Histoplasma capsulatum

Background

Microbiology

• Dimorphic fungus; mold at room temperature, yeast at >37º C
  • Mold: aerial hyphae with macroconidia
    • Mold form is highly infectious, associated with lab-related outbreaks
    • Mycelia have a typical appearance of spiked spherical conidia
  • Yeast:
    • Non-infectious, once hanging out in your body
    • Narrow-based budding
• H. capsulatum var. capsulatum most common worldwide, in various clades
• H. capsulatum var. duboisii present in western Africa, has larger yeast forms
  • Can take up to 7 days to grow

Epidemiology

Distribution of histoplasmosis

• Endemic in many parts of the world
  • Ohio and Mississippi River Valley systems (Central/Eastern US)
  • Probably up through St. Lawrence River as well
  • Probably more broadly distributed, including Central and South America, South and East Asia, and Australia
  • H. capsulatum var. duboisii in western Africa
• Typically found in moist soil enriched with bat or bird droppings, which helps it to sporulate
  • Disturbing the soil aerosolizes it, allowing the microconidia to be inhaled
  • Microconidia can be transported for miles by air currents

Pathophysiology

• Inhaled microconidia reach the alveolii and are phagocytosed by alveolar macrophages
  • Innoculum size can be smaller with immunodeficiency
  • Size of innoculation affects disease severity and progression
• Microconidia transform into budding yeasts, in a process that is dependent on macrophage calcium and iron
• They multiply inside macrophages, and translocate through the lymphatics
• Cellular immunity developed around 2 weeks later
  • Response depends on IL-12 and TNF-alpha
  • Organize to form granulomas to contain the infection
• Latent infection can reactivate, but rare
  • Most common with infliximab
• In impaired cellular immunity, infection can become disseminated

Clinical Manifestations

• Often asymptomatic; in endemic areas, 50-80% of people skin-test positive or have radiographic evidence of previous infection
• Can cross tissue planes

Acute pulmonary histoplasmosis

• Fever, chill, malaise, headaches, myalgias, anorexia, cough, dyspnea, and chest pain
• Pneumonitis on chest x-ray, often with adenopathy
  • "Buckshot" appearance? (Mandell)
• Can have rheumatologic sequelae in 5-10%, with arthralgias, arthritis, and erythema nodosum
• Can have pericarditis from the inflammatory response
• Hilar adenopathy can necrotize
• Usually self-limited, no need to treat unless longer than a month

Progressive disseminated histoplasmosis

• Usually, though not exclusively, in immunocompromised pations
  • Risk factors include CD4 <200, very old or very young, and therapeutic immunosuppression (pred, MMF, tac, MTX, TNF-alpha, other biologics
• Can be rapidly-progressing and acute, or more subacute

Acute progressive disseminated histoplasmosis

• Fever, weight loss, organomegaly, thrombocytopenia
• Meningitis or focal brain lesions
• Oral and GI mucosal ulcerations
• Adrenal insufficiency

Chronic progressive disseminated histoplasmosis

• In normal hosts
• Absent or low-grade fever
• Longer course
• Most common finding is oropharyngeal lesion: deep, well-circumscribed, unrated, and painless
  • Mimics squamous cell carcinoma
• Can also have hepatosplenomegaly, chronic meningitis, or chronic granulomatous hepatitis

Chronic cavitary histoplasmosis

• Typically seen in bullous emphysema
• Productive cough, dyspnea, low-grade fever, night sweats, weight loss
  • Hemoptysis is rare
  • Progressive without treatment
• Chest x-ray shows upper-lobe infiltrations, vacitation, and pleural thickening, similar to tuberculosis

Fibrosing mediastinitis

• Rare but serious
• Progressive fibrosis around hilar/mediatinal lymphadenopathy, wither unilateral or bilateral
• Can present with a SVC syndrome, obstruction of pulmonary vessels, or airway obstruction
• Can also present with recurrent pneumonias, hemoptysis, or respiratory failure
• 30% mortality

Other complications

• Ophthalmic uveitis
• Meningitis
• Endocarditis

African histoplasmosis

• H. capsulatum vars. capsulatum and duboisii coexist in Africa
• var. duboisii has more skin and skeletal manifestations
  • Ulcers, nodules, or psoriaform lesions that can spontaneously resolve
    • Can cause a cold abscess, without inflammation
  • Osteolytic bone lesions are common (50%) of cases
    • Skull and ribs most common
    • Can have sinus formation and cystic bone lesions
  • May not have any evidence on CXR of prior pulmonary histoplasmosis
  • Can also present with progressive disseminated disease, with fevers and multiorgan involvement
    • Combianation of granulomas and pus
    • Larger yeast is harder for macrophages to engulf

Diagnosis

• Fungal culture of sputum (chronic cavitary), or blood or bone marrow aspirate (disseminated), or CSF (CNS histo)
  • Mold and yeast forms depending on the temperature
  • Best stain is GMS (Giemsa m…. silver)
  • Seen within the macrophages
• Serology can be done for antigen or antibody
  • Serology may be negative in immunosuppressed patients
  • Antigen of urine (best), BAL fluid, and serum if available
    • Urine is best, but only 40% sensitive in cavitary, up to 95% in AIDS patients
    • Cross-reacts with other endemic fungi; false-positives with antithymocyte globulin
• PCR is possible
  • 16S PCR

Management

• In general, mild infections are treated with itraconazole and severe infections with amphotericin B

Syndrome	Treatment
Acute pulmonary histoplasmosis
Mild, self-resolving	If resolves within a month, no need to treat
Mild, ongoing symptoms	Itraconazole 200 mg po TID x3d then itra 200 mg po daily or BID for 6-12 weeks
Moderate to severe	Liposomal amphotericin B 3-5 mg/kg/d for 1-2 weeks, followed by itraconazole 200 mg TID x3d then itraconazole 200 mg BID x12wk Methylpred 0.5-1 mg/kg IV daily for first 1-2 weeks if respiratory complications
Chronic cavitary pulmonary histoplasmosis	Itraconazole 200 mg TID x3d then daily or BID for at least 1 year (18-24 months may have lower relapse)
Complications
Pericarditis	NSAIDs if mild Prednisone 0.5-1 mg/kg daily then taper over 1-2 weeks, plus itra (as above) for 6-12 weeks if hemodynamic compromise May need therapeutic pericardiocentesis
Rheumatologic	NSAIDs if mild, prednisone and itraconazole (as for pericarditis) if severe
Mediastinal lymphadenitis	Usually no treatment. Follow guide for acute pulmonary histoplasmosis.
Mediastinal granuloma	Usually no treatment. Standard itraconazole protocol for 6-12 weeks if symptomatic.
Mediastinal fibrosis	Antifungals not recommended. Treat only if there is suspicion of mediastinal granuloma. May need stenting of obstructed pulmonary vessels.
Broncholithiasis	Antifungals not recommended. May need surgery.
Progressive disseminated histoplasmosis	Follow antigen levels during therapy and for 12 months after to monitor for relapse
Mild to moderate	Itraconazole for 12 months
Moderately severe to severe	Liposomal amphotericin B 3 mg/kg for 1-2 weeks then oral itraconazole for at least 12 months
Immunosuppressed	May need lifelong suppressive therapy with itraconazole 200 mg po daily
CNS histoplasmosis	Liposomal amphotericin B 5 mg/kg daily for 4-6 weeks (total 175 mg/kg) followed by itraconazole for at least 1 year, until resolution of CSF abnormalities
Pregnancy	Liposomal amphotericin B 3-5 mg/kg for 4-6 weeks
Children	As per above guidelines, with amphotericin B deoxycholate 1 mg/kg and itraconazole 2.5-5 mg/kg bid (max 400 mg daily)
Prophylaxis	Itraconazole 200 mg po daily recommended if HIV with CD4 <150 and more than 10 cases per 100 patient-years

Note: therapeutic drug level monitoring is recommended for itraconazole

Source: IDSA guidelines 2007