DESCRIPTION
- Sexually transmitted disease
- Primary stage:
- Painless papule, pustule, or ulcer
- Secondary stage:
- Spread to regional lymph nodes
- Fluctuant inguinal lymphadenopathy (buboes)
- Lymphadenopathy may be unilateral or bilateral
- Responsive to antibacterial therapy
- Tertiary stage:
- If untreated, significant tissue damage and destruction may result
- Endemic in Southeast Asia, Latin America, parts of Africa, and the Caribbean
- Increasing incidence among men who have sex with men
- Also known as:
- Struma
- Tropical bubo
- Nicolas–Favre–Durand disease
ETIOLOGY
Chlamydia trachomatis
serotypes L1, L2, and L3
DIAGNOSIS
SIGNS AND SYMPTOMS
History
- Primary genital lesions:
- Incubation: 3–30 days after sexual exposure to
C. trachomatis
- Painless genital chancre lasts 2–3 days (rarely, a papule or vesicle)
- Often transient and not noticed
- May present as proctitis
- Secondary stage:
- Systemic symptoms:
- Fever and malaise
- Myalgias
- Lymphadenopathy; usually inguinal:
- May ulcerate and drain pus
- Proctitis:
- Rectal bleeding
- Tenesmus
- Constipation
- Tertiary stage:
- Symptoms mimic inflammatory bowel disease or proctocolitis
- Elephantiasis
- Strictures
Physical-Exam
- Primary stage:
- Painless papule, pustule, or ulcer
- Usually anogenital region
- Secondary stage:
- Tender inguinal adenopathy:
- Occurs 1–3 wk after initial inoculation
- Adenopathy is unilateral in 2/3 of cases
- Buboes (large inguinal lymph nodes) form in inguinal and femoral chains
- Groove sign: Scarred or coalescent buboes above and below inguinal ligament give a linear depression parallel to the inguinal ligament (seen in 30%)
- Anal-receptive patients may develop hemorrhagic proctocolitis
- Perirectal lymphatic inflammation causes fistulae and strictures
- Tertiary disease (invasive if untreated):
- Chronic proctocolitis:
- Abdominal pain
- Rectal bleeding
- Genital strictures
- Perineal and perianal fistulae
- Elephantiasis of the ipsilateral leg
DIAGNOSIS TESTS & NTERPRETATION
Lab
- Standard
Chlamydia
DNA probes
do not
test for lymphogranuloma venereum (LGV) strain
- False-positive VDRL in 20%
- Serologic testing and culture are the standard
- Complement fixation titers >1:64 are consistent with LGV infection
Diagnostic Procedures/Surgery
Bubo aspiration—specific but expensive and impractical
DIFFERENTIAL DIAGNOSIS
- Genital herpes (ulcers usually not seen in LGV)
- Syphilis—nodes nontender, longer incubation
- Chancroid—multiple ulcers, no systemic symptoms
- Granuloma inguinale—lesions painless and bleed easily
TREATMENT
PRE HOSPITAL
No pre-hospital issues
INITIAL STABILIZATION/THERAPY
No field or ED stabilization required
ED TREATMENT/PROCEDURES
If large, buboes may need to be aspirated or drained to avoid or minimize scarring
MEDICATION
First Line
Doxycycline: 100 mg PO BID for 3 wk
Second Line
- Azithromycin: 1,000 mg PO weekly for 3 wk
- Erythromycin: 500 mg PO QID for 3 wk
Pregnancy Considerations
Erythromycin is the recommended regimen in pregnancy and during lactation
FOLLOW-UP
DISPOSITION
Admission Criteria
Hospitalization is rarely needed (i.e., severe systemic symptoms)
Discharge Criteria
Immunocompetent patient without systemic involvement
Issues for Referral
- Outpatient follow-up is required to confirm diagnosis and cure
- Rectal infection may require retreatment
FOLLOW-UP RECOMMENDATIONS
- Ensure that sexual partners are tested and treated
- Sexual contacts within 60 days should be tested and treated with antichlamydial therapy
PEARLS AND PITFALLS
- Diagnosis is based on clinical suspicion, epidemiologic patterns, and exclusion of other etiologies
- Consider this diagnosis in men who have sex with men
- Treat to avoid tertiary disease which is not responsive to antibiotic therapy alone
- Treatment course is at least 3 wk of antibiotics
ADDITIONAL READING
- Centers for Disease Control and Prevention: 2002 guidelines for treatment of sexually transmitted diseases. Available at:
http://www.cdc.gov/std/treatment/2010/STD-Treatment-2010-RR5912.pdf#page=28
.
- McLean CA, Stoner BP, Workowski KA. Treatment of lymphogranuloma venereum.
Clin Infect Dis
. 2007;44:S147–S152.
- White JA. Manifestations and management of lymphogranuloma venereum.
Curr Opin Infect Dis
. 2009;22:57–66.
- White J, Ison C. Lymphogranuloma venereum: What does the clinician need to know?
Clin Med
. 2008;8:327–330.
CODES
ICD9
099.1 Lymphogranuloma venereum
ICD10
A55 Chlamydial lymphogranuloma (venereum)
MALARIA
Jordan Moskoff
BASICS
DESCRIPTION
- Protozoan infection transmitted through the Anopheles mosquito
- Incubation period 8–16 days
- Periodicity of the disease is due to the life cycle of the protozoan:
- Exoerythrocytic phase: Immature sporozoites migrate to liver, where they rapidly multiply into mature parasites (merozoites).
- Erythrocytic phase: Mature parasites are released into circulation and invade RBCs.
- Replication within RBCs followed 48–72 hr later by RBC lysis and release of merozoites into circulation, repeating cycle
- Fever corresponds to RBC lysis.
- Plasmodium falciparum:
- Cause of most cases and almost all deaths
- Usually presents as an acute, overwhelming infection
- Able to infect red cells of all ages:
- Results in greater degree of hemolysis and anemia
- Causes widespread capillary obstruction:
- Results in end-organ hypoxia and dysfunction
- More moderate infection in people who are on or who have recently stopped prophylaxis with an agent to which the P. falciparum is resistant
- Post-traumatic immunosuppression may cause relapse of malaria in patients who have lived in endemic areas.
- Plasmodium vivax and Plasmodium ovale:
- May present with an acute febrile illness
- Dormant liver stages (hypnozoites) that may cause relapse 6–11 mo after initial infection
- Plasmodium malariae:
- May persist in the bloodstream at low levels up to 30 yr
ETIOLOGY
- Transmission usually occurs from the bite of infected female Anopheles mosquito.
- North American transmission possible:
- Anopheles mosquitoes on east and west coasts of US.
- Transmission may also occur through infected blood products and shared needles.
Pediatric Considerations
- Sickle cell trait protective
- Cerebral malaria more common in children
- In highly endemic areas with minimal lab capability, all children presenting with febrile illness may be treated.