If symptoms of histoplasmosis infection occur, they start within 3 to 17 days after exposure; the typical time is 12–14 days. Most affected individuals have clinically silent manifestations and show no apparent ill effects. The
acute phase of histoplasmosis is characterized by nonspecific respiratory symptoms, often cough or flu-like.
Chest X-ray findings are normal in 40–70% of cases. Chronic histoplasmosis cases can resemble
tuberculosis; disseminated histoplasmosis affects multiple organ systems and is fatal unless treated. While histoplasmosis is the most common cause of
mediastinitis, this remains a relatively rare disease. Severe infections can cause
hepatosplenomegaly,
lymphadenopathy, and adrenal enlargement.
Presumed ocular histoplasmosis syndrome causes
chorioretinitis, where the
choroid and
retina of the eyes are scarred, resulting in a loss of vision not unlike
macular degeneration. Despite its name, the relationship to
Histoplasma is controversial. Distinct from POHS, acute ocular histoplasmosis may rarely occur in immunodeficiency.
Complications In the absence of proper treatment, and especially in
immunocompromised individuals, complications can arise. These include recurrent pneumonia,
respiratory failure, fibrosing mediastinitis,
superior vena cava syndrome, pulmonary vessel obstruction, and progressive fibrosis of lymph nodes. Fibrosing mediastinitis is a serious complication and can be fatal.
People who smoke and people with structural
lung disease have a higher probability of developing chronic cavitary histoplasmosis. After healing of lesions, hard, calcified lymph nodes can erode the walls of the airway, causing
hemoptysis. ==Mechanisms==