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Published on: June 11, 2011
Trimethoprim-sulfamethoxazole-induced Steven Johnson syndrome in an HIV-infected patient
Syed Ahmed Taqi1, Syed Ahmed Zaki, Angadi Rajasab Nilofer
1Department of Oral Pathology and Microbiology, Bharthi Vidyapeeth University Dental College and Hospital, Navi Mumbai, India.
Abstract:
Trimethoprim-sulfamethoxazole (TMP/SMX) is a widely prescribed antimicrobial for the management of several uncomplicated infections. It is commonly used for the treatment and prophylaxis of Pneumocystis jirovecii pneumonia (PCP) in the HIV-infected population. The adverse reaction to TMP/SMX is more frequent and severe in HIV-infected patients as compared to the general population. Here, we report a case of Stevens-Johnson syndrome (SJS) secondary to TMP/SMX. The patient had a generalized cutaneous reaction with involvement of the eyes, oral cavity, and genitals. He had elevated hepatic alanine aminotransferase and aspartate aminotransferase enzyme. TMP/SMX therapy was stopped and supportive treatment was started. His condition improved after eight days of stopping TMP/SMX therapy.
Insights
Trimethoprim-sulfamethoxazole (TMP/SMX) can cause severe Stevens-Johnson syndrome (SJS) in HIV patients. Promptly discontinuing TMP/SMX and providing supportive care led to this patient
Area of Science:
- Pharmacology
- Immunology
- Dermatology
Background:
- Trimethoprim-sulfamethoxazole (TMP/SMX) is a common antibiotic for various infections.
- It is frequently used for Pneumocystis jirovecii pneumonia (PCP) prophylaxis in HIV-infected individuals.
- HIV-infected patients exhibit a higher incidence and severity of adverse reactions to TMP/SMX.
Observation:
- A case report details a patient experiencing Stevens-Johnson syndrome (SJS) after TMP/SMX treatment.
- The patient presented with a widespread mucocutaneous reaction affecting the eyes, oral cavity, and genitals.
- Laboratory findings included elevated liver enzymes (alanine aminotransferase and aspartate aminotransferase).
Findings:
- Discontinuation of TMP/SMX therapy was followed by supportive care.
- The patient's condition showed improvement eight days after cessation of the antibiotic.
- This case highlights a severe adverse drug reaction to TMP/SMX in an HIV-positive individual.
Implications:
- Clinicians should maintain a high index of suspicion for severe cutaneous adverse reactions (SCARs) like SJS with TMP/SMX use, especially in HIV patients.
- Early recognition and withdrawal of the offending agent are crucial for managing TMP/SMX-induced SJS.
- This case underscores the importance of careful monitoring and risk-benefit assessment when prescribing TMP/SMX to immunocompromised populations.
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