AI Article Synopsis

  • Pseudomonal ecthyma gangrenosum is usually seen in immunosuppressed individuals but can be rare and serious when associated with specific antibiotic-resistant strains.
  • The case discussed involves a 30-year-old woman with acute myeloid leukemia who developed a necrotic skin lesion post-chemotherapy, ultimately identified as colistin & carbapenem-resistant.
  • Timely recognition and treatment with the right antibiotics and surgical intervention are crucial for recovery, especially in patients with compromised immune systems in hem-oncology.

Article Abstract

Pseudomonal ecthyma gangrenosum is a well-known condition in immunosuppressed patients. However, ecthyma gangrenosum associated with is a rare entity that requires early recognition and optimal antibiotic and surgical management. We herein report the first case of colistin & carbapenem-resistant ecthyma gangrenosum in an acute myeloid leukemia patient. A 30-year-old female with acute myeloid leukemia received induction chemotherapy at the National Institute of Blood Diseases and Bone Marrow Transplantation hospital. Post-chemotherapy, she developed fever and a necrotic erythematous papule on right forearm. Colistin-susceptible carbapenem-resistant was isolated in cultures. Susceptibility testing was performed by microbroth dilution method. Worsening necrotic lesion prompted surgical debridement. Histopathology of debrided tissue revealed necrotic inflammation, and tissue cultures grew colistin-resistant carbapenem-resistant (colistin minimum inhibitory concentration >4 µg/mL). We speculate that colistin resistance was acquired due to impaired antibiotic penetration in necrotic nidus. A higher incidence of carbapenem-resistant associated ecthyma gangrenosum is anticipated in hem-oncology patients, and timely diagnosis, appropriate antibiotics, and surgical debridement remain the only potential cure.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9152185PMC
http://dx.doi.org/10.1177/2050313X221102113DOI Listing

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