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These studies suggest lisinopril can cause skin rashes as a potential side effect in some patients.
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Lisinopril, an angiotensin-converting enzyme (ACE) inhibitor, is widely used for managing hypertension and congestive heart failure. However, it has been associated with various adverse effects, including skin rashes. This article synthesizes research findings on the occurrence and characteristics of skin rashes induced by lisinopril.
Research has shown that lisinopril can induce inflammatory reactions in the skin. A study involving guinea pigs demonstrated that continuous infusion of lisinopril led to significant intradermal inflammation, suggesting a direct inflammatory response to the drug. This indicates that lisinopril can provoke skin reactions through inflammatory pathways.
Several case reports have documented the clinical presentation of skin rashes associated with lisinopril. For instance, a 38-year-old male developed persistent, moderately itchy skin eruptions on his face and upper chest while on lisinopril therapy. The rash was characterized by "juicy" annular lesions with darker centers and erythematous papules on the upper trunk. Another case involved a man in his 40s who experienced a rapidly progressive skin eruption after starting lisinopril, characterized by tender, erythematous patches and plaques.
Histopathological examination of skin biopsies from patients with lisinopril-induced rashes often reveals neutrophilic infiltrates in the sebaceous glands. This finding is consistent with neutrophilic sebaceous adenitis (NSA), a rare condition that has been linked to various medications, including lisinopril.
In a multicenter study comparing lisinopril with atenolol, skin rashes were reported in a small percentage of patients (1.7% for lisinopril and 2.0% for atenolol). This suggests that while skin rashes are not exceedingly common, they are a recognized adverse effect of lisinopril therapy. The study also highlighted that other adverse effects, such as cough and proteinuria, were more frequently observed with lisinopril.
Discontinuing lisinopril often leads to the resolution of the rash, although this is not always immediate. In some cases, additional treatments such as corticosteroids may be required to manage severe skin reactions. It is crucial for healthcare providers to monitor patients for skin reactions and consider alternative antihypertensive therapies if necessary.
Proper patient selection and the identification of risk factors can help mitigate the risk of adverse skin reactions. Patients with a history of drug-induced rashes or those with autoimmune conditions may be at higher risk and should be monitored closely.
Lisinopril, while effective for managing hypertension and heart failure, can induce skin rashes in some patients. These rashes can vary in presentation and severity, often involving inflammatory and neutrophilic responses. Clinicians should be aware of this potential side effect and manage it through careful patient monitoring, discontinuation of the drug if necessary, and appropriate symptomatic treatment. Further research is needed to fully understand the mechanisms behind lisinopril-induced skin reactions and to develop strategies for prevention and management.
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