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Diagnostic Delay of Spinal Tuberculosis Causing Medullary Compression. 导致髓质受压的脊柱结核的诊断延迟。
IF 1.1 Q4 INFECTIOUS DISEASES Pub Date : 2024-05-03 eCollection Date: 2024-01-01 DOI: 10.1155/2024/5118600
Krestine Corydon, Matilde Bjørn Ørum, Kristoffer Backman Nøhr, Kristina Öbrink-Hansen

We present a case of a Philippine woman in her late twenties, diagnosed with spinal tuberculosis after surgical intervention due to medullary compression. The diagnosis was preceded by four months of unexplained back pain. Differential diagnoses included ulcer, liver-gallbladder disease, musculoskeletal causes, and cancer. This case highlights the importance of considering tuberculosis as a differential diagnosis in patients from high-endemic areas to avoid diagnostic delay and the risk of disease progression.

我们介绍了一例菲律宾妇女的病例,她 20 多岁,由于髓质受压,在接受手术治疗后被确诊为脊柱结核。确诊前曾有四个月原因不明的背部疼痛。鉴别诊断包括溃疡、肝胆疾病、肌肉骨骼疾病和癌症。该病例强调了将结核病作为高端流行病地区患者的鉴别诊断的重要性,以避免诊断延误和疾病恶化的风险。
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引用次数: 0
Non-O1, Non-O139 Vibrio cholerae Bacteremia in an Autoimmune Pancreatitis Patient. 一名自身免疫性胰腺炎患者的非 O1、非 O139 霍乱弧菌菌血症。
IF 1.1 Q4 INFECTIOUS DISEASES Pub Date : 2024-05-03 eCollection Date: 2024-01-01 DOI: 10.1155/2024/7219952
Cheng-Jing Gu, Ming-Dong Ding, Da-Ming Zhou, Jie Li, Wen-Qing Yu, Yong-Lin Yang

Over 200 different serogroups of Vibrio cholerae based on O-polysaccharide specificity have been described worldwide, including the two most important serogroups, O1 and O139. Non-O1/non-O139 V. cholerae serogroups generally do not produce the cholera-causing toxin but do sporadically cause gastroenteritis and extra-intestinal infections. Recently, however, bloodstream infections caused by non-O1/non-O139 V. cholerae are being increasingly reported, and these infections are associated with high mortality in immunocompromised hosts. We describe a case of non-O1/non-O139 V. cholerae bacteremia in a patient with autoimmune pancreatitis and stenosis of the intra- and extrahepatic bile ducts. The clinical manifestations of bacteremia were fever and mild digestive symptoms. The blood cultures showed V. cholerae, which was identified as a non-O1, non-O139 serogroup by slide agglutination tests and PCR. The bloodstream infection of the patient was likely caused by the consumption of contaminated seafood at a banquet. The patient recovered after the administration of a third-generation cephalosporin. Non-O1/non-O139 V. cholerae infection presents with or without gastrointestinal manifestations; close attention should be paid to the possibility of disseminated non-O1/non-O139 V. cholerae infection in high-risk patients.

根据 O 型多糖的特异性,全世界已发现 200 多个不同的霍乱弧菌血清群,其中包括两个最重要的血清群 O1 和 O139。非 O1/ 非 O139 霍乱弧菌血清群一般不产生导致霍乱的毒素,但偶尔会引起肠胃炎和肠道外感染。然而,最近由非 O1/ 非 O139 霍乱弧菌引起的血流感染的报道越来越多,这些感染与免疫力低下的宿主的高死亡率有关。我们描述了一例患有自身免疫性胰腺炎和肝内外胆管狭窄的非 O1/ 非 O139 型霍乱弧菌菌血症患者。菌血症的临床表现为发热和轻微的消化道症状。血液培养显示霍乱弧菌,通过玻片凝集试验和 PCR 鉴定为非 O1、非 O139 血清群。患者的血液感染很可能是在一次宴会上食用了受污染的海鲜所致。患者在使用第三代头孢菌素后痊愈。非 O1/ 非 O139 型霍乱弧菌感染会出现或不出现胃肠道表现;应密切关注高危患者感染非 O1/ 非 O139 型霍乱弧菌的可能性。
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引用次数: 0
Pott's Paraplegia in a 2 Years Female: A Rare Presentation at an Early Age. 一名两岁女童的波特氏截瘫:罕见的幼年病例
IF 1.1 Q4 INFECTIOUS DISEASES Pub Date : 2024-04-27 eCollection Date: 2024-01-01 DOI: 10.1155/2024/5575592
Preeti Basnet, Anish Joshi, Saurab Karki, Anil Jung Thapa, Prayash Poudel, Anugya Sapkota, Manoj Shrestha, Shreebridhi Pande

Introduction: Potts disease is extrapulmonary skeletal tuberculosis mostly affecting the thoracolumbar spine. It destroys the disc space, adjacent vertebral bodies, and spinal elements, leading to cord compression and paraplegia.

Methods: This is a case report study of a 29-month-old toddler who presented to our hospital with bilateral lower limb weakness.

Results: On clinical, laboratory, and radiological examination, she was diagnosed with Pott's spine, started on antitubercular therapy, and planned for surgery in her follow-up.

Conclusion: Tuberculosis of the spine is still prevalent in developing countries, mainly in children. Complications of the disease can be devastating because of its ability to cause bone destruction, spinal deformity, and paraplegia. So, in a tuberculosis-endemic region, clinical suspicion should be there for Potts disease when a child presents with paraplegia of the lower limbs. Children can develop tuberculosis which can spread to the spine despite vaccination. The prognosis of spinal tuberculosis is improved by early diagnosis and rapid intervention.

简介波茨病是一种肺外骨骼结核病,主要侵犯胸腰椎。它破坏椎间盘间隙、邻近椎体和脊柱元素,导致脊髓受压和截瘫:这是一个病例报告,研究对象是一名 29 个月大的幼儿,因双下肢无力到我院就诊:根据临床、实验室和放射学检查,她被诊断为波特氏脊柱炎,开始接受抗结核治疗,并计划在后续治疗中进行手术:结论:脊柱结核在发展中国家仍然很普遍,主要发生在儿童身上。结论:脊柱结核在发展中国家仍然很普遍,主要发生在儿童身上,由于该病能够导致骨质破坏、脊柱畸形和截瘫,其并发症可能是毁灭性的。因此,在结核病流行的地区,当儿童出现下肢截瘫时,临床上应怀疑是否患有波茨病。尽管接种了疫苗,儿童仍有可能患上结核病,并扩散到脊柱。早期诊断和快速干预可改善脊柱结核的预后。
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引用次数: 0
Delayed Surgical Treatment of a CE1 Lung Cyst Resulting in Pericystectomy of CE4 Cyst. CE1 肺囊肿延迟手术治疗导致 CE4 囊肿周围切除术。
IF 1.1 Q4 INFECTIOUS DISEASES Pub Date : 2024-03-14 eCollection Date: 2024-01-01 DOI: 10.1155/2024/5167805
Gian Luca D'Alessandro, Agostina Pontarelli, Armanda Leka, Dino Casazza, Raffaella Lissandrin, Tommaso Manciulli, Annarita Botta, Roberto Parrella, Enrico Brunetti, Pietro Rinaldi

Lung is the second most common locationof cystic echinococcosis (CE), after the liver. Diagnosis of lung CE is often incidental, and clinical manifestations depend on the location and size of the cyst, the most common being chest pain, shortness of breath, expectoration of fragments of endocyst, and haemoptysis. Surgery is the primary treatment, with a minor role for medical therapy. Delayed diagnosis and treatment may have important consequences. We present a case of lung CE in whichsurgical treatment was delayed due to the first wave of COVID-19. Since surgery could not be performed immediately, the patient was kept on albendazole and the cyst stage moved from CE1 to CE3a, to CE4, eventually requiring a more aggressive pericystectomy instead of the commonly performed endocystectomy. The clinical and imaging characteristics of a rare CE4 cyst of the lung are reported.

肺是囊性棘球蚴病(CE)的第二大常见部位,仅次于肝脏。肺囊性棘球蚴病的诊断往往是偶然的,临床表现取决于囊肿的位置和大小,最常见的表现是胸痛、气短、排出内囊碎片和咯血。手术是主要治疗方法,药物治疗作用较小。延误诊断和治疗可能会造成严重后果。我们介绍了一例肺 CE 病例,该病例的手术治疗因第一波 COVID-19 而延误。由于无法立即进行手术,患者一直服用阿苯达唑,囊肿阶段从CE1到CE3a,再到CE4,最终需要进行更积极的囊周切除术,而不是通常进行的囊内切除术。本文报告了一例罕见的 CE4 肺囊肿的临床和影像学特征。
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引用次数: 0
Unmasking the Enigma: Influenza Vaccine and the Rare Case of Post-Vaccination Pericarditis. 揭开谜底:流感疫苗与接种后心包炎的罕见病例。
IF 1.1 Q4 INFECTIOUS DISEASES Pub Date : 2024-03-09 eCollection Date: 2024-01-01 DOI: 10.1155/2024/2729208
Ekrem Yetiskul, Alaukika Agarwal, Gaetano Di Pietro, Faris Qaqish, Salman Khan, Shahkar Khan

Acute pericarditis is an inflammatory condition involving the pericardium, the double-layered sac that surrounds the heart. It is characterized by chest pain, typically pleuritic and sharp, along with other clinical and laboratory findings indicative of pericardial inflammation. While acute pericarditis following influenza vaccination is rare, it has been reported in medical literature. The relationship between vaccinations, including the influenza vaccine, and pericarditis is particularly interesting, as it has implications for public health and vaccination programs. Understanding the pathophysiological mechanisms behind vaccine-induced pericarditis and recognizing the clinical presentation are essential for healthcare professionals to diagnose, manage, and educate patients appropriately.

急性心包炎是一种涉及心包的炎症,心包是环绕心脏的双层囊。其特征是胸痛,典型的胸膜炎性剧痛,以及其他表明心包炎症的临床和实验室检查结果。虽然接种流感疫苗后发生急性心包炎的情况很少见,但医学文献中也有报道。包括流感疫苗在内的疫苗接种与心包炎之间的关系尤其引人关注,因为它对公共卫生和疫苗接种计划具有重要意义。了解疫苗诱发心包炎背后的病理生理机制并识别其临床表现对于医护人员诊断、管理和教育患者至关重要。
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引用次数: 0
Aspergillus fumigatus Epidural Abscess and Postsurgical Wound Infection in an Immunocompetent Host. 免疫功能正常的宿主硬膜外脓肿和手术后伤口感染的曲霉菌。
IF 1.1 Q4 INFECTIOUS DISEASES Pub Date : 2024-02-29 eCollection Date: 2024-01-01 DOI: 10.1155/2024/8104167
Nadine Montreuil, Andres Martinez, Leon Budrie, Shriya Goyal, Tanya Quiroz, Christine Vu, Folusakin Ayoade, Candice A Sternberg

In this case, we present an immunocompetent patient who had a wound infection secondary to Aspergillus fumigatus after undergoing a neurosurgical procedure that was complicated by an epidural abscess. The patient was treated with voriconazole and responded favorably. We highlight the need for awareness of the possibility of an Aspergillus infection in people without any obvious immunocompromise and advocate for the inclusion of this opportunistic fungus in the workup of postneurosurgical infections and dura-based collections. A brief review of relevant literature is also included.

在本病例中,我们介绍了一名免疫功能正常的患者,该患者在接受神经外科手术后继发了伤口感染,并发硬膜外脓肿。患者接受了伏立康唑治疗,效果良好。我们强调有必要认识到无明显免疫力低下者感染曲霉菌的可能性,并主张将这种机会性真菌纳入神经外科术后感染和硬脑膜脓肿的检查中。本文还简要回顾了相关文献。
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引用次数: 0
A Man in His Forties with Recurrent Cat-Scratch Disease. 一名四十多岁的男子反复患猫抓病。
IF 1.1 Q4 INFECTIOUS DISEASES Pub Date : 2024-02-27 eCollection Date: 2024-01-01 DOI: 10.1155/2024/4411133
Sara López-Rueda, Benjamin Valente-Acosta, Adrian Murillo-Zolezzi, Francisco Moreno-Sánchez, Irma Hoyo-Ulloa, Jesús Javier Baquera-Heredia

Cat-scratch disease (CSD) is a self-limited zoonotic infection transmitted by felines caused by the Gram-negative bacillus Bartonella henselae. It usually presents with lymphadenopathy and constitutional symptoms that resolve within eight weeks, with, or without antibiotic treatment. The diagnosis is made by serology, molecular diagnosis in a biopsy, or a positive culture. The recurrence or reactivation of B. henselae has rarely been reported. We present the case of a 45-year-old man with a history of CSD two years before who presented to the clinic with groin lymphadenopathy. The patient had a history of close contact with felines though no known risk exposure was reported. The diagnosis was made with a positive serology suggestive of recent infection along with histopathological changes suggestive of CSD. Subsequently, azithromycin was administered with complete resolution of symptoms.

猫抓病(CSD)是由革兰氏阴性杆菌鸡矢藤巴顿氏菌引起的猫科动物自限性传染病。该病通常表现为淋巴结肿大和全身症状,经抗生素治疗或不经抗生素治疗均可在八周内缓解。诊断可通过血清学、活检中的分子诊断或阳性培养进行。鸡疫杆菌复发或再活化的报道很少。我们接诊了一例 45 岁的男性患者,他两年前曾患 CSD,后因腹股沟淋巴结病就诊。患者有与猫科动物密切接触的历史,但没有报告已知的风险暴露。血清学检查呈阳性,提示近期感染,组织病理变化提示 CSD,因此确诊。随后,患者接受了阿奇霉素治疗,症状完全缓解。
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引用次数: 0
Extrapulmonary Tuberculosis Leading to Abdominal Wall Mass in Young Patient. 导致年轻患者腹壁肿块的肺外结核病
IF 1 Q4 INFECTIOUS DISEASES Pub Date : 2024-02-05 eCollection Date: 2024-01-01 DOI: 10.1155/2024/9924307
Mohadeseh Karimi, Ali AtashAbParvar

Background: Tuberculosis is a bacterial infection that is caused by Mycobacterium tuberculosis. Tuberculosis has arguably been the largest killer of humans historically, and it remains one of the most important infectious causes of death in the world. Tuberculosis can be classified into different forms and it manifests as pulmonary and out pulmonary, respectively, in 85% and 15% of cases. Only a few cases of tuberculosis with abdominal wall involvement have been reported. Case Presentation. Herein, we present a 27-year-old Persian woman, presented with asymmetric abdominal bulging in the right side of the periumbilical area since 6 months before admission that has no pain or secretion. The patient was oriented and not ill or toxic in general appearance. Vital signs were within normal ranges. An abdominal physical examination revealed a mobile, well-bordered, nontender mass 3 × 3 centimeter (cm) in diameter palpated in the right periumbilical area. The patient underwent surgery which revealed a cystic lesion that was carefully resected. In histopathology examination of the specimen resection, tuberculosis was confirmed.

Conclusion: We report a rare case of extrapulmonary tuberculosis that was identified at the abdominal wall. Due to the high number of cases of TB and the development of extrapulmonary forms that can present in an unusual location as an abdominal wall which are difficult to diagnose, it is very important to keep in mind the differential diagnosis of tuberculosis.

背景:结核病是由结核分枝杆菌引起的细菌感染。结核病可以说是人类历史上最大的杀手,至今仍是世界上最重要的传染性死亡原因之一。结核病可分为不同的形式,85%和 15%的病例分别表现为肺结核和肺外结核。腹壁受累的肺结核病例仅有少数报道。病例介绍。本病例是一名 27 岁的波斯妇女,入院前 6 个月出现右侧脐周不对称腹部隆起,无疼痛或分泌物。患者神志清楚,全身无不适或中毒症状。生命体征在正常范围内。腹部体格检查发现,右侧脐周触及一个直径为 3 × 3 厘米(cm)的活动、边界清楚、无触痛的肿块。患者接受了手术治疗,手术仔细切除了囊性病变。切除标本的组织病理学检查证实了结核病:我们报告了一例罕见的腹壁肺外结核病例。由于肺结核病例较多,而且肺外结核可能出现在腹壁这种难以诊断的异常部位,因此牢记肺结核的鉴别诊断非常重要。
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引用次数: 0
Genitourinary Blastomycosis in a Young Male Patient: A Case Report and Review of Diagnostic Challenges 一名年轻男性患者的泌尿生殖系统布氏杆菌病:病例报告和诊断难题回顾
IF 1.1 Q4 INFECTIOUS DISEASES Pub Date : 2023-12-19 DOI: 10.1155/2023/4713948
Emily Hillman, Hangcheng Fu, Randa Obid, U. Anele
Disseminated blastomycosis is an endemic fungal infection that rarely manifests with genitourinary involvement. We present a unique case of a 28-year-old professional male gamer with a remote history of hemoptysis and cervical lymphadenopathy who presented with hematospermia, lower urinary tract symptoms (LUTS), and persistent groin abscesses after left orchiectomy at an outside hospital. He underwent drainage of groin abscess and prostate biopsy for an abnormal digital rectal exam which revealed disseminated blastomycosis requiring systemic, long-term antifungal treatment. We have also included a review of literature to note clinical patterns in presentations and highlight the diagnostic challenges that this infection presents.
播散性囊霉菌病是一种地方性真菌感染,很少表现为泌尿生殖系统受累。我们介绍了一例独特的病例,患者是一名 28 岁的职业男性游戏玩家,曾有咯血和颈部淋巴结病史,在一家外院接受左侧睾丸切除术后出现血精、下尿路症状(LUTS)和持续性腹股沟脓肿。他接受了腹股沟脓肿引流术,并因数字直肠检查异常而接受了前列腺活检,结果显示他患上了播散性囊霉菌病,需要长期全身抗真菌治疗。我们还对文献进行了回顾,以注意临床表现的模式,并强调这种感染所带来的诊断难题。
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引用次数: 0
Persistent, Poorly Responsive Immune Thrombocytopenia Secondary to Asymptomatic COVID-19 Infection in a Child 一名儿童继发于无症状 COVID-19 感染的持续性、反应性差的免疫性血小板减少症
IF 1.1 Q4 INFECTIOUS DISEASES Pub Date : 2023-12-15 DOI: 10.1155/2023/3298520
C. Mettananda, Senani Williams
Immune thrombocytopenic purpura (ITP) secondary to asymptomatic COVID-19 infection, especially in children, is not reported. Furthermore, persistent, treatment-resistant ITP secondary to COVID-19 is not reported. We report a previously healthy 14-year-old Asian boy who developed secondary ITP following an asymptomatic COVID-19 infection and is having a relapsing and remitting cause with poor response to immunosuppressants even after 21 months following the diagnosis. This case emphasizes the importance of testing for COVID-19 in newly diagnosed ITP patients and the need for follow-up platelet counts in patients who recover from COVID-19 as it may follow into developing secondary ITP yet being asymptomatic until you present with a bleeding complication of ITP. The poor response to standard immunosuppression warrants more understanding of the pathophysiology of persistently low platelets following COVID-19 infection. Long-term sequelae of the disease highlight the importance of getting vaccinated for COVID-19 despite COVID-19 being no longer a global emergency.
因无症状感染 COVID-19 而继发免疫性血小板减少性紫癜(ITP)的病例(尤其是儿童)尚未见报道。此外,继发于 COVID-19 的持续性、耐药性 ITP 也未见报道。我们报告了一名之前身体健康的 14 岁亚洲男孩,他在无症状感染 COVID-19 后继发了 ITP,即使在确诊后 21 个月仍出现复发和缓解,且对免疫抑制剂反应不佳。本病例强调了对新诊断的 ITP 患者进行 COVID-19 检测的重要性,以及对从 COVID-19 感染中康复的患者进行血小板计数随访的必要性,因为 COVID-19 感染可能会导致继发性 ITP,但患者在出现 ITP 出血并发症之前并无症状。由于对标准免疫抑制的反应不佳,因此需要进一步了解 COVID-19 感染后血小板持续偏低的病理生理学。尽管COVID-19已不再是全球紧急事件,但该疾病的长期后遗症凸显了接种COVID-19疫苗的重要性。
{"title":"Persistent, Poorly Responsive Immune Thrombocytopenia Secondary to Asymptomatic COVID-19 Infection in a Child","authors":"C. Mettananda, Senani Williams","doi":"10.1155/2023/3298520","DOIUrl":"https://doi.org/10.1155/2023/3298520","url":null,"abstract":"Immune thrombocytopenic purpura (ITP) secondary to asymptomatic COVID-19 infection, especially in children, is not reported. Furthermore, persistent, treatment-resistant ITP secondary to COVID-19 is not reported. We report a previously healthy 14-year-old Asian boy who developed secondary ITP following an asymptomatic COVID-19 infection and is having a relapsing and remitting cause with poor response to immunosuppressants even after 21 months following the diagnosis. This case emphasizes the importance of testing for COVID-19 in newly diagnosed ITP patients and the need for follow-up platelet counts in patients who recover from COVID-19 as it may follow into developing secondary ITP yet being asymptomatic until you present with a bleeding complication of ITP. The poor response to standard immunosuppression warrants more understanding of the pathophysiology of persistently low platelets following COVID-19 infection. Long-term sequelae of the disease highlight the importance of getting vaccinated for COVID-19 despite COVID-19 being no longer a global emergency.","PeriodicalId":9608,"journal":{"name":"Case Reports in Infectious Diseases","volume":"4 2","pages":""},"PeriodicalIF":1.1,"publicationDate":"2023-12-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139000955","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
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Case Reports in Infectious Diseases
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