eMedicine Specialties > Infectious Diseases > Parasitic Infections

Onchocerciasis: Differential Diagnoses & Workup

Author: Mary Nettleman, MD, MS, Chair, Department of Medicine, Michigan State University
Coauthor(s): Apoorv Kalra, MD, Assistant Professor of Medicine, Michigan State University
Contributor Information and Disclosures

Updated: Apr 16, 2009

Differential Diagnoses

Food Allergies
Pinta
Hypersensitivity Reactions, Delayed
Scabies
Leprosy
Syphilis
Lichen Planus
Treponematosis (Endemic Syphilis)
Loa loa infection
Vitamin A Deficiency
Lymphatic filariasis
Yaws

Other Problems to Be Considered

Atopic dermatitis
Contact dermatitis
Insect bites
Chronic eczema
Malnutrition
Streptocerciasis
Superficial mycoses
Glaucoma
Trachoma
Vitiligo

Workup

Laboratory Studies

  • Pathological diagnosis
    • Traditionally, a diagnosis of onchocerciasis requires demonstration of microfilariae in a skin-snip biopsy sample (see Procedures). This technique yields high specificity (100%) in experienced hands but low sensitivity (20%-50%) in early stages of infection.
    • The diagnosis may also be made by direct examination of surgical specimens obtained by excision of nodules.
  • Immunodiagnosis
    • Antibody detection does not distinguish between active and past infections. Various antibodies have been tested, as follows:
      • Ov16 card test: Antibodies against this antigen have been shown to yield high sensitivity (approximately 80%) and specificity (approximately 85%) and may yield positive results in early infections when skin-snip results are negative.20,21 Capillary blood samples are collected by finger prick. The immunochromatographic card test is used to detect the presence of immunoglobulin G4 (IgG4) antibodies to recombinant Ov16 antigen.
      • Recombinant hybrid proteins (OvH2 and OvH3): This test is based on hybrid proteins of two separate Onchocerca proteins (Ov20 and Ov33). High sensitivity (>95%) and specificity (>95%) has been described in this enzyme-linked immunoassay (ELISA)–based antibody detection test.22
      • An ELISA-based test using a cocktail of 3 antigens (Ov7, Ov11, Ov16) has also been used to detect antibodies. A comparison study showed that a mixture of these 3 proteins yielded a sensitivity of approximately 97% and a specificity 100%, superior to those of the recombinant Ov16 card test.23
      • Testing for a low–molecular-weight antigen fraction of female O volvulus parasite yields sensitivity and specificity similar to those of skin-snip testing.24
    • Antigen detection: Oncho-27 antigens have been studied in the diagnosis of Onchocerca infections. The advantage of this test is that it uses urine or tears for testing. In a study of 456 patients in a hyperendemic area of Cameroon, this technique yielded a sensitivity and specificity of 100%.25
  • Nucleic acid amplification tests: Polymerase chain reaction (PCR) using material from skin-snips or skin scratches provides high sensitivity and specificity, superior to older methods.26,3 However, the limited availability of technical expertise, as well as the high cost of the test, restricts its use in resource-limited settings.

Imaging Studies

  • Ultrasonography may reveal nonpalpable nodules, although this is not useful as a screening test. Ultrasonography of an adult worm in a nodule reveals a homogeneous echogenic area containing echodense particles with a lateral acoustic shadow.

Other Tests

  • Diethylcarbamazine (DEC) patch test: Based on the principle of Mazzotti reaction, topical application of DEC in a cream base (DEC patch) elicits localized cutaneous reactions (pruritus, maculopapular eruptions, dermal edema) in response to dying microfilariae.27 Earlier studies reported varying degree of sensitivity (30%-92%) in patients with positive skin-snip results. Severe cutaneous reactions may require steroid therapy or hospitalization. Higher concentrations of DEC and longer patch times increase the sensitivity.28 However, false-positive reactions may occur in patients with other filarial diseases such as Loa loa infection.

Procedures

  • Skin snip
    • In this technique, a razor blade is used to remove tiny skin samples (3-5 mg) from multiple sites (iliac crests, shoulder blades); they are then placed in saline to observe microfilariae emerging from the skin samples. Alternatively, sclerocorneal punch samples can be used to obtain skin-tissue specimens.
    • The sensitivity is low in the prepatent disease stage, areas of low prevalence, and areas of mass ivermectin use.
    • Skin-snip biopsy specimens can also be used to detect microfilariae using nucleic acid amplification.
  • Nodule resection (nodulectomy, onchocercomectomy): Although this is the most invasive method, surgical removal of nodules has both diagnostic (if adult worm is observed) and therapeutic potential (elimination of the adult worms in that nodule).

Histologic Findings

Microscopic examination of excised onchocercomata reveals cross-sections of adult worms with eosinophils and lymphocytes at the periphery of the nodule.

More on Onchocerciasis

Overview: Onchocerciasis
Differential Diagnoses & Workup: Onchocerciasis
Treatment & Medication: Onchocerciasis
Follow-up: Onchocerciasis
Multimedia: Onchocerciasis
References

References

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Further Reading

Keywords

onchocerciasis, onchocercosis, river blindness, volvulosis, craw-craw, Robles disease, Onchocerca volvulus, O volvulus, Simulium fly, blinding disease, papular dermatitis, leopard skin, sowda, sowdah, Nakalaga syndrome, ocular onchocerciasis, ocular onchocercosis, onchodermatitis, onchocercomata

Contributor Information and Disclosures

Author

Mary Nettleman, MD, MS, Chair, Department of Medicine, Michigan State University
Mary Nettleman, MD, MS is a member of the following medical societies: American College of Physicians, Association of Professors of Medicine, Central Society for Clinical Research, Infectious Diseases Society of America, and Society of General Internal Medicine
Disclosure: Nothing to disclose.

Coauthor(s)

Apoorv Kalra, MD, Assistant Professor of Medicine, Michigan State University
Disclosure: Nothing to disclose.

Medical Editor

Daniel R Lucey, MD, MPH, Chief, Fellowship Program Director, Department of Internal Medicine, Division of Infectious Diseases, Washington Hospital Center; Professor, Department of Internal Medicine, Uniformed Services University of the Health Sciences
Daniel R Lucey, MD, MPH is a member of the following medical societies: Alpha Omega Alpha and American College of Physicians
Disclosure: Nothing to disclose.

Pharmacy Editor

Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine
Disclosure: Nothing to disclose.

Managing Editor

John W King, MD, Professor of Medicine, Section of Infectious Diseases, Louisiana State University Health Sciences Center; Director, Viral Therapeutics Clinics for Hepatitis; Consulting Staff, Department of Infectious Diseases, Overton Brook Veterans Affairs Medical Center
John W King, MD is a member of the following medical societies: American Association for the Advancement of Science, American College of Physicians, American Federation for Medical Research, American Society for Microbiology, Association of Subspecialty Professors, Infectious Diseases Society of America, and Sigma Xi
Disclosure: emedicine $50.00 author of chapter

CME Editor

Eleftherios Mylonakis, MD, Clinical and Research Fellow, Department of Internal Medicine, Division of Infectious Diseases, Massachusetts General Hospital
Eleftherios Mylonakis, MD is a member of the following medical societies: American Association for the Advancement of Science, American College of Physicians, American Society for Microbiology, and Infectious Diseases Society of America
Disclosure: Nothing to disclose.

Chief Editor

Burke A Cunha, MD, Professor of Medicine, State University of New York School of Medicine at Stony Brook; Chief, Infectious Disease Division, Winthrop-University Hospital
Burke A Cunha, MD is a member of the following medical societies: American College of Chest Physicians, American College of Physicians, and Infectious Diseases Society of America
Disclosure: Nothing to disclose.

 
 
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