Acanthocheilonemiasis
National Organization for Rare Disorders, Inc.
Important
It is possible that the main title of the report Acanthocheilonemiasis
is not the name you expected. Please check the synonyms listing to find
the alternate name(s) and disorder subdivision(s) covered by this report.
Synonyms
- Dipetalonemiasis
- Dipetalonema perstans
- Mansonella perstans
- Acanthocheilonemiasis perstans
Disorder Subdivisions
General Discussion
Acanthocheilonemiasis is a rare tropical infectious disease caused by a parasite known as Acanthocheilonema perstans, which belongs to a group of parasitic diseases known as filarial diseases (nematode). This parasite is found, for the most part, in Africa. Symptoms of infection may include red, itchy skin (pruritis), abdominal and chest pain, muscular pain (myalgia), and areas of localized swelling (edema). In addition, the liver and spleen may become abnormally enlarged (hepatosplenomegaly). Laboratory testing may also reveal abnormally elevated levels of certain specialized white blood cells (eosinophilia). The parasite is transmitted through the bite of small flies (A. coliroides).
Symptoms
Initially people with Acanthocheilonemiasis may have no symptoms. Symptoms occur more frequently in people who visit the areas where this parasite is common (endemic), than in people who are native to that area. One common laboratory finding, in people who have recently returned from infected areas, is abnormally high levels of specialized white blood cells (eosinophilia). Generally there are no symptoms associated with the laboratory finding.
When symptoms appear they may include itchy skin (pruritis), abdominal pain, chest pain, muscle pains (myalgias), and/or areas of swelling under the skin (subcutaneous). Examination by a physician may reveal an abnormally enlarged liver and spleen (hepatosplenomegaly), and abnormally high levels of granular white blood cells (eosinophilia). The adult worm (nematode) may lodge in the tissues of the abdomen and chest causing inflammation and immune reactions. This may result in inflammation of the lining of the lungs (pleuritis) and/or the membranes that surround the heart (pericarditis).
The early or prelarval form (microfilariae) of Acanthocheilonema perstans can be isolated from the blood from patients with Acanthocheilonemiasis. Generally this disease is diagnosed by the examination under a microscope of a thick blood smear taken from the patient.
Causes
Acanthocheilonemiasis is a rare infectious disease caused by long "thread- like" worms, Acanthocheilonema perstans, also known as Dipetalonema perstans. The disease is transmitted by a small black insect (midge), called A. Cailicoides.
Affected Populations
Acanthocheilonema perstans, the parasite that causes Acanthocheilonemiasis is common in central Africa and in some areas of South America. This disorder affects males and females in equal numbers.
Related Disorders
Symptoms of the following disorders can be similar to those of Acanthocheilonemiasis. Comparisons may be useful for a differential diagnosis:
Filariasis is a group of rare infectious diseases caused by parasitic worms. These disorders are characterized by abnormal changes with the lymph glands (lymphadenopathy) and chronic obstruction of the flow of lymphatic fluid. This may result in the extreme swelling of the legs and/or genitalia (elephantiasis). This parasite enters the body by a mosquito bite. (For more information on this disorder, choose "Filariasis" as your search term in the Rare Disease Database.)
Other tropical diseases can cause similar symptoms to Acanthocheilonemiais. For more information choose "Tropical" as your search term in the Rare Disease Database.
Standard Therapies
Acanthocheilonemiasis is treated by means of the administration of antifilarial drugs, some of which are newer than others. Ivermectin or diethyl-carbamazine (DEC) are frequently prescribed. Occasionally, surgery may be required to remove large adult worms. Mild cases of acanthocheilonemiasis do not require treatment.
Investigational Therapies
Information on current clinical trials is posted on the Internet at www.clinicaltrials.gov. All studies receiving U.S. government funding, and some supported by private industry, are posted on this government web site.
For information about clinical trials being conducted at the NIH Clinical Center in Bethesda, MD, contact the NIH Patient Recruitment Office:
Tollfree: (800) 411-1222 TTY: (866) 411-1010 Email: prpl@cc.nih.gov
For information about clinical trials sponsored by private sources, contact: www.centerwatch.com
Research on tropical diseases is ongoing. The development of a vaccine is also being investigated. For more information on these disorders contact the World Health Organization (WHO) listed in the Resources section below.
References
TEXTBOOKS Stein JH, Hutton JJ, Kohler PO, et al., eds. Internal Medicine. 4th ed. Mosby-Yearbook, Inc., St. Louis, MO. 1994:1966; 2280.
JOURNAL ARTICLES Huynh T, Thean J, Maini R. Dipetalonema reconditum in the human eye. Br J Ophthalmol. 2001;85:1391-92.
Tripathi RP, Tripathi R, Bhaduri AP, et al. Antifilarial activity of some 2H-1-benzopyran-2-ones (coumarins). Acta Trop. 2000;76:101-06.
Zahner H, Schares G. Experimental chemotherapy of filariasis: comparative evaluation of the efficacy of filaricidal compounds in Mastomys coucha infected with Litomosoides carinii, Acanthocheilonema vitae, Brugia malaya and B. pahangi. Acta Trop. 1993;52:221-66.
Resources
Centers for Disease Control and Prevention
1600 Clifton Road NE Atlanta, GA 30333 Tel: (404)639-3534 Tel: (800)311-3435 Email: http://www.cdc.gov/netinfo.htm Internet: http://www.cdc.gov/
NIH/National Institute of Allergy and Infectious Diseases
6610 Rockledge Drive MSC 6612 Bethesda, MD 20892-6612 Tel: (301)496-5717 Fax: (301)402-3573 TDD: (800)877-8339 Internet: http://www.niaid.nih.gov/
World Health Organization (WHO) Regional Office for the Americas (AMRO)
Pan American Health Organization (PAHO) 525 23rd Street NW Washington, DC 20037 Tel: (202)974-3000 Fax: (202)974-3663 Email: postmaster@paho.org Internet: http://www.who.ch/
For a Complete Report
This is an abstract of a report from the National Organization for Rare Disorders, Inc.® (NORD). A copy of the complete report can be obtained for a small fee by visiting the NORD website. The complete report contains additional information including symptoms, causes, affected population, related disorders, standard and investigational treatments (if available), and references from medical literature. For a full-text version of this topic, see http://www.rarediseases.org/search/rdblist.html.
The information provided in this report is not intended for diagnostic purposes. It is provided for
informational purposes only. NORD recommends that affected individuals seek the advice or counsel of
their own personal physicians.
It is possible that the title of this topic is not the name you selected. Please check the Synonyms
listing to find the alternate name(s) and Disorder Subdivision(s) covered by this report
This disease entry is based upon medical information available through the date at the end of the
topic. Since NORD's resources are limited, it is not possible to keep every entry in the Rare Disease
Database completely current and accurate. Please check with the agencies listed in the Resources section
for the most current information about this disorder.
For additional information and assistance about rare disorders, please contact the National Organization
for Rare Disorders at P.O. Box 1968, Danbury, CT 06813-1968; phone (203) 744-0100; web site
www.rarediseases.org or email orphan@rarediseases.org
Last Updated:
3/25/2005
Copyright
1986, 1993, 1997, 2005
National Organization for Rare Disorders, Inc.
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