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1.
Am J Med ; 134(2): e101-e108, 2021 02.
Article in English | MEDLINE | ID: mdl-33091391

ABSTRACT

BACKGROUND: The Centers for Disease Control and Prevention and New York State Department of Health recently identified the Capital District of New York (CDNY) as an emerging endemic area for blastomycosis. However, no clinical or epidemiological description of blastomycosis in the CDNY has been published. METHODS: We performed a retrospective analysis of blastomycosis cases at Albany Medical Center (AMC) and Albany Stratton Veterans Affairs Medical Center (VAMC) from January 1, 2000, through June 1, 2019. Patients were identified via an institution-approved informatics system at the hospital's microbiology laboratory. RESULTS: We identified 20 patients diagnosed with blastomycosis over the past 2 decades. There was a nearly 9-fold increase in the annual number of cases in 2016-2019 compared with 2000-2015. The majority of patients resided in the CDNY (90%), and 65% lived within the Mohawk River valley. Most cases (85%) were assumed to be malignancies or non-mycotic infections prior to diagnosis, with median time between presentation and diagnosis of 53 days. CONCLUSIONS: Our data support recent reports that blastomycosis is an emerging disease in the CDNY. Most patients were misdiagnosed as malignancy or non-mycotic infection, which led to treatment delays.


Subject(s)
Blastomyces , Blastomycosis/epidemiology , Communicable Diseases, Emerging/epidemiology , Endemic Diseases/statistics & numerical data , Adolescent , Adult , Aged , Blastomycosis/microbiology , Female , Humans , Male , Middle Aged , New York/epidemiology , Young Adult
2.
J Hand Surg Am ; 42(11): 932.e1-932.e6, 2017 Nov.
Article in English | MEDLINE | ID: mdl-28666674

ABSTRACT

Isolated blastomycosis hand infections are extremely rare, and are often clinically unsuspected, leading to delays in clinical diagnosis. Conclusive diagnosis often necessitates fungal cultures and histopathological demonstration of budding yeasts in tissues. In this report, we describe the rare occurrence of isolated blastomycotic hand infection, without any other organ involvement, in a 42-year-old male patient. Analyzing tissue specimens with frozen section has been shown in the past to demonstrate granulomatous inflammation and yeast forms of the organism; however, as demonstrated in this patient, the presence of pseudoepitheliomatous cells may deceptively appear as malignant, causing substantial concern and anxiety. Definitive diagnosis often necessitates fungal culture and histopathological examination with special fungal stains including polymerase chain reaction for speciation.


Subject(s)
Blastomycosis/diagnosis , Blastomycosis/therapy , Multimodal Imaging/methods , Osteomyelitis/diagnosis , Osteomyelitis/therapy , Adult , Antifungal Agents/administration & dosage , Biopsy, Needle , Combined Modality Therapy , Drainage/methods , Edema/diagnosis , Edema/etiology , Finger Joint/diagnostic imaging , Finger Joint/physiopathology , Follow-Up Studies , Hand/physiopathology , Humans , Immunohistochemistry , Magnetic Resonance Imaging/methods , Male , Osteomyelitis/microbiology , Positron-Emission Tomography/methods , Rare Diseases , Treatment Outcome
3.
Semin Respir Crit Care Med ; 32(6): 775-82, 2011 Dec.
Article in English | MEDLINE | ID: mdl-22167405

ABSTRACT

Pneumocystis (carinii) jiroveci pneumonia can occur in immunocompromised individuals, especially hematopoietic stem and solid organ transplant recipients and those receiving immunosuppressive agents, and is the most common opportunistic infection in persons with advanced human immunodeficiency virus (HIV) infection. The Pneumocystis genus was initially mistaken as a trypanosome and later as a protozoan. Genetic analysis identified the organism as a unicellular fungus. Pneumocystis jiroveci is the species responsible for human infections. A slow indolent time course with symptoms of pneumonia progressing over weeks to months is characteristic in HIV-infected patients. Fulminant respiratory failure associated with fever and dry cough is typical in non-HIV-infected patients. Definitive diagnosis relies on histopathological testing of sputum, induced or sampled by fiberoptic bronchoscopy with bronchoalveolar lavage. The first-line drug for treatment and prevention is trimethoprim-sulfamethoxazole.


Subject(s)
Pneumocystis carinii/pathogenicity , Pneumonia, Pneumocystis , Adrenal Cortex Hormones/therapeutic use , Anti-Infective Agents/therapeutic use , Chemoprevention , Humans , Immunocompromised Host , Pneumocystis carinii/cytology , Pneumocystis carinii/immunology , Pneumonia, Pneumocystis/complications , Pneumonia, Pneumocystis/diagnosis , Pneumonia, Pneumocystis/drug therapy , Pneumonia, Pneumocystis/epidemiology , Pneumonia, Pneumocystis/prevention & control
4.
Am J Infect Control ; 39(8): 697-700, 2011 Oct.
Article in English | MEDLINE | ID: mdl-21641085

ABSTRACT

BACKGROUND: Control measures were instituted in a neonatal intensive care unit (NICU) in Syracuse, New York, when a neonatologist became ill with mumps after returning from Africa. Two health care providers (HCPs) who worked with the neonatologist developed parotitis within 13 days of exposure. Outbreak control included furloughing the neonatologist and the 2 HCPs until after 5 days of the onset of parotitis, cohorting and isolating all exposed infants in the NICU, and implementing droplet precautions. All susceptible HCPs were immunized, and all HCPs were required to wear surgical masks when within 3 feet of patients. RESULTS: Five HCPs developed parotitis. The neonatologist and 2 of the HCPs were confirmed cases, and 2 other HCPs did not meet the case definition. Twenty-six HCPs who worked in other units of the hospital besides the NICU developed nonspecific signs and symptoms of illness. Of the 2,904 HCPs tested, 287 (10%) had negative antibody results, and 153 (8%) were age 40 years or older. Of the 287 HCPs with negative antibody titers, 200 (70%) received the mumps-measles-rubella vaccine in response to this effort. No cases of mumps were reported in exposed infants, children, or adult patients during the time of exposure. CONCLUSION: Infection control efforts, including vaccinating susceptible HCPs and instituting droplet precautions, might have prevented mumps infection in the NICU patients.


Subject(s)
Cross Infection/prevention & control , Disease Outbreaks/prevention & control , Health Personnel , Infant, Premature, Diseases/prevention & control , Infection Control/methods , Intensive Care Units, Neonatal , Mumps/prevention & control , Adult , Cross Infection/epidemiology , Cross Infection/transmission , Cross Infection/virology , Humans , Infant, Newborn , Infant, Premature , Infant, Premature, Diseases/epidemiology , Infant, Premature, Diseases/virology , Measles-Mumps-Rubella Vaccine/administration & dosage , Middle Aged , Mumps/diagnosis , Mumps/epidemiology , Mumps/transmission , Mumps virus/immunology , New York/epidemiology , Patient Isolation , Young Adult
6.
Am J Health Syst Pharm ; 61(12): 1235-41, 2004 Jun 15.
Article in English | MEDLINE | ID: mdl-15259752

ABSTRACT

PURPOSE: The epidemiology, virology, and transmission of West Nile virus (WNV) are reviewed, and the clinical features, diagnosis, and treatment of WNV infection are examined. SUMMARY: WNV infection is caused by a flavivirus transmitted from birds to humans through the bite of culicine mosquitoes. WNV was discovered in the blood of a febrile woman from Uganda's West Nile province in 1937. The first case of domestically acquired WNV infection was reported in the United States in 1999 in New York. Since then, WNV infection has spread rapidly across the United States, with 9306 confirmed cases and 210 deaths reported from 45 states in 2003. It is still not clear how WNV was introduced into North America. WNV is a small, single-stranded RNA virus and a member of the Japanese encephalitis virus antigenic complex. While most humans infected with WNV are asymptomatic, some may develop an influenza-like illness. Disease surveillance remains the cornerstone for the early recognition and control of WNV. We describe one case of WNV infection with an update on the disease. Strategies for the prevention and control of this infection are reviewed. CONCLUSION: There is no established treatment for WNV infection. Currently, prevention and control are the only measures that help decrease the morbidity and mortality associated with WNV infection. As the number of cases escalates and the geographic distribution of WNV infection widens, the epidemic will continue to pose a major challenge to clinicians in the coming years. There is an urgent need for more research on the pathogenesis and treatment of WNV infection.


Subject(s)
Culicidae , Insect Vectors , West Nile Fever , West Nile virus/pathogenicity , Animals , Communicable Disease Control , Culex/virology , Culicidae/virology , Ecology , Humans , Male , Middle Aged , United States/epidemiology , West Nile Fever/diagnosis , West Nile Fever/epidemiology , West Nile Fever/prevention & control , West Nile Fever/transmission
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