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A rare case of scedosporium apiospermum osteomyelitis in an immunocompetent patient 免疫功能正常患者患上杏孢子菌骨髓炎的罕见病例
IF 1.5 Q4 INFECTIOUS DISEASES Pub Date : 2024-01-01 DOI: 10.1016/j.idcr.2024.e01929
Aayushi J. Rajani, Darshankumar Raval, Rohit Chitale, Ravindra Durvasula, Justin Oring, Ross Powers

Scedosporium, a widespread filamentous fungus found in diverse environments, has experienced a rise in cases due to escalating malignancies and chronic immunosuppression. Clinical manifestations span mycetoma, airway involvement, and various infections, with osteomyelitis being a notable complication. We present a case of a 77-year-old female initially displaying cutaneous Scedosporium signs, which progressed to osteomyelitis. The patient, with a history of trauma, chronic low dose steroid use, and underlying conditions, presented with a foot injury caused by her dog. Despite initial management, worsening symptoms led to the identification of Scedosporium. A comprehensive approach involving debridement, antimicrobial therapy, and reduction of immunosuppression resulted in clinical improvement. The rarity of zoonotic transmission, diagnostic challenges, and antifungal efficacy are also discussed. The patient's positive trajectory emphasizes early diagnosis, targeted treatment, and vigilance in managing immunosuppression. An adaptable treatment protocol is proposed based on risk factors. Considering the rising opportunistic fungal infections and delayed culture results, initiating empirical antifungals based on clinical judgment and regional prevalence is vital for favorable outcomes.

角孢子菌是一种广泛存在于各种环境中的丝状真菌,由于恶性肿瘤和慢性免疫抑制的不断升级,角孢子菌病例也在不断增加。临床表现包括真菌瘤、气道受累和各种感染,其中骨髓炎是一种显著的并发症。我们介绍了一例 77 岁女性患者的病例,她最初出现皮肤孢子丝菌征象,后来发展为骨髓炎。患者有外伤史、长期使用低剂量类固醇药物史和基础疾病史,她的脚是被狗咬伤的。尽管进行了初步治疗,但由于症状不断恶化,最终确诊为Scedosporium。经过清创、抗菌治疗和减少免疫抑制等综合治疗后,临床症状有所好转。本文还讨论了人畜共患传播的罕见性、诊断难题和抗真菌疗效。该患者的积极发展轨迹强调了早期诊断、针对性治疗以及在管理免疫抑制时保持警惕。根据风险因素提出了一套可调整的治疗方案。考虑到机会性真菌感染的增加和培养结果的延迟,根据临床判断和地区流行情况启动经验性抗真菌药物治疗对取得良好疗效至关重要。
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引用次数: 0
A true challenge: Disseminated tuberculosis with tuberculous meningitis in a patient with underlying chronic liver disease 真正的挑战一名患有慢性肝病的散播性肺结核患者合并结核性脑膜炎
IF 1.1 Q4 INFECTIOUS DISEASES Pub Date : 2024-01-01 DOI: 10.1016/j.idcr.2024.e02065
Harika Kalangi , Laura Rivera Boadla , David C. Perlman , Stanley R. Yancovitz , Vani George , Nadim Salomon

Tuberculous meningitis (TBM) is a potentially life-threatening form of tuberculosis (TB) that affects the central nervous system. Its management in patients with concomitant chronic liver disease (CLD) presents unique challenges due to altered drug metabolism with potentially impaired spinal fluid drug penetration and hepatotoxicity. The standard regimen for TBM includes isoniazid (INH) and rifampin (RIF), and Pyrazinamide (PZA) which are metabolized by the liver and may cause hepatotoxicity, which can exacerbate preexisting liver disease. Thus, careful consideration is required to balance therapeutic efficacy with potential drug-induced hepatotoxicity. Regular monitoring of liver function tests and clinical response is essential to minimize adverse effects and optimize treatment outcomes. Further research is needed to establish evidence-based guidelines for the tailored management of TBM in this vulnerable patient subset. Overall, the treatment of TBM in patients with severe liver disease should be individualized and closely monitored.

结核性脑膜炎(TBM)是一种影响中枢神经系统、可能危及生命的结核病(TB)。由于药物代谢发生改变,脊髓液药物渗透性和肝毒性可能受损,因此对合并慢性肝病(CLD)的患者的治疗面临独特的挑战。治疗 TBM 的标准方案包括异烟肼 (INH) 和利福平 (RIF),以及吡嗪酰胺 (PZA),这些药物经肝脏代谢,可能引起肝毒性,从而加重原有的肝病。因此,需要慎重考虑如何在疗效与药物可能引起的肝毒性之间取得平衡。定期监测肝功能检测和临床反应对于减少不良反应和优化治疗效果至关重要。需要开展进一步研究,以制定循证指南,为这一易感患者亚群量身定制 TBM 治疗方案。总之,严重肝病患者的 TBM 治疗应个体化并进行密切监测。
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引用次数: 0
Diffuse gingival hypertrophied Kaposi sarcoma as an initial presentation of HIV Infection 弥漫性牙龈肥大卡波西肉瘤是艾滋病毒感染的初期表现
IF 1.5 Q4 INFECTIOUS DISEASES Pub Date : 2024-01-01 DOI: 10.1016/j.idcr.2024.e02003
Abinet Meno Abose , Tibebu Amare , Mierafe Daniel , Anteneh Gebeyehu

Kaposi sarcoma is an indolent angio-proliferative spindle- cell tumor derived from endothelial and immune cells infected with Human herpes virus type 8(HHV-8). In the era of highly active antiretroviral (HAART), Kaposi sarcoma is a rare form of initial presentation of HIV infection [1]. The author presents a case of diffuse gingival hypertrophied Kaposi sarcoma in 18-year-old male newly diagnosed RVI patient. After confirming the diagnosis patient started on HAART and mouth care. Surgical excision is the first line of treatment with HAART, since this patient has low CD4 count of 30 cells/mm3 which will complicate the surgery. So, we are waiting for CD4 count to increase above 200 cells/mm3 to undergo surgical excision. The case is representative of HIV complexity and aimed to bring awareness of unusual presentation of HIV.This case also reminds us how important early initiation of HAART is.

卡波西肉瘤(Kaposi sarcoma)是一种由感染人类疱疹病毒 8 型(HHV-8)的内皮细胞和免疫细胞衍生出来的不显性血管增生性纺锤形细胞肿瘤。在高活性抗逆转录病毒(HAART)时代,卡波西肉瘤是一种罕见的艾滋病病毒感染初期表现形式[1]。作者介绍了一例新诊断为 RVI 的 18 岁男性患者的弥漫性牙龈肥大卡波西肉瘤病例。确诊后,患者开始接受 HAART 治疗和口腔护理。手术切除是 HAART 的第一线治疗方法,因为该患者的 CD4 细胞数低至 30 cells/mm3,这将使手术复杂化。因此,我们正在等待 CD4 细胞数增加到 200 cells/mm3 以上时再进行手术切除。这个病例代表了艾滋病的复杂性,旨在让人们认识到艾滋病的不寻常表现。
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引用次数: 0
Toscana virus (TOSV) meningitis with atypical characteristics: Report of two cases 具有非典型特征的托斯卡纳病毒(TOSV)脑膜炎:两个病例的报告
IF 1.1 Q4 INFECTIOUS DISEASES Pub Date : 2024-01-01 DOI: 10.1016/j.idcr.2024.e02034
Roberta Maria Antonello , Giuseppe Formica , Letizia Attala , Dario Mannini , Lorenzo Zammarchi , Alessandro Bartoloni , Massimo Antonio Di Pietro

Toscana virus (TOSV) is an emerging cause of central nervous system (CNS) infections, especially in endemic countries during summer. Cerebrospinal fluid (CSF) is usually clear, with < 500 leukocytes/mm3, normal glucose (> 60 % serum glucose) and normal (< 45 mg/dL) to slightly increased protein levels. Here we present two cases of TOSV meningitis with misleading CSF characteristics observed at Santa Maria Annunziata Hospital (Bagno a Ripoli, Florence, Italy). Case 1 presented with signs and symptoms of meningitis. CSF was opalescent on macroscopic examination, with 1192 cells/mm3, hypoglycorrhachia (30 % serum glucose) and hyperproteinorachia (228.0 mg/dL). TOSV meningitis was confirmed with serology. Case 2 presented with headache, vomiting and mild neck stiffness. CSF was slightly turbid, with 1092 cells/mm3, normal glucose (61 % serum glucose) and slightly increased protein (77.0 mg/dL) levels. TOSV meningitis was confirmed with serology and molecular test on CSF. We performed a literature review including cases of TOSV neuroinvasive infections in which CSF characteristics were reported. Pleocytosis > 500 cells/mm3 was reported in 12/62 (19.4 %) patients, hypoglycorrhachia in 3/62 (4.8 %) patients, mild hyperproteinorachia (45 - 75 mg/dL) in 7/62 (11.3 %) patients and severe hyperproteinorachia (> 75 mg/dL) in 40/62 (64.5 %) patients. TOSV should be considered in the differential diagnosis of CNS infections in endemic areas during the warm season even when CSF examination shows atypical results.

托斯卡纳病毒(TOSV)是一种新出现的中枢神经系统(CNS)感染病因,尤其是在夏季流行的国家。脑脊液(CSF)通常是透明的,白细胞数为 500 个/立方毫米,葡萄糖含量正常(血清葡萄糖含量为 60%),蛋白质含量正常(45 毫克/分升)或略有升高。在此,我们介绍两例在圣玛丽亚-安努齐亚塔医院(意大利佛罗伦萨巴尼奥-里波利)观察到的具有误导性 CSF 特征的 TOSV 脑膜炎病例。病例 1 出现脑膜炎的体征和症状。脑脊液宏观检查呈乳白色,细胞数为 1192 个/立方毫米,血糖过低(血清葡萄糖含量为 30%),蛋白过高(228.0 毫克/分升)。经血清学检查,确诊为 TOSV 脑膜炎。病例 2 表现为头痛、呕吐和轻度颈部僵硬。脑脊液略显浑浊,细胞数为 1092 个/立方毫米,葡萄糖含量正常(血清葡萄糖含量为 61%),蛋白质含量略有升高(77.0 毫克/分升)。通过对脑脊液进行血清学和分子检测,确诊为 TOSV 脑膜炎。我们进行了文献回顾,其中包括有 CSF 特征报道的 TOSV 神经侵袭性感染病例。据报道,12/62(19.4%)例患者出现 500 个/立方毫米的多形核,3/62(4.8%)例患者出现低蛋白血症,7/62(11.3%)例患者出现轻度高蛋白血症(45 - 75 mg/dL),40/62(64.5%)例患者出现重度高蛋白血症(75 mg/dL)。在温暖季节,即使脑脊液检查结果不典型,也应将 TOSV 列入流行地区中枢神经系统感染的鉴别诊断中。
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引用次数: 0
A higher area under the concentration-time curve/minimum inhibitory concentration target as a potential prognostic factor for vancomycin treatment of methicillin-resistant Staphylococcus aureus meningitis: A case report 万古霉素治疗耐甲氧西林金黄色葡萄球菌脑膜炎的潜在预后因素--较高的浓度-时间曲线下面积/最低抑制浓度目标值:病例报告
IF 1.1 Q4 INFECTIOUS DISEASES Pub Date : 2024-01-01 DOI: 10.1016/j.idcr.2024.e02035
Kenichi Nakazono , Hiroki Saito , Ayaka Ohkubo , Hidetaka Onodera , Haruaki Wakatake , Yuta Katsuta , Junpei Tada , Hiroyuki Kunishima , Takashi Matsuzaki

The area under the concentration-time curve (AUC)/minimum inhibitory concentration (MIC) – guided approach is recommended for vancomycin therapeutic drug monitoring in severe methicillin-resistant Staphylococcus aureus (MRSA) infection. However, evidence regarding the efficacy of vancomycin AUC-guided strategies for the treatment of systemic infections is limited. This case report describes the successful treatment of MRSA meningitis, with vancomycin using a higher AUC/MIC target. A 61-year-old woman who underwent ventriculoperitoneal (VP) shunt placement for subarachnoid hemorrhage, developed MRSA meningitis due to shunt infection. Vancomycin was administered intravenously, with concurrent monitoring of serum and cerebrospinal fluid (CSF) vancomycin concentrations and AUC/MIC. On post-operative day (POD) 24 of VP shunt placement, the vancomycin trough concentration and AUC/MIC were 12.0 μg/mL and 515, respectively, with persistently positive CSF culture. On POD 28, the trough concentration and AUC/MIC were 18.6 μg/mL and 610, respectively. There were no major adverse events, and CSF culture turned negative on POD 30. The vancomycin CSF-to-serum ratio was approximately 41 %. For patients with MRSA meningitis, we suggest an optimal therapeutic range with a vancomycin AUC/MIC target near the upper limit of the therapeutic window.

在严重耐甲氧西林金黄色葡萄球菌(MRSA)感染中,万古霉素治疗药物监测推荐采用浓度-时间曲线下面积(AUC)/最低抑菌浓度(MIC)指导法。然而,有关万古霉素 AUC 指导策略治疗全身感染疗效的证据却很有限。本病例报告介绍了使用万古霉素较高的 AUC/MIC 目标值成功治疗 MRSA 脑膜炎的案例。一名因蛛网膜下腔出血而接受脑室腹腔(VP)分流术的 61 岁女性因分流术感染而患上 MRSA 脑膜炎。患者静脉注射万古霉素,同时监测血清和脑脊液(CSF)中万古霉素的浓度和 AUC/MIC。VP 分流术后第 24 天(POD),万古霉素谷浓度和 AUC/MIC 分别为 12.0 μg/mL 和 515,CSF 培养持续阳性。在 POD 28,谷浓度和 AUC/MIC 分别为 18.6 μg/mL 和 610。没有出现重大不良反应,POD 30时CSF培养转为阴性。万古霉素 CSF 与血清的比值约为 41%。对于 MRSA 脑膜炎患者,我们建议最佳治疗范围为万古霉素 AUC/MIC 目标值接近治疗窗的上限。
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引用次数: 0
Peritonsillar abscess caused by hypervirulent Klebsiella pneumoniae: A case report and literature review 高化脓性肺炎克雷伯菌引起的扁桃体周围脓肿: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.e02113
Kazuya Mizobata , Daichi Murakami , Ryo Ueda , Yuki Suzuki , Yusuke Koizumi , Hisakazu Yano , Masamitsu Kono , Muneki Hotomi
Klebsiella pneumoniae is a pathogenic bacterium responsible for otorhinolaryngology-head and neck infections. Hypervirulent K. pneumoniae (hvKp), an alarming subtype of K. pneumoniae, causes life-threatening hematogenous infection. However, there are few reports on the character of hvKp strain in the field of otorhinolaryngology-head and neck surgery. We report the case of a 60-year-old Japanese man with a peritonsillar abscess caused by hvKp. K. pneumoniae isolated from pus was positive in a string test. Genetic analysis revealed that the strain had K2, rmpA and aerobactin genes. There was no evidence of hematogenous infections such as bacteremia and liver abscess, and there was improvement by surgical drainage and intravenous antimicrobial treatment. To the best of our knowledge, this is the first reported case of peritonsillar abscess caused by hvKp that did not have hematogenous infections. The string test is a simple and inexpensive method for screening hvKp. This case highlights the need for strategies to inhibit the spread of these highly virulent strains by early drainage and appropriate antimicrobial treatment.
肺炎克雷伯菌是一种导致耳鼻喉科--头颈部感染的致病细菌。高病毒性肺炎克雷伯菌(hvKp)是肺炎克雷伯菌的一个令人担忧的亚型,可引起危及生命的血源性感染。然而,在耳鼻咽喉头颈外科领域,有关 hvKp 菌株特性的报道很少。我们报告了一例由 hvKp 引起腹腔脓肿的 60 岁日本男性病例。从脓液中分离出的肺炎双球菌在串联试验中呈阳性。基因分析显示,该菌株含有 K2、rmpA 和 aerobactin 基因。没有证据显示出现菌血症和肝脓肿等血源性感染,手术引流和静脉抗菌治疗后病情有所好转。据我们所知,这是首例由 hvKp 引起的腹腔周围脓肿,且没有血源性感染的报道。串联检测是一种简单而廉价的筛查 hvKp 的方法。本病例强调了通过早期引流和适当的抗菌治疗来抑制这些高致病性菌株扩散的策略的必要性。
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引用次数: 0
A first case of subdural empyema due to Staphylococcus saccharolyticus 首例由糖溶葡萄球菌引起的硬膜下气肿病例
IF 1.1 Q4 INFECTIOUS DISEASES Pub Date : 2024-01-01 DOI: 10.1016/j.idcr.2024.e02109
Masahiko Kaneko , Tomoki Shinohara , Yuya Masuda , Kenichi Ishikawa , Hisaharu Shikata , Chie Sakisuka , Daisuke Syoda , Akira Fukui , Kiichirou Zenke
Staphylococcus saccharolyticus, an anaerobic coagulase-negative staphylococcal species, is a member of the normal skin microbiota. It can be a rare cause of human infectious disease and is usually considered a contaminant, but some rare reports have described deep-seated infections caused by S. saccharolyticus. Intracranial subdural empyema, a life-threatening condition that requires early diagnosis and emergency intervention, can be caused by various pathogens. A 54-year-old man with no pre-existing medical conditions other than hypertension was transferred to our emergency department because of progressively worsening consciousness impairment. As non-contrast head computed tomography revealed hematoma-like collection in the subdural space, urgent drainage was performed via multiple burr holes. Perioperative tissue culture yielded monomicrobial growth of S. saccharolyticus after 4 days. Meropenem was administered in the immediate postoperative period, and later replaced with Penicillin G for six weeks. The patient is now in good clinical condition more than 18 months after treatment. This represents the first reported case of subdural empyema caused by S. saccharolyticus in an immunocompetent adult patient with a review of the pertinent literature. S. saccharolyticus should be added to the list of anaerobic microorganisms that can to cause subdural empyema. Prolonged anaerobic culture is critical to improve the yield of this possibly underestimated pathogen.
糖溶性葡萄球菌是一种厌氧凝固酶阴性葡萄球菌,是正常皮肤微生物群中的一员。它可能是人类传染病的罕见病因,通常被认为是一种污染物,但也有一些罕见报告描述了由溶糖葡萄球菌引起的深层感染。颅内硬膜下水肿是一种危及生命的疾病,需要早期诊断和紧急干预,可由多种病原体引起。一名54岁的男子除高血压外无其他疾病,因意识障碍逐渐加重而转入我院急诊科。由于非对比度头部计算机断层扫描显示硬膜下腔有血肿样聚集,因此紧急进行了多孔引流。4 天后,围手术期组织培养发现了单菌生长的糖溶菌。术后立即使用了美罗培南,随后又用青霉素 G 代替,持续了六周。治疗 18 个多月后,患者目前临床状况良好。这是首例免疫功能正常的成年患者因糖溶性沙雷菌引起硬膜下腔积液的病例,相关文献对此进行了综述。应将糖溶性沙雷氏菌列入可导致硬膜下水肿的厌氧微生物名单。长期厌氧培养对于提高这种可能被低估的病原体的检出率至关重要。
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引用次数: 0
Multimodal imaging findings of multiple evanescent white dot syndrome in COVID-19 patients COVID-19 患者多发白点综合征的多模态成像发现
IF 1.1 Q4 INFECTIOUS DISEASES Pub Date : 2024-01-01 DOI: 10.1016/j.idcr.2024.e02110
Natalie Chen , Mark Mandell , Parnian Arjmand

Purpose

To describe the multimodal imaging findings of a rare case of multiple evanescent white dot syndrome (MEWDS) associated with COVID-19.

Methods

A case report was analyzed and described alongside COVID-19 associated MEWDS cases identified in the current literature.

Results

A healthy 20-year-old man was evaluated after a three-day history of blurry vision occurring two months after COVID-19 infection. Multimodal imaging revealed signs of typical MEWDS, with optical coherence tomography angiography (OCT-A) demonstrating homogenous reflectivity. Six additional cases were reported in the literature, displaying clinical symptoms and imaging consistent with typical MEWDS but demonstrating higher rates of incomplete visual recovery and treatment use.

Conclusions

COVID-19 associated MEWDS is a novel condition. This is the first known case of COVID-19 associated MEWDS with reported OCT-A findings in an otherwise healthy patient. Although posterior uveitis following COVID-19 infection is rare, clinicians should remain informed on the best practices for diagnosing and caring for patients with MEWDS.
目的描述一例罕见的与 COVID-19 相关的多发白点综合征(MEWDS)的多模态成像结果。结果一名 20 岁的健康男性在感染 COVID-19 两个月后出现视力模糊,三天后接受了评估。多模态成像显示了典型的 MEWDS 征象,光学相干断层血管成像(OCT-A)显示了同质反射。文献中还报道了另外六例病例,其临床症状和影像学表现与典型的 MEWDS 一致,但视力恢复不完全和使用治疗的比例较高。这是已知的首例与 COVID-19 相关的 MEWDS 病例,报告的 OCT-A 结果显示,患者原本是健康的。虽然 COVID-19 感染后葡萄膜后炎非常罕见,但临床医生仍应了解诊断和护理 MEWDS 患者的最佳方法。
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引用次数: 0
An uncommon liver abscess secondary to an ingested foreign body: A case report 继发于吞食异物的罕见肝脓肿:病例报告
IF 1.5 Q4 INFECTIOUS DISEASES Pub Date : 2024-01-01 DOI: 10.1016/j.idcr.2024.e01934
Ahmed Hadj Taieb , Mohamed Ali Chaouch , Aymen Kaouach , Sadok Ben Jabra , Mohamed Zayati , Besma Gafsi , Emna Mili , Faouzi Noomen

Introduction

This article discusses a case study involving a unique occurrence of a hepatic abscess caused by the presence of an ingested foreign body. Hepatic abscesses, characterized by pus accumulation within liver tissue, often result from various infections, with some cases having unidentified origins.

Case presentation

This study focuses on a 75-year-old man who presented at an emergency department with persistent pain in the right upper abdomen and fever for ten days. Diagnostic tests revealed a low-density, multiloculated mass in the liver and a hyperdense linear structure near the duodenum, indicating a hepatic abscess originating from duodenal perforation due to a foreign body that had migrated from ingestion. The patient underwent antibiotic treatment and a surgical procedure involving laparotomy to extract the foreign object and drain the abscess.

Conclusion

this case study underscores the rare occurrence of hepatic abscesses caused by ingested foreign bodies. Swift and accurate diagnosis, along with appropriate treatment involving foreign body removal and abscess drainage, are pivotal for favorable patient outcomes. The choice of treatment strategy impacts hospital stay duration, and understanding potential complications from foreign body ingestion enhances patient management and care.

导言本文讨论了一个病例研究,该病例涉及因摄入异物导致肝脓肿的独特病例。肝脓肿的特征是肝脏组织内的脓液积聚,通常由各种感染引起,有些病例起因不明。病例介绍本研究的重点是一名 75 岁的男性,他因右上腹持续疼痛和发热十天到急诊科就诊。诊断性检查发现肝脏内有一个低密度、多灶性肿块,十二指肠附近有一个高密度线状结构,这表明肝脓肿源于十二指肠穿孔,而穿孔的原因是摄入的异物移位。患者接受了抗生素治疗,并进行了开腹手术,取出异物并引流脓肿。迅速、准确的诊断,以及包括异物取出和脓肿引流在内的适当治疗,对患者的预后至关重要。治疗策略的选择会影响住院时间的长短,而了解异物摄入可能引起的并发症则能加强对患者的管理和护理。
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引用次数: 0
Secondary hemophagocytic syndrome in an acquired immunodeficiency syndrome and Alpha-thalassemia patient infected with Talaromyces marneffei: A case report and literature review 一名获得性免疫缺陷综合征和阿尔法地中海贫血患者感染马内菲他拉酵母菌后出现继发性嗜血细胞综合征: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.e01954
Qingqing Wu, Yixiu Yu, Shenhong Feng, Bingqian Fang, Renzhi Zheng, Weidong Sun, Jianzhi Zhao

Hemophagocytic lymphohistiocytosis (HLH) is a life-threatening disease characterized by a hyperinflammatory syndrome and impairment of multiple organ systems. Talaromycosis marneffei (TSM) is an opportunistic infection mostly found in immunosuppressed populations, such as those with acquired immunodeficiency syndrome (AIDS), and is prevalent in southern China. However, HLH secondary to TSM is extremely rare and has only been reported in isolated cases. A 30-year-old patient with recurrent high fever and progressive cytopenia was diagnosed with HLH secondary to disseminated TSM with AIDS and Alpha-thalassemia. The patient remained in sustained remission without recurrence after effective treatment with antifungals and glucocorticoids.

嗜血细胞淋巴组织细胞增多症(HLH)是一种危及生命的疾病,其特征是高炎症综合征和多个器官系统受损。马拉色菌病(TSM)是一种机会性感染,多见于免疫抑制人群,如获得性免疫缺陷综合征(AIDS)患者,在中国南方很普遍。然而,继发于TSM的HLH极为罕见,仅有个别病例报道。一名 30 岁的患者反复发高烧并伴有进行性全血细胞减少,被诊断为继发于艾滋病和阿尔法地中海贫血的播散性 TSM 的 HLH。在使用抗真菌药物和糖皮质激素进行有效治疗后,患者病情持续缓解,没有复发。
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