Background: The Jarisch-Herxheimer reaction is an inflammatory reaction that occurs within 12 hours after administration of antibiotic therapy for spirochaeta species like Treponema pallidum. The reaction includes fever, headache, reappearing or worsening of skin lesions, lymphadenopathy, pharyngitis, malaise, and myalgias. Case presentation: We present a 27-year-old man complaining of high fever 4 hours after the injection of benzathine penicillin. The patient also complained of headaches, body aches and aches. There were no complaints of shortness of breath, itching, skin blisters, red eyes, or sores on the genitals. History of take any medication was denial by the patient. After treatment by giving antipyretics and corticosteroids and ge...
We report the case of a 44 year-old female, who presented a long-lasting, clinically atypical, secon...
Patients who present with papular rashes have a wide differential diagnosis particularly in the sett...
We report the case of a 44 year-old female, who presented a long-lasting, clinically atypical, secon...
The Jarisch-Herxheimer reaction (JHR) typically occurs after the initiation of antibiotic treatment ...
Multistage and reinfection of syphilis, which developed genital chancre after secondary syphilis is ...
It has long been acknowledged that syphilis is a disease with a diverse range of presentations. We h...
Introduction: The Jarisch-Herxheimer reaction, a febrile inflammatory reaction that often occurs aft...
Copyright © 2014 Vineet Punia et al. This is an open access article distributed under the Creative C...
A 61-year-old HIV+ male presented for regular follow up and complained of a rash. Past history was n...
ABSTRACTCoinfection between syphilis and Human Immunodeficiency Virus (HIV) could have varied clinic...
The importance of treating leptospirosis with penicillin is emphasized by two case reports and a rev...
Background: Drug-induced hypersensitivity syndrome (DIHS) is characterized by a severe multiorgan hy...
We present a case of Weil\u27s disease complicated by a Jarisch-Herxheimer reaction (JHR) after init...
BACKGROUND: Drug-Induced Hypersensitivity Syndrome (DIHS) is a severe and rare systemic reaction tri...
Purpose: To report a patient previously treated for primary and secondary syphilis who presented wit...
We report the case of a 44 year-old female, who presented a long-lasting, clinically atypical, secon...
Patients who present with papular rashes have a wide differential diagnosis particularly in the sett...
We report the case of a 44 year-old female, who presented a long-lasting, clinically atypical, secon...
The Jarisch-Herxheimer reaction (JHR) typically occurs after the initiation of antibiotic treatment ...
Multistage and reinfection of syphilis, which developed genital chancre after secondary syphilis is ...
It has long been acknowledged that syphilis is a disease with a diverse range of presentations. We h...
Introduction: The Jarisch-Herxheimer reaction, a febrile inflammatory reaction that often occurs aft...
Copyright © 2014 Vineet Punia et al. This is an open access article distributed under the Creative C...
A 61-year-old HIV+ male presented for regular follow up and complained of a rash. Past history was n...
ABSTRACTCoinfection between syphilis and Human Immunodeficiency Virus (HIV) could have varied clinic...
The importance of treating leptospirosis with penicillin is emphasized by two case reports and a rev...
Background: Drug-induced hypersensitivity syndrome (DIHS) is characterized by a severe multiorgan hy...
We present a case of Weil\u27s disease complicated by a Jarisch-Herxheimer reaction (JHR) after init...
BACKGROUND: Drug-Induced Hypersensitivity Syndrome (DIHS) is a severe and rare systemic reaction tri...
Purpose: To report a patient previously treated for primary and secondary syphilis who presented wit...
We report the case of a 44 year-old female, who presented a long-lasting, clinically atypical, secon...
Patients who present with papular rashes have a wide differential diagnosis particularly in the sett...
We report the case of a 44 year-old female, who presented a long-lasting, clinically atypical, secon...