A 63-year-old immunocompromised male with a history of renal transplant and stage III large B-cell non-Hodgkin lymphoma undergoing rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP) therapy presented with fever and a disseminated pustular eruption. Initial laboratory values indicated septicemia. Differential diagnoses included Sweet's syndrome, septic emboli, and leukocytoclastic vasculitis. Punch biopsies and bacterial cultures confirmed disseminated methicillin-sensitive (MSSA) infection. Histopathology revealed intraepidermal vesiculopustules and bacterial cocci colonies in the superficial dermis, suggesting hematogenous spread. The patient's indwelling venous access port was identified as the infection source and removed. Treatment included antibiotics such as cefepime, vancomycin, fluconazole, and acyclovir, as well as filgrastim for neutropenia. Following port removal and a four-week course of ceftriaxone, the patient's condition improved. This case highlights the importance of clinicopathologic correlation in diagnosing and managing disseminated staphylococcal infections in immunocompromised patients. The rare presentation of vesiculopustular eruptions secondary to MSSA emphasizes the need for prompt identification and treatment to prevent severe complications. This report contributes to the limited literature on disseminated staphylococcal infections presenting as vesiculopustular eruptions in immunocompromised individuals.
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http://dx.doi.org/10.7759/cureus.67516 | DOI Listing |
Infect Drug Resist
September 2024
Department of Emergency, Third Affiliated Hospital of Wenzhou Medical University (Rui'an People's Hospital), Wenzhou, Zhejiang, People's Republic of China.
infection is readily disseminated, yet the multiple septic arthritis and extensive migratory skin and soft tissue infections it causes are uncommon and challenging to treat. The infection can be life-threatening, with a mortality rate of 15-31%. Early, targeted antibiotic therapy is critical to improve prognosis.
View Article and Find Full Text PDFCureus
August 2024
Dermatology, Texas Tech University Health Sciences Center, Lubbock, USA.
J Oral Biol Craniofac Res
September 2024
Oral Health Sciences Center, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Background: Early diagnosis of neonatal osteomyelitis is often challenging due to the rarity of such cases and here we are presenting 2 case reports to add to the existing deficient literature: A 15-day-old male infant presented with swelling and pus discharge from the anterior region of the mandible. Repeated culture and sensitivity tests revealed a transition from disseminated methicillin-sensitive S. aureus sepsis to methicillin-resistant sepsis.
View Article and Find Full Text PDFHeliyon
April 2024
State Key Laboratory for Diagnosis and Treatment of Infectious Diseases, National Clinical Research Center for Infectious Diseases, Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Existing studies revealed high clonal diversity among bacteremia isolates, especially for methicillin-sensitive (MSSA) strains. A 66-year-old male patient presenting with a widespread methicillin-sensitive (MSSA) infection, accompanied by concurrent carbapenem-resistant (CRKP) bloodstream infection.To evaluate the evolution of the present isolate, whole genome sequencing and bioinformatics analysis were performed for all available MSSA isolates.
View Article and Find Full Text PDFAccess Microbiol
February 2024
Staphylococcal and Streptococcus Reference Laboratory, United Kingdom Health Security Agency, 61 Colindale Avenue, London, NW9 5EQ, UK.
Background: Panton-Valentine leukocidin (PVL) (SA) is an emergent public health concern. PVL toxin has been mostly associated with methicillin-sensitive (MSSA)-related skin and soft tissue infections occurring in high-risk groups such as people who inject drugs (PWID). The emergence of PVL methicillin-resistant (MRSA) infection is causing severe and life-threatening disease in PWID.
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