{"title":"Febrile Pancytopenia and Hemophagocytosis From Disseminated Histoplasmosis in HIV/AIDS Patients: Two Cases and a Review of Combined Antifungal and Steroid Therapy.","authors":"Chinelo Animalu, Nupur Singh, Kenneth Cory Guice, Kase Maner","doi":"10.1155/crdi/2623694","DOIUrl":"https://doi.org/10.1155/crdi/2623694","url":null,"abstract":"<p><p>Hemophagocytosis is a clinical condition characterized by the engulfment of bone marrow cellular elements, including erythrocytes, leukocytes, platelets, and their precursors, by activated macrophages. It has been associated with several infectious organisms, including the Epstein-Barr virus (EBV) and histoplasmosis. Human immunodeficiency virus (HIV) has been known to trigger hemophagocytosis in the presence or absence of other infections. Disseminated histoplasmosis is a common opportunistic infection in advanced patients with acquired immunodeficiency syndrome (AIDS) in endemic areas; however, the best treatment for histoplasmosis associated with hemophagocytosis is uncertain. This article presents two cases of patients with AIDS secondary to uncontrolled HIV who were admitted with fever, malaise, low CD4 + counts, and a history of noncompliance with antiretroviral therapy (ART). Both patients had pancytopenia, markedly elevated serum ferritin, and elevated liver transaminases. The diagnosis of histoplasmosis was confirmed by positive fungal blood cultures, buffy coat smears showing intracellular fungal organisms, and positive urine <i>Histoplasma</i> antigen. Bone marrow biopsies revealed <i>Histoplasma capsulatum</i> (<i>H. capsulatum</i>) in Grocott methenamine silver (GMS) stains and fungal cultures, histiocytes with intracellular red blood cells, and precursors of granulocytes, consistent with hemophagocytosis. Both patients received amphotericin B but remained febrile and pancytopenic, eventually requiring corticosteroid therapy. We present our experience with these patients and discuss the management of hemophagocytosis in patients with AIDS with disseminated histoplasmosis. We also completed a literature review and created a list of all known cases of disseminated histoplasmosis complicated by HIV/AIDS and hemophagocytosis and listed previous treatments.</p>","PeriodicalId":9608,"journal":{"name":"Case Reports in Infectious Diseases","volume":"2025 ","pages":"2623694"},"PeriodicalIF":1.0,"publicationDate":"2025-04-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12021483/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143964078","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}
{"title":"The Pathogenic Potential of <i>Slackia exigua</i>: A Case Study of Bacteremia in a Patient With Oral Infection.","authors":"Gang Zhou, Lisa Cornelius, Dhammika H Navarathna","doi":"10.1155/crdi/2079663","DOIUrl":"https://doi.org/10.1155/crdi/2079663","url":null,"abstract":"<p><p><i>Slackia exigua</i> is an anaerobic, Gram-positive, nonspore-forming bacterium that is typically part of the normal oral microbiota. It is generally considered biochemically inert and is often dismissed as a nonpathogenic contaminant in clinical cultures, particularly in respiratory samples. However, in this case study, we report a rare instance of <i>S</i>. <i>exigua</i> bacteremia in a patient with multiple medical comorbidities who was hospitalized after reporting to Emergency Department due to fatigue and right ear pain. The patient subsequently developed signs of persistent symptoms of septicemia, prompting an extensive investigation. Blood cultures identified <i>S</i>. <i>exigua</i> as the causative agent. This case underscores the importance of thorough culture workup and clinical correlation, especially in immunocompromised patients and patients with multiple medical comorbidities. Comprehensive dental care and the administration of targeted antibiotic therapy resulted in the patient's full recovery. This report highlights the potential pathogenic role of <i>S</i>. <i>exigua</i> in certain clinical scenarios and emphasizes the need for awareness of its possible implications in systemic infections.</p>","PeriodicalId":9608,"journal":{"name":"Case Reports in Infectious Diseases","volume":"2025 ","pages":"2079663"},"PeriodicalIF":1.0,"publicationDate":"2025-04-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12014268/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144062457","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}
Seth Krueger, Michael Carcella, Caroline Dillon, Darrell McBride
{"title":"<i>Salmonella</i> Endocarditis: Rare Bacteremia Causing Mural Infective Endocarditis.","authors":"Seth Krueger, Michael Carcella, Caroline Dillon, Darrell McBride","doi":"10.1155/crdi/3830316","DOIUrl":"https://doi.org/10.1155/crdi/3830316","url":null,"abstract":"<p><p>Current guidelines do not recommend routine cardiac imaging in patients with gram-negative bacteremia, as gram-negative infective endocarditis is rare. Nongastrointestinal <i>Salmonella</i> infections causing endocarditis are even more uncommon, especially in the developed world. We present the case of a 60-year-old female with <i>Salmonella</i> bacteremia, ultimately found to have a right atrial mural endocarditis involving an implantable cardioverter-defibrillator and an indwelling venous catheter. The vegetation and indwelling devices were removed from the operating room due to the high concern of embolization if performed percutaneously, and she completed 6 weeks of antibiotic therapy. Both indwelling devices were later replaced once treatment was completed, and there was no evidence of recurrence at the 8-month follow-up. This case proves that in those with cardiac implantable electronic devices and other indwelling devices which enter the heart, who are found to have atypical bacteremia, may benefit from cardiac imaging as a part of their workup.</p>","PeriodicalId":9608,"journal":{"name":"Case Reports in Infectious Diseases","volume":"2025 ","pages":"3830316"},"PeriodicalIF":1.0,"publicationDate":"2025-04-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12011455/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143980457","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}
Haolei Liu, Hailu Jiao, Jun Feng, Hui Gao, Shikui Wu
{"title":"A Case Report of COVID-19 With Tracheobronchial Aspergillosis.","authors":"Haolei Liu, Hailu Jiao, Jun Feng, Hui Gao, Shikui Wu","doi":"10.1155/crdi/4627040","DOIUrl":"https://doi.org/10.1155/crdi/4627040","url":null,"abstract":"<p><p>The concurrence of COVID-19 and tracheobronchial aspergillosis (TBA) is rarely documented in clinical practice. This report presents a case of TBA in a patient diagnosed with COVID-19 prior to the administration of immunosuppressive agents. This case underscores the necessity of considering fungal infections in patients with COVID-19, even during the early stages of the disease. The combination of timely bronchoscopy, antiviral therapy, and antifungal treatment resulted in favorable therapeutic outcomes for the patient.</p>","PeriodicalId":9608,"journal":{"name":"Case Reports in Infectious Diseases","volume":"2025 ","pages":"4627040"},"PeriodicalIF":1.0,"publicationDate":"2025-04-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12009674/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143962117","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}
Susan Alessandra Rodriguez Gonzalez, Linda Banegas, Edwin Mauricio Cantillano Quintero, Jesús Domínguez-Rojas
{"title":"Severe Dengue With Hyperinflammatory State and Associated Acute Pancreatitis.","authors":"Susan Alessandra Rodriguez Gonzalez, Linda Banegas, Edwin Mauricio Cantillano Quintero, Jesús Domínguez-Rojas","doi":"10.1155/crdi/8029446","DOIUrl":"https://doi.org/10.1155/crdi/8029446","url":null,"abstract":"<p><p>The increase in the incidence of dengue cases in the region has led to the identification of multiple complications associated with the disease. The present study presents the case of an adolescent girl with severe dengue in a hyperinflammatory state, who presented mild acute pancreatitis. This complication, although infrequent, can be harmful. In the clinical case presented, the patient presented severe dengue, according to the clinical diagnosis. In addition, polyserositis was observed, with positive NS1, IgG, and IgM, elevated transaminases above 1000 U/L and elevated levels of inflammatory markers such as ferritin, LDH, procalcitonin, and decreased fibrinogen. The diagnosis of acute pancreatitis was established based on two main criteria: elevated serum lipase/amylase and imaging studies. The patient did not experience significant abdominal pain; however, she manifested intense and persistent nausea for a period of 3 days. Despite presenting no other risk factors for acute pancreatitis, the patient was suffering from an infectious process. Treatment consisted of a complete 24-h fast and adequate hydration, which resulted in a progressive improvement in the patient's condition.</p>","PeriodicalId":9608,"journal":{"name":"Case Reports in Infectious Diseases","volume":"2025 ","pages":"8029446"},"PeriodicalIF":1.0,"publicationDate":"2025-04-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12009173/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143968200","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}
Lisle Blackbourn, Elisa Yoo, Michael D Lunt, Umair Hamid
{"title":"Acute Myelopathy as Initial Presentation of Disseminated Histoplasmosis: A Case Report.","authors":"Lisle Blackbourn, Elisa Yoo, Michael D Lunt, Umair Hamid","doi":"10.1155/crdi/1124517","DOIUrl":"https://doi.org/10.1155/crdi/1124517","url":null,"abstract":"<p><p>Histoplasmosis is a fungal infection caused by the fungus <i>Histoplasma capsulatum</i> that can rarely present with central nervous system (CNS) manifestations that include meningitis, encephalitis, focal brain or spinal cord lesions, and stroke syndromes. Because of this variation from patient to patient, CNS histoplasmosis is a difficult clinical diagnosis to make, which can be further hindered by no highly sensitive diagnostic testing available. Here, we present a unique case of a 46-year-old male immunocompromised due to type 1 diabetes mellitus with disseminated histoplasmosis as an acute presentation of myelopathy. Patient had left leg weakness for a few days prior to presentation and a neurological exam remarkable for signs of acute thoracic myelopathy, specifically concerning for Brown-Séquard syndrome. MRI imaging demonstrated an enhancing thoracic spinal cord lesion along with multiple cerebral enhancing lesions, bilateral adrenal masses, and innumerable pulmonary nodules. Biopsy results demonstrated yeast forms consistent with Histoplasma species.</p>","PeriodicalId":9608,"journal":{"name":"Case Reports in Infectious Diseases","volume":"2025 ","pages":"1124517"},"PeriodicalIF":1.0,"publicationDate":"2025-04-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11986188/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143973580","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}
{"title":"Cefepime-Induced Encephalopathy in a Patient With Uncompromised Renal Function: A Case Report.","authors":"Aayusha Dhakal, Ozone Gautam","doi":"10.1155/crdi/6650287","DOIUrl":"10.1155/crdi/6650287","url":null,"abstract":"<p><p>Cefepime, a fourth-generation cephalosporin, is widely used in the treatment of infections caused by resistant Gram-negative bacteria especially <i>Pseudomonas aeruginosa</i>, or in severe infections, septic shock, and infections in immunocompromised patients. As it crosses the blood-brain barrier, it can cause neurotoxicity which has mostly been reported in patients with impaired renal function. Patients can present with drowsiness, confusion, delirium, agitation, stupor, or coma, and sometimes with generalized myoclonus and seizures within two to six days after starting the antibiotic. This is a rare case report where a patient with intact kidney function presented with confusion and incoherence. After excluding the possible causes for encephalopathy, cefepime-induced encephalopathy was diagnosed and the patient gradually improved after discontinuing the medication. This case is an unusual presentation of symptoms in a patient with normal kidney function, which necessitates further studies to establish other potential risk factors of cefepime-induced neurotoxicity.</p>","PeriodicalId":9608,"journal":{"name":"Case Reports in Infectious Diseases","volume":"2025 ","pages":"6650287"},"PeriodicalIF":1.0,"publicationDate":"2025-03-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11972131/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143794683","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}
{"title":"Antibiotic-Resistant <i>Shigella sonnei</i> Bacteremia in an Immunocompetent Postgastric Bypass Patient Without Typical Risk Factors.","authors":"Alejandra Gutierrez, Shovendra Gautam","doi":"10.1155/crdi/9910105","DOIUrl":"10.1155/crdi/9910105","url":null,"abstract":"<p><p><i>Shigella</i> bacteremia, though rare, is a serious condition that highlights the importance of recognizing potential complications in patients with <i>Shigella</i> infections. In this paper, we present a case of <i>Shigella</i> bacteremia in a 53-year-old female s/p a Roux-en-Y gastric bypass revision four months prior, presenting with acute onset of nausea, vomiting, and persistent, explosive, watery diarrhea which started one day after she consumed pork chops and ground beef. Initial laboratory tests indicated leukocytosis and hypokalemia. Human immunodeficiency virus (HIV), rapid plasma regain (RPR), and Hepatitis C were nonreactive. A computed tomography (CT) scan of the abdomen and pelvis showed no intestinal wall thickening or any other acute abnormalities. Blood cultures identified a <i>Shigella sonnei</i> infection that was resistant to multiple antibiotics. She was treated with intravenous meropenem. <i>Shigella</i> bacteremia is a rare complication of <i>Shigella</i> infection and requires thorough investigation to identify potential underlying factors. Antibiotic susceptibilities should also be assessed, given the increasing resistance of <i>Shigella</i> strains to previously effective treatments.</p>","PeriodicalId":9608,"journal":{"name":"Case Reports in Infectious Diseases","volume":"2025 ","pages":"9910105"},"PeriodicalIF":1.0,"publicationDate":"2025-03-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11968168/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143779318","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}
{"title":"An Imported Case of Gigantic Amoebic Liver Abscess in a 24-Year-Old Woman in Singapore.","authors":"Edwin Chong Yu Sng, Jean-Marc Chavatte","doi":"10.1155/crdi/6230349","DOIUrl":"10.1155/crdi/6230349","url":null,"abstract":"<p><p>A liver abscess can be due to several different microbiological aetiologies. While pyogenic liver abscess is most frequently encountered, amoebic liver abscess and hydatid cyst caused by the parasites, <i>Entamoeba histolytica</i> and <i>Echinococcus granulosus,</i> respectively, should be considered whenever there is epidemiological exposure. As parasitic infections are now rarely seen in clinical practice in developed countries with improvement in sanitation, lack of clinical experience in managing amoebic liver abscesses and overlapping clinical and imaging features between amoebic and pyogenic liver abscesses may lead to delay in diagnosis. In particular, although amoebic liver abscesses respond well to treatment if diagnosed early, they can progress and rupture with high mortality if treatment is delayed. Hence, early diagnosis and prompt initiation of antimicrobials are crucial to prevent complications and death. This case report highlights a case of a very large 21 cm ALA in a young lady to illustrate the challenges faced during diagnostic evaluation.</p>","PeriodicalId":9608,"journal":{"name":"Case Reports in Infectious Diseases","volume":"2025 ","pages":"6230349"},"PeriodicalIF":1.0,"publicationDate":"2025-03-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11949589/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143728726","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}
Kevin Andrew Smith, Alejandra Méndez, Lindsey J Reese
{"title":"A Man Living in the Wilderness Presents With a Unique Case of <i>Erysipelothrix rhusiopathiae</i> Causing Primary CNS Infection.","authors":"Kevin Andrew Smith, Alejandra Méndez, Lindsey J Reese","doi":"10.1155/crdi/6625621","DOIUrl":"10.1155/crdi/6625621","url":null,"abstract":"<p><p>We report the first published case of <i>Erysipelothrix rhusiopathiae</i> causing subdural empyema. This 66-year-old male patient had relevant exposure history including living in a tent in the woods and having direct contact with wildlife. His main symptom which triggered his presentation was diplopia with exam findings consistent with a left partial oculomotor nerve palsy. Initial attempts at less invasive source control via burr holes alone failed. He was treated successfully with craniectomy and aqueous penicillin G with a duration of 6 weeks following surgery. CNS infection as the primary manifestation of <i>Erysipelothrix rhusiopathiae</i> has been reported in only one other case based on our review of the literature. This pathogen demonstrates an ability to manifest infection in many ways and remains susceptible to narrow spectrum beta-lactams.</p>","PeriodicalId":9608,"journal":{"name":"Case Reports in Infectious Diseases","volume":"2025 ","pages":"6625621"},"PeriodicalIF":1.0,"publicationDate":"2025-03-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11944679/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143717985","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}