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= Visceral Leishmaniasis =
{{Infobox disease
| name = Visceral leishmaniasis
| image = Amastigotes in a chorionic villus.jpg
| caption = Amastigotes of ''Leishmania'' in a chorionic villus
| field = Infectious disease
| symptoms = Fever, weight loss, enlargement of the spleen and liver
| complications = Anemia, secondary infections
| causes = ''Leishmania'' parasites
| risks = Malnutrition, poverty, immunosuppression
| diagnosis = Microscopy, serology, PCR
| treatment = Antimonial drugs, amphotericin B, miltefosine
| prevention = Vector control, bed nets
}}


'''Visceral leishmaniasis''' (VL), also known as kala-azar, is the most severe form of leishmaniasis, a disease caused by protozoan parasites of the genus ''Leishmania''. Visceral leishmaniasis affects the body's internal organs, such as the spleen, liver, and bone marrow, and is fatal if left untreated.  
'''Visceral leishmaniasis''', also known as '''kala-azar''', is a severe form of [[leishmaniasis]] caused by protozoan parasites of the ''[[Leishmania]]'' genus. It is transmitted by the bite of infected [[sandflies]]. The disease is characterized by irregular bouts of fever, substantial weight loss, swelling of the spleen and liver, and anemia.


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==Epidemiology==
title='''{{PAGENAME}}'''
Visceral leishmaniasis is endemic in parts of the [[Indian subcontinent]], [[East Africa]], and [[Brazil]]. It is estimated that 50,000 to 90,000 new cases occur annually, with a significant number of deaths if untreated. The disease is closely associated with poverty, malnutrition, and environmental changes that increase exposure to sandflies.
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== Overview ==
==Pathophysiology==
Visceral leishmaniasis is characterized by fever, weight loss, splenomegaly (enlargement of the spleen), hepatomegaly (enlargement of the liver), and anemia. The disease is transmitted through the bites of infected female phlebotomine sandflies.  
The ''Leishmania'' parasites invade the host's [[reticuloendothelial system]], primarily affecting the spleen, liver, and bone marrow. The parasites multiply within macrophages, leading to the characteristic symptoms of the disease. The immune response to the infection can cause further damage to the host tissues.


[[File:Visceral-Leishmaniasis-in-Ethiopia-An-Evolving-Disease-pntd.0003131.g001.jpg|thumb|500px|A phlebotomine sandfly, the vector of ''Leishmania'' parasites.]]
==Clinical Presentation==
Patients with visceral leishmaniasis typically present with prolonged fever, weight loss, and splenomegaly. Hepatomegaly and lymphadenopathy may also be observed. Anemia and leukopenia are common laboratory findings. If left untreated, the disease can be fatal due to complications such as secondary infections and severe anemia.


== Causative Agent ==
==Diagnosis==
The disease is caused by several species of the ''Leishmania'' genus, primarily ''Leishmania donovani'' and ''Leishmania infantum'' (also known as ''Leishmania chagasi'' in Latin America).
Diagnosis of visceral leishmaniasis is confirmed by identifying the parasites in tissue samples, such as bone marrow or spleen aspirates, using microscopy. Serological tests and polymerase chain reaction (PCR) are also used to detect ''Leishmania'' DNA or antibodies.


== Transmission ==
==Treatment==
VL is transmitted to humans through the bite of infected female phlebotomine sandflies, which acquire the parasite by feeding on infected animals or humans.  
The treatment of visceral leishmaniasis involves the use of antileishmanial drugs. Pentavalent antimonials, such as sodium stibogluconate, have been the mainstay of treatment. Liposomal amphotericin B is also effective and is often used in cases of drug resistance or intolerance. Miltefosine, an oral drug, is another option for treatment.


== Epidemiology ==
==Prevention==
Visceral leishmaniasis is endemic in parts of Asia, Africa, South America, and the Mediterranean region. It is estimated that there are 50,000 to 90,000 new cases of VL worldwide each year.
Preventive measures focus on reducing exposure to sandflies. This includes the use of insecticide-treated bed nets, indoor residual spraying, and environmental management to reduce sandfly breeding sites. Public health education and improving socio-economic conditions are also crucial in controlling the spread of the disease.


== Clinical Manifestations ==
==History==
After an incubation period that can range from weeks to months, individuals infected with VL may develop:
The disease was first described in the 19th century, and significant contributions to its understanding were made by scientists such as Sir [[Upendra Nath Brahmachari]], who developed a treatment for kala-azar.
* Persistent fever
* Weight loss
* Fatigue
* Enlargement of the spleen and liver
* Anemia and leukopenia


== Diagnosis ==
[[File:Scientist Sir Upendra Nath Brahmachari.png|thumb|Sir Upendra Nath Brahmachari, who developed a treatment for kala-azar]]
Diagnosis of VL is based on clinical signs and confirmed through laboratory tests, including:
* Serological tests to detect antibodies against ''Leishmania'' parasites
* Parasitological examination of bone marrow, spleen, or lymph node aspirates
* Molecular tests, such as PCR, to identify ''Leishmania'' DNA


[[File:Parasites of the tropical diseases Kala-Azar and Oriental So Wellcome V0022616.jpg|thumb|Microscopic view of ''Leishmania'' parasites in a spleen aspirate.]]
==Also see==
* [[Leishmaniasis]]
* [[Cutaneous leishmaniasis]]
* [[Mucocutaneous leishmaniasis]]
* [[Sandfly]]


== Treatment ==
==References==
Treatment for VL typically involves the administration of antileishmanial drugs, such as:
* World Health Organization. "Leishmaniasis." WHO, 2023.
* Amphotericin B
* Centers for Disease Control and Prevention. "Parasites - Leishmaniasis." CDC, 2023.
* Miltefosine
* Pentavalent antimonials


Early diagnosis and treatment are crucial to prevent fatal outcomes and reduce the risk of developing post-kala-azar dermal leishmaniasis (PKDL), a complication that can occur after treatment.
{{Infectious diseases}}
{{Neglected tropical diseases}}


== Prevention and Control ==
Prevention of VL focuses on reducing contact with sandflies and controlling the sandfly population. Strategies include:
* Use of insecticide-treated bed nets
* Indoor residual spraying with insecticides
* Personal protective measures, such as wearing long-sleeved clothing and applying insect repellent
== External Links ==
* [https://www.who.int/health-topics/leishmaniasis#tab=tab_1 World Health Organization - Leishmaniasis]
* [https://www.cdc.gov/parasites/leishmaniasis/index.html CDC - Parasites - Leishmaniasis]
== References ==
<references/>
* ''Control of the Leishmaniases'' by the World Health Organization
* ''Leishmaniasis: Epidemiology, Control and Prevention'' edited by David Claborn
[[Category:Tropical diseases]]
[[Category:Parasitic diseases]]
[[Category:Parasitic diseases]]
[[Category:Neglected tropical diseases]]
[[Category:Infectious diseases]]
[[Category:Infectious diseases]]
{{stub}}

Revision as of 02:43, 11 December 2024

Visceral leishmaniasis
Amastigotes of Leishmania in a chorionic villus
ICD-10
ICD-9
DiseasesDB
MedlinePlus
eMedicine
MeSH ID

Visceral leishmaniasis, also known as kala-azar, is a severe form of leishmaniasis caused by protozoan parasites of the Leishmania genus. It is transmitted by the bite of infected sandflies. The disease is characterized by irregular bouts of fever, substantial weight loss, swelling of the spleen and liver, and anemia.

Epidemiology

Visceral leishmaniasis is endemic in parts of the Indian subcontinent, East Africa, and Brazil. It is estimated that 50,000 to 90,000 new cases occur annually, with a significant number of deaths if untreated. The disease is closely associated with poverty, malnutrition, and environmental changes that increase exposure to sandflies.

Pathophysiology

The Leishmania parasites invade the host's reticuloendothelial system, primarily affecting the spleen, liver, and bone marrow. The parasites multiply within macrophages, leading to the characteristic symptoms of the disease. The immune response to the infection can cause further damage to the host tissues.

Clinical Presentation

Patients with visceral leishmaniasis typically present with prolonged fever, weight loss, and splenomegaly. Hepatomegaly and lymphadenopathy may also be observed. Anemia and leukopenia are common laboratory findings. If left untreated, the disease can be fatal due to complications such as secondary infections and severe anemia.

Diagnosis

Diagnosis of visceral leishmaniasis is confirmed by identifying the parasites in tissue samples, such as bone marrow or spleen aspirates, using microscopy. Serological tests and polymerase chain reaction (PCR) are also used to detect Leishmania DNA or antibodies.

Treatment

The treatment of visceral leishmaniasis involves the use of antileishmanial drugs. Pentavalent antimonials, such as sodium stibogluconate, have been the mainstay of treatment. Liposomal amphotericin B is also effective and is often used in cases of drug resistance or intolerance. Miltefosine, an oral drug, is another option for treatment.

Prevention

Preventive measures focus on reducing exposure to sandflies. This includes the use of insecticide-treated bed nets, indoor residual spraying, and environmental management to reduce sandfly breeding sites. Public health education and improving socio-economic conditions are also crucial in controlling the spread of the disease.

History

The disease was first described in the 19th century, and significant contributions to its understanding were made by scientists such as Sir Upendra Nath Brahmachari, who developed a treatment for kala-azar.

Sir Upendra Nath Brahmachari, who developed a treatment for kala-azar

Also see

References

  • World Health Organization. "Leishmaniasis." WHO, 2023.
  • Centers for Disease Control and Prevention. "Parasites - Leishmaniasis." CDC, 2023.