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1.
J Fam Pract ; 68(2): 113; 114; 116, 2019 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-30870537

RESUMEN

Was a recent change in diet to blame for this patient's rash?


Asunto(s)
Dieta Cetogénica/efectos adversos , Prurito/diagnóstico , Prurito/etiología , Adulto , Dorso , Diagnóstico Diferencial , Femenino , Humanos , Tórax
2.
Open Forum Infect Dis ; 6(11): ofz442, 2019 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-31696143

RESUMEN

Shewanella infections are uncommon in immunocompetent hosts. We report 6 cases of Shewanella algae infection in young, healthy Naval Special Warfare trainees in San Diego during 2 consecutive El Niño seasons, defining a unique population at risk and adding to the epidemiologic understanding of this potentially virulent organism.

3.
J Spec Oper Med ; 16(3): 16-19, 2016.
Artículo en Inglés | MEDLINE | ID: mdl-27734437

RESUMEN

Thrombotic microangiopathy (TMA) syndromes represent a spectrum of illnesses that share common clinical and pathologic features of microangiopathic hemolytic anemia, thrombocytopenia, and organ injury from pathologic small-vessel thrombosis. At least nine primary TMA syndromes have been described and classified based on common probable etiologies, diagnostic criteria, and treatments. The most recognized of the TMA syndromes include thrombotic thrombocytopenic purpura (TTP) and hemolytic-uremic syndrome (HUS). Advanced laboratory techniques are required to distinguish between these syndromes; however, all patients should initially be treated with plasma exchange for presumed ADAMTS13 deficiency-mediated TMA. The authors present a case of a TMA syndrome in a Navy SEAL (Sea, Air, Land) candidate.


Asunto(s)
Personal Militar , Microangiopatías Trombóticas/diagnóstico , Proteína ADAMTS13/sangre , Humanos , Masculino , Intercambio Plasmático , Síndrome , Microangiopatías Trombóticas/enzimología , Microangiopatías Trombóticas/terapia , Adulto Joven
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