Your browser doesn't support javascript.
loading
Severe rhabdomyolysis as a rare complication of human granulocytic anaplasmosis.
Peng, Chun-Yu; Desai, Prarthana; Saleh, Mohammed; Daniel, Ocheita.
Afiliación
  • Peng CY; Internal Medicine Department, Danbury Hospital, Danbury, CT, USA.
  • Desai P; Internal Medicine Department, Danbury Hospital, Danbury, CT, USA.
  • Saleh M; Internal Medicine Department, Danbury Hospital, Danbury, CT, USA.
  • Daniel O; Internal Medicine Department, Danbury Hospital, Danbury, CT, USA.
IDCases ; 36: e01942, 2024.
Article en En | MEDLINE | ID: mdl-38699527
ABSTRACT
Human granulocytic anaplasmosis (HGA) is a tick-borne illness caused by infection with Anaplasma phagocytophilum. Although rare, rhabdomyolysis and acute renal failure are potential complications of HGA. We present the case of an 86-year-old male who exhibited severe myopathy, rhabdomyolysis, and acute renal failure necessitating hemodialysis. Treatment with doxycycline resulted in partial renal function improvement, allowing discontinuation of dialysis after 8 weeks. This case underscores the importance of considering rhabdomyolysis as a manifestation of HGA, particularly in individuals residing in or traveling to endemic areas.
Palabras clave

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: IDCases Año: 2024 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: IDCases Año: 2024 Tipo del documento: Article