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Author: Mark A Crowe, MD, Assistant Clinical Instructor, Department of Medicine, Division of Dermatology, University of Washington School of Medicine

Mark A Crowe is a member of the following medical societies: American Academy of Dermatology and North American Clinical Dermatologic Society

Coauthor(s): Mark A Hall, MD, Staff Physician, Dermatology Service, Walter Reed Army Medical Center

Editors: Janet Fairley, MD, Professor, Program Director, Section Chief, Department of Dermatology, Medical College of Wisconsin; Richard P Vinson, MD, Assistant Clinical Professor, Department of Dermatology, Texas Tech University School of Medicine; Consulting Staff, Mountain View Dermatology, PA; Paul Krusinski, MD, Director of Dermatology, Professor, Department of Internal Medicine, Fletcher Allen Health Care, University of Vermont; Joel M Gelfand, MD, MSCE, Medical Director, Clinical Studies Unit, Assistant Professor, Department of Dermatology, Associate Scholar, Center for Clinical Epidemiology and Biostatistics, University of Pennsylvania; Dirk M Elston, MD, Director, Department of Dermatology, Geisinger Medical Center

Author and Editor Disclosure

Synonyms and related keywords: soft chancre, Haemophilus ducreyi, H ducreyi, sexually transmitted disease, STD, genital ulcer, bubo

Background

Chancroid is a sexually transmitted genital ulcer disease (GUD) caused by the gram-negative bacillus Haemophilus ducreyi. It is characterized by the presence of painful ulcers and inflammatory inguinal adenopathy. Chancroid is often referred to as a soft chancre because the lesions are usually not indurated. In contrast, a syphilitic chancre is nontender and indurated.

Pathophysiology

H ducreyi produces a potent cytolethal distending toxin, which is an important virulence factor in the pathogenesis of chancroid, probably contributing to both the generation and the slow healing of ulcers.

Chancroid facilitates human immunodeficiency virus transmission. The chemokine receptors CCR5 and CXCR4 belong to the class of 7 transmembrane G-protein–coupled receptors, and their natural ligands are key players in the recruitment of immune cells to sites of inflammation. CCR5 and CXCR4 are the 2 main co-receptors essential for HIV entry. Macrophages in lesions of chancroid have significantly increased expression of CCR5 and CXCR4 compared with peripheral blood cells, and CD4 T cells had significant up-regulation of CCR5. The beta-chemokine RANTES (regulated on activation, normal T cell expressed and secreted) are important ligands for CCR5. RANTES is present throughout the papular and pustular stages of chancroid infection but is not present in uninfected control skin.

Together with the disruption of mucosal and skin barriers, the presence of cells with up-regulated HIV-1 co-receptors in H ducreyi–infected lesions provides an environment that facilitates the acquisition of HIV-1 infection. Effective and early treatment of genital ulceration, and chancroid in particular, is an important part of any strategy to control the spread of HIV infection in tropical countries.

Frequency

United States

Chancroid is rarely reported in the United States, but regional outbreaks and some endemic transmission occur, principally among migrant farm workers and poor inner city residents.

International

Because of a lack of readily available, accurate diagnostic tests, the global incidence of chancroid is unknown. An estimated 6 million cases of chancroid occur each year. Chancroid is common in many of the world's poorest regions such as areas of Africa, Asia, and the Caribbean. These regions also have some of the highest rates of HIV infection in the world, and chancroid is common in all 18 countries where adult HIV prevalence surpasses 8%. In addition to regional outbreaks, individual cases are reported sporadically in the developed world, usually in individuals who have recently returned from chancroid endemic areas or occasionally within the context of localized urban outbreaks, which may be associated with commercial sex work.

Mortality/Morbidity

  • Chancroid produces painful ulcers on the genitals, often (50%) associated with unilateral tender inguinal lymphadenitis (ie, a bubo). Left untreated, the buboes can form fluctuant abscesses that spontaneously rupture, resulting in a nonhealing ulcer.
  • Chancroid has been shown to be a major cofactor in the transmission of HIV-1 infection. This relationship has been especially significant in the heterosexual spread of HIV in Africa.

Sex

Males develop the disease most often, with a male-to-female ratio of 3-25:1.

  • Uncircumcised men develop chancroid more often than circumcised men. Patients who are uncircumcised do not respond as well to treatment as those who are circumcised.
  • Chancroid is more common in heterosexual men.
  • Female prostitutes, either with active disease in the form of genital ulcers or as asymptomatic carriers, are an important reservoir for infection.

Age

Chancroid is most prevalent in sexually active and promiscuous males, with a mean patient age of 30 years.



History

  • After an incubation period of 3-7 days, the patient develops painful, erythematous papules at the site of contact. The papules become pustular and then rupture, usually forming 1-3 painful ulcers.
  • Men usually have symptoms directly related to the painful genital lesions or inguinal tenderness. Most females are asymptomatic but may present with less obvious symptoms, such as dysuria, dyspareunia, vaginal discharge, pain on defecation, or rectal bleeding. Constitutional symptoms, such as malaise and low-grade fevers, may be present.
  • Most commonly, males report a history of recent contact with a prostitute. In addition, men who are infected are less likely to have used condoms and more likely to report a history of more than 2 sexual partners in the preceding 3 months.
  • Oral sex has also been documented in the transmission of chancroid.

Physical

  • A small papule is the initial lesion at the site of infection. The papule rapidly becomes pustular and eventually ulcerates. The ulcer enlarges, develops ragged undermined borders, and is surrounded by a rim of erythema. The border of the ulcer is not indurated as in syphilis. A grayish fibrinous membrane covers the base of the ulcer. Autoinoculation results in multiple sites of infection in various stages of evolution.
  • In men, the most common site of infection is the foreskin, but it may also occur less commonly on the shaft, the glans, or the meatus of the penis. In women, ulcers most commonly occur on the labia majora, but they may also occur on the labia minora, the thighs, the perineum, or the cervix.
  • As many as 50% of patients have tender, fixed, inguinal lymphadenopathy, usually unilaterally, that when fluctuant is called a bubo and is highly specific for chancroid (see Media Files 2-3).
  • A probable diagnosis can be made if all the following criteria are met:

    • The patient has one or more painful genital ulcers.
    • The patient has no evidence of Treponema pallidum infection by darkfield examination of ulcer exudate or by a serologic test for syphilis performed at least 7 days after onset of ulcers.
    • The clinical presentation, appearance of genital ulcers, and if present, regional lymphadenopathy are typical for chancroid.
    • Test results for herpes simplex virus (HSV) performed on the ulcer exudate are negative.
  • The combination of a painful ulcer and tender inguinal adenopathy, symptoms occurring in one third of patients, suggests a diagnosis of chancroid; when accompanied by suppurative inguinal adenopathy, these signs are almost pathognomonic.

Causes

  • H ducreyi (a short gram-negative bacillus) causes chancroid.
  • See Pathophysiology.
  • Chancroid is closely associated with prostitution. H ducreyi can survive only in subgroups of the population with a sufficient turnover of sex partners. Chancroid is not a sustainable infection in sexual networks with low rates of partner change.



Behcet Disease
Herpes Simplex
Lymphogranuloma Venereum
Syphilis

Other Problems to be Considered

Extracutaneous Crohn disease
Fixed drug eruption



Lab Studies

  • The diagnosis of chancroid based solely on the ulcer's appearance is accurate only in 30-50% of cases. In areas of high prevalence, the accuracy for clinical diagnosis of chancroid is as high as 80%; however, in areas where the disease is less common, the clinical basis for diagnosing chancroid leads to overdiagnosis. Considerable overlap exists between the major causes of GUD: herpes simplex, syphilis, chancroid, and often co-infection with 2 diseases at the same time. Co-infection with syphilis or HSV occurs in as many as 10% of patients. Realizing that no etiology can be found in 25-50% of all cases of GUD is important.
  • Gram staining may show gram-negative coccobacilli singly, in clusters, or in various morphological forms described as "schools of fish,railroad tracks," or "fingerprints." The organisms are visualized extracellularly more often than intracellularly and tend to occur in close proximity to polymorphonuclear leukocytes.
    • Gram staining of an ulcer specimen is not highly specific or sensitive. Interpretation is hampered by polymicrobial contamination. However, slides with gram-negative coccobacilli in parallel rows or in a clustered school of fish pattern have been reported to have a sensitivity of 62% and a specificity of 99% for chancroid.
    • Direct microscopy should not be used in the routine diagnosis of chancroid.
  • Culture is now the accepted standard for diagnosis in most areas, but even in an experienced laboratory, it is only 60-80% sensitive. Numerous selective artificial media have been developed, but 2 media are commonly used. Nairobi medium consists of a biplate of (1) gonococcal agar base with 2% bovine hemoglobin and 5% fetal calf serum and (2) Mueller-Hinton agar with 5% chocolatized horse blood. Both media contained vancomycin (3 µg/ml) and 1% CVA (ie, cephalothin, vancomycin, and amphotericin B) enrichment. The use of both media together increases the yield of positive cultures. Most H ducreyi organisms are resistant to vancomycin, but some strains are inhibited by its presence. Therefore, negative cultures in the setting of high suspicion should prompt screening for vancomycin-sensitive organisms.
    • A simple inexpensive medium containing gonococcal agar base supplemented with 5% Fildes' extract and unchocolated horse blood or a medium containing 0.2% activated charcoal instead of fetal calf serum are suitable alternatives for diagnostic purposes in resource poor countries.
    • H ducreyi is a fastidious organism. Patients' specimens must either be plated out directly on an appropriate culture medium or sent to the microbiology laboratory for culture as soon as possible. There is no widely available transport medium.
    • Studies have shown cultures to be less sensitive in women than in men.
  • Purulent material aspirated from intact buboes is almost always sterile.
  • Polymerase chain reaction (PCR) amplification is replacing culture as the diagnostic test of choice in some major medical centers. PCR amplification using a variety of primers may provide a useful alternative to culture for the detection of H ducreyi. Although PCR assays perform well on samples prepared from H ducreyi cultures, they are less sensitive when used to test genital ulcer specimens.
  • A multiplex PCR (M-PCR) assay has been developed for the simultaneous amplification of DNA targets from H ducreyi, T pallidum, and HSV types 1 and 2 and appears more sensitive than standard diagnostic tests for the detection of these etiologic agents in genital ulcer specimens. The M-PCR assay has been developed but is not yet commercially available.
  • Monoclonal antibody–based technology has the potential to provide a simple, inexpensive, rapid, and sensitive means of detecting H ducreyi in genital ulcer specimens, but no assay kits are commercially available.
  • Serology has limited usefulness in the routine diagnosis of chancroid infection.
  • Tissue biopsy is not a recommended diagnostic method for chancroid but may be useful as a means to exclude malignancy in nonhealing or atypical ulcers.
  • Serologic tests for syphilis include Venereal Disease Research Laboratory (VDRL) test, rapid plasma reagin (RPR) test, and a darkfield examination.
  • Tests for HSV include a Tzanck smear, direct fluorescence microscopy, and culture.
  • HIV testing should be performed in all patients who have genital ulcers caused by H ducreyi.
  • Patients should be retested for syphilis and HIV 3 months after the diagnosis of chancroid if the initial test results were negative.
  • Consider tests for other STDs, including hepatitis B, Chlamydia trachomatis, and gonorrhea.
  • As PCR and other techniques become available, cultures may be indicated to obtain a specimen for antibiotic sensitivity testing.

Histologic Findings

Histologic features from a biopsy sample of a chancroid ulcer may be sufficiently distinct to permit a presumptive diagnosis. Lesions show 3 zones. The most superficial zone is narrow and consists of neutrophils, fibrin, erythrocytes, and necrotic tissue. The second zone is wider and contains newly formed blood vessels with marked endothelial cell proliferation. The lumina of many of these vessels are occluded, leading to thrombosis. The deepest zone is composed of a dense infiltrate of plasma cells and lymphoid cells. Ducrey bacilli are seldom demonstrable on biopsy samples. Tissue biopsy is not a recommended diagnostic method for chancroid but may be useful as a means to exclude malignancy in nonhealing or atypical ulcers.



Medical Care

  • Local therapy includes gentle topical cleansing, soaks, and measures to reduce edema.
  • Patients with nonfluctuant buboes respond well to antibiotics, and the lesions do not need to be drained.
  • If appropriate therapy is provided and no clinical improvement is evident, the clinician must consider whether the diagnosis is correct, whether the patient is co-infected with another STD, whether the patient is infected with HIV, whether the treatment was used as instructed, and whether the H ducreyi strain is resistant to the prescribed antimicrobial.
  • In resource poor settings, where diagnostic facilities are not readily available, the World Health Organization advocates the use of a syndromic approach for the therapy of GUD.
    • The syndromic approach for the therapy of STDs delivers effective treatment quickly to people when they first come for care and is focused on the most common STDs that can be cured, including syphilis, gonorrhea, chlamydia, chancroid, trichomoniasis, and candidiasis.
    • The syndromic approach does not require the use of expensive tests, which often are not available. People who may have more than one STD infection are treated with the most effective drug available. In some undeveloped regions, 6 out of every 10 patients with an STD have 2 or more different infections at the same time. This approach also emphasizes treatment during the first visit. Treating curable STDs as soon as possible limits future spread of STDs, including HIV.
    • STD syndromes that cause similar signs and symptoms are included in a simple flow chart to help health care workers use the syndromic approach to make a diagnose and begin appropriate therapy.
    • Using the syndromic approach is as follows:
      • Men who present with a urethral discharge are treated for both gonorrhea and chlamydia.
      • Women who present with lower abdominal pain are treated for gonorrhea, chlamydia, and other bacteria.
      • Women who present with vaginal discharge and cervicitis are treated for gonorrhea and chlamydia.
      • Women who present with vaginal discharge and vaginitis are treated for trichomoniasis and candidiasis.
      • Men or women who present with genital ulcers are treated for syphilis, chancroid, and genital herpes.
    • Treating people with STDs in this way is less expensive long term because more people are cured the first time they come for care and the spread of STD may be limited.
    • The recommended drugs for STDs should be selected based upon cost, availability, and local resistance patterns.
    • A proper supply of STD drugs and training programs for health care workers are essential.
    • With the syndromic approach there is less emphasis placed on identifying the cause of a particular STD. This may be difficult for some health care workers to accept when they have been trained to identify the specific cause of a disease before starting therapy. However, in a setting where rapid therapy is of utmost importance and sophisticated laboratories are not available the syndromic approach provides effective treatment.
    • Prompt, effective therapy and education of patients helps them decide to use condoms, change their risky sexual behavior, and convince their partner to get treatment.

Surgical Care

  • Fluctuant buboes should be drained under local anesthesia. Insert a large-gauge needle into the bubo, passing through normal tissue from the side or the top of the lesion rather than the bottom, thus avoiding continuous dependent drainage and fistula formation (see Media File 4).
  • Incision and drainage is an effective method for treating fluctuant buboes and may be preferable to traditional needle aspiration considering the frequency of required repeat aspirations in some studies.
  • If circumcision is needed, it should be completed after the patient successfully completes treatment with antibiotics.

Activity

Patients should refrain from sexual activity until ulcers are healed. Untreated chancroid ulcers may persist for 1-3 months. Chancroid ulcers treated with the appropriate antibiotic agent resolve within 7-14 days.



Recommended antibiotic regimens are generally all effective and well tolerated. Studies have shown that patients who are infected with HIV do not respond to therapy as well as patients who are HIV negative, and patients who are uncircumcised may not respond to therapy as well as patients who are circumcised.

Virtually all strains of H ducreyi are resistant to penicillin and tetracycline. Trimethoprim and sulfamethoxazole is no longer used because of the development of high rates of resistance. Worldwide, several isolates with intermediate resistance to either ciprofloxacin or erythromycin have been reported.

Relapses after antibiotic therapy occur in as many as 5% of patients and are more common in patients who are uncircumcised or are also infected with HIV. If they are not infected with HIV, repeating the original therapy is usually effective.

Some specialists suggest using the erythromycin 7-day regimen for treating HIV-infected persons because the data concerning the therapeutic efficacy of ceftriaxone and azithromycin regimens in HIV-infected patients are limited.

Because treatment is often accompanied by treatment for gonococcal infections, it is important to be aware of changes to the CDC guidelines for STDs. In April 2007, the Centers for Disease Control and Prevention (CDC) updated treatment guidelines for gonococcal infection and associated conditions. Fluoroquinolone antibiotics are no longer recommended to treat gonorrhea in the United States. The recommendation was based on analysis of new data from the CDC's Gonococcal Isolate Surveillance Project (GISP). The data from GISP showed the proportion of gonorrhea cases in heterosexual men that were fluoroquinolone-resistant (QRNG) reached 6.7%, an 11-fold increase from 0.6% in 2001.
 
The data were published in the April 13, 2007 issue of the Morbidity and Mortality Weekly Report. This limits treatment of gonorrhea to drugs in the cephalosporin class (eg, ceftriaxone 125 mg IM once as a single dose). Fluoroquinolones may be an alternative treatment option for disseminated gonococcal infection if antimicrobial susceptibility can be documented. For more information, see the CDC's Antibiotic-Resistant Gonorrhea Web site, CDC Updated Gonococcal treatment recommendations (April 2007), or Medscape Medical News on CDC Issues - New Treatment Recommendations for Gonorrhea.

Drug Category: Antibiotics

Empiric antimicrobial therapy must be comprehensive and should cover all likely pathogens in the context of the clinical setting. The syndromic approach to therapy of GUD may be appropriate in some settings.

Drug NameCeftriaxone (Rocephin)
DescriptionThird-generation cephalosporin with broad-spectrum, gram-negative activity; lower efficacy against gram-positive organisms; higher efficacy against resistant organisms. Arrests bacterial growth by binding to 1 or more penicillin-binding proteins.
Adult Dose250 mg IM once; not to exceed 4 g
Pediatric Dose>7 days: 25-50 mg/kg/d IV/IM; not to exceed 125 mg/d
Infants and children: 50-75 mg/kg/d IV/IM divided q12h; not to exceed 2 g/d
ContraindicationsDocumented hypersensitivity
InteractionsProbenecid may increase ceftriaxone levels; coadministration with ethacrynic acid, furosemide, and aminoglycosides may increase nephrotoxicity
PregnancyB - Usually safe but benefits must outweigh the risks.
PrecautionsAdjust dose in renal impairment; caution in breastfeeding women and in persons allergic to penicillin

Drug NameAzithromycin (Zithromax)
DescriptionTreats mild-to-moderate microbial infections. More expensive than other therapies.
Adult Dose1 g PO once
Pediatric Dose10 mg/kg PO once; not to exceed 500 mg/d
ContraindicationsDocumented hypersensitivity; hepatic impairment; coadministration with pimozide
InteractionsMay increase toxicity of theophylline, warfarin, and digoxin; effects are reduced with coadministration of aluminum and/or magnesium antacids; nephrotoxicity and neurotoxicity may occur when coadministered with cyclosporine
PregnancyB - Usually safe but benefits must outweigh the risks.
PrecautionsSite reactions can occur with IV route; bacterial or fungal overgrowth may result with prolonged antibiotic use; may increase hepatic enzymes and cholestatic jaundice; caution in patients with impaired hepatic function, prolonged QT intervals, or pneumonia; caution in patients who are hospitalized, debilitated, or elderly

Drug NameErythromycin (E.E.S., E-Mycin, Ery-Tab)
DescriptionInhibits bacterial growth, possibly by blocking dissociation of peptidyl tRNA from ribosomes, causing RNA-dependent protein synthesis to arrest. For treatment of staphylococcal and streptococcal infections. In children, age, weight, and severity of infection determine proper dosage. When bid dosing is desired, half-total daily dose may be taken q12h. For more severe infections, double the dose.
Adult Dose500 mg PO qid for 7 d
Pediatric Dose20 mg/kg PO 2 h prior to procedure, followed by 10 mg/kg 6 h after initial dose
30-50 mg/kg/d (15-25 mg/lb/d) PO divided q6-8h; double dose for severe infection
ContraindicationsDocumented hypersensitivity; hepatic impairment
InteractionsCoadministration may increase toxicity of theophylline, digoxin, carbamazepine, and cyclosporine; may potentiate anticoagulant effects of warfarin; coadministration with lovastatin and simvastatin increases risk of rhabdomyolysis
PregnancyB - Usually safe but benefits must outweigh the risks.
PrecautionsCaution in liver disease; estolate formulation may cause cholestatic jaundice; GI adverse effects are common (give doses pc); discontinue use if nausea, vomiting, malaise, abdominal colic, or fever occur

Drug NameCiprofloxacin (Cipro)
DescriptionFluoroquinolone that inhibits bacterial DNA synthesis and, consequently, growth by inhibiting DNA gyrase and topoisomerases, which are required for replication, transcription, and translation of genetic material. Quinolones have broad activity against gram-positive and gram-negative aerobic organisms. Has no activity against anaerobes. Continue treatment for at least 2 d (7-14 d typical) after signs and symptoms have disappeared. CDC no longer recommends fluoroquinolones for gonorrhea because of increased resistance.
Adult Dose500 mg PO bid for 3 d
Pediatric Dose<18 years: Not recommended
³18 years: Administer as in adults
ContraindicationsDocumented hypersensitivity
InteractionsAntacids, iron salts, and zinc salts may reduce serum levels; administer antacids 2-4 h before or after taking fluoroquinolones; cimetidine may interfere with metabolism of fluoroquinolones; reduces therapeutic effects of phenytoin; probenecid may increase serum concentrations
May increase toxicity of theophylline, caffeine, cyclosporine, and digoxin (monitor digoxin levels); may increase effects of anticoagulants (monitor PT)
PregnancyC - Safety for use during pregnancy has not been established
PrecautionsDosage adjustments (adult adjustments)
CrCl (mL/min) <10: 50% of PO or IV dose q12h
HD: 0.25-0.5 g PO or 0.2-0.4 g IV q12h
During peritoneal dialysis: 0.25-0.5 g PO or 0.2-0.4 g IV q8h
In prolonged therapy, perform periodic evaluations of organ system functions (eg, renal, hepatic, hematopoietic); adjust dose in renal function impairment; superinfections may occur with prolonged or repeated antibiotic therapy
Not drug of first choice in pediatric patients because of increased incidence of adverse events (including arthropathy) compared with controls; no data for dose for pediatric patients with renal impairment (ie, CrCl <50 mL/min)



Further Outpatient Care

  • Patients should receive follow-up care to ensure resolution of the disease. Clinical improvement should occur over 7 days, and healing should be complete in 2 weeks with appropriate antibiotic therapy. Healing is slower for some uncircumcised men who have ulcers under the foreskin. Lymphadenopathy may be slow to resolve and may require needle aspiration if a significant bubo is present.
  • Because of the highly infectious nature of chancroid, routine treatment of contacts of men with chancroid is recommended even if they are asymptomatic. All sexual contacts during the 10 days prior to the development of the genital lesion should be treated.
  • Empirical treatment of high-risk women has been shown to significantly decrease the prevalence of disease.
  • Isolation or quarantine is not required, but patients must avoid sexual contact until all lesions, including discharging regional lymph nodes, are healed.

Deterrence/Prevention

  • Eradication of chancroid is a feasible public health objective. H ducreyi has a short duration of infectivity and requires frequent contacts to spread within a population. Humans are the only reservoir for H ducreyi, and rates of infection can be easily reduced through a variety of methods. Simple washing with soap and water within a few hours of sexual exposure is effective in reducing risk of chancroid.
  • Instituting a condom policy directed at protecting sex workers and their clients from exposure to STDs and improving curative services are among the most effective strategies.
  • Offering regular examination and treatment for registered sex workers or monthly presumptive antibiotic treatment to women at risk have both been shown to dramatically reduce the prevalence of chancroid. Antibiotic treatment of the highest-risk populations can reduce chancroid transmission in the short term and lead to a rapid decline in chancroid prevalence in a community.
  • Breaking the chancroid transmission cycle in any of these ways can markedly reduce the prevalence of chancroid even when other conditions favor its spread.

Complications

  • Phimosis, balanoposthitis, and rupture of buboes with fistula formation and scarring are reported complications.

Prognosis

  • The prognosis is excellent if chancroid is treated properly and if no co-infection with HIV is present.
  • As many as 5% of patients have a relapse of their disease and usually respond to a repeat course of their original therapy.
  • No adverse effects of chancroid on pregnancy outcome have been reported.
  • Chancroid-infected patients who have HIV should be monitored closely because they are more likely to experience treatment failure and to have ulcers that heal slowly.

Patient Education



Medical/Legal Pitfalls

  • Failure to evaluate and treat co-infections, such as syphilis, herpes simplex, or HIV, is a pitfall.

Special Concerns

  • Confirmed cases should be reported to the Division of Sexually Transmitted Diseases at the Centers for Disease Control and Prevention (CDC).
  • Mother-to-infant transmission has not been reported. Because sexual contact is the only known route of transmission, the diagnosis of chancroid in infants and young children is strong evidence of sexual abuse.



Media file 1:  Chancroid usually starts as a small papule that rapidly becomes pustular and eventually ulcerates. The ulcer enlarges, develops ragged undermined borders, and is surrounded by a rim of erythema. Unlike syphilis, lesions are tender and the border of the ulcer is not indurated. Courtesy of Hon Pak, MD.
Click to see larger pictureClick to see detailView Full Size Image
Media type:  Photo

Media file 2:  This patient shows the characteristic lesions of chancroid. The bubo on the right side drained spontaneously. The bubo in the left inguinal canal required needle aspiration.
Click to see larger pictureClick to see detailView Full Size Image
Media type:  Photo

Media file 3:  Close-up view of the chancroid ulcers in Media File 2.
Click to see larger pictureClick to see detailView Full Size Image
Media type:  Photo

Media file 4:  Large fluctuant buboes should be drained with local anesthesia and a large-gauge needle inserted through surrounding healthy skin. The insertion site should be superior or lateral to the bubo to prevent chronic drainage from the site.
Click to see larger pictureClick to see detailView Full Size Image
Media type:  Photo



  • Afonina G, Leduc I, Nepluev I, Jeter C, Routh P, Almond G, et al. Immunization with the Haemophilus ducreyi hemoglobin receptor HgbA protects against infection in the swine model of chancroid. Infect Immun. Apr 2006;74(4):2224-32. [Medline].
  • Annan NT, Lewis DA. Treatment of chancroid in resource-poor countries. Expert Rev Anti Infect Ther. Apr 2005;3(2):295-306. [Medline].
  • Ballard RC. Syndromic case management of STDs in Africa. Afr Health. Mar 1998;20(3):13-5. [Medline].
  • Bogaerts J, Vuylsteke B, Martinez Tello W, Mukantabana V, Akingeneye J, Laga M, et al. Simple algorithms for the management of genital ulcers: evaluation in a primary health care centre in Kigali, Rwanda. Bull World Health Organ. 1995;73(6):761-7. [Medline].
  • Bong CT, Bauer ME, Spinola SM. Haemophilus ducreyi: clinical features, epidemiology, and prospects for disease control. Microbes Infect. Sep 2002;4(11):1141-8. [Medline].
  • Centers for Disease Control and Prevention. Update to CDC's Sexually transmitted diseases treatment guidelines, 2006: fluoroquinolones no longer recommended for treatment of gonococcal infections. MMWR [serial online]. Apr 13 2007;56(14):332-336. Available at http://www.cdc.gov/mmwr/preview/mmwrhtml/mm5614a3.htm?s_cid=mm5614a3_e.
  • Centers for Disease Control and Prevention. Sexually transmitted diseases treatment guidelines 2006. MMWR [serial online]. 2006;55:Available at http://www.cdc.gov/std/treatment/2006/toc.htm.
  • Cole LE, Toffer KL, Fulcher RA, San Mateo LR, Orndorff PE, Kawula TH. A humoral immune response confers protection against Haemophilus ducreyi infection. Infect Immun. Dec 2003;71(12):6971-7. [Medline].
  • Dallabetta GA, Gerbase AC, Holmes KK. Problems, solutions, and challenges in syndromic management of sexually transmitted diseases. Sex Transm Infect. Jun 1998;74 Suppl 1:S1-11. [Medline].
  • Dangor Y, Ballard RC, da L Exposto F, Fehler G, Miller SD, Koornhof HJ. Accuracy of clinical diagnosis of genital ulcer disease. Sex Transm Dis. Oct-Dec 1990;17(4):184-9. [Medline].
  • DiCarlo RP, Armentor BS, Martin DH. Chancroid epidemiology in New Orleans men. J Infect Dis. Aug 1995;172(2):446-52. [Medline].
  • Ducrey A. Experimentelle Untersuchungen uber den Ansteckungsstof des weichen Schankers und uber die Bubonen. Monats Prakt Dermatol. 1889;9:387-405.
  • Ernst AA, Marvez-Valls E, Martin DH. Incision and drainage versus aspiration of fluctuant buboes in the emergency department during an epidemic of chancroid. Sex Transm Dis. Jul-Aug 1995;22(4):217-20. [Medline].
  • Fleming DT, Wasserheit JN. From epidemiological synergy to public health policy and practice: the contribution of other sexually transmitted diseases to sexual transmission of HIV infection. Sex Transm Infect. Feb 1999;75(1):3-17. [Medline].
  • Fulcher RA, Cole LE, Janowicz DM, Toffer KL, Fortney KR, Katz BP, et al. Expression of Haemophilus ducreyi collagen binding outer membrane protein NcaA is required for virulence in swine and human challenge models of chancroid. Infect Immun. May 2006;74(5):2651-8. [Medline].
  • Hammond GW. A history of the detection of Haemophilus ducreyi, 1889-1979. Sex Transm Dis. Mar-Apr 1996;23(2):93-6. [Medline].
  • Hollier LM, Workowski K. Treatment of sexually transmitted diseases in women. Obstet Gynecol Clin North Am. Dec 2003;30(4):751-75, vii-viii. [Medline].
  • Htun Y, Morse SA, Dangor Y, Fehler G, Radebe F, Trees DL, et al. Comparison of clinically directed, disease specific, and syndromic protocols for the management of genital ulcer disease in Lesotho. Sex Transm Infect. Jun 1998;74 Suppl 1:S23-8. [Medline].
  • Humphreys TL, Schnizlein-Bick CT, Katz BP, Baldridge LA, Hood AF, Hromas RA, et al. Evolution of the cutaneous immune response to experimental Haemophilus ducreyi infection and its relevance to HIV-1 acquisition. J Immunol. Dec 1 2002;169(11):6316-23. [Medline].
  • Joseph AK, Rosen T. Laboratory techniques used in the diagnosis of chancroid, granuloma inguinale, and lymphogranuloma venereum. Dermatol Clin. Jan 1994;12(1):1-8. [Medline].
  • Kulkarni K, Lewis DA, Ison CA. Expression of the cytolethal distending toxin in a geographically diverse collection of Haemophilus ducreyi clinical isolates. Sex Transm Infect. Aug 2003;79(4):294-7. [Medline].
  • Lewis DA. Chancroid: clinical manifestations, diagnosis, and management. Sex Transm Infect. Feb 2003;79(1):68-71. [Medline][Full Text].
  • Lewis DA. Chancroid: from clinical practice to basic science. AIDS Patient Care STDS. Jan 2000;14(1):19-36. [Medline].
  • Lewis DA. Diagnostic tests for chancroid. Sex Transm Infect. Apr 2000;76(2):137-41. [Medline].
  • Lewis DA, Stevens MK, Latimer JL, Ward CK, Deng K, Blick R, et al. Characterization of Haemophilus ducreyi cdtA, cdtB, and cdtC mutants in in vitro and in vivo systems. Infect Immun. Sep 2001;69(9):5626-34. [Medline].
  • Mackay IM, Harnett G, Jeoffreys N, et al. Detection and discrimination of herpes simplex viruses, Haemophilus ducreyi, Treponema pallidum, and Calymmatobacterium (Klebsiella) granulomatis from genital ulcers. Clin Infect Dis. May 15 2006;42(10):1431-8.
  • Martin DH, Mroczkowski TF. Dermatologic manifestations of sexually transmitted diseases other than HIV. Infect Dis Clin North Am. Sep 1994;8(3):533-82. [Medline].
  • Martin DH, Sargent SJ, Wendel GD Jr, McCormack WM, Spier NA, Johnson RB. Comparison of azithromycin and ceftriaxone for the treatment of chancroid. Clin Infect Dis. Aug 1995;21(2):409-14. [Medline].
  • Mayaud P, Ka-Gina G, Grosskurth H. Effectiveness, impact and cost of syndromic management of sexually transmitted diseases in Tanzania. Int J STD AIDS. 1998;9 Suppl 1:11-4. [Medline].
  • Mertz KJ, Weiss JB, Webb RM, Levine WC, Lewis JS, Orle KA, et al. An investigation of genital ulcers in Jackson, Mississippi, with use of a multiplex polymerase chain reaction assay: high prevalence of chancroid and human immunodeficiency virus infection. J Infect Dis. Oct 1998;178(4):1060-6. [Medline].
  • Mroczkowski TF, Martin DH. Genital ulcer disease. Dermatol Clin. Oct 1994;12(4):753-64. [Medline].
  • O'Farrell N. Soap and water prophylaxis for limiting genital ulcer disease and HIV-1 infection in men in sub-Saharan Africa. Genitourin Med. Aug 1993;69(4):297-300. [Medline].
  • O'Farrell N. Targeted interventions required against genital ulcers in African countries worst affected by HIV infection. Bull World Health Organ. 2001;79(6):569-77. [Medline].
  • O'Farrell N, Hoosen AA, Coetzee KD, van den Ende J. Genital ulcer disease: accuracy of clinical diagnosis and strategies to improve control in Durban, South Africa. Genitourin Med. Feb 1994;70(1):7-11. [Medline].
  • Patterson K, Olsen B, Thomas C, Norn D, Tam M, Elkins C. Development of a rapid immunodiagnostic test for Haemophilus ducreyi. J Clin Microbiol. Oct 2002;40(10):3694-702. [Medline].
  • Pillay A, Hoosen AA, Loykissoonlal D, Glock C, Odhav B, Sturm AW. Comparison of culture media for the laboratory diagnosis of chancroid. J Med Microbiol. Nov 1998;47(11):1023-6. [Medline].
  • Plummer FA, D'Costa LJ, Nsanze H, Dylewski J, Karasira P, Ronald AR. Epidemiology of chancroid and Haemophilus ducreyi in Nairobi, Kenya. Lancet. Dec 3 1983;2(8362):1293-5. [Medline].
  • Rome ES. Sexually transmitted diseases: testing and treating. Adolesc Med. Jun 1999;10(2):231-41, vi. [Medline].
  • Rosen T, Brown TJ. Cutaneous manifestations of sexually transmitted diseases. Med Clin North Am. Sep 1998;82(5):1081-104, vi. [Medline].
  • Roy-Leon JE, Lauzon WD, Toye B, Singhal N, Cameron DW. In vitro and in vivo activity of combination antimicrobial agents on Haemophilus ducreyi. J Antimicrob Chemother. Sep 2005;56(3):552-8. [Medline].
  • Schmid GP. Treatment of chancroid, 1997. Clin Infect Dis. Jan 1999;28 Suppl 1:S14-20. [Medline].
  • Schmid GP, Faur YC, Valu JA, Sikandar SA, McLaughlin MM. Enhanced recovery of Haemophilus ducreyi from clinical specimens by incubation at 33 versus 35 degrees C. J Clin Microbiol. Dec 1995;33(12):3257-9. [Medline].
  • Schmid GP, Sanders LL Jr, Blount JH, Alexander ER. Chancroid in the United States. Reestablishment of an old disease. JAMA. Dec 11 1987;258(22):3265-8. [Medline].
  • Schulte JM, Schmid GP. Recommendations for treatment of chancroid, 1993. Clin Infect Dis. Apr 1995;20 Suppl 1:S39-46. [Medline].
  • Spinola SM, Fortney KR, Katz BP, Latimer JL, Mock JR, Vakevainen M, et al. Haemophilus ducreyi requires an intact flp gene cluster for virulence in humans. Infect Immun. Dec 2003;71(12):7178-82. [Medline].
  • Steen R. Eradicating chancroid. Bull World Health Organ. 2001;79(9):818-26. [Medline].
  • Steen R. Sex, soap and antibiotics: the case for chancroid eradication. Int J STD AIDS. 2001;12(Suppl 2):147.
  • Steen R, Dallabetta G. Genital ulcer disease control and HIV prevention. J Clin Virol. Mar 2004;29(3):143-51. [Medline].
  • Telzak EE, Chiasson MA, Bevier PJ, Stoneburner RL, Castro KG, Jaffe HW. HIV-1 seroconversion in patients with and without genital ulcer disease. A prospective study. Ann Intern Med. Dec 15 1993;119(12):1181-6. [Medline].
  • Trager JD. Sexually transmitted diseases causing genital lesions in adolescents. Adolesc Med Clin. Jun 2004;15(2):323-52. [Medline].
  • Tyndall M, Malisa M, Plummer FA, Ombetti J, Ndinya-Achola JO, Ronald AR. Ceftriaxone no longer predictably cures chancroid in Kenya. J Infect Dis. Feb 1993;167(2):469-71. [Medline].
  • Van der Veen F, Fransen L. Drugs for STD management in developing countries: choice, procurement, cost, and financing. Sex Transm Infect. Jun 1998;74 Suppl 1:S166-74. [Medline].
  • Weiss HA, Thomas SL, Munabi SK, Hayes RJ. Male circumcision and risk of syphilis, chancroid, and genital herpes: a systematic review and meta-analysis. Sex Transm Infect. Apr 2006;82(2):101-9; discussion 110. [Medline].
  • World Health Organization. Management of sexually transmitted diseases. World Health Organization. Available at http://www.who.int/en/.
  • World Health Organization. Syndromic Case Management of STD (Sexually Transmitted Diseases)- A Guide for Decision-makers, Health Care Workers, and Communicators. World Health Organization. Available at www.who.int/en/.

Chancroid excerpt

Article Last Updated: Jan 30, 2007