的穿刺液显示存在 C 群链球菌。到了第五天,第一天采集的血液培养物检测出一种革兰氏阴性螺旋体,随后确定为 H. cinaedi。患者曾与其男性伴侣发生口交,这表明存在潜在的传播途径。这一点意义重大,因为 H. cinaedi 最初是从男男性行为者(MSM)的直肠培养物中发现的,这增加了通过口交进行咽部传播的可能性。在我们的患者中,虽然没有从腹膜周围脓肿的抽吸物中分离出 H.cinaedi,但其在血液培养中的存在以及缺乏其他潜在的菌血症来源,使得脓肿很可能是原发感染部位。本病例强调了将 H. cinaedi 作为免疫功能正常患者的潜在病原体的重要性,尤其是在 MSM 病例中。H. cinaedi通过口交传播的可能性及其在发生扁桃体周围脓肿中的作用(这是一种以前未报道过的关联)需要进一步研究。
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引用次数: 0
Unilateral dystrophic circumferential calcified ureteral stenosis with hydronephrosis associated with multisystem inflammatory syndrome in adults following coronavirus disease 2019 2019年冠状病毒病成人单侧萎缩性环状钙化输尿管狭窄伴肾积水,并伴有多系统炎症综合征
IF 1.1 Q4 INFECTIOUS DISEASES Pub Date : 2024-01-01 DOI: 10.1016/j.idcr.2024.e02082
Makoto Hibino, Yuta Kasai, Hikari Higa, Shigehiro Watanabe, Riko Kamada, Shunichi Tobe, Kazunari Maeda, Tetsuri Kondo
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引用次数: 0
Miliaria crystallina complicating infectious spondylodiscitis 感染性脊柱盘炎并发的结晶性睫状体炎
IF 1.1 Q4 INFECTIOUS DISEASES Pub Date : 2024-01-01 DOI: 10.1016/j.idcr.2024.e02076
Olfa Jomaa, Mouna Brahem, Habib Hajji, Mahbouba Ardhaoui, Rihab Sarraj, Mohamed Younes, Rebeh Bougossa, Fatma Elarbi

We report the case of miliaria crystallina complicating infectious spondylodiscitis in the lumbar region in a 66-year old woman. The eruption was concomitant with a persistent malignant fever and consisted of diffuse vesicular lesions spread all over the body with regress after resolution of fever.

我们报告了一名 66 岁女性腰部感染性脊椎盘炎并发结晶粟粒疹的病例。发病时伴有持续恶性发热,全身出现弥漫性水泡状皮损,退热后皮损消退。
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引用次数: 0
Severe meningitis and infectious aneurysm rupture of the middle cerebral artery following mechanical thrombectomy in infective endocarditis: A case report 感染性心内膜炎机械血栓切除术后出现严重脑膜炎和大脑中动脉感染性动脉瘤破裂:病例报告
IF 1.1 Q4 INFECTIOUS DISEASES Pub Date : 2024-01-01 DOI: 10.1016/j.idcr.2024.e02086
Yeting Luo, Zhijuan Lu, Yunhui Zhu, Zhaohui Lai

Introduction

Infective endocarditis (IE) is known to precipitate several severe complications, often culminating in dire outcomes. In this report, we present the case of a 33-year-old female with IE, which was further complicated by the occurrence of brain infarction, meningitis, and infectious aneurysm.

Case report

A 33-year-old female patient, presenting with left limb weakness persisting for a duration of 15 h, was admitted to our medical facility. A head MRI scan disclosed the presence of an acute cerebral infarction located in the left hemisphere, and subsequent CT angiography confirmed an occlusion of the M1 segment of the left middle cerebral artery. Consequently, the patient underwent mechanical thrombectomy as an intervention. Several days later, echocardiography revealed the presence of a 6.5 × 3.2 mm vegetation on the anterior mitral valve cusp, while blood cultures returned positive for Streptococcus mitis. A diagnosis of IE was established, and antibiotic therapy tailored to the microbiological sensitivities was promptly initiated. However, on the ninth day of her hospitalization, the patient's clinical condition deteriorated significantly due to the emergence of critical complications, including meningitis and a infectious aneurysm. Despite the implementation of aggressive antibiotic therapy, her condition continued to worsen, ultimately resulting in her demise on the sixteenth day of hospitalization, precipitated by the rupture of the infectious aneurysm.

Conclusions

The occurrence of infective endocarditis alongside brain infarction, meningitis, and infectious aneurysm in a single patient represents a rare, intricate, and gravely serious clinical scenario. In such instances, the responsibility for management should be vested in a multidisciplinary team of healthcare professionals.
导言众所周知,感染性心内膜炎(IE)会引发多种严重并发症,最终往往导致可怕的后果。在本报告中,我们介绍了一名 33 岁女性 IE 患者的病例,该病例因脑梗塞、脑膜炎和感染性动脉瘤的发生而变得更加复杂。头部核磁共振扫描显示左侧大脑半球存在急性脑梗塞,随后的 CT 血管造影证实左侧大脑中动脉 M1 段闭塞。因此,患者接受了机械性血栓切除术作为介入治疗。几天后,超声心动图检查发现二尖瓣前瓣尖上有一个 6.5 × 3.2 毫米的植被,同时血液培养结果显示链球菌阳性。IE 诊断成立,并根据微生物敏感性迅速开展了抗生素治疗。然而,在住院的第九天,由于出现了脑膜炎和感染性动脉瘤等严重并发症,患者的临床状况明显恶化。结论在一名患者身上同时出现感染性心内膜炎、脑梗塞、脑膜炎和感染性动脉瘤是一种罕见、复杂和严重的临床表现。在这种情况下,由多学科医护人员组成的团队应承担起处理责任。
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引用次数: 0
Pulmonary coccidioidomycosis in China: Case reports and literature review 中国的肺球孢子菌病:病例报告和文献综述
IF 1.1 Q4 INFECTIOUS DISEASES Pub Date : 2024-01-01 DOI: 10.1016/j.idcr.2024.e02102
Huanhuan Bi , Feng Hou , Weizhong Han , JiaXing Sun , DunQiang Ren , Min Zhuang , Chunling Zhang , Hongmei Wang
Coccidioidomycosis is a fungal infection commonly found in the tropical regions of southwestern United States, such as Arizona, the Central Valley of California, parts of New Mexico, and western Texas. The endemic regions also extend into northern Mexico and include focal endemic areas in sections of Central America and Argentina. Coccidioides species have also been reported in central and southern Utah, Nevada, and the central part of Washington State., the pathogenic bacteria commonly colonize the lungs. China, which is outside the traditionally established endemic area, is witnessing a rise in reported cases of pulmonary coccidioidomycosis. Meanwhile, the comorbidities of the disease began to become complicated. We reported two Chinese patients with pulmonary coccidioidomycosis complicated by organizing pneumonia and reviewed 42 cases of Chinese patients in the literature from 1958 to 2024. Out of the 44 patients from 13 different provinces (Including Hong Kong Special Administrative Region and Taiwan), the average age was (43.08 ± 3.03) years. Among them, 34 (76.7 %) were male, while 10 (23.3 %) were female, cough/sputum (81.8 %) are the most common symptoms, the cases are concentrated in coastal areas. 27(61.4 %) were Imported and 17(38.6 %) were domestic primary cases, showing a higher proportion of imported cases compared to domestic primary cases. Misdiagnosis and mistreatment have a significant impact on patients, the combination of new technologies and traditional pathology diagnosis have substantially promoted precise diagnosis for clinician in non-endemic areas. Interestingly, the histopathological findings of the two patients we report showed evident organizing pneumonia and an increased eosinophil count, the application of corticosteroid drugs notably improved the patients' conditions. Overall, at least 84.1 % of patients had a favorable prognosis. Considering the changing epidemiology of pulmonary coccidioidomycosis, Chinese healthcare providers should be cautious about their patients' travel history, particularly among male individuals.
球孢子菌病是一种真菌感染,常见于美国西南部的热带地区,如亚利桑那州、加利福尼亚州中央谷地、新墨西哥州部分地区和得克萨斯州西部。流行地区还延伸到墨西哥北部,包括中美洲和阿根廷部分地区的重点流行区。在犹他州中部和南部、内华达州和华盛顿州中部也有球孢子虫物种的报道,致病菌通常在肺部定殖。中国不在传统的流行区内,但报告的肺球孢子菌病病例却在增加。同时,该病的合并症也开始变得复杂。我们报告了两例肺球孢子菌病并发组织化肺炎的中国患者,并回顾了1958年至2024年间42例中国患者的文献。在来自 13 个不同省份(包括香港特别行政区和台湾)的 44 例患者中,平均年龄为(43.08 ± 3.03)岁。咳嗽/咳痰(81.8%)是最常见的症状,病例主要集中在沿海地区。27例(61.4%)为进口病例,17例(38.6%)为国内原发病例,显示进口病例的比例高于国内原发病例。误诊误治对患者的影响很大,新技术与传统病理诊断的结合大大促进了非流行区临床医生的精确诊断。有趣的是,我们报告的两名患者的组织病理学检查结果显示明显的组织性肺炎和嗜酸性粒细胞计数增加,应用皮质类固醇药物明显改善了患者的病情。总体而言,至少 84.1% 的患者预后良好。考虑到肺球孢子菌病流行病学的变化,中国的医疗服务提供者应谨慎对待患者的旅行史,尤其是男性患者。
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引用次数: 0
Isolated retrobulbar optic neuritis after Klebsiella pneumoniae infection: A rare case report and literature review 肺炎克雷伯菌感染后的孤立性球后视神经炎:罕见病例报告和文献综述
IF 1.1 Q4 INFECTIOUS DISEASES Pub Date : 2024-01-01 DOI: 10.1016/j.idcr.2024.e02106
Qing Wang , Shijie Duan , Shikun Deng , Shenghui Yu
A new invasive Klebsiella pneumoniae liver abscess syndrome (IKPLAS) has been described. It is often described as primary liver abscess and metastatic infection in multiple systems. Patients often develop endogenous endophthalmitis (EE), when the infection affects the eyes. Isolated optic neuritis (ON) is an unusual manifestation of Klebsiella pneumoniae (K. pneumoniae) infection associated ocular complications. We report a rare case of isolated retrobulbar optic neuritis in a 33-year-old young man on the 4th day of admission with severe pneumonia as the first symptom. Cerebrospinal fluid (CSF) analysis showed higher protein levels (1.12 g/l) but aquaporin-4 (AQP4) & myelin oligodendrocyte glycoprotein (MOG) antibodies were negative. Pulse therapy with intravenous methylprednisolone (1 g daily for 3 days, followed by tapering for a total of 2 months) and immunoglobulin (37.5 g daily for 5 days) was effective on his ON. We suggest that this was a form of para-infectious optic neuritis (PON) triggered by K. pneumoniae infection. K. pneumoniae antigens induced para-infectious demyelination of the optic nerve may be involved in visual impairment.
一种新的侵袭性肺炎克雷伯氏菌肝脓肿综合征(IKPLAS)已被描述。它通常被描述为原发性肝脓肿和多个系统的转移性感染。当感染波及眼睛时,患者通常会出现内源性眼内炎(EE)。孤立性视神经炎(ON)是肺炎克雷伯菌(K. pneumoniae)感染引起眼部并发症的一种不常见表现。我们报告了一例罕见的孤立性球后视神经炎病例,患者是一名 33 岁的年轻男性,入院第 4 天,以重症肺炎为首发症状。脑脊液(CSF)分析显示蛋白质水平较高(1.12 克/升),但水汽蛋白-4(AQP4)和amp;髓鞘少突胶质细胞糖蛋白(MOG)抗体阴性。静脉注射甲基强的松龙(每天 1 克,连续 3 天,然后逐渐减量,共 2 个月)和免疫球蛋白(每天 37.5 克,连续 5 天)的脉冲疗法对他的ON有效。我们认为这是一种由肺炎双球菌感染引发的副感染性视神经炎(PON)。肺炎克氏菌抗原诱导的视神经副感染性脱髓鞘可能与视力损伤有关。
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引用次数: 0
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