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Acute hematogenous disseminated pulmonary tuberculosis and tuberculous meningitis following in vitro fertilization and embryo transfer: A case report 体外受精和胚胎移植后出现急性血行播散性肺结核和结核性脑膜炎:病例报告
IF 1.1 Q4 INFECTIOUS DISEASES Pub Date : 2024-01-01 DOI: 10.1016/j.idcr.2024.e02096
Mingyi Li , Xuejuan Yang , Qi Zhou , Jinxiu Wang , Xicheng Wang , Lin Mao
With the extensive development of assisted reproductive technology, in vitro fertilization and embryo transfer (IVF-ET) have enabled successful pregnancies for some infertility patients. However, pregnancy leads to endocrine and immune function changes that result in decreased immunity, providing an opportunity for mycobacterium tuberculosis infection or reactivation. Hematogenous disseminated pulmonary tuberculosis is a dangerous complication of pregnancy after IVF-ET, which can lead to adverse outcomes. In this case report, we present a patient with normal immune function who developed hematogenous disseminated tuberculosis after IVF-ET. We retrospectively analyzed the clinical manifestations, test results and imaging findings of the patient while reviewing relevant literature. We recommend conducting genital tuberculosis screening and screening for latent tuberculosis infection before IVF-ET. Healthcare providers should maintain high vigilance for active tuberculosis during pregnancy when unexplained high fever, cough with sputum production, early vaginal bleeding occurs despite repeated broad-spectrum antibiotic treatment.
随着辅助生殖技术的广泛发展,体外受精和胚胎移植(IVF-ET)使一些不孕症患者成功怀孕。然而,妊娠会导致内分泌和免疫功能发生变化,导致免疫力下降,为结核分枝杆菌感染或再活化提供了机会。血行播散性肺结核是体外受精-胚胎移植术后妊娠的一种危险并发症,可导致不良后果。在本病例报告中,我们介绍了一名免疫功能正常的患者,她在接受体外受精-胚胎移植(IVF-ET)后发生了血行播散性肺结核。我们回顾性分析了患者的临床表现、检验结果和影像学检查结果,同时查阅了相关文献。我们建议在进行体外受精-胚胎移植(IVF-ET)前进行生殖器结核筛查和潜伏结核感染筛查。如果在反复使用广谱抗生素治疗后仍出现不明原因的高热、咳嗽并伴有痰、早期阴道出血等症状,医护人员应高度警惕妊娠期活动性结核。
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引用次数: 0
Tuberculosis and Takayasu's arteritis: An enigmatic association 肺结核与高安氏动脉炎:神秘的关联
IF 1.5 Q4 INFECTIOUS DISEASES Pub Date : 2024-01-01 DOI: 10.1016/j.idcr.2024.e01938
Gawahir A. Ali, Wael Goravey

There is indirect evidence signifying a potential link between tuberculosis and Takayasu’s arteritis (TAK); however, the exact mechanism and relationship between TKA and Mycobacterium tuberculosis (TB) remain to be elucidated. This case intends to highlight the association between TB and TKA, as early detection can avoid devastating consequences.

有间接证据表明,结核病与高安氏动脉炎(TAK)之间存在潜在联系;然而,TKA 与结核分枝杆菌(TB)之间的确切机制和关系仍有待阐明。本病例旨在强调结核病与高加索动脉炎之间的关系,因为早期发现可以避免破坏性后果。
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引用次数: 0
Invasive pneumococcal serotype 3 infection following pneumococcal vaccination in a hematopoietic stem cell transplant patient: A case report 造血干细胞移植患者接种肺炎球菌疫苗后感染侵袭性肺炎球菌血清 3 型:病例报告
IF 1.5 Q4 INFECTIOUS DISEASES Pub Date : 2024-01-01 DOI: 10.1016/j.idcr.2024.e01936
Kazuhiro Ishikawa, Nobuyoshi Mori

Given the high mortality rate of invasive pneumococcal disease (IPD) in hematopoietic stem cell transplant (HSCT) recipients, vaccination is recommended. These recipients respond to most vaccines; however, their immune response is typically weaker during the first months or years after transplantation, compared with that of healthy individuals. Here, we report a case of IPD with serotype 3 pneumonia and empyema in an HSCT recipient who had received three doses of the 13-valent pneumococcal conjugate vaccine (PCV) and one dose of the 23-valent pneumococcal polysaccharide vaccine; furthermore, the recipient had no relapse, graft-versus-host disease, or use of immunosuppressive agents after allogeneic HSCT for acute myeloid leukemia. Moreover, we discussed the characteristics of serotype 3 Streptococcus pneumoniae, a case series of breakthrough infections with S. pneumoniae in HSCT recipients who received pneumococcal vaccines, and the potential implications for the upcoming PCV15 and PCV20 vaccines for serotype 3.

鉴于造血干细胞移植(HSCT)受者患侵袭性肺炎球菌疾病(IPD)的死亡率很高,因此建议接种疫苗。这些受者对大多数疫苗都有反应;然而,与健康人相比,他们在移植后最初几个月或几年内的免疫反应通常较弱。在此,我们报告了一例 IPD 合并血清 3 型肺炎和肺水肿的造血干细胞移植受者,该受者曾接种过三针 13 价肺炎球菌结合疫苗 (PCV) 和一针 23 价肺炎球菌多糖疫苗;此外,该受者在接受异基因造血干细胞移植治疗急性髓性白血病后没有复发、移植物抗宿主疾病或使用免疫抑制剂。此外,我们还讨论了血清型 3 肺炎链球菌的特征、造血干细胞移植受者接种肺炎球菌疫苗后发生肺炎链球菌突破性感染的系列病例,以及即将推出的血清型 3 PCV15 和 PCV20 疫苗的潜在意义。
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引用次数: 0
A non-surgical approach: Ampicillin's success in Listeria monocytogenes endocarditis 非手术疗法:氨苄西林成功治疗单核细胞增多性李斯特菌心内膜炎
IF 1.5 Q4 INFECTIOUS DISEASES Pub Date : 2024-01-01 DOI: 10.1016/j.idcr.2024.e01965
Natalia Ramos-Ospina , Pablo Andrés Moncada-Vallejo

Background

Listeria monocytogenes, a Gram-positive bacillus, primarily affects immunocompromised individuals. Endocarditis is a rare but severe complication of L. monocytogenes bacteremia, irrespective of native or prosthetic valves. While there is no standardized treatment, the use of ampicillin proves effective in most cases. Surgical intervention is reserved for cases involving valve dehiscence, heart failure, or myocardial abscess.

Case presentation

A 54-year-old female, with mitral valve replacement, presented with fever, chest pain and dyspnea at rest. Patient was initially diagnosed with bacterial pneumonia; however, subsequent evaluation revealed L. monocytogenes bacteremia, resulting in endocarditis. Surgical management was contraindicated due to multiple prior valve replacement surgeries. Symptoms resolution, along with improvements in echocardiographic and clinical parameters, was achieved through extended antibiotic treatment only with no surgical intervention.

Conclusion - key takeaways

This case underscores the critical importance of individualized treatment approaches in endocarditis, particularly in patients with surgery approach contraindication, and emphasized the success achieved through ampicillin-based management.

背景单核细胞增多性李斯特菌是一种革兰氏阳性杆菌,主要影响免疫力低下的人。心内膜炎是单核细胞增多性李斯特菌血症的一种罕见但严重的并发症,不论是原生瓣膜还是人工瓣膜。虽然没有标准化的治疗方法,但使用氨苄西林对大多数病例都有效。病例介绍 一位 54 岁的女性患者因发热、胸痛和休息时呼吸困难而接受二尖瓣置换术。患者最初被诊断为细菌性肺炎,但随后的评估发现其患有单核细胞增多症菌血症,导致心内膜炎。由于患者之前接受过多次瓣膜置换手术,因此禁忌手术治疗。本病例强调了心内膜炎个体化治疗方法的重要性,尤其是对有手术禁忌症的患者,并强调了氨苄西林治疗所取得的成功。
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引用次数: 0
A case of prosthetic valve endocarditis and aortic abscess due to Bacillus cereus 一例由蜡样芽孢杆菌引起的人工瓣膜心内膜炎和主动脉脓肿病例
IF 1.5 Q4 INFECTIOUS DISEASES Pub Date : 2024-01-01 DOI: 10.1016/j.idcr.2024.e01940
Akina Fukushima , Takaaki Kobayashi , Yoshihito Otsuka , Naoto Hosokawa , Sandra Moody , Miyu Takagi , Akihito Yoshida

Bacillus cereus (B. cereus) is commonly found in the environment and is often considered a blood culture contaminant. However, in patients with specific risk factors such as intravenous drug use, central venous access catheters, immunosuppression, or prosthetic valves, B. cereus can cause severe infections. Herein, we present a case of prosthetic valve endocarditis (PVE) caused by B. cereus in an 84-year-old woman with a history of aortic valve replacement for aortic stenosis five years earlier. She presented with anorexia, and her physical examination revealed tenderness in the left upper quadrant of the abdomen. Blood culture grew B. cereus, and a CT scan showed splenic infarction, raising suspicion of PVE. Transesophageal echocardiogram (TEE) revealed an abscess around the left coronary cusp of the aortic valve and a 15 mm vegetation. Due to the patient's high risk for post-operative complications and her unwillingness to undergo surgery, the surgery was deferred. Instead, she was successfully treated with six weeks of intravenous vancomycin and discharged home. Follow-up TEE demonstrated resolution of the vegetation and valvular abscess. At her six-month post-discharge evaluation, no signs of active infection were noted including fever or worsening heart failure. Although surgery is typically recommended for most cases of PVE, conservative treatment can be considered as an alternative option for selected patients.

蜡样芽孢杆菌(B. cereus)常见于环境中,通常被认为是一种血液培养污染物。然而,在具有特定风险因素(如静脉注射药物、中心静脉通路导管、免疫抑制或人工瓣膜)的患者中,蜡样芽孢杆菌可导致严重感染。在此,我们介绍了一例由蜡样芽孢杆菌引起的人工瓣膜心内膜炎(PVE)病例,患者是一名 84 岁的女性,五年前曾因主动脉瓣狭窄进行过主动脉瓣置换术。她出现厌食,体格检查显示左上腹有压痛。血液培养培养出了蜡样芽孢杆菌,CT 扫描显示脾脏梗塞,这引起了对 PVE 的怀疑。经食道超声心动图(TEE)显示,主动脉瓣左冠状尖周围有脓肿和一个 15 毫米的植被。由于患者术后并发症风险较高,且不愿接受手术,因此手术被推迟。她接受了为期六周的万古霉素静脉注射治疗,并成功出院回家。随访的 TEE 显示植被和瓣膜脓肿已经消退。在她出院后六个月的评估中,没有发现任何活动性感染的迹象,包括发烧或心衰恶化。虽然大多数 PVE 病例通常都建议进行手术治疗,但对于选定的患者,保守治疗也可作为一种替代选择。
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引用次数: 0
Infective endocarditis caused by Lactococcus garvieae: A case report and review of the literature 加维氏乳球菌引起的感染性心内膜炎:病例报告和文献综述
IF 1.5 Q4 INFECTIOUS DISEASES Pub Date : 2024-01-01 DOI: 10.1016/j.idcr.2024.e01941
Izumi Kitagawa , Noriyoshi Ishikawa , Ryohei Ono

Lactococcus garvieae is a Gram-positive coccus that can be easily misidentified as Enterococcus spp. or streptococci. Infection with L. garvieae is associated with the consumption of raw fish and unpasteurized dairy products. Although rare, it can cause infective endocarditis (IE). Herein, we report a case in which aortic valve replacement (AVR) was required for IE caused by L. garvieae.

A 79-year-old Japanese man with a history of hypertension, myocardial infarction, gastroesophageal reflux disease (GERD), and abdominal aortic aneurysm presented with loss of appetite, myalgia, and difficulty in moving. Physical examination revealed a diastolic murmur, an Osler’s node on the right first toe, dental caries, and a palpable spleen, suggesting IE. Transthoracic echocardiography revealed a large, mobile vegetation on the aortic valve, which was associated with severe aortic regurgitation. Blood cultures revealed L. garvieae. The patient received antibiotic therapy, underwent AVR, and recovered without major complications. To date, 30 cases of L. garvieae-associated IE have been reported. We reviewed and summarized all cases of L. garvieae-associated IE including our case.

加维氏乳球菌是一种革兰氏阳性球菌,很容易被误认为是肠球菌属或链球菌。感染加维氏乳球菌与食用生鱼和未经巴氏消毒的乳制品有关。虽然罕见,但它可引起感染性心内膜炎(IE)。一名 79 岁的日本男子曾患高血压、心肌梗死、胃食管反流病(GERD)和腹主动脉瘤,出现食欲不振、肌痛和行动不便。体格检查发现患者有舒张期杂音,右脚第一趾有奥斯勒结节,龋齿,脾脏可触及,提示有 IE。经胸超声心动图显示,主动脉瓣上有一大片移动的植被,并伴有严重的主动脉瓣反流。血液培养发现了加维氏菌。患者接受了抗生素治疗,接受了主动脉瓣置换术,康复后未出现重大并发症。迄今为止,与加维氏菌相关的 IE 已有 30 例报道。我们回顾并总结了包括本病例在内的所有加维氏菌相关 IE 病例。
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引用次数: 0
A rare skin reaction in an elderly woman after exposure to prophylaxis for rabies: A case report 一名老年妇女在接触狂犬病预防药后出现罕见皮肤反应:病例报告
IF 1.5 Q4 INFECTIOUS DISEASES Pub Date : 2024-01-01 DOI: 10.1016/j.idcr.2024.e01974
Luiz Euribel Prestes-Carneiro , Paola Andressa Xavier Mente , Luana Dalla Costa , Ana Paula Lagisck , Eder Gatti Fernandes

Introduction

Rabies is a zoonosis caused by viruses of the family Rhabdoviridae. Prophylaxis with the rabies vaccine and immunoglobulins, depending on the severity of the case, is recommended. After vaccination, mild, moderate, or severe adverse events (AE) are described. Although rare, severe skin reactions may occur, increasing the risk of anaphylaxis.

Case report

An 84-year-old woman was attacked by a stray unknown cat, leaving her with bites and scratches in the neck region and multiple injuries. The case was classified as severe. About 3 h after the first dose of the rabies vaccine, disseminated purplish spots appeared on her lower limbs, worsening significantly after the second dose, requiring hospitalization for the application of the third dose under observation, dermatology evaluation, and collection of skin tissue for biopsy. She was discharged 24 h after the third vaccination, and the purple spots cleared gradually. The biopsy suggested an adverse reaction to the vaccine components. Immunohistochemistry of the rabies virus antigen in dermal nerve fillets was negative. The seroconversion post rabies vaccine showed IgG antibody values below the reference levels.

Conclusion

Vaccination against rabies is extremely important; however, AEs may occur. Our patient developed an important AE and required hospitalization. After complete vaccination, the serum was not converted. A similar case was not previously described, and the case report is important for the creation of jurisprudence on rabies vaccination in elderly patients in Brazil.

导言狂犬病是由狂犬病毒科病毒引起的人畜共患疾病。根据病例的严重程度,建议使用狂犬病疫苗和免疫球蛋白进行预防。疫苗接种后会出现轻度、中度或重度不良反应 (AE)。病例报告 一位 84 岁的妇女被一只不知名的流浪猫袭击,颈部被咬伤和抓伤,身上多处受伤。该病例被列为重症。接种第一剂狂犬病疫苗约 3 小时后,她的下肢出现散在紫斑,接种第二剂后病情明显加重,需要住院接种第三剂,并接受观察、皮肤科评估和采集皮肤组织进行活检。第三次接种 24 小时后,她出院了,紫斑也逐渐消退。活检结果表明她对疫苗成分产生了不良反应。皮肤神经片中狂犬病毒抗原的免疫组化结果为阴性。狂犬病疫苗接种后的血清转换显示 IgG 抗体值低于参考水平。我们的患者出现了严重的不良反应,需要住院治疗。在完成疫苗接种后,血清中的抗体没有发生转化。以前没有类似病例的描述,该病例报告对巴西老年患者狂犬病疫苗接种法的制定具有重要意义。
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引用次数: 0
Two cases of misleading Epstein-Barr virus infection and the role of EBV-DNA 两例误导性 Epstein-Barr 病毒感染和 EBV DNA 的作用。
IF 1.5 Q4 INFECTIOUS DISEASES Pub Date : 2024-01-01 DOI: 10.1016/j.idcr.2024.e02001
Luca Pipitò , Alessandra Murabito , Antonio Cascio

Two atypical cases of infectious mononucleosis in two teenagers with initially negative serology and non-evocative blood examinations are reported. The first patient had recently traveled to Africa, and Epstein-Barr virus negative serology led us to make many extensive investigations. The second patient complained of asthenia for a month, and PET/CT was performed to suspicion of lymphoma. PET scan revealed hypermetabolic lymph nodes in the supradiaphragmatic and subdiaphragmatic stations, along with18F-FDG uptake in the spleen and pharynx, raising more suspicion of lymphoma. Fortunately, Epstein-Barr virus DNA testing was performed and turned positive in both cases, and Epstein-Barr virus serology subsequently became positive. Diagnosing EBV infection can be challenging in rare cases, as EBV-specific serology may be negative in the early stages and confounding factors may be present. Therefore, Epstein-Barr virus DNA testing should be considered early in the diagnostic algorithm to prevent unnecessary investigations in similar cases.

本病例报告了两个非典型传染性单核细胞增多症病例,这两名青少年最初血清学检查呈阴性,血液检查也无异常。第一例患者最近曾去非洲旅行,Epstein-Barr 病毒血清学阴性导致我们进行了许多广泛的检查。第二名患者主诉气喘一个月,我们对其进行了正电子发射计算机断层扫描(PET/CT),怀疑其患有淋巴瘤。正电子发射计算机断层扫描显示,膈上和膈下淋巴结高代谢,脾脏和咽部也有 18F-FDG 摄取,这使我们更加怀疑淋巴瘤。幸运的是,对两个病例都进行了爱泼斯坦-巴氏病毒 DNA 检测,结果均为阳性,随后爱泼斯坦-巴氏病毒血清学检测也呈阳性。在罕见病例中,诊断 EBV 感染可能具有挑战性,因为 EBV 特异性血清学在早期可能呈阴性,而且可能存在干扰因素。因此,在诊断算法中应尽早考虑进行 Epstein-Barr 病毒 DNA 检测,以避免在类似病例中进行不必要的检查。
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引用次数: 0
Disseminated cysticercosis and neurocysticercosis with classic starry-sky appearance in an adolescent vegetarian Indian male 一名吃素的印度男性青少年身上伴有典型星空外观的散发性囊尾蚴病和神经囊尾蚴病
IF 1.1 Q4 INFECTIOUS DISEASES Pub Date : 2024-01-01 DOI: 10.1016/j.idcr.2024.e02079
Himanshu Jindal , Priyanka Gupta , Hardika Arora , P. Purushothaman
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引用次数: 0
Shoulder shake-up: Unveiling the unusual case of acute melioidosis 肩部震动揭开急性瓜虫病不寻常病例的面纱
IF 1.1 Q4 INFECTIOUS DISEASES Pub Date : 2024-01-01 DOI: 10.1016/j.idcr.2024.e02040
Yash Khatod , Neetha Thayil Ramankutty , Deepak Kumar , Vibhor Tak , Neha Gupta , Rengarajan Rajagopal , Suvinay Saxena

Background

Melioidosis is one of the emerging infections in India and is often neglected due to lack of awareness among clinicians. The diseases usually present as multifocal or focal abscesses with bacteremia, yet the isolated septic monoarthritic complicated with septic venous thrombosis is a rare presentation.

Case

This case report describes a 48-year-old male business executive with diabetes and alcoholism who developed septic arthritis caused by Burkholderia pseudomallei and no clear history of exposure to the organism. The patient initially experienced fever, chills, fatigue, reduced urine output, and signs of early sepsis. Despite initial improvement with fluid therapy and antibiotics, the patient's fever persisted. Meticulous clinical examination revealed signs of inflammation and movement restriction in the left shoulder which letter on became obvious and the main complaints of patient. Blood cultures confirmed the presence of B. pseudomallei. Imaging showed septic arthritis, osteomyelitis, lymphadenitis, and venous thrombosis in the left shoulder. Surgical debridement was performed, and the tissue cultures showed the growth of the same pathogen. This led to significant clinical improvement and with prolonged course of antibiotics, complete resolution of symptoms and normal joint function was achieved.

Conclusion

This case report serves to highlight the rare and atypical presentation of Melioidosis and the importance of suspecting this infection in nonendemic regions underscoring the probable impact of climate change. Early diagnosis, effective source control measures and prolonged antibiotic therapy, emerges as pivotal factors contributing to favorable outcomes in such cases.

背景髓样脓肿病是印度新出现的传染病之一,由于临床医生缺乏认识,该病常常被忽视。本病例报告描述了一名患有糖尿病和酗酒的 48 岁男性企业高管,他患上了由假马来伯克霍尔德菌(Burkholderia pseudomallei)引起的化脓性关节炎,但没有明确的病菌接触史。患者最初出现发热、寒战、乏力、尿量减少和早期败血症症状。尽管经过输液治疗和抗生素治疗后病情初步好转,但患者仍持续发烧。仔细的临床检查发现,患者左肩有炎症和活动受限的迹象,随后这些症状逐渐明显,并成为患者的主要主诉。血液培养证实患者感染了假马勒氏杆菌。影像学检查显示左肩有化脓性关节炎、骨髓炎、淋巴结炎和静脉血栓。手术清创后,组织培养显示出相同的病原体。结论:本病例报告强调了梅里埃病的罕见和非典型表现,以及在非流行地区怀疑这种感染的重要性,并强调了气候变化可能带来的影响。早期诊断、有效的病源控制措施和长期抗生素治疗是此类病例取得良好疗效的关键因素。
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引用次数: 0
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