Disseminated histoplasmosis
Updates to Article Attributes
Disseminated histoplasmosis, also known as progressive disseminated histoplasmosis, is a severe form of histoplasmosis infection typically seen in immunosuppressed patients, especially in the setting of HIV infection. It results from haematogeneous dissemination of the infection, involving multiple organs and systems and associating a high mortality1.
Terminology
Although it is sometimes referred to as extrapulmonary histoplasmosis, lung involvement is one of the commonest manifestations of this condition2.
Epidemiology
Dissemination of the disease is fairly uncommon and may occur in 1 in 2000 acute infections3.
Risk factors
HIV infection, especially with less than 150 cells/μL CD41,4
Immunosuppressive medications4
Biologic agents (infliximab, etanercept)3
Immune disorders (idiopathic CD4 lymphocytopenia, Job's syndrome, common variable immunodeficiency)
Extremes of ages
Clinical presentation
Clinical presentation includes systemic symptoms such as fever, weight loss and fatigue and local systems depending on the organs involved, with frequent progressive shortness of breath and diarrhoea1,3.
Physical examination may reveal hepatoesplenomegaly, lymphadenopathy and skin and oral lesions1.
Location
Lungs: parenchymal disease2.
Gastrointestinal: any site of the digestive tube can be involved, with potential bleeding or perforation1,4.
Liver and spleen: haemophagocytic lymphohistiocytosis with macrophage activation syndrome1.
Kidneys: granulomatous nephritis1.
Adrenal glands: adrenal insuficciency1,3.
Central nervous system: meninges, brain or spinal cord lesions1.
-</ul><h4>Clinical presentation</h4><p>Clinical presentation includes systemic symptoms such as fever, weight loss and fatigue and local systems depending on the organs involved, with frequent progressive shortness of breath and diarrhoea<sup>1,3</sup>. </p><p>Physical examination may reveal hepatoesplenomegaly, lymphadenopathy and skin and oral lesions<sup>1</sup>. <br></p><p></p><p></p>- +</ul><h4>Clinical presentation</h4><p>Clinical presentation includes systemic symptoms such as fever, weight loss and fatigue and local systems depending on the organs involved, with frequent progressive shortness of breath and diarrhoea<sup>1,3</sup>.</p><p>Physical examination may reveal hepatoesplenomegaly, lymphadenopathy and skin and oral lesions<sup>1</sup>. </p><h4>Location</h4><ul>
- +<li><p>Lungs: parenchymal disease<sup>2</sup>. </p></li>
- +<li><p>Gastrointestinal: any site of the digestive tube can be involved, with potential bleeding or perforation<sup>1,4</sup>.</p></li>
- +<li><p>Liver and spleen: haemophagocytic lymphohistiocytosis with macrophage activation syndrome<sup>1</sup>.</p></li>
- +<li><p>Kidneys: granulomatous nephritis<sup>1</sup>.</p></li>
- +<li><p>Adrenal glands: adrenal insuficciency<sup>1,3</sup>. </p></li>
- +<li><p>Central nervous system: meninges, brain or spinal cord lesions<sup>1</sup>.</p></li>
- +<li><p> </p></li>
- +</ul><p><br></p><p></p><p></p><p></p>
Systems changed:
- Haematology