AI Article Synopsis

  • A 63-year-old man with a renal transplant and lymphoma undergoing chemotherapy (R-CHOP) developed fever and a widespread pustular rash, which were linked to septicemia.
  • After ruling out other conditions, tests confirmed a methicillin-sensitive Staphylococcus aureus (MSSA) infection, primarily from his infected venous access port.
  • Treatment involved removing the port and using a combination of antibiotics, leading to improvement, highlighting the significance of proper diagnosis and management of similar infections in immunocompromised patients.

Article Abstract

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://www.ncbi.nlm.nih.gov/pmc/articles/PMC11416146PMC
http://dx.doi.org/10.7759/cureus.67516DOI Listing

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Article Synopsis
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