Multisystem Bacterial Infections
Typhoid and paratyphoid fever
Pathophysiology and epidemiology
- Systemic Salmonella infection with S. typhi or S. paratyphoid.
- After malaria, commonest serious tropical disease in returning travellers from Asia (esp. South and Southeast); also found in Africa and South America.
- 1-3 weeks incubation.
- Not to be confused with typhus, an infection by Rickettsia typhi.
Presentation
- Insidious onset of fever, headache, malaise, and constipation. Diarrhoea and vomiting can occur but are less common.
- Other features: rose spots (macules on chest and abdo), hepatosplenomegaly, lymphadenopathy, dry cough, neurological symptoms, bradycardia.
Paratyphoid fever:
- Similar to typhoid fever, but more abrupt onset and milder course.
Investigations
- Blood and stool cultures.
- FBC and LFTs may be deranged.
Management
Leptospirosis
Pathophysiology and epidemiology
- Infection with the spirochete genus Leptospira.
- Transmitted to humans in urine of rats, dogs, and other mammals, either directly or in urine-contaminated water.
- Can be acquired in the UK, but most UK cases are acquired abroad.
- 1-2 weeks incubation.
Presentation
- Biphasic course, with bacteraemic flu-like phase followed 1-3 days later by immune phase.
- Immune phase may be mild (e.g. fever and myalgia), but severe manifestations include Weil's disease, characterised by haemorrhage, conjunctival suffusion (redness without exudate), jaundice, and hepatorenal failure.
- Less commonly, there may be GI, respiratory, or CNS manifestations.
Investigations
- FBC: ↑neutrophils, and sometimes ↓Hb and ↓PLT.
- Deranged renal and liver function tests.
- Diagnosis: IgM serology (>7 days).
Management
- Penicillins or tetracyclines.
- Antibiotics are still given in the immune phase, despite the fact that they may confer little benefit.
Whipple's disease
Pathophysiology and epidemiology
- Infection by the Gram +ve rod Tropheryma whipplei.
- Ubiquitous in environment, and often linked to soil or animal exposure e.g. farmer.
- Minimal immune response by patients suggests specific immunodeficiency as a risk factor.
- Patients are 90% male, mean age 50, usually white.
Presentation
- Joints: typically migratory large joins arthralgia, which may precede other symptoms by >5 years. Often misdiagnosed as a seronegative arthritis.
- GI: chronic intermittent diarrhoea, colicky abdo pain, malabsorption, weight loss.
Less common:
- CNS: usually dementia/confusion, less commonly, ophthalmoplegia, nystagmus, seizures, myoclonus.
- Cardiac: usually endocarditis, less commonly myo/pericarditis.
- Others: fever, lymphadenopathy, skin hyperpigmentation, cough, uveitis.
- In rare cases, it can present with one/some of these features alone.
Investigations
- Bloods: ↓Hb, ↑WBC, ↑CRP, ↑PT (vit K malabsorption).
- Diagnosis is by tissue biopsy, usually small bowel from upper GI endoscopy, testing sample with Periodic acid‐Schiff stain (+ve) and PCR.
- CSF PCR in all, due to potential morbidity of CNS involvement. Other sites only sampled (e.g. joints, lymph nodes) if symptomatic and GI features absent.
- Very difficult to culture, so even in endocarditis it is only diagnosed from histology of resected valves.
Management
Complications and prognosis
- Uniformly fatal without treatment.
- Immune reconstitution inflammatory syndrome (IRIS) in first weeks of treatment.
- Relapses, often in CNS, if inadequately treated.
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