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Post operative abdominal wall mucormycosis infection after laparotomy for bowel perforation 肠穿孔开腹手术后腹壁粘液瘤病感染。
IF 1.5 Q4 INFECTIOUS DISEASES Pub Date : 2024-01-01 DOI: 10.1016/j.idcr.2024.e01998
Neha Kumta , Lawrence Huang , Gururaj Nagaraj , Lindsey Papacostas , Shradha Subedi

Mucormycosis is a devastating disease with a high mortality rate, typically affecting immunosuppressed individuals. Postoperative surgical site infections due to mucromycosis are rare, with only a handful of cases reported in the literature. Here, we describe a fatal case of post operative abdominal wound infection caused by mucormycosis in an immunocompetent man in his 70 s, who developed the infection following a laparotomy for bowel perforation. Initially, the growth of fungal species from a superficial wound swab was not considered significant until the patient exhibited signs of worsening sepsis. Limited operative debridement was performed for prognostication, in accordance with the family’s wishes. There was evidence of extensive significant invasive fungal infection, marked by necrosis extending into the abdominal wall fat and muscle. The patient was then transitioned to comfort measures and subsequently died. This case emphasizes the importance of maintaining a high level of clinical suspicion for mucormycosis, even in patients with minimal risk factors, and highlights the importance of prompt and aggressive treatment.

粘孢子菌病是一种破坏性疾病,死亡率很高,通常会影响免疫抑制患者。粘孢子菌病引起的术后手术部位感染非常罕见,文献中仅有少数病例报道。在此,我们描述了一例由粘孢子菌病引起的腹部伤口感染的致命病例,患者是一名 70 多岁的免疫功能正常的男性,在因肠穿孔进行开腹手术后发生感染。起初,从浅表伤口拭子中发现的真菌生长并不明显,直到患者出现败血症恶化的迹象。根据家属的意愿,为了预后进行了有限的手术清创。有证据表明存在广泛的严重侵袭性真菌感染,其特征是坏死延伸至腹壁脂肪和肌肉。患者随后转入舒适治疗,最终死亡。本病例强调了临床上高度怀疑粘孢子菌病的重要性,即使是风险因素极低的患者也不例外,并强调了及时积极治疗的重要性。
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引用次数: 0
Multidrug-resistant aeromonas caviae causing cystitis in a renal failure patient 耐多药鱼腥酵母菌导致一名肾衰竭患者膀胱炎
IF 1.1 Q4 INFECTIOUS DISEASES Pub Date : 2024-01-01 DOI: 10.1016/j.idcr.2024.e01999
Jiao Zhou , Tianbing Xiao , Yuqing Huang , Jianrong Tang , Xiaobing Zhang , Bei Jia , Jianguo Wu

A 49-year-old female with multiple myeloma complicated by renal failure had dysuria. The urine culture revealed multidrug-resistant aeromonas caviae during her hospital stay. Her symptoms and signs significantly improved after receiving a seven-day course of piperacillin-tazobactam treatment. She had no history of urinary tract infections(UTIs). On follow-up, she felt clinically well. Aeromonas caviae is a rare cause of UTI. We review previous cases of aeromonas caviae UTIs. The purpose of this case report is to assist in the diagnosis and management of aeromonas caviae cystitis.

一名患有多发性骨髓瘤并发肾衰竭的 49 岁女性出现排尿困难。住院期间,尿液培养发现了耐多药的鱼腥酵母菌。在接受了为期七天的哌拉西林-他唑巴坦治疗后,她的症状和体征明显好转。她没有尿路感染(UTI)病史。随访时,她感觉临床症状良好。鱼腥单胞菌是UTI的罕见病因。我们回顾了以前的鱼雷单胞菌UTI病例。本病例报告旨在帮助诊断和治疗腔隙气单胞菌膀胱炎。
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引用次数: 0
Bilateral scrofuloderma: An incessant entity 双侧瘰疬性皮肤病:绵延不绝的实体
IF 1.1 Q4 INFECTIOUS DISEASES Pub Date : 2024-01-01 DOI: 10.1016/j.idcr.2024.e02097
Parakriti Gupta , Ivneet Kour , Varsha Gupta , Varinder Saini , Lipika Singhal
Scrofuloderma is most common presentation of cutaneous tuberculosis in India. A 15-years-old immunocompetent male presented with bilateral cervical necrotising lesions and was treated with ATTx9 months, without improvement. Patient was diagnosed with scrofuloderma and ZN staining revealed 2+acid-fast bacilli. Cartridge-based nucleic acid amplification test showed rifampicin resistance. Patient was initiated on shorter regimen, but deferred treatment owing to technical portal problems. After 3 months, neck swelling had enlarged and he was started on multi-drug regimen x24 months. This underlines requisite to consider scrofuloderma in differentials of bilateral cervical lesions and to periodically monitor compliance to prevent subsequent emergence of resistance.
瘰疬性皮肤病是印度最常见的皮肤结核病。一名 15 岁免疫功能正常的男性出现双侧颈部坏死性病变,接受 ATT 治疗 9 个月,病情未见好转。患者被诊断为瘰疬性皮肤病,ZN 染色显示有 2+ 酸性快速杆菌。盒式核酸扩增检测显示利福平耐药。患者开始接受较短疗程的治疗,但由于门户技术问题而推迟了治疗。3 个月后,患者的颈部肿胀扩大,又开始使用多种药物治疗 x24 个月。这突出表明,在鉴别双侧颈部病变时必须考虑瘰疬性皮肤病,并定期监测患者的依从性,以防止出现耐药性。
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引用次数: 0
Is Shigella an under-recognized pathogen? A case of pyogenic cervical spondylitis caused by Escherichia coli and Shigella flexneri infection 志贺氏菌是一种未得到充分认识的病原体吗?一例由大肠杆菌和柔性志贺氏菌感染引起的化脓性颈椎炎病例
IF 1.5 Q4 INFECTIOUS DISEASES Pub Date : 2024-01-01 DOI: 10.1016/j.idcr.2024.e01930
Jiafeng Zhang , Yaoting Liu , Hongkun Wu , Lin Zhou

Shigella typically causes gastrointestinal infections, and extra-intestinal manifestations are rare. We report the first known case of pyogenic cervical spondylitis co-infected with Escherichia coli and Shigella flexneri, highlighting the diagnostic challenges and clinical implications. A 53-year-old woman presented with neck pain for one month. MRI revealed C6 and C7 vertebrae abscesses. The patient underwent anterior cervical debridement and bone-graft fusion. Intraoperative pus culture grew Escherichia coli, while metagenomic next-generation sequencing detected both Escherichia coli and Shigella species. Intravenous imipenem 500 mg every 6 h was administered, leading to full wound healing at a 6-month follow-up. This case emphasizes the importance of considering Shigella infection in the differential diagnosis of pyogenic spondylitis and demonstrates the utility of a multi-pronged diagnostic approach.

志贺氏菌通常会引起胃肠道感染,而肠道外表现则很少见。我们报告了第一例已知的大肠埃希菌和柔性志贺氏菌共同感染化脓性颈椎炎的病例,强调了诊断上的挑战和临床意义。一名 53 岁的妇女因颈部疼痛一个月前来就诊。核磁共振成像显示 C6 和 C7 椎体脓肿。患者接受了颈椎前路清创术和植骨融合术。术中脓液培养出大肠埃希菌,元基因组下一代测序检测出大肠埃希菌和志贺氏杆菌。每 6 小时静脉注射亚胺培南 500 毫克,6 个月后伤口完全愈合。该病例强调了在化脓性脊柱炎的鉴别诊断中考虑志贺氏菌感染的重要性,并展示了多管齐下诊断方法的实用性。
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引用次数: 0
Epididymal alveolar echinococcosis and tuberculosis co-infection: A case report 附睾肺泡棘球蚴病与结核病合并感染:病例报告
IF 1.5 Q4 INFECTIOUS DISEASES Pub Date : 2024-01-01 DOI: 10.1016/j.idcr.2024.e01966
Chuanchuan Liu , Hainin Fan

Alveolar echinococcosis (AE) is a common and significant public health problem caused by the larvae of the Echinococcus multilocularis. The occurrence of epididymal AE is rare and often overlooked in combination with mycobacterium tuberculosis infection. We report a case of a 34-year-old man who presented with right-sided scrotal enlargement with pain. Physical examination revealed an enlarged right scrotum with rupture. CT examination showed a blurred border and non-enhancing lesion on the right epididymis. Postoperative pathology and molecular biology identified an epididymal E. multilocularis infection. We report this rare case to emphasise the difficulty of preoperative diagnosis and the importance of complete surgical excision of the lesion.

肺泡棘球蚴病(AE)是由多形棘球蚴引起的一种常见的重大公共卫生问题。附睾棘球蚴病非常罕见,而且往往与结核分枝杆菌感染同时发生而被忽视。我们报告了一例 34 岁男子的病例,他出现右侧阴囊肿大并伴有疼痛。体格检查显示右侧阴囊肿大伴有破裂。CT 检查显示右侧附睾边界模糊,病变不增强。术后病理和分子生物学检查确定为附睾多形伊蚊感染。我们报告这一罕见病例是为了强调术前诊断的难度和手术彻底切除病灶的重要性。
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引用次数: 0
A case report of using gauze packing to treat postoperative chest bleeding after left pneumonectomy for secondary rifampicin-resistant tuberculosis 使用纱布包扎治疗继发性耐利福平肺结核左肺切除术后胸腔出血的病例报告
IF 1.5 Q4 INFECTIOUS DISEASES Pub Date : 2024-01-01 DOI: 10.1016/j.idcr.2024.e01953
Qibin Liu , Xiaoman Zhou , Li Yao, Feng Xu, Penggang Tang, Ting Li, Di Yang, Fang Liu, Jian Sheng , Yuhui Jiang , Xiyong Dai , Xianxiang Chen

One patient with rifampin-resistant tuberculosis underwent emergency left pneumonectomy and thoracic gauze packing for hemoptysis due to recurrent hemoptysis after transcatheter arterial embolization. Vital signs were maintained by mechanical ventilation and medication. Tracheotomy and anti-tuberculosis treatment were performed. After half a year of follow-up, the patient's condition was stable.

一名耐利福平肺结核患者因经导管动脉栓塞术后反复咯血而接受了紧急左肺切除术和胸腔纱布填塞术。通过机械通气和药物治疗维持了生命体征。进行了气管切开术和抗结核治疗。经过半年的随访,患者病情稳定。
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引用次数: 0
An unusual case of Brodie’s abscess in the humerus of an adult female 一名成年女性肱骨中的布罗迪脓肿罕见病例
IF 1.5 Q4 INFECTIOUS DISEASES Pub Date : 2024-01-01 DOI: 10.1016/j.idcr.2024.e01977
Priya Samuel , Andrew Brack , John C. Lam

Brodie’s abscess is a manifestation of subacute to chronic osteomyelitis, characterized as intraosseous abscess formation, usually on the metaphysis of the long tubular bones in the lower extremities of male pediatric patients. Clinically, Brodie’s abscess presents with atraumatic bone pain of an insidious onset, with absence of systemic findings. Delay in diagnosis is common, as diagnostic imaging, followed by biopsy for culture and histologic examination are generally required to secure a diagnosis of Brodie’s abscess. Treatment of Brodie’s abscess is non-standardized, and usually consists of surgical debridement and antibacterial therapy. Despite the variability in therapeutic approaches, outcomes of Brodie’s abscess treated with surgery and antibiotics are favourable. Herein we report a case of a delayed diagnosis of Brodie’s abscess in the upper extremity of an adult female. While she improved with treatment of Brodie’s abscess, the case serves to remind clinicians to consider this entity in adult individuals who present with atraumatic bone pain.

布罗迪脓肿是亚急性至慢性骨髓炎的一种表现,其特点是骨内脓肿形成,通常发生在男性儿童患者下肢长管状骨的干骺端。临床上,布罗迪脓肿表现为隐匿性起病的创伤性骨痛,无全身症状。诊断延迟很常见,因为通常需要进行诊断性影像学检查,然后进行活组织培养和组织学检查,才能确诊布罗迪脓肿。布罗迪脓肿的治疗并不规范,通常包括手术清创和抗菌治疗。尽管治疗方法多种多样,但通过手术和抗生素治疗布罗迪脓肿的效果还是不错的。在此,我们报告了一例延迟诊断的成年女性上肢布罗迪脓肿病例。虽然她在接受布罗迪脓肿治疗后病情有所好转,但该病例也提醒临床医生,在成年患者出现非创伤性骨痛时应考虑到这种情况。
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引用次数: 0
Insight into ocular complications of West Nile Virus: A case report of chorioretinal scarring 西尼罗河病毒眼部并发症透视:脉络膜视网膜瘢痕病例报告
IF 1.1 Q4 INFECTIOUS DISEASES Pub Date : 2024-01-01 DOI: 10.1016/j.idcr.2024.e02095
Hamza Inayat , Anna Branch , James J. Armstrong , Verena Juncal , Courtney Casserly

Purpose

This case report aims to emphasize the significance of the ocular manifestations in individuals with West Nile Virus (WNV) infection, with primary neurological involvement. By presenting a case of chorioretinal scarring secondary to WNV, we highlight the importance of a thorough ophthalmological evaluation in suspected cases of WNV to identify potential sight-threatening complications.

Observations

A 63-year-old woman presented with neurological symptoms following a trip to Denver, USA, including headaches, fever, and decreased consciousness. Despite initial treatment for suspected meningoencephalitis, her condition deteriorated, leading to focal seizures and profound weakness. Ophthalmological examination revealed chorioretinal lesions consistent with WNV retinopathy.

Conclusions

and Importance: WNV can present with neurological symptoms, and ocular complications can lead to significant visual impairment. This case report highlights the importance of asking individuals with suspected WNV about ocular symptoms. Despite the absence of a preventive treatment for ocular manifestations, clinicians must stay attentive to ocular symptoms in patients to mitigate potential complications, such as chorioretinal neovascularization, which can be treated with anti-vascular endothelial growth factor therapy injections.
目的 本病例报告旨在强调西尼罗河病毒(WNV)感染者的眼部表现对神经系统原发性受累的重要性。通过介绍一例继发于 WNV 的脉络膜视网膜瘢痕病例,我们强调了对 WNV 疑似病例进行全面眼科评估以识别潜在的危及视力并发症的重要性。尽管最初对她进行了疑似脑膜脑炎的治疗,但她的病情还是恶化了,导致局灶性癫痫发作和极度虚弱。眼科检查发现脉络膜视网膜病变与 WNV 视网膜病变一致:WNV可表现为神经系统症状,眼部并发症可导致严重的视力损伤。本病例报告强调了向疑似 WNV 患者询问眼部症状的重要性。尽管目前还没有针对眼部表现的预防性治疗方法,但临床医生必须时刻关注患者的眼部症状,以减少潜在并发症的发生,如脉络膜视网膜新生血管,可通过注射抗血管内皮生长因子疗法进行治疗。
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引用次数: 0
Disseminated Ureaplasma infection: A case report of septic polyarthritis in a patient on Rituximab therapy 播散性解脲支原体感染:一例利妥昔单抗治疗患者的脓毒性多关节炎病例报告
IF 1.1 Q4 INFECTIOUS DISEASES Pub Date : 2024-01-01 DOI: 10.1016/j.idcr.2024.e02101
Michael Axenhus , Jesper Ericson , Agata Rysinska , Annelie Petterson , Desiree Friis

Introduction

Immunocompromised individuals, such as those undergoing Rituximab therapy, are susceptible to severe infections by these organisms. We present a rare case of polyarticular septic arthritis caused by disseminated Ureaplasma urealyticum in a Rituximab-treated patient.

Presentation of case

A 38-year-old male with a history of schizophrenia and multiple sclerosis presented with intense pain, swelling, and fever, along with limited joint mobility. Despite initial treatment with antibiotics and surgical intervention, the patient's condition deteriorated. PCR assays confirmed the presence of Ureaplasma urealyticum, prompting a change in antibiotic therapy. With focused antimicrobial treatment and supportive care, the patient exhibited gradual improvement, although reinfection occurred one month after discharge, necessitating additional surgical interventions and antibiotic therapy.

Discussion

Septic arthritis due to Ureaplasma urealyticum is exceedingly rare but can occur in immunocompromised patients undergoing Rituximab therapy. Accurate pathogen identification using PCR assays is crucial for optimizing therapeutic outcomes in such cases. Treatment typically involves a combination of surgical debridement and tailored antimicrobial therapy with agents effective against Ureaplasma species. Close monitoring for disease recurrence and joint function is essential for long-term management.

Conclusion

This case highlights the diagnostic challenges and therapeutic complexities of septic arthritis caused by Ureaplasma urealyticum in immunocompromised patients undergoing Rituximab treatment. Interdisciplinary collaboration and the use of PCR assays for accurate pathogen identification are crucial for successful outcomes in such cases. Clinicians should consider the unique susceptibility of immunocompromised individuals to rare pathogens and tailor antimicrobial therapy accordingly.
导言接受利妥昔单抗治疗等免疫功能低下者很容易受到这些微生物的严重感染。病例介绍一名 38 岁男性患者,有精神分裂症和多发性硬化症病史,出现剧烈疼痛、肿胀和发热,关节活动受限。尽管最初使用了抗生素和手术治疗,但患者的病情还是恶化了。PCR 检测证实患者体内存在尿解支原体,这促使患者改变了抗生素疗法。讨论尿解支原体引起的化脓性关节炎极为罕见,但可发生在接受利妥昔单抗治疗的免疫功能低下患者中。使用 PCR 检测法准确鉴定病原体对于优化此类病例的治疗效果至关重要。治疗通常包括外科清创和使用对解脲脲原体有效的药物进行定制抗菌治疗。本病例凸显了接受利妥昔单抗治疗的免疫功能低下患者中尿解脲原体引起的化脓性关节炎的诊断挑战和治疗复杂性。跨学科合作和使用 PCR 检测法准确鉴定病原体对于此类病例的成功治疗至关重要。临床医生应考虑到免疫功能低下者对罕见病原体的独特敏感性,并相应地调整抗菌治疗。
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引用次数: 0
Herpes zoster ophthalmicus following recombinant zoster vaccine: A case report and brief literature review 接种重组带状疱疹疫苗后出现带状疱疹眼炎:病例报告和简要文献综述
IF 1.1 Q4 INFECTIOUS DISEASES Pub Date : 2024-01-01 DOI: 10.1016/j.idcr.2024.e02070
Joshua M. Garcia, Ramez I. Haddadin

Purpose

Immunizations have long been pivotal in preventing diseases like HZ (herpes zoster), caused by VZV (varicella zoster virus). This study aims to evaluate the efficacy and safety of the RZV (recombinant zoster vaccine) compared to the ZVL (zoster vaccine live) and to report rare adverse events following RZV administration.

Observation

Herein, we report an unusual case of a 59-year-old man who developed a V1-limited rash with a positive HZ PCR (polymerase chain reaction) test following administration of RZV in the United States.

Conclusion

The development of RZV has significantly improved the prevention of HZ compared to ZVL. Nevertheless, rare adverse events, such as dermatomal reactions, underscore the importance of ongoing monitoring and research into the immunomodulatory effects of RZV. Physicians should continue to administer the RZV to patients but be cognizant that reactivation may rarely subsequently occur.

Case Presentation

The patient with a history of benign prostatic hyperplasia was treated at an outside hospital two days after receiving the RZV complaining of paresthesia and a rash on his nasolacrimal area and forehead. The patient presented to the ED (emergency department), 9 days post-vaccination due to persistence of his symptoms despite use of amoxicillin, valacyclovir, and an unidentified eye drop. The dose of valacyclovir was increased, and he completed 1 g TID (three times a day) PO (per orally) for 10 days with subsequent resolution of symptoms. A positive PCR test confirmed the diagnosis of HZ. Topical mupirocin ointment was initiated and the patient was referred for ophthalmologic evaluation.

目的长期以来,免疫接种在预防由 VZV(水痘带状疱疹病毒)引起的 HZ(带状疱疹)等疾病方面发挥着关键作用。本研究旨在评估 RZV(重组带状疱疹疫苗)与 ZVL(带状疱疹活疫苗)相比的有效性和安全性,并报告接种 RZV 后出现的罕见不良反应。结论与 ZVL 相比,RZV 的开发大大提高了 HZ 的预防效果。尽管如此,罕见的不良反应(如皮疹反应)凸显了持续监测和研究 RZV 免疫调节作用的重要性。病例介绍该患者有良性前列腺增生病史,在接受 RZV 治疗两天后在一家外院就诊,主诉感觉麻痹,鼻泪管部位和前额出现皮疹。接种疫苗 9 天后,尽管使用了阿莫西林、伐昔洛韦和一种不明眼药水,但症状仍持续存在,于是患者来到急诊科就诊。他增加了伐昔洛韦的剂量,并连续 10 天口服 1 克伐昔洛韦(一天三次),症状随之缓解。PCR 检测呈阳性,确诊为 HZ。患者开始外用莫匹罗星软膏,并被转到眼科进行评估。
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引用次数: 0
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