Rare case of severe rhabdomyolysis secondary to human granulocytic anaplasmosis
| Autor: | Jasanjeet Jawanda |
|---|---|
| Rok vydání: | 2020 |
| Předmět: |
medicine.medical_specialty
Leukopenia Human granulocytic anaplasmosis biology business.industry Constitutional symptoms Incidence (epidemiology) 030208 emergency & critical care medicine General Medicine medicine.disease biology.organism_classification Anaplasma phagocytophilum Dermatology Serology 03 medical and health sciences 0302 clinical medicine Emergency Medicine medicine Etiology medicine.symptom business Rhabdomyolysis |
| Zdroj: | The American Journal of Emergency Medicine. 38:1543.e1-1543.e2 |
| ISSN: | 0735-6757 |
| DOI: | 10.1016/j.ajem.2020.03.066 |
| Popis: | Anaplasma phagocytophilum (AP) is the causative agent of human granulocytic anaplasmosis (HGA), a tick-borne illness with highest incidence in north-eastern regions of the United States. This condition presents with vague constitutional symptoms and has been associated with laboratory derangements such as leukopenia, thrombocytopenia and transaminitis1. Rhabdomyolysis, however, is not one of these associations. We report a case of confirmed HGA associated with severe rhabdomyolysis, where no other cause was identified. The etiology of rhabdomyolysis secondary to AP infection is still unknown. A presumptive diagnosis of HGA can be made in the presence of fever, non-specific symptoms such as myalgias, laboratory derangements such as leukopenia and thrombocytopenia in an individual residing in an endemic area3. Serological confirmation should not delay treatment, given the rapid progression of this dangerous infection. Rhabdomyolysis should also be considered as part of supporting data in the diagnostic consideration for HGA. |
| Databáze: | OpenAIRE |
| Externí odkaz: |
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