首页 > 最新文献

Case Reports in Infectious Diseases最新文献

英文 中文
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
Bacteroides fragilis Acute Hematogenous Osteomyelitis in a Young Female with Sickle Cell Disease 一名患有镰状细胞病的年轻女性体内的脆弱拟杆菌急性血源性骨髓炎
IF 1.1 Q4 INFECTIOUS DISEASES Pub Date : 2023-12-05 DOI: 10.1155/2023/6340222
Nada Bassam Hamieh, Hiba Abdul Hamid Abou Layla, Rola Ali Ali, Zeina Bayram, Abdul Rahman Bizri
Patients with sickle cell disease are at increased risk for multiple infections including osteomyelitis. The most reported causative organisms are Salmonella spp. and Staphylococcus aureus. Anaerobic infections including Bacteroides fragilis are not commonly seen. Here, we report the first case of a 28-year-old female patient with sickle cell disease and acute hematogenous Bacteroides fragilis tibial osteomyelitis. Diagnosis was made by isolating the organism from blood and tibial fluid cultures. The patient was successfully managed with a course of intravenous followed by oral antibiotics and percutaneous drainage of collection and responded well. This case report will shed light on the importance of Bacteroides fragilis as a causative organism for osteomyelitis in sickle cell disease patients, thereby affecting the management of these patients.
镰状细胞病患者发生包括骨髓炎在内的多种感染的风险增加。报告最多的致病菌是沙门氏菌和金黄色葡萄球菌。包括脆弱拟杆菌在内的厌氧感染并不常见。在此,我们报告一例28岁女性镰状细胞病合并急性血源性脆弱拟杆菌性胫骨骨髓炎的病例。诊断是通过从血液和胫骨液培养中分离出生物体。患者成功地进行了一个疗程的静脉注射,随后口服抗生素和经皮引流收集,反应良好。本病例报告将阐明脆弱拟杆菌作为镰状细胞病患者骨髓炎的致病生物的重要性,从而影响这些患者的管理。
{"title":"Bacteroides fragilis Acute Hematogenous Osteomyelitis in a Young Female with Sickle Cell Disease","authors":"Nada Bassam Hamieh, Hiba Abdul Hamid Abou Layla, Rola Ali Ali, Zeina Bayram, Abdul Rahman Bizri","doi":"10.1155/2023/6340222","DOIUrl":"https://doi.org/10.1155/2023/6340222","url":null,"abstract":"Patients with sickle cell disease are at increased risk for multiple infections including osteomyelitis. The most reported causative organisms are Salmonella spp. and Staphylococcus aureus. Anaerobic infections including Bacteroides fragilis are not commonly seen. Here, we report the first case of a 28-year-old female patient with sickle cell disease and acute hematogenous Bacteroides fragilis tibial osteomyelitis. Diagnosis was made by isolating the organism from blood and tibial fluid cultures. The patient was successfully managed with a course of intravenous followed by oral antibiotics and percutaneous drainage of collection and responded well. This case report will shed light on the importance of Bacteroides fragilis as a causative organism for osteomyelitis in sickle cell disease patients, thereby affecting the management of these patients.","PeriodicalId":9608,"journal":{"name":"Case Reports in Infectious Diseases","volume":"117 39","pages":""},"PeriodicalIF":1.1,"publicationDate":"2023-12-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138599450","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
A Case of Trueperella bernardiae Bacteremia due to a PICC-Associated Infection in a Paraplegic Patient 一例截瘫患者因 PICC 相关感染引发的伯纳氏真菌菌血症病例
IF 1.1 Q4 INFECTIOUS DISEASES Pub Date : 2023-12-04 DOI: 10.1155/2023/6238339
Carter Chapman, Jacob Nichols
Trueperella bernardiae is a Gram-positive bacterium known to cause a wide variety of opportunistic infections in humans. We report a novel case of T. bernardiae bacteremia in a paraplegic patient due to a peripherally inserted central catheter- (PICC-) associated infection that was treated successfully with piperacillin/tazobactam.
伯纳真perella bernardiae是一种革兰氏阳性细菌,已知可引起人类多种机会性感染。我们报告了一个新的病例T. bernardiae菌血症在截瘫患者由于周围插入中心导管(PICC)相关感染,成功地治疗了哌拉西林/他唑巴坦。
{"title":"A Case of Trueperella bernardiae Bacteremia due to a PICC-Associated Infection in a Paraplegic Patient","authors":"Carter Chapman, Jacob Nichols","doi":"10.1155/2023/6238339","DOIUrl":"https://doi.org/10.1155/2023/6238339","url":null,"abstract":"Trueperella bernardiae is a Gram-positive bacterium known to cause a wide variety of opportunistic infections in humans. We report a novel case of T. bernardiae bacteremia in a paraplegic patient due to a peripherally inserted central catheter- (PICC-) associated infection that was treated successfully with piperacillin/tazobactam.","PeriodicalId":9608,"journal":{"name":"Case Reports in Infectious Diseases","volume":"34 29","pages":""},"PeriodicalIF":1.1,"publicationDate":"2023-12-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138601391","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
A Case of Myroides odoratimimus Bacteremia due to a Tunneled Dialysis Catheter-Associated Infection in a Paraplegic Patient 截瘫患者隧道透析导管相关感染致多效米氏菌血症1例
Q4 INFECTIOUS DISEASES Pub Date : 2023-11-11 DOI: 10.1155/2023/3089837
Carter Chapman, Barrett Meeks, Liam Ung, Jacob Nichols
Myroides odoratimimus is a Gram-negative opportunistic pathogen known to rarely cause a wide range of opportunistic infections in humans. We report a novel case of M. odoratimimus bacteremia in a paraplegic patient with an extensive medical history likely due to a tunneled dialysis catheter infection that was successfully treated with levofloxacin.
芳香密蝇是一种革兰氏阴性机会性病原体,已知很少引起人类广泛的机会性感染。我们报告了一个新的病例M. odoratimimus菌血症截瘫患者广泛的病史可能是由于隧道透析导管感染,成功治疗左氧氟沙星。
{"title":"A Case of Myroides odoratimimus Bacteremia due to a Tunneled Dialysis Catheter-Associated Infection in a Paraplegic Patient","authors":"Carter Chapman, Barrett Meeks, Liam Ung, Jacob Nichols","doi":"10.1155/2023/3089837","DOIUrl":"https://doi.org/10.1155/2023/3089837","url":null,"abstract":"Myroides odoratimimus is a Gram-negative opportunistic pathogen known to rarely cause a wide range of opportunistic infections in humans. We report a novel case of M. odoratimimus bacteremia in a paraplegic patient with an extensive medical history likely due to a tunneled dialysis catheter infection that was successfully treated with levofloxacin.","PeriodicalId":9608,"journal":{"name":"Case Reports in Infectious Diseases","volume":"36 15","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-11-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135042822","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
Flea-Borne Typhus Presenting with Acalculous Cholecystitis and Severe Anemia. 蚤传斑疹伤寒表现为无结石性胆囊炎和严重贫血。
IF 1.1 Q4 INFECTIOUS DISEASES Pub Date : 2023-11-03 eCollection Date: 2023-01-01 DOI: 10.1155/2023/5510295
Ramya Varadarajan, Ashmi P Patel, Keyvon Rashidi, Albert Oh, Rashmeen Rahman, Ryan Neal

Background: Flea-borne typhus (FBT), an uncommon illness in the United States, typically presents as a high continuous fever with commonly associated symptoms including headache, myalgias, and rashes on the trunk and extremities. Patients infected with FBT may also present with atypical symptoms. As such, the combination of its relatively low incidence in the United States coupled with its variability in associated symptoms poses a diagnostic challenge for clinicians; early empiric treatment with doxycycline is warranted prior to a definitive diagnosis to reduce the risk of damage to vital organs. Case Report. This case describes a 54-year-old male who presented to an emergency room in Houston, Texas, with one week of constant right upper quadrant abdominal pain and fevers up to 40°C. The patient was initially diagnosed with Grade III severe acute cholangitis after abdominal ultrasound revealed gallbladder sludge and wall thickening without ductal dilatation, but a subsequent endoscopic retrograde cholangiopancreatography was unremarkable. Following intermittent fevers and worsening anemia, the patient was started on oral doxycycline for atypical infection, and an infectious disease workup subsequently returned a positive titer for Rickettsia typhi. He experienced rapid symptomatic and clinical improvement, and the patient was discharged home with a final diagnosis of flea-borne typhus.

Conclusion: Albeit uncommon, the presentation of this patient's symptoms and final diagnosis of flea-borne typhus demonstrates the importance of (1) keeping atypical infections such as FBT in the differential diagnosis and (2) beginning empiric treatment to prevent damage to vital organs if suspicion of FBT is high.

背景:跳蚤传播的斑疹伤寒(FBT)在美国是一种不常见的疾病,通常表现为持续高烧,通常伴有头痛、肌痛和躯干和四肢皮疹等相关症状。感染FBT的患者也可能出现非典型症状。因此,其在美国的发病率相对较低,加上相关症状的可变性,对临床医生提出了诊断挑战;在明确诊断之前,早期经验性地使用强力霉素治疗是必要的,以减少对重要器官损害的风险。病例报告。本病例描述了一名54岁男性,他在德克萨斯州休斯顿的急诊室就诊,持续一周的右上腹腹痛和高达40°C的发烧。患者最初被诊断为III级严重急性胆管炎,腹部超声显示胆囊淤泥和壁增厚,无导管扩张,但随后的内镜逆行胆管造影未见明显变化。在间歇性发热和贫血恶化后,患者开始口服强力霉素治疗非典型感染,随后的传染病检查显示伤寒立克次体滴度呈阳性。他经历了迅速的症状和临床改善,患者出院回家,最终诊断为跳蚤传播的斑疹伤寒。结论:虽然罕见,但该患者的症状和最终诊断表明:(1)在鉴别诊断中保持非典型感染(如FBT)的重要性;(2)在怀疑FBT的情况下开始经经验治疗,以防止重要器官受损。
{"title":"Flea-Borne Typhus Presenting with Acalculous Cholecystitis and Severe Anemia.","authors":"Ramya Varadarajan, Ashmi P Patel, Keyvon Rashidi, Albert Oh, Rashmeen Rahman, Ryan Neal","doi":"10.1155/2023/5510295","DOIUrl":"10.1155/2023/5510295","url":null,"abstract":"<p><strong>Background: </strong>Flea-borne typhus (FBT), an uncommon illness in the United States, typically presents as a high continuous fever with commonly associated symptoms including headache, myalgias, and rashes on the trunk and extremities. Patients infected with FBT may also present with atypical symptoms. As such, the combination of its relatively low incidence in the United States coupled with its variability in associated symptoms poses a diagnostic challenge for clinicians; early empiric treatment with doxycycline is warranted prior to a definitive diagnosis to reduce the risk of damage to vital organs. <i>Case Report</i>. This case describes a 54-year-old male who presented to an emergency room in Houston, Texas, with one week of constant right upper quadrant abdominal pain and fevers up to 40°C. The patient was initially diagnosed with Grade III severe acute cholangitis after abdominal ultrasound revealed gallbladder sludge and wall thickening without ductal dilatation, but a subsequent endoscopic retrograde cholangiopancreatography was unremarkable. Following intermittent fevers and worsening anemia, the patient was started on oral doxycycline for atypical infection, and an infectious disease workup subsequently returned a positive titer for <i>Rickettsia typhi</i>. He experienced rapid symptomatic and clinical improvement, and the patient was discharged home with a final diagnosis of flea-borne typhus.</p><p><strong>Conclusion: </strong>Albeit uncommon, the presentation of this patient's symptoms and final diagnosis of flea-borne typhus demonstrates the importance of (1) keeping atypical infections such as FBT in the differential diagnosis and (2) beginning empiric treatment to prevent damage to vital organs if suspicion of FBT is high.</p>","PeriodicalId":9608,"journal":{"name":"Case Reports in Infectious Diseases","volume":"2023 ","pages":"5510295"},"PeriodicalIF":1.1,"publicationDate":"2023-11-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10637845/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"89716981","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Enterovirus-Rhinovirus-Induced Acute Respiratory Distress Syndrome in Adults: A Case Report and Short Literature Review. 成人肠病毒-鼻病毒致急性呼吸窘迫综合征1例报告及简短文献回顾
IF 1.1 Q4 INFECTIOUS DISEASES Pub Date : 2023-11-03 eCollection Date: 2023-01-01 DOI: 10.1155/2023/8887955
Eirini Avgoustou, Aikaterini Spyridaki, Giorgos Pothitos, Antonios Papadopoulos, Spyridon Kois, Foula Vassilara

Enteroviruses and rhinoviruses (EV-RV) are small RNA viruses that usually cause the common cold and asthma exacerbations. Although EV-RV-induced acute respiratory distress syndrome (ARDS) is common in children, only scattered reports of ARDS in adults have been published. The diagnosis has been greatly facilitated by the advent of molecular techniques, namely, real-time polymerase chain reaction (RT-PCR). EV-RV can cause ARDS by stimulating a cytokine cascade. No antiviral therapy has yet been approved, and treatment is entirely supportive. Herein, we report a rare case of EV-RV infection in an afebrile adult with dyspnea that rapidly progressed to acute lung injury and ARDS. EV-RV was isolated with multiple real-time PCR in nasopharyngeal and bronchial specimens, while no other pathogen was detected. We also present an up-to-date review of relevant literature, in an attempt to stress the importance of the early identification of viral culprits, which can minimize the use of invasive diagnostic procedures and antibiotic agents.

肠病毒和鼻病毒(EV-RV)是小RNA病毒,通常引起普通感冒和哮喘加重。虽然ev - rv引起的急性呼吸窘迫综合征(ARDS)在儿童中很常见,但在成人中只发表了零星的ARDS报告。分子技术的出现极大地促进了诊断,即实时聚合酶链反应(RT-PCR)。EV-RV可通过刺激细胞因子级联引起ARDS。目前还没有抗病毒治疗被批准,治疗完全是支持性的。在此,我们报告了一例罕见的EV-RV感染病例,该病例发生在一名患有呼吸困难的发热成人中,并迅速发展为急性肺损伤和ARDS。采用多重实时荧光定量PCR从鼻咽和支气管标本中分离出EV-RV,未检出其他病原体。我们还对相关文献进行了最新的回顾,试图强调早期识别病毒罪魁祸首的重要性,这可以最大限度地减少侵入性诊断程序和抗生素的使用。
{"title":"Enterovirus-Rhinovirus-Induced Acute Respiratory Distress Syndrome in Adults: A Case Report and Short Literature Review.","authors":"Eirini Avgoustou, Aikaterini Spyridaki, Giorgos Pothitos, Antonios Papadopoulos, Spyridon Kois, Foula Vassilara","doi":"10.1155/2023/8887955","DOIUrl":"10.1155/2023/8887955","url":null,"abstract":"<p><p>Enteroviruses and rhinoviruses (EV-RV) are small RNA viruses that usually cause the common cold and asthma exacerbations. Although EV-RV-induced acute respiratory distress syndrome (ARDS) is common in children, only scattered reports of ARDS in adults have been published. The diagnosis has been greatly facilitated by the advent of molecular techniques, namely, real-time polymerase chain reaction (RT-PCR). EV-RV can cause ARDS by stimulating a cytokine cascade. No antiviral therapy has yet been approved, and treatment is entirely supportive. Herein, we report a rare case of EV-RV infection in an afebrile adult with dyspnea that rapidly progressed to acute lung injury and ARDS. EV-RV was isolated with multiple real-time PCR in nasopharyngeal and bronchial specimens, while no other pathogen was detected. We also present an up-to-date review of relevant literature, in an attempt to stress the importance of the early identification of viral culprits, which can minimize the use of invasive diagnostic procedures and antibiotic agents.</p>","PeriodicalId":9608,"journal":{"name":"Case Reports in Infectious Diseases","volume":"2023 ","pages":"8887955"},"PeriodicalIF":1.1,"publicationDate":"2023-11-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10637844/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"89716980","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Comment on "Pneumocystis jirovecii Pneumonia in a HIV-Infected Patient with a CD4 Count Greater Than 400 Cells/μL and Atovaquone Prophylaxis". 评论“CD4计数大于400细胞/μL的HIV感染患者的吉氏肺孢子虫肺炎和阿托伐醌预防”。
IF 1.1 Q4 INFECTIOUS DISEASES Pub Date : 2023-10-23 eCollection Date: 2023-01-01 DOI: 10.1155/2023/9793264
Gilles Nevez, Claire Hoffmann, Solène Le Gal
{"title":"Comment on \"<i>Pneumocystis jirovecii</i> Pneumonia in a HIV-Infected Patient with a CD4 Count Greater Than 400 Cells/<i>μ</i>L and Atovaquone Prophylaxis\".","authors":"Gilles Nevez,&nbsp;Claire Hoffmann,&nbsp;Solène Le Gal","doi":"10.1155/2023/9793264","DOIUrl":"https://doi.org/10.1155/2023/9793264","url":null,"abstract":"<jats:p />","PeriodicalId":9608,"journal":{"name":"Case Reports in Infectious Diseases","volume":"2023 ","pages":"9793264"},"PeriodicalIF":1.1,"publicationDate":"2023-10-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10615577/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"71421011","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Persistent Vulvar Itch Unresponsive to Treatment: A Case of Vulvar Schistosomiasis Caused by Schistosoma mansoni and a Brief Review of Literature. 持续性外阴瘙痒治疗无效:一例由曼氏血吸虫引起的外阴血吸虫病病例及文献复习。
IF 1.1 Q4 INFECTIOUS DISEASES Pub Date : 2023-10-18 eCollection Date: 2023-01-01 DOI: 10.1155/2023/9913905
Anthony Gyening-Yeboah, Solomon E Quayson

Background: Vulvar schistosomiasis is a female genital schistosomiasis (FGS), which occurs because of the damage caused by the presence of schistosome ova within the vulva. FGS is mostly misdiagnosed as a sexually transmitted infection. There is no reported case of vulvar schistosomiasis from Schistosoma mansoni in an immunocompetent or immunocompromised person in Ghanaian medical literature; however, there is a reported case of S. haematobium in an immunocompromised person. This is the first case of vulvar schistosomiasis from S. mansoni infection in an immunocompromised person. This case report discusses the need to consider vulvar schistosomiasis in patients with itchiness of the vulva. Case Presentation. A sixty-nine-year-old married woman presents with a persistent vulvar itch that is unresponsive to treatment. A clinical diagnosis of vulvar lichen planus unresponsive to medical therapy was made. A histopathological diagnosis of vulvar schistosomiasis was, however, made. Ziehl-Neelsen stain revealed the ova of Schistosoma mansoni. Symptoms resolved on administration of oral praziquantel.

Conclusion: Vulvar schistosomiasis must be considered in clinical history-taking and investigation of signs and symptoms related to itchiness of the vulva. Ziehl-Neelsen staining is a helpful histopathology armamentarium to determine the species of schistosome ova.

背景:外阴血吸虫病是一种女性生殖器血吸虫病(FGS),其发生是由于外阴内存在血吸虫卵造成的损害。FGS大多被误诊为性传播感染。在加纳医学文献中,没有报道免疫功能正常或免疫功能低下的人患上曼氏血吸虫外阴血吸虫病的病例;然而,据报道,一名免疫功能低下的人出现了一例埃及血吸虫。这是第一例免疫功能低下的人感染曼氏血吸虫引起的外阴血吸虫病。本病例报告讨论了外阴瘙痒患者是否需要考虑外阴血吸虫病。案例介绍。一位69岁的已婚妇女出现持续的外阴瘙痒,对治疗没有反应。临床诊断为外阴扁平苔藓对药物治疗无反应。然而,对外阴血吸虫病进行了组织病理学诊断。Ziehl-Neelsen染色显示曼氏血吸虫卵。口服吡喹酮后症状缓解。结论:外阴血吸虫病在临床病史采集和外阴瘙痒相关体征、症状调查中应予以重视。Ziehl-Neelsen染色是一种有助于确定血吸虫卵种类的组织病理学方法。
{"title":"Persistent Vulvar Itch Unresponsive to Treatment: A Case of Vulvar Schistosomiasis Caused by <i>Schistosoma mansoni</i> and a Brief Review of Literature.","authors":"Anthony Gyening-Yeboah,&nbsp;Solomon E Quayson","doi":"10.1155/2023/9913905","DOIUrl":"10.1155/2023/9913905","url":null,"abstract":"<p><strong>Background: </strong>Vulvar schistosomiasis is a female genital schistosomiasis (FGS), which occurs because of the damage caused by the presence of schistosome ova within the vulva. FGS is mostly misdiagnosed as a sexually transmitted infection. There is no reported case of vulvar schistosomiasis from <i>Schistosoma mansoni</i> in an immunocompetent or immunocompromised person in Ghanaian medical literature; however, there is a reported case of <i>S. haematobium</i> in an immunocompromised person. This is the first case of vulvar schistosomiasis from <i>S. mansoni</i> infection in an immunocompromised person. This case report discusses the need to consider vulvar schistosomiasis in patients with itchiness of the vulva. <i>Case Presentation</i>. A sixty-nine-year-old married woman presents with a persistent vulvar itch that is unresponsive to treatment. A clinical diagnosis of vulvar lichen planus unresponsive to medical therapy was made. A histopathological diagnosis of vulvar schistosomiasis was, however, made. Ziehl-Neelsen stain revealed the ova of <i>Schistosoma mansoni</i>. Symptoms resolved on administration of oral praziquantel.</p><p><strong>Conclusion: </strong>Vulvar schistosomiasis must be considered in clinical history-taking and investigation of signs and symptoms related to itchiness of the vulva. Ziehl-Neelsen staining is a helpful histopathology armamentarium to determine the species of schistosome ova.</p>","PeriodicalId":9608,"journal":{"name":"Case Reports in Infectious Diseases","volume":"2023 ","pages":"9913905"},"PeriodicalIF":1.1,"publicationDate":"2023-10-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10599860/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"54227787","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Lenacapavir with Fostemsavir in a Multidrug-Resistant HIV-Infected Hemodialysis Patient. Lenacapavir联合Fostemsavir治疗一名耐多药HIV感染的血液透析患者。
IF 1 Q4 INFECTIOUS DISEASES Pub Date : 2023-10-18 eCollection Date: 2023-01-01 DOI: 10.1155/2023/8865265
Ferdinand Bigirimana, Sigi Van den Wijngaert, Christelle Fosso, Karolien Stoffels, Charlotte Martin, Evelyne Maillart, Philippe Clevenbergh

We report a hemodialysis MDR HIV-infected patient switched to fostemsavir with lenacapavir plus lamivudine for more than a year. She maintained a suppressed viral replication and did not present any clinical or biological drug-related side effects. The combination of lenacapavir plus fostemsavir looks promising in terms of safety and efficacy even in patients with end-stage renal disease awaiting renal transplant. Both drugs are first in class ARVs so that there is no cross resistance with previous drugs, maintaining their efficacy against MDR HIV.

我们报告了一名血液透析耐多药HIV感染患者,在一年多的时间里,改用福司韦加乐那帕韦和拉米夫定治疗。她保持了受抑制的病毒复制,没有出现任何临床或生物学上与药物有关的副作用。即使在等待肾移植的终末期肾病患者中,乐那帕韦与福司韦的联合用药在安全性和有效性方面也很有希望。这两种药物都是一流的抗逆转录病毒药物,因此与以前的药物没有交叉耐药性,保持了它们对耐多药艾滋病毒的疗效。
{"title":"Lenacapavir with Fostemsavir in a Multidrug-Resistant HIV-Infected Hemodialysis Patient.","authors":"Ferdinand Bigirimana, Sigi Van den Wijngaert, Christelle Fosso, Karolien Stoffels, Charlotte Martin, Evelyne Maillart, Philippe Clevenbergh","doi":"10.1155/2023/8865265","DOIUrl":"10.1155/2023/8865265","url":null,"abstract":"<p><p>We report a hemodialysis MDR HIV-infected patient switched to fostemsavir with lenacapavir plus lamivudine for more than a year. She maintained a suppressed viral replication and did not present any clinical or biological drug-related side effects. The combination of lenacapavir plus fostemsavir looks promising in terms of safety and efficacy even in patients with end-stage renal disease awaiting renal transplant. Both drugs are first in class ARVs so that there is no cross resistance with previous drugs, maintaining their efficacy against MDR HIV.</p>","PeriodicalId":9608,"journal":{"name":"Case Reports in Infectious Diseases","volume":"2023 ","pages":"8865265"},"PeriodicalIF":1.0,"publicationDate":"2023-10-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10599868/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"54227786","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Capnocytophaga canimorsus Infection in a 38-Year-Old Male after a Dog Bite. 38岁男性犬咬伤后嗜狼细胞感染1例。
IF 1.1 Q4 INFECTIOUS DISEASES Pub Date : 2023-10-16 eCollection Date: 2023-01-01 DOI: 10.1155/2023/9917898
Ahmad Ahsen, Philip Korsun, Fadi Albahra, Ranjit Nair, Zain Tariq

Here, we present a unique case of a 38-year-old male with a history of alcohol use disorder and multiple sexual partners, who presented with fulminant sepsis with shock, multiorgan failure, and livedo racemosa after a dog bite the week prior. The patient was intubated on arrival and was started on vasopressors and antibiotics. Eventually, the patient's clinical status improved, and he was transferred out of the intensive care unit. Blood cultures tested positive for oxidase-positive Gram-negative rods two days after collection, and species identification showed Capnocytophaga canimorsus.

在这里,我们介绍了一个独特的病例,一名38岁的男性有酒精使用障碍史,有多个性伴侣,在前一周被狗咬伤后,他出现了伴有休克、多器官衰竭和外消旋活菌的暴发性败血症。患者在抵达时插管,并开始服用血管升压药和抗生素。最终,患者的临床状况有所改善,他被转移出重症监护室。采集后两天,血液培养物的氧化酶阳性革兰氏阴性杆菌检测呈阳性,物种鉴定显示犬无细胞自噬菌。
{"title":"<i>Capnocytophaga canimorsus</i> Infection in a 38-Year-Old Male after a Dog Bite.","authors":"Ahmad Ahsen,&nbsp;Philip Korsun,&nbsp;Fadi Albahra,&nbsp;Ranjit Nair,&nbsp;Zain Tariq","doi":"10.1155/2023/9917898","DOIUrl":"10.1155/2023/9917898","url":null,"abstract":"<p><p>Here, we present a unique case of a 38-year-old male with a history of alcohol use disorder and multiple sexual partners, who presented with fulminant sepsis with shock, multiorgan failure, and livedo racemosa after a dog bite the week prior. The patient was intubated on arrival and was started on vasopressors and antibiotics. Eventually, the patient's clinical status improved, and he was transferred out of the intensive care unit. Blood cultures tested positive for oxidase-positive Gram-negative rods two days after collection, and species identification showed <i>Capnocytophaga canimorsus</i>.</p>","PeriodicalId":9608,"journal":{"name":"Case Reports in Infectious Diseases","volume":"2023 ","pages":"9917898"},"PeriodicalIF":1.1,"publicationDate":"2023-10-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10593545/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"50157130","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Case Reports in Infectious Diseases
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1