ChineseChina UKUK DeutschlandDeutschland FranceFrance РоссияРоссия 한국한국 ไทยไทย Việt NamViệt Nam العربيةالعربية ҚазақстанҚазақстан EspañaEspaña MyanmarMyanmar DaiDai

Linking China’s Premium Healthcare · Serving Global Health Needs

Breaking down language, channel and process barriers in cross-border care — making the best doctors your personal doctors.
300 Grade-A partner hospitals · 3,000+ leading experts · one-stop service across all specialties

One-Stop Medical Care in China

  • International flights · Airport pickup · Nearby hotels
  • Multilingual interpreters · Full medical escort
  • Expert matching · Hospital fast-track
  • Full-cycle treatment · Post-op follow-up
Sign in
Home > West Medicine > Internal Medicine > Infectious Diseases
A48.400

Brazilian Purpuric Fever

传染科

Common symptoms

休克、血压下降、腹泻、腹痛、胃肠道出血、神志不清、发绀、少尿

The pathology of disease

Brazilian purpuric fever (BPF) is an acute fulminant pediatric disease first recognized in São Paulo, Brazil in 1984, presenting with high fever, abdominal pain, vomiting, purpuric rash, and shock with rapid death. Over 90% had purulent conjunctivitis ~2 weeks before. A 1985 Pan American/CDC task force defined it as a new disease (BPF); in 1986, H. influenzae biogroup aegyptius (HIBA) was isolated from blood/CSF/purpura of typical patients.

Common Symptoms

Shock; hypotension; diarrhea; abdominal pain; GI bleeding; confusion; cyanosis; oliguria

Causes and Pathogenesis

(1) Etiology: Originally Koch-Weeks bacillus, named H. aegyptius by Pittman (1950), then H. influenzae biogroup aegyptius (HIBA) after Killa (1976) noted its phenotype resembled H. influenzae biotype IV. BPF-clone HIBA from typical patients carries a 0.024 MDa plasmid (control conjunctivitis strains have 0.002 MDa or none); whole-cell electrophoresis, 16+23S RNA probing, and extracellular protein studies distinguish BPF clones from controls. (2) Pathogenesis: HIBA invades eye/nose/throat and multiplies locally; invasive BPF clones cause bacteremia and release endotoxin (mean 675 µg/L in patients vs 25 µg/L in healthy children)—endotoxin likely causes multiorgan damage. Autopsy shows widespread petechiae/purpura, microthrombi in small vessels, hemorrhage/necrosis, cerebral edema without inflammation, pulmonary congestion/edema/hemorrhage, adrenal hemorrhage, marked lymphoid depletion, and ischemic necrosis of distal extremities/ears/nose—no vasculitis.

Treatment

Drug therapy, rehabilitation

Preventive Measures

Curing conjunctivitis does not prevent BPF; some recommend topical ampicillin/chloramphenicol plus several days of systemic treatment. Surveillance in endemic areas tracks BPF clones and predicts outbreaks.

Department to Visit

It is recommended to visit the Infectious Diseases department; an appointment can be booked on this platform before the visit.

Warm reminder: The above information is for health science reference only and cannot replace professional medical diagnosis. If you have related symptoms, please seek medical attention at a regular hospital promptly.