Fever and leukocytosis have many possible etiologies in injection drug users. We present a case of a 22-year-old woman with fever and leukocytosis that were presumed secondary to cotton fever, a rarely recognized complication of injection drug use, after an extensive workup. Cotton fever is a benign, self-limited febrile syndrome characterized by fevers, leukocytosis, myalgias, nausea and vomiting, occurring in injection drug users who filter their drug suspensions through cotton balls. While this syndrome is commonly recognized amongst the injection drug user population, there is a paucity of data in the medical literature. We review the case presentation and available literature related to cotton fever. I njection drug use is associated with many infectious and non-infectious complications. The most common associated complications faced by managing physicians are soft-tissue infections, overdose, intoxication, and withdrawal.1 A frequent and challenging triage dilemma in this population is that of fever with active injection drug use. Despite numerous unsuccessful attempts to develop discriminating decision rules to guide ambulatory triage in these cases, clinicians are still unable to reliably exclude occult infections such as endocarditis and osteomyelitis. 2,3 This often results in short-term hospitalization of these patients, with accrual of health care expenditures. 4 An infrequently recognized cause of fever in injection drug users is cotton fever, a poorly characterized systemic febrile inflammatory syndrome seen in this population. Ironically, while there is a paucity of literature and awareness in the medical community, cotton fever is a wellrecognized syndrome amongst injection drug users. Originally coined in 1975, cotton fever was described as a benign selflimited febrile syndrome occurring in injection drug users who filtered their drug suspensions through cotton balls. 5 We present a case of presumed cotton fever in an active injection heroin user, in whom the diagnosis was only considered upon hearing the patient reference the syndrome after substantial workup had been completed. Additionally, a review of the medical literature and a discussion of the current theories about the pathophysiology of cotton fever are presented.
CASE REPORTA 22-year-old woman presented to an outside hospital 4 hours after developing acute onset of fevers, headache, abdominal pain and radiating back pain, which began 20 minutes after injecting heroin. She did not endorse any visual symptoms, chest pain, dyspnea, or rashes. Initial vital signs were notable for a temperature of 39°C and heart rate of 102 beats per minute. At the time, the remainder of her exam was reported as normal except for diffuse abdominal tenderness. In the setting of acute back pain, a lumbar spine MRI was obtained and interpreted as consistent with an L3-S2 epidural abscess. Blood cultures were drawn, and the patient was started on vancomycin and ceftriaxone. Twelve hours after initiation of symptoms, the patient was transferred to our instituti...