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Corrigendum: Optic neuropathy and congenital glaucoma associated with probable Zika virus infection in Venezuelan patients. 勘误:委内瑞拉患者视神经病变和先天性青光眼可能与寨卡病毒感染相关。
Pub Date : 2018-08-31 eCollection Date: 2018-08-01 DOI: 10.1099/jmmcr.0.005161
C Gustavo De Moraes, Michele Pettito, Juan B Yepez, Anavaj Sakuntabhai, Etienne Simon-Loriere, Mussaret B Zaidi, Matthieu Prot, Claude Ruffie, Susan S Kim, Rando Allikmets, Joseph D Terwilliger, Joseph H Lee, Gladys E Maestre

[This corrects the article DOI: 10.1099/jmmcr.0.005145.].

[更正文章DOI: 10.1099/jmmcr.0.005145.]。
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引用次数: 2
Guillain Barré syndrome associated with bladder instillation of Bacille Calmette Guérin (BCG). 膀胱灌注卡介苗(BCG)相关的格林-巴氏综合征。
Pub Date : 2018-08-20 eCollection Date: 2018-08-01 DOI: 10.1099/jmmcr.0.005164
Karmel Webb, Pradhib Venkatesan

Introduction: Guillain Barré Syndrome (GBS) has rarely been associated with tuberculosis and has been previously reported after Bacille Calmette Guérin (BCG) vaccination, but we report an association of GBS with intra-vesical BCG instillations followed by the clinical picture of disseminated BCGosis.

Case presentation: A 68-year-old man with bladder carcinoma had a transurethral tumour resection followed by repeated BCG instillations. Catheterization for his eighth dose was traumatic, causing frank haematuria. Ten days later he presented with fevers, myalgia and dyspnoea. Chest X-ray on admission showed micronodular shadowing and a computed tomography scan showed miliary changes in the lungs. Disseminated BCGosis infection was suspected and his symptoms did improve after starting rifamipicin, isoniazid and ethambutol. Over 2 weeks post-admission he developed an unsteady gait, reduced pin-prick sensation below both knees and fingertips, reduced proprioception in both toes and ankles, with absent reflexes in his lower limbs and diminished reflexes in his upper limbs. Nerve conduction studies showed a purely demyelinating sensori-motor peripheral neuropathy in upper and lower limbs, characteristic of GBS.

Conclusion: To our knowledge this is the first case report of GBS following bladder instillation of BCG. Given the millions of cases of tuberculosis and millions of doses of administered BCG, GBS must be a very rare adverse effect.

吉兰巴罗综合征(GBS)很少与结核病相关,以前曾有报道在卡介苗(Bacille Calmette gusamurin, BCG)接种后发生,但我们报告了吉兰巴罗综合征与膀胱内卡介苗注射后出现弥散性BCGosis的临床表现有关。病例介绍:一名68岁男性膀胱癌经尿道肿瘤切除术后反复注射卡介苗。第8剂导管插管是创伤性的,引起了明显的血尿。10天后,他出现发烧、肌痛和呼吸困难。入院时的胸部x光片显示微结节影,计算机断层扫描显示肺部的军事变化。怀疑播散性BCGosis感染,在开始使用利福平、异烟肼和乙胺丁醇后症状有所改善。入院后2周多,患者出现步态不稳,双膝和指尖以下针刺感减少,双趾和踝关节本体感觉减少,下肢反射缺失,上肢反射减弱。神经传导研究显示,上肢和下肢有纯粹脱髓鞘的感觉-运动周围神经病变,这是GBS的特征。结论:据我们所知,这是首例膀胱注射卡介苗后发生GBS的病例。鉴于数以百万计的结核病病例和数以百万计的卡介苗剂量,GBS一定是一种非常罕见的不良反应。
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引用次数: 6
Measles during arbovirus outbreak: a diagnostic challenge. 虫媒病毒暴发期间的麻疹:诊断挑战。
Pub Date : 2018-08-10 eCollection Date: 2018-08-01 DOI: 10.1099/jmmcr.0.005156
Ann-Claire Gourinat, Cécile Cazorla, Anne Pfannstiel, Thomas Tran
Introduction. Dengue fever is a major public health problem in New Caledonia, like in many Pacific Islands Countries and territories. In 2017 New Caledonia faced multiple circulations of arboviruses with a major outbreak of dengue and a co-circulating Zika virus. New Caledonia is considered as a non-endemic territory for measles since the mid 1990’s. Case presentation. A 41-year-old male presented fever, headache, sinusitis and exanthematous maculopapular rash. A clinical diagnosis of arbovirus was first suspected due to the local epidemic context. A few days later the patient was admitted to the main hospital. The real time RT-PCR for dengue and Zika virus were negative on the first blood sample. A drug reaction with eosinophilia and systemic symptoms (DRESS) syndrome and other infectious diseases including measles were then suspected. ELISA tests for measles were positive for IgM and equivocal for IgG. A throat swab was immediately shipped to a reference laboratory for measles nucleic acid testing. After a week, the patient recovered and the presence of measles RNA was confirmed. No secondary cases were reported among contacts of the patient and the source of his infection could not be ascertained. Conclusion. Diagnosis of measles during an arbovirus outbreak in a country where measles disease is rare can be a pitfall for healthcare professionals. The introduction of measles via returned travellers or tourists from areas where measles remains endemic is a real threat to countries with high vaccine coverage.
导言:与许多太平洋岛屿国家和领土一样,登革热是新喀里多尼亚的一个主要公共卫生问题。2017年,新喀里多尼亚面临多重虫媒病毒传播,同时爆发了登革热和寨卡病毒共同传播。自1990年代中期以来,新喀里多尼亚被视为麻疹非流行地区。病例介绍:41岁男性,表现为发热、头痛、鼻窦炎及黄斑丘疹。由于当地的流行情况,首次怀疑虫媒病毒的临床诊断。几天后,病人住进了大医院。首份血样登革和寨卡病毒实时RT-PCR检测均为阴性。然后怀疑有嗜酸性粒细胞增多和全身症状(DRESS)综合征的药物反应以及包括麻疹在内的其他传染病。麻疹ELISA检测IgM阳性,IgG不明确。咽拭子立即被送往参比实验室进行麻疹核酸检测。一周后,患者康复并确认麻疹RNA的存在。该患者的接触者中未报告继发病例,其感染源无法确定。结论:在麻疹疾病罕见的国家,在虫媒病毒暴发期间诊断麻疹可能是卫生保健专业人员的一个陷阱。通过从麻疹流行地区返回的旅行者或游客传播麻疹,对疫苗覆盖率高的国家构成了真正的威胁。
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引用次数: 2
Rare Elizabethkingia anophelis meningitis case in a Danish male. 丹麦男性罕见伊丽莎白按蚊脑膜炎病例。
Pub Date : 2018-08-09 eCollection Date: 2018-08-01 DOI: 10.1099/jmmcr.0.005163
Hans Linde Nielsen, Irene Harder Tarpgaard, David Fuglsang-Damgaard, Philip Kjettinge Thomsen, Sylvain Brisse, Michael Dalager-Pedersen

Introduction: Elizabethkingia anophelis is a Gram-negative, aerobic, non-motile rod belonging to the family Flavobacteriaceae. Over the last 5 years, it has emerged as an opportunistic human pathogen involved in neonatal meningitis and sepsis, as well as nosocomial outbreaks. It has been isolated from the midgut of the Anopheles gambiae mosquito, but there is no evidence for a role of the mosquito in human infections, and very little is known regarding the routes of transmission to humans. Recent studies, primarily from South-East Asia, suggest that E. anophelis, and not Elizabethkingia meningoseptica, is the predominant human pathogen of this genus. However, identification to the species level has been difficult due to the limitations of the current MALDI-TOF MS (matrix-associated laser desorption ionization-time of flight MS) systems for correct species identification.

Case presentation: Here, we present a rare case of E. anophelis meningitis in a Danish male, who had a travel exposure to Malaysia 7 weeks before hospitalization. A multidrug-resistant Elizabethkingia species was isolated from blood and cerebrospinal fluid, and genomic sequencing was used to characterize the phylogenetic position of the isolate, which was determined as associated with previously described sublineage 11. The patient was successfully treated with intravenous moxifloxacin and rifampicin for 2 weeks with no major sequelae, but we did not find the source of transmission.

Conclusion: All clinical microbiologists should be aware of the present limitations of the MALDI-TOF MS systems for correct species identification, and therefore we recommend the use of genome sequencing for the correct identification at the species and sublineage level.

伊莉莎白杆菌(Elizabethkingia anophelis)是一种革兰氏阴性、需氧、非运动的杆菌,属于黄杆菌科。在过去5年中,它已作为一种机会性人类病原体出现,涉及新生儿脑膜炎和败血症以及院内暴发。它已从冈比亚按蚊的中肠中分离出来,但没有证据表明这种蚊子在人类感染中起作用,而且对传播给人类的途径所知甚少。最近主要来自东南亚的研究表明,该属的主要人类病原体是按蚊,而不是伊丽莎白脑膜炎杆菌。然而,由于现有的基质相关激光解吸电离飞行时间质谱(MALDI-TOF MS)系统在正确的物种识别方面的局限性,对物种水平的识别一直很困难。病例介绍:在此,我们报告一例罕见的按蚊脑膜炎病例,患者为丹麦男性,住院前7周曾到马来西亚旅行。从血液和脑脊液中分离出一种多重耐药的elizabeth ethkingia物种,并使用基因组测序来表征该分离物的系统发育位置,确定其与先前描述的亚谱系11相关。患者静脉注射莫西沙星和利福平治疗成功2周,无重大后遗症,但未发现传播源。结论:所有临床微生物学家都应该意识到MALDI-TOF MS系统在正确的物种鉴定方面的局限性,因此我们建议使用基因组测序在物种和亚谱系水平上进行正确的鉴定。
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引用次数: 13
Ehrlichiosis presenting as severe sepsis and meningoencephalitis in an immunocompetent adult. 埃立克体病表现为严重败血症和脑膜脑炎在免疫能力的成年人。
Pub Date : 2018-07-27 eCollection Date: 2018-09-01 DOI: 10.1099/jmmcr.0.005162
Stephanie L Buzzard, Brittany D Bissell, Melissa L Thompson Bastin

Introduction: Ehrlichia are obligate intracellular pathogens transmitted to vertebrates by ticks.

Case presentation: We report the case of a 59-year-old man who presented to the University of Kentucky Albert B. Chandler Medical Center (Lexington, KY, USA) after being found fallen down in the woods. A lumbar puncture revealed what appeared to be bacterial meningitis, yet cerebrospinal fluid cultures, Gram stains and a meningitis/encephalitis panel were inconclusive. However, an Ehrlichia DNA PCR of the blood resulted as being positive for Ehrlichia chaffeensis antibodies. The patient received a 14 day course of doxycycline, and recovered from his multiple organ failure. The aetiology of the ehrlichial meningoencephalitis was likely transmission through a tick-bite, due to the patient's outdoor exposure.

Conclusion: While it is rare to see Ehrlichia as a cause of meningitis, this illness can progress to severe multisystem disease with septic shock, meningoencephalitis or acute respiratory distress syndrome (ARDS). Those with compromised immunity are at a higher risk of developing the more severe form of the disease and have higher case fatality rates.

埃立克体是一种专性细胞内病原体,通过蜱传播给脊椎动物。病例介绍:我们报告一名59岁的男子,他被发现在树林里摔倒后,来到肯塔基大学阿尔伯特B.钱德勒医学中心(美国肯塔基州列克星敦)。腰椎穿刺显示似乎是细菌性脑膜炎,但脑脊液培养、革兰氏染色和脑膜炎/脑炎小组没有结论。然而,血液的埃利希体DNA PCR结果为沙非埃利希体抗体阳性。患者接受了14天的强力霉素疗程,并从多器官衰竭中恢复过来。埃利希型脑膜脑炎的病因可能是由于患者的户外暴露而通过蜱叮咬传播。结论:虽然很少看到埃利希体作为脑膜炎的原因,但这种疾病可发展为感染性休克、脑膜脑炎或急性呼吸窘迫综合征(ARDS)等严重的多系统疾病。免疫力受损的人患更严重疾病的风险更高,病死率也更高。
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引用次数: 6
A case of hepato-biliary infection secondary to cryptosporidium in a patient on tacrolimus. 他克莫司致隐孢子虫继发肝胆感染1例。
Pub Date : 2018-07-20 eCollection Date: 2018-08-01 DOI: 10.1099/jmmcr.0.005159
Sajal Gupta, Alison Johnson, Simon Meyrick, Angharad P Davies, R Chalmers

Introduction: Cryptosporidium infection is known to cause hepato-biliary involvement, mainly in association with T-cell immune deficiency. Hepato-biliary involvement in association with milder immunosuppression is less well described. We describe the first case, to our knowledge, of Cryptosporidium hominis hepato-biliary infection associated with tacrolimus in a patient with nephrotic syndrome.

Case presentation: A 14 year old girl who had been on tacrolimus for nephrotic syndrome presented with diarrhea due to C. hominis. Nineteen days after her initial presentation she attended hospital with abdominal pain and deranged liver function tests. An ultrasound scan showed a thickened gall bladder. Her symptoms settled and her liver function tests returned to normal after treatment with nitazoxanide.

Conclusion: Cryptosporidium should be considered in the differential diagnosis of both diarrhea and hepato-biliary symptoms and abnormal liver function tests, even in the presence of relatively mild immunosuppression. Nitazoxanide was an effective treatment in this case.

简介:隐孢子虫感染已知可引起肝胆受累,主要与t细胞免疫缺陷有关。肝胆受累与轻度免疫抑制相关的描述较少。我们描述了第一个病例,据我们所知,人隐孢子虫肝胆感染与他克莫司相关的肾病综合征患者。病例介绍:一个14岁的女孩谁曾在他克莫司肾病综合征提出腹泻由于人原梭菌。初次就诊19天后,她因腹痛和肝功能检查紊乱而入院。超声扫描显示胆囊增厚。经硝唑昔尼特治疗后,患者症状消退,肝功能检查恢复正常。结论:即使存在相对轻微的免疫抑制,在腹泻和肝胆症状及肝功能检查异常时也应考虑隐孢子虫的鉴别诊断。Nitazoxanide是一种有效的治疗方法。
{"title":"A case of hepato-biliary infection secondary to cryptosporidium in a patient on tacrolimus.","authors":"Sajal Gupta,&nbsp;Alison Johnson,&nbsp;Simon Meyrick,&nbsp;Angharad P Davies,&nbsp;R Chalmers","doi":"10.1099/jmmcr.0.005159","DOIUrl":"https://doi.org/10.1099/jmmcr.0.005159","url":null,"abstract":"<p><strong>Introduction: </strong>Cryptosporidium infection is known to cause hepato-biliary involvement, mainly in association with T-cell immune deficiency. Hepato-biliary involvement in association with milder immunosuppression is less well described. We describe the first case, to our knowledge, of <i>Cryptosporidium hominis</i> hepato-biliary infection associated with tacrolimus in a patient with nephrotic syndrome.</p><p><strong>Case presentation: </strong>A 14 year old girl who had been on tacrolimus for nephrotic syndrome presented with diarrhea due to <i>C. hominis</i>. Nineteen days after her initial presentation she attended hospital with abdominal pain and deranged liver function tests. An ultrasound scan showed a thickened gall bladder. Her symptoms settled and her liver function tests returned to normal after treatment with nitazoxanide.</p><p><strong>Conclusion: </strong>Cryptosporidium should be considered in the differential diagnosis of both diarrhea and hepato-biliary symptoms and abnormal liver function tests, even in the presence of relatively mild immunosuppression. Nitazoxanide was an effective treatment in this case.</p>","PeriodicalId":73559,"journal":{"name":"JMM case reports","volume":"5 8","pages":"e005159"},"PeriodicalIF":0.0,"publicationDate":"2018-07-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6152403/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"36587036","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: 3
Cyberlindnera jadinii (teleomorph Candida utilis) candidaemia in a patient with aplastic anaemia: a case report. 再生障碍性贫血患者念珠菌血症1例报告。
Pub Date : 2018-07-10 eCollection Date: 2018-08-01 DOI: 10.1099/jmmcr.0.005160
Pauline Treguier, Marion David, Gilles Gargala, Vincent Camus, Aspasia Stamatoullas, Anne-Lise Menard, Pascal Lenain, Nathalie Contentin, Emilie Lemasle, Helene Lanic, Hervé Tilly, Fabrice Jardin, Stéphane Lepretre

Introduction: We present what is believed to be the first report of candidaemia caused by Cyberlindnera (Pichia) jadinii (teleomorph of Candida utilis) in a patient with an aplastic anaemia.

Case presentation: The patient, a 21-year-old male, presented with hepatic cytolysis, cutaneous and pulmonary involvement, and septic shock. Cyberlindnera jadinii was identified by aerobic blood culture and MS. The patient initially received multiple and combined antifungal therapy, but continued to have persistent skin lesions and fever. He was successfully treated by emergency haploidentical haematopoietic stem cell transplantation, combined with triple antifungal therapy and supportive care.

Conclusion: Cyberlindnera jadinii, teleomorph of Candida utilis, which is not usually invasive, can lead to an opportunistic invasive infection in unhealthy adult patients. For treatment of the invasive candida infection, it is necessary to combine antifungal therapy and supportive care.

简介:我们提出了被认为是由念珠菌(假丝酵母的远变形)在再生障碍性贫血患者引起念珠菌血症的第一份报告。病例介绍:患者,21岁男性,表现为肝细胞溶解,皮肤和肺部受累,感染性休克。通过有氧血培养和ms鉴定出jadinii,患者最初接受了多种和联合抗真菌治疗,但持续出现皮肤损伤和发烧。通过紧急单倍体造血干细胞移植,结合三联抗真菌治疗和支持性护理,成功治疗。结论:利用念珠菌的远变形念珠菌(Cyberlindnera jadinii)通常不具有侵袭性,但在不健康的成人患者中可导致机会性侵袭性感染。侵袭性念珠菌感染的治疗应结合抗真菌治疗和支持性护理。
{"title":"<i>Cyberlindnera jadinii</i> (teleomorph <i>Candida utilis</i>) candidaemia in a patient with aplastic anaemia: a case report.","authors":"Pauline Treguier,&nbsp;Marion David,&nbsp;Gilles Gargala,&nbsp;Vincent Camus,&nbsp;Aspasia Stamatoullas,&nbsp;Anne-Lise Menard,&nbsp;Pascal Lenain,&nbsp;Nathalie Contentin,&nbsp;Emilie Lemasle,&nbsp;Helene Lanic,&nbsp;Hervé Tilly,&nbsp;Fabrice Jardin,&nbsp;Stéphane Lepretre","doi":"10.1099/jmmcr.0.005160","DOIUrl":"https://doi.org/10.1099/jmmcr.0.005160","url":null,"abstract":"<p><strong>Introduction: </strong>We present what is believed to be the first report of candidaemia caused by <i>Cyberlindnera</i> (<i>Pichia</i>) <i>jadinii</i> (teleomorph of <i>Candida utilis</i>) in a patient with an aplastic anaemia.</p><p><strong>Case presentation: </strong>The patient, a 21-year-old male, presented with hepatic cytolysis, cutaneous and pulmonary involvement, and septic shock. <i>Cyberlindnera jadinii</i> was identified by aerobic blood culture and MS. The patient initially received multiple and combined antifungal therapy, but continued to have persistent skin lesions and fever. He was successfully treated by emergency haploidentical haematopoietic stem cell transplantation, combined with triple antifungal therapy and supportive care.</p><p><strong>Conclusion: </strong><i>Cyberlindnera jadinii</i>, teleomorph of <i>Candida utilis</i>, which is not usually invasive, can lead to an opportunistic invasive infection in unhealthy adult patients. For treatment of the invasive candida infection, it is necessary to combine antifungal therapy and supportive care.</p>","PeriodicalId":73559,"journal":{"name":"JMM case reports","volume":"5 8","pages":"e005160"},"PeriodicalIF":0.0,"publicationDate":"2018-07-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6152400/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"36587037","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: 9
Staphylococcus haemolyticus epididymo-orchitis and bacteraemia: a case report. 附睾-睾丸炎溶血葡萄球菌合并菌血症1例。
Pub Date : 2018-07-05 eCollection Date: 2018-07-01 DOI: 10.1099/jmmcr.0.005157
Christina Pindar, Roberto A Viau

Introduction: Although more often recognized as a culprit in female urinary tract infection, coagulase-negative staphylococci (CoNS) can cause severe genitourinary infections in men. While positive blood cultures with CoNS are usually thought to be contaminants, in the setting of a severe genito-urinary infection they can represent true infection.

Case presentation: We present the case of a 70-year-old male without a central venous catheter or urinary catheter who developed Staphylococcus haemolyticus bloodstream infection secondary to epididymo-orchitis.

Conclusion: This case highlights the importance of prompt recognition of serious CoNS infections, including bacteraemia, in the setting of CoNS genitourinary tract infections.

导语:虽然凝固酶阴性葡萄球菌(con)通常被认为是女性尿路感染的罪魁祸首,但它可以导致男性严重的泌尿生殖系统感染。虽然含有con的阳性血培养通常被认为是污染物,但在严重的泌尿生殖系统感染的情况下,它们可能代表真正的感染。病例介绍:我们提出的情况下,70岁的男性没有中心静脉导管或尿导管谁发展的溶血性葡萄球菌血液感染继发附睾睾丸炎。结论:本病例强调了在con泌尿生殖道感染的情况下,及时识别包括菌血症在内的严重con感染的重要性。
{"title":"<i>Staphylococcus haemolyticus</i> epididymo-orchitis and bacteraemia: a case report.","authors":"Christina Pindar,&nbsp;Roberto A Viau","doi":"10.1099/jmmcr.0.005157","DOIUrl":"https://doi.org/10.1099/jmmcr.0.005157","url":null,"abstract":"<p><strong>Introduction: </strong>Although more often recognized as a culprit in female urinary tract infection, coagulase-negative staphylococci (CoNS) can cause severe genitourinary infections in men. While positive blood cultures with CoNS are usually thought to be contaminants, in the setting of a severe genito-urinary infection they can represent true infection.</p><p><strong>Case presentation: </strong>We present the case of a 70-year-old male without a central venous catheter or urinary catheter who developed <i>Staphylococcus haemolyticus</i> bloodstream infection secondary to epididymo-orchitis.</p><p><strong>Conclusion: </strong>This case highlights the importance of prompt recognition of serious CoNS infections, including bacteraemia, in the setting of CoNS genitourinary tract infections.</p>","PeriodicalId":73559,"journal":{"name":"JMM case reports","volume":"5 7","pages":"e005157"},"PeriodicalIF":0.0,"publicationDate":"2018-07-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6159547/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"36546542","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: 7
Mycobacterium xenopi systemic infection in a domestic fiery-shouldered conure bird (Pyrrhura egregia). 家养赤肩野禽的异种分枝杆菌全身感染。
Pub Date : 2018-07-04 eCollection Date: 2018-07-01 DOI: 10.1099/jmmcr.0.005158
Guillaume St-Jean, Carl A Gagnon, Hafid Soualhine, Manon Tremblay, Andrée-Anne Beaulieu, Doris Sylvestre

Introduction: Mycobacterium xenopi is a rare opportunistic pathogen mainly causing infections in immunocompromised human patients or those with underlying chronic structural lung disease. Cases of disease in veterinary medicine remain scarce. Few animal species, including birds, are suspected of being vectors of the disease and there has not yet been a report of clinical disease in birds. We report the first case, to our knowledge, of systemic infection in a domestic bird.

Case presentation: A female fiery-shouldered conure was submitted after death for necropsy following episodes of heavy breathing. The necropsy revealed multiple granulomatous lesions within the liver, air sacs and kidneys. Ziehl-Neelsen stains demonstrated the presence of numerous intralesional acid-fast bacilli. PCR assays and culture confirmed the presence of M. xenopi.

Conclusion: Through this case we hope to describe the characteristics of M. xenopi disease in birds and the possible close relationship between animal and human infections.

摘要:异种分枝杆菌是一种罕见的条件致病菌,主要在免疫功能低下的人类患者或伴有慢性结构性肺部疾病的患者中引起感染。兽医领域的疾病病例仍然很少。很少有动物物种,包括鸟类,被怀疑是该疾病的媒介,尚未有鸟类临床疾病的报告。我们报告的第一个病例,据我们所知,全身性感染的家禽。病例介绍:一名女性肩背发红,死后因呼吸急促而接受尸检。尸检显示肝脏、肺泡及肾脏内多处肉芽肿病变。Ziehl-Neelsen染色显示病灶内存在大量抗酸杆菌。PCR检测和培养证实了非洲棘球蚴的存在。结论:通过本病例,我们希望能够描述禽种棘支原体病的特点,以及动物与人感染之间可能存在的密切关系。
{"title":"<i>Mycobacterium xenopi</i> systemic infection in a domestic fiery-shouldered conure bird (<i>Pyrrhura egregia</i>).","authors":"Guillaume St-Jean,&nbsp;Carl A Gagnon,&nbsp;Hafid Soualhine,&nbsp;Manon Tremblay,&nbsp;Andrée-Anne Beaulieu,&nbsp;Doris Sylvestre","doi":"10.1099/jmmcr.0.005158","DOIUrl":"https://doi.org/10.1099/jmmcr.0.005158","url":null,"abstract":"<p><strong>Introduction: </strong><i>Mycobacterium xenopi</i> is a rare opportunistic pathogen mainly causing infections in immunocompromised human patients or those with underlying chronic structural lung disease. Cases of disease in veterinary medicine remain scarce. Few animal species, including birds, are suspected of being vectors of the disease and there has not yet been a report of clinical disease in birds. We report the first case, to our knowledge, of systemic infection in a domestic bird.</p><p><strong>Case presentation: </strong>A female fiery-shouldered conure was submitted after death for necropsy following episodes of heavy breathing. The necropsy revealed multiple granulomatous lesions within the liver, air sacs and kidneys. Ziehl-Neelsen stains demonstrated the presence of numerous intralesional acid-fast bacilli. PCR assays and culture confirmed the presence of <i>M. xenopi</i>.</p><p><strong>Conclusion: </strong>Through this case we hope to describe the characteristics of <i>M. xenopi</i> disease in birds and the possible close relationship between animal and human infections.</p>","PeriodicalId":73559,"journal":{"name":"JMM case reports","volume":"5 7","pages":"e005158"},"PeriodicalIF":0.0,"publicationDate":"2018-07-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6159546/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"36546543","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: 2
Extensively drug-resistant (XDR) Pseudomonas aeruginosa identified in Lima, Peru co-expressing a VIM-2 metallo-β-lactamase, OXA-1 β-lactamase and GES-1 extended-spectrum β-lactamase. 广泛耐药(XDR)铜绿假单胞菌在秘鲁利马共表达一种VIM-2金属β-内酰胺酶、OXA-1 β-内酰胺酶和GES-1广谱β-内酰胺酶。
Pub Date : 2018-06-21 eCollection Date: 2018-07-01 DOI: 10.1099/jmmcr.0.005154
Paul Ríos, Claudio Rocha, William Castro, Maria Vidal, Enrique Canal, Manuela Bernal, Nathanael D Reynolds, Drake H Tilley, Mark P Simons

Introduction: Pseudomonas aeruginosa has the ability to acquire plasmids and other mobile genetic elements that confer resistance to antibiotics. Bacterial genes encoding different β-lactamases (bla), such as metallo-β-lactamases (MBLs) and extended-spectrum β-lactamases (ESBL), can confer resistance to multiple classes of β-lactam antibiotics.

Case presentation: An 83 year old female was admitted in 2012 to the Peruvian Naval Hospital, Centro Médico Naval 'Cirujano Mayor Santiago Távara' (CEMENA), in Lima, Peru. A midstream urine sample was collected and sent to the local CEMENA laboratory for routine urine culture. P. aeruginosa was isolated and initial antibiotic susceptibility testing showed it to be sensitive to imipenem. The clinicians started a course of meropenem, but the patient did not improve. After 5 days, a second urine culture was performed and a P. aeruginosa was isolated again, but this time the strain showed resistance to imipenem. The treatment course was changed to fosfomycin and the patient improved. Phenotypic and molecular laboratory testing to characterize the antibiotic resistance were performed, demonstrating the presence of both MBL and ESBL genes.

Conclusion: To our knowledge, this is the first report of a P. aeruginosa XDR clinical isolate that co-expresses an MBL (VIM-2), OXA-1 beta-lactamase and the ESBL (GES-1) in Peru. It is also the first report of a VIM carbapenemase in Peru.

铜绿假单胞菌有能力获得质粒和其他可移动的遗传元素,赋予抗生素耐药性。细菌基因编码不同的β-内酰胺酶(bla),如金属β-内酰胺酶(MBLs)和广谱β-内酰胺酶(ESBL),可赋予对多种β-内酰胺类抗生素的耐药性。病例介绍:一名83岁女性于2012年入住秘鲁利马的秘鲁海军医院(Cirujano Mayor Santiago Távara)。采集中游尿液样本,送往当地CEMENA实验室进行常规尿液培养。分离得到铜绿假单胞菌,初步药敏试验显示其对亚胺培南敏感。临床医生开始了一个疗程的美罗培南,但病人并没有好转。5天后,进行第二次尿液培养,再次分离出铜绿假单胞菌,但这次菌株对亚胺培南表现出耐药性。改用磷霉素治疗,病情好转。进行了表征抗生素耐药性的表型和分子实验室检测,证明存在MBL和ESBL基因。结论:据我们所知,这是秘鲁首次报道铜绿假单胞菌XDR临床分离株共表达MBL (VIM-2)、OXA-1 β -内酰胺酶和ESBL (GES-1)。这也是秘鲁首次报道VIM碳青霉烯酶。
{"title":"Extensively drug-resistant (XDR) <i>Pseudomonas aeruginosa</i> identified in Lima, Peru co-expressing a VIM-2 metallo-β-lactamase, OXA-1 β-lactamase and GES-1 extended-spectrum β-lactamase.","authors":"Paul Ríos,&nbsp;Claudio Rocha,&nbsp;William Castro,&nbsp;Maria Vidal,&nbsp;Enrique Canal,&nbsp;Manuela Bernal,&nbsp;Nathanael D Reynolds,&nbsp;Drake H Tilley,&nbsp;Mark P Simons","doi":"10.1099/jmmcr.0.005154","DOIUrl":"https://doi.org/10.1099/jmmcr.0.005154","url":null,"abstract":"<p><strong>Introduction: </strong><i>Pseudomonas aeruginosa</i> has the ability to acquire plasmids and other mobile genetic elements that confer resistance to antibiotics. Bacterial genes encoding different β-lactamases (bla), such as metallo-β-lactamases (MBLs) and extended-spectrum β-lactamases (ESBL), can confer resistance to multiple classes of β-lactam antibiotics.</p><p><strong>Case presentation: </strong>An 83 year old female was admitted in 2012 to the Peruvian Naval Hospital, Centro Médico Naval 'Cirujano Mayor Santiago Távara' (CEMENA), in Lima, Peru. A midstream urine sample was collected and sent to the local CEMENA laboratory for routine urine culture. <i>P. aeruginosa</i> was isolated and initial antibiotic susceptibility testing showed it to be sensitive to imipenem. The clinicians started a course of meropenem, but the patient did not improve. After 5 days, a second urine culture was performed and a <i>P. aeruginosa</i> was isolated again, but this time the strain showed resistance to imipenem. The treatment course was changed to fosfomycin and the patient improved. Phenotypic and molecular laboratory testing to characterize the antibiotic resistance were performed, demonstrating the presence of both MBL and ESBL genes.</p><p><strong>Conclusion: </strong>To our knowledge, this is the first report of a <i>P. aeruginosa</i> XDR clinical isolate that co-expresses an MBL (VIM-2), OXA-1 beta-lactamase and the ESBL (GES-1) in Peru. It is also the first report of a VIM carbapenemase in Peru.</p>","PeriodicalId":73559,"journal":{"name":"JMM case reports","volume":"5 7","pages":"e005154"},"PeriodicalIF":0.0,"publicationDate":"2018-06-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6159545/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"36546541","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: 9
期刊
JMM case reports
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