IDCasesPub Date : 2025-01-01DOI: 10.1016/j.idcr.2025.e02207
Mikiyas G. Teferi , Abel K. Gulma , Meron T. Akalu , Getaw W. Hassen , Elias M. Gashaw , Nahom D. Gerer
{"title":"Mumps-associated hepatitis: A rare clinical presentation","authors":"Mikiyas G. Teferi , Abel K. Gulma , Meron T. Akalu , Getaw W. Hassen , Elias M. Gashaw , Nahom D. Gerer","doi":"10.1016/j.idcr.2025.e02207","DOIUrl":"10.1016/j.idcr.2025.e02207","url":null,"abstract":"<div><h3>Introduction</h3><div>Mumps is a viral infection that principally affects the salivary glands, but it results in a range of complications, including orchitis, pancreatitis, and meningoencephalitis. Hepatic involvement is exceedingly rare and underreported in adults. Here, we present a peculiar case of mumps-associated hepatitis, highlighting its diagnostic challenges, clinical course, and management.</div></div><div><h3>Case presentation</h3><div>An unvaccinated 20-year-old male presented with a two-week history of fever, malaise, and bilateral parotid gland swelling, along with nausea, anorexia, and right upper quadrant discomfort. Tender parotid gland enlargement, scleral icterus, and bilateral testicular tenderness were noted on examination. The laboratory results revealed that the liver enzymes were significantly high, with a positive mumps virus IgM serology test; the following conditions were excluded: hepatitis A, B, C, Epstein–Barr, and cytomegalovirus. The patient was treated conservatively through hydration maintenance, pain relief, and rest. Consistent with a self-limiting course of mumps associated with hepatitis, liver functions normalized over four weeks.</div></div><div><h3>Discussion</h3><div>Mumps virus is an RNA paramyxovirus that affects glandular tissues. Although rare, case reports suggest that transient hepatitis can result from direct viral invasion or immune-mediated injury. The diagnosis requires high clinical suspicion, as symptoms overlap with other causes of viral hepatitis. The main treatment focuses on providing constant supportive care, which is usually sufficient, and the prognosis tends to be favorable.</div></div><div><h3>Conclusion</h3><div>Hepatitis is a rare but possible complication of mumps, especially in patients who have elevated liver enzymes. This case serves as a reminder that all healthcare professionals must be vigilant in atypical presentations of mumps to guarantee appropriate treatment and avoid unnecessary tests.</div></div>","PeriodicalId":47045,"journal":{"name":"IDCases","volume":"40 ","pages":"Article e02207"},"PeriodicalIF":1.1,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143697277","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}
IDCasesPub Date : 2025-01-01DOI: 10.1016/j.idcr.2024.e02120
Oviya Selvam , Yogindher Singh R. , M.D. Gowthaman , Manobalan K. , K. Subashree
{"title":"Mycotic cyst: Case report","authors":"Oviya Selvam , Yogindher Singh R. , M.D. Gowthaman , Manobalan K. , K. Subashree","doi":"10.1016/j.idcr.2024.e02120","DOIUrl":"10.1016/j.idcr.2024.e02120","url":null,"abstract":"<div><div>Phaeohyphomycotic cyst is a common subcutaneous form of phaeohyphomycosis in which patients can present with subcutaneous plaques, nodules, etc., It is an infrequent presentation and is most reported in immunocompromised individuals. Diagnosis is confirmed by histopathological and mycological demonstration of the organism. The treatment is by surgical excision with systemic antifungals. We report a rare case of asymptomatic Mycotic cyst in an immunocompetent individual.</div></div>","PeriodicalId":47045,"journal":{"name":"IDCases","volume":"39 ","pages":"Article e02120"},"PeriodicalIF":1.1,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11697273/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142933008","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}
IDCasesPub Date : 2025-01-01DOI: 10.1016/j.idcr.2024.e02132
Biruk Amare, Andrew Mangano, Moumita Sarker, Sagun Adhikari
{"title":"Disseminated Mycobacterium Chelonae infection in an immunocompromised adult: An uncommon etiology of skin infection","authors":"Biruk Amare, Andrew Mangano, Moumita Sarker, Sagun Adhikari","doi":"10.1016/j.idcr.2024.e02132","DOIUrl":"10.1016/j.idcr.2024.e02132","url":null,"abstract":"<div><div><em>Mycobacterium Chelonae</em> is a rapidly growing nontuberculous mycobacterium (NTM) that is ubiquitous in the environment and is associated with skin and soft tissue infections (1). Because <em>Mycobacterium Chelonae</em> is an opportunistic infection, it can present as skin abscess, cellulitis, osteomyelitis, pulmonary infection or disseminated infections, particularly in individuals with compromised immune systems or underlying lung conditions such as cystic fibrosis or bronchiectasis. <em>M.Chelonae</em> is one of the most pathogenic rapidly growing mycobacteria (RGM). Diagnosing RGM and distinguishing it from Mycobacterium tuberculosis is important because public health tracking and management is different in these two organisms. Antibiotic susceptibility testing can also provide valuable clues to the species identification of RGM as each species has a specific in vitro antibiotic susceptibility pattern (2). Although incidence of <em>M. Chelonae</em> is increasing, these infections often remain misdiagnosed. This case report discusses the clinical presentation, diagnostic challenges, the rationale for early empiric treatment, and therapeutic options for <em>M. Chelonae</em> infection, emphasizing the importance of timely intervention in immunocompromised individuals.</div></div>","PeriodicalId":47045,"journal":{"name":"IDCases","volume":"39 ","pages":"Article e02132"},"PeriodicalIF":1.1,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11732071/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142984910","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":"Scrub typhus associated with reactive arthritis: A case report and literature review","authors":"Shinya Yamanaka , Kazuhiro Ishikawa , Miyako Kon , Junko Aoki , Kunimichi Saeki , Junta Tanaka","doi":"10.1016/j.idcr.2024.e02143","DOIUrl":"10.1016/j.idcr.2024.e02143","url":null,"abstract":"<div><div>Scrub typhus (tsutsugamushi disease) is an acute febrile illness caused by <em>Orientia tsutsugamushi</em>, often found in Asia and Oceania. The presence of an eschar, characterized by a crust, is a key diagnostic finding. Many symptoms of this disease are already known, however reactive arthritis following scrub typhus is very rare. Here, we present a case of 79-year-old man who was referred to our hospital because of continuous fever and left shoulder pain. We found 4-fold rise in <em>Orientia tsutugamushi</em>-specific IgG titer using paired serum samples and <em>Orientia</em> sp. genes by real-time PCR from a crust of right thigh. And the left shoulder joint image was consistent with aseptic arthritis; thus we diagnosed as scrub typhus with reactive arthritis. This case highlights the importance of recognizing reactive arthritis as a symptom of scrub typhus. In this report, we also review published cases of reactive arthritis associated with scrub typhus, and we suppose that this arthritis related to this infection may recover after antibiotic use and have a good prognosis. Physicians' awareness of newly appeared arthritis may contribute to facilitate early diagnosis, and may improve the course of such patients.</div></div>","PeriodicalId":47045,"journal":{"name":"IDCases","volume":"39 ","pages":"Article e02143"},"PeriodicalIF":1.1,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11753909/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143029698","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}
IDCasesPub Date : 2025-01-01DOI: 10.1016/j.idcr.2024.e02141
Mohamed Adam Mahamud , Claude M. Muvunyi , Ayman Ahmed , Emmanuel Edwar Siddig
{"title":"Comprehensive management of actinomycetoma in a young male: A case report from Somalia","authors":"Mohamed Adam Mahamud , Claude M. Muvunyi , Ayman Ahmed , Emmanuel Edwar Siddig","doi":"10.1016/j.idcr.2024.e02141","DOIUrl":"10.1016/j.idcr.2024.e02141","url":null,"abstract":"<div><div>Mycetoma is a neglected tropical disease that predominantly affects individuals in low socioeconomic strata, primarily in tropical and subtropical regions. This case report describes a 20-year-old male student from Bahdo City, Somalia, who presented with a persistent cervical mass following a history of trauma. The patient exhibited vital signs within normal limits, and imaging studies, including ultrasound and computed tomography, revealed well-defined cystic masses. A Fine Needle Aspiration cytology confirmed the diagnosis of actinomycetoma by revealing sheets of neutrophils, multinucleated giant cells, and branching filamentous bacteria structures. The patient was treated with co-trimoxazole and amikacin, resulting in significant improvement after three months, highlighting the critical role of early diagnosis and appropriate medical management in enhancing patient outcomes. This report emphasizes the importance of thorough clinical evaluation and the use of cytological methods, particularly in resource-limited settings, to expedite the diagnosis and treatment of actinomycetoma.</div></div>","PeriodicalId":47045,"journal":{"name":"IDCases","volume":"39 ","pages":"Article e02141"},"PeriodicalIF":1.1,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11758836/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143048114","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}
IDCasesPub Date : 2025-01-01DOI: 10.1016/j.idcr.2025.e02180
Ujjwayini Ray , Soma Dutta, Arpita Sutradhar
{"title":"Histoplasmosis – More common than we realize","authors":"Ujjwayini Ray , Soma Dutta, Arpita Sutradhar","doi":"10.1016/j.idcr.2025.e02180","DOIUrl":"10.1016/j.idcr.2025.e02180","url":null,"abstract":"<div><div>Histoplasmosis is primarily associated with immunocompromised individuals; however, its presentation in immunocompetent patients is increasingly recognized. This series of 5 cases from eastern India, a potential Histoplasmosis hotspot, describes five immunocompetent individuals with the disease. It emphasizes the diverse clinical spectrum of Histoplasmosis, often mimicking other conditions, thereby complicating diagnosis. Four patients presented with adrenal masses, emphasizing the importance of considering histoplasmosis in the differential diagnosis of adrenal enlargement. One patient developed hemophagocytic lymphohistiocytosis (HLH), underscoring the severe complications associated with disseminated histoplasmosis. Additionally, one patient exhibited localized disease, demonstrating the variable clinical presentations of this infection. Our findings emphasize the need for heightened clinical suspicion of histoplasmosis in patients with adrenal masses or unexplained fever, even in immunocompetent individuals in a relevant epidemiological setting. Early diagnosis and appropriate antifungal therapy are crucial for optimal outcomes.</div></div>","PeriodicalId":47045,"journal":{"name":"IDCases","volume":"39 ","pages":"Article e02180"},"PeriodicalIF":1.1,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143396273","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}
IDCasesPub Date : 2025-01-01DOI: 10.1016/j.idcr.2025.e02200
Saori Ikeda , Noriyo Yanagawa
{"title":"Pneumocystis pneumonia with multiple nodules on computed tomography","authors":"Saori Ikeda , Noriyo Yanagawa","doi":"10.1016/j.idcr.2025.e02200","DOIUrl":"10.1016/j.idcr.2025.e02200","url":null,"abstract":"<div><div>As is well known to us that pneumocystis pneumonia (PCP) is one of opportunistic infections, there are not so many cases that computed tomography (CT) reveals multiple nodules, especially in non-HIV PCP. In this case, a 47-year-old female with acute myeloid leukemia has developed PCP. Two years prior to this presentation, she had undergone hematopoietic stem cell transplantation (HSCT) and had not experienced any recurrence. CT showed multiple nodules and segmental consolidation with subpleural sparing. Considering that it is refractory to levofloxacin, that β-d glucan is elevated, that PCP PCR was positive in the analysis of bronchial lavage fluid, and that other viral and fungal infections are unlikely, we clinically diagnosed as PCP. Although multiple nodules were thought to be atypical for PCP, CT performed 12 days after starting trimethoprim/sulfamethoxazole to confirm radiological efficacy demonstrated resolution of the nodules as well as consolidation. The significance of the present report lies in the fact that PCP should be kept in mind in the differential diagnosis when there are multiple nodules detected on CT in post-HSCT patients.</div></div>","PeriodicalId":47045,"journal":{"name":"IDCases","volume":"40 ","pages":"Article e02200"},"PeriodicalIF":1.1,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143683208","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":"Meningitis caused by Streptococcus pyogenes triggered by malignant otitis externa: A case report","authors":"Ayako Shirai , Daisuke Ono , Kazuyuki Mimura , Kei Yamamoto , Takayuki Kawamura , Yujin Nozaki , Sunao Tanaka , Masaomi Yamamoto , Hideaki Ohno , Kunihisa Tsukada , Hideaki Oka","doi":"10.1016/j.idcr.2025.e02214","DOIUrl":"10.1016/j.idcr.2025.e02214","url":null,"abstract":"<div><div>A previously healthy 58-year-old male initially presented to a healthcare facility with otorrhea in his left ear, accompanied by a scab in both the auricle and ear canal, with a lesion protruding from the left cavity and oozing discharge (day 0). The following day, the patient was transferred to our facility with fever and altered consciousness. Imaging studies, including computed tomography and magnetic resonance imaging, revealed a soft tissue mass in the left maxillary, ethmoid and sphenoid sinuses, and diffuse pus within the subdural space over the bilateral frontoparietal regions. Cerebrospinal fluid (CSF) analysis showed elevated opening pressure, increased white blood cell count, predominance of polymorphonuclear leukocytes, elevated protein levels, and reduced glucose levels compared to the serum. <em>Streptococcus pyogenes</em> was identified in ear discharge, CSF, and blood cultures using matrix-assisted laser desorption ionization time-of-flight mass spectrometry. The presence of a papilloma in the left nasal cavity suggested that malignant otitis externa (MOE) served as the entry point for infection, leading to meningitis. The patient was treated with a combination of ceftriaxone and vancomycin, followed by ceftriaxone and cefotaxime, surgical resection of the tumor, and local debridement for infection control. To date, this is the first reported case of <em>S. pyogenes</em>-induced meningitis secondary to MOE. Although rare, the detection of <em>S. pyogenes</em> in otitis externa emphasizes the necessity of comprehensive evaluation of ear pathology to enable effectively source control as well as manage related infections and complications.</div></div>","PeriodicalId":47045,"journal":{"name":"IDCases","volume":"40 ","pages":"Article e02214"},"PeriodicalIF":1.1,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143747977","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}
IDCasesPub Date : 2025-01-01DOI: 10.1016/j.idcr.2025.e02148
Bingkun Li , Tiantian Li , Qian Lu , Dong Liang , Cunwei Cao
{"title":"Severe disseminated Talaromyces marneffei infection in idiopathic CD4 lymphopenia","authors":"Bingkun Li , Tiantian Li , Qian Lu , Dong Liang , Cunwei Cao","doi":"10.1016/j.idcr.2025.e02148","DOIUrl":"10.1016/j.idcr.2025.e02148","url":null,"abstract":"<div><div>Idiopathic CD4 lymphopenia (ICL) is a rare non–HIV-related syndrome, characterized by a reduced CD4 T-cell count and a predisposition to various opportunistic infections. However, <em>Talaromyces marneffei</em> (TM) infection has rarely been reported in ICL patients. Here, we report a previously healthy 48-year-old male patient who presented with fever, headache, fatigue, vomiting, and poor appetite. Mycological cultures from blood, bone marrow, liver and spleen were positive for TM. The immunodeficiency evaluation revealed a CD4 T-lymphocyte count of 32 cells/μL, with a negative HIV test. After receiving co-treatment with amphotericin B and voriconazole, the patient showed clinical improvement. At 1-year follow-up, the CD4 T-cell count remained decreased despite the complete resolution of symptoms. The appearance of disseminated TM infection in non-HIV patients should prompt an investigation for the possibility of ICL, as the clinical manifestations can be severe.</div></div>","PeriodicalId":47045,"journal":{"name":"IDCases","volume":"39 ","pages":"Article e02148"},"PeriodicalIF":1.1,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11763228/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143048156","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}
IDCasesPub Date : 2025-01-01DOI: 10.1016/j.idcr.2025.e02167
Xin Xiang , Jian Zheng , Cheng-Wei Ma , Lei Ruan, Jing-Zheng Zhuang, Qing-Chun Li
{"title":"Perforated colon cancer complicated by necrotizing soft tissue infection: A case report and literature review","authors":"Xin Xiang , Jian Zheng , Cheng-Wei Ma , Lei Ruan, Jing-Zheng Zhuang, Qing-Chun Li","doi":"10.1016/j.idcr.2025.e02167","DOIUrl":"10.1016/j.idcr.2025.e02167","url":null,"abstract":"<div><div>Necrotizing soft tissue infections (NSTIs) are rare but life-threatening complications of colorectal cancer, often overlooked during patient diagnosis and treatment. NSTIs progress rapidly, leading to significant tissue damage and elevated mortality rates. This report presents the case of a 71-year-old male who presented with abdominal pain and distention, later diagnosed with perforated colon cancer and NSTI of the left abdominal wall. Following admission, the patient developed septic shock and acute kidney injury. Emergency surgery was performed, including radical resection of the colon cancer, proximal colostomy, and extensive debridement of necrotic tissue. Postoperatively, Continuous Renal Replacement Therapy (CRRT) was used alongside standard treatments, contributing to a relatively rapid recovery. At the 30-month follow-up, no evidence of tumor recurrence was observed.</div></div>","PeriodicalId":47045,"journal":{"name":"IDCases","volume":"39 ","pages":"Article e02167"},"PeriodicalIF":1.1,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143157741","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}