eMedicine Specialties > Pulmonology > Infectious Lung Diseases

Histoplasmosis: Differential Diagnoses & Workup

Author: Jazeela Fayyaz, DO, Senior Fellow, Department of Pulmonology, Lenox Hill Hospital
Coauthor(s): Klaus-Dieter Lessnau, MD, FCCP, Clinical Associate Professor of Medicine, New York University School of Medicine; Medical Director, Pulmonary Physiology Laboratory; Director of Research in Pulmonary Medicine, Department of Medicine, Section of Pulmonary Medicine, Lenox Hill Hospital
Contributor Information and Disclosures

Updated: Aug 14, 2009

Differential Diagnoses

Aspergillosis
Pneumococcal Infections
Blastomycosis
Pneumocystis Carinii Pneumonia
Carcinoid Lung Tumors
Pneumonia, Aspiration
Chlamydial Pneumonias
Pneumonia, Bacterial
Coccidioidomycosis
Pneumonia, Fungal
Legionella pneumonias
Pneumonia, Viral
Lung Cancer, Oat Cell (Small Cell)
Sarcoidosis
Lymphoma, Mediastinal
Tuberculosis
Mediastinal Cysts
Mycoplasma Infections
Pancoast Syndrome

Workup

Laboratory Studies

  • CBC count
    • Mild anemia may be present in chronic pulmonary histoplasmosis.
    • In acute progressive disseminated histoplasmosis, pancytopenia occurs in 70-90% of patients, with a platelet count less than 70,000. Pancytopenia may occur at a lower rate in chronic progressive disseminated histoplasmosis.
  • Alkaline phosphatase: levels are elevated in acute progressive disseminated histoplasmosis and chronic pulmonary histoplasmosis.8
  • Marked elevations in lactate dehydrogenase levels may be seen in AIDS patients with disseminated histoplasmosis.9
  • Sputum cultures
    • Positive yields occur in approximately 15% patients with acute pulmonary histoplasmosis.
    • Culture results are positive in 60-85% of specimens from patients with chronic pulmonary histoplasmosis.8
  • Blood cultures
    • Blood culturing should be performed in all patients, and results are positive in 50-70% of patients with progressive  disseminated histoplasmosis.8
    • Results are rarely positive in patients with other types of histoplasmosis.
  • Complement-fixing antibodies
    • Titer is considered positive at reciprocal dilutions greater than 1:8. A titer with dilutions greater than 1:32 suggests active histoplasmosis infection. Cross-reactivity with antigens from Blastomyces dermatitidis and Coccidioides immitis may cause a false-positive test result. False positive tests may also occur in persons with lymphoma, tuberculosis,  or sarcoidosis.4
    • Positive results are expected in 5-15% of cases of acute pulmonary infection 3 weeks after exposure. This figure increases to 75-95% at 6 weeks in cases of symptomatic infection. Test results usually normalize over months, with resolution of infection.
    • Test results may remain positive in 70-90% of cases associated with chronic pulmonary histoplasmosis or chronic progressive disseminated histoplasmosis.6
  • Immunoprecipitating antibodies
    • This test detects antibodies to 2 glycoproteins, H and M.
    • Anti-M antibody is detected in 50-80% of patients and remains elevated for years.
    • Anti-H antibody is detected in only 10-20% of patients and becomes undetectable within 6 months in the absence of continued infection. Anti-H antibody is more specific for active histoplasmosis.8
  • Serum and urine antigen detection10
    • These are useful in individuals who are immunocompromised when antibody production may be impaired.
    • Detection rates in cases of acute progressive disseminated histoplasmosis are 50% with serum assay and 90% with urine assay. Lower detection rates are observed in acute or chronic pulmonary histoplasmosis.3
    • Cross-reactivity with Blastomyces and Coccidioides species causes false-positive results.
    • Some patients with acute histoplasmosis may have high serum levels of angiotensin-converting enzyme.11 This may cause a diagnostic confusion with sarcoidosis, particularly if the patient with histoplasmosis also has hilar adenopathy.
    • Urine antigen levels may be used to follow the patient's course.4
    • In making the diagnosis of progressive disseminated histoplasmosis, blood cultures, blood antigen, urine antigen, and Histoplasma immunodiffusion and complement fixation should be obtained.6

Imaging Studies

  • Chest radiography
    • In acute pulmonary histoplasmosis, findings on chest radiography are usually normal. Occasionally, hilar and mediastinal nodes are enlarged. Patchy infiltrates, predominately in the lower lung fields, may be present. In cases of exposure to high inoculum, diffuse pulmonary involvement correlates with a reticular nodular or miliary pattern on chest radiography. Cavitations are rarely present.
    • Histoplasmomas are healed pulmonary lesions that appear as residual nodules on chest radiography. These coin lesions usually are 1-4 cm in diameter. When yeast forms are present in the core, continued fibrosis in response to the yeast antigens adds to the fibrotic capsule, slowly enlarging the lesions.
    • Hilar lymphadenopathy is rare in chronic pulmonary histoplasmosis, although calcified nodes from prior healed infections may be present. Cavitations, predominantly in the upper lobes, are present in 90% of patients. Underlying emphysematous changes are common. Progressive fibrotic scarring is present in long-standing cases.
    • In chronic progressive disseminated histoplasmosis, chest radiography findings usually do not reveal any active pulmonary disease.
    • In acute progressive disseminated histoplasmosis, hilar lymphadenopathy with diffuse nodular infiltrates is common, occurring in 50% of patients. Findings on chest radiography are normal in 33% of patients initially, but radiographs may reveal pulmonary involvement as the disease progresses.6
  • CT scanning
    • Head CT scanning is useful in detecting the presence of cerebral histoplasmosis prior to performing a lumbar puncture.
    • Abdominal CT scanning is useful if adrenal involvement is suspected, especially with subacute progressive disseminated histoplasmosis, which results in adrenal infection in 80% of patients. Bilateral adrenal enlargement usually is detectable.3
  • Echocardiography: Transthoracic or transesophageal echocardiography may be helpful if valvular involvement is suspected; endocarditis with Histoplasma species is rarely associated with positive blood cultures.

Other Tests

  • Pulmonary function testing
    • Determine the extent of pulmonary involvement by evaluating the degree of restrictive defect, the presence of a small airway obstruction, the extent of diffusion impairment, and the presence of hypoxemia.
    • Monitor the progression of pulmonary disease in patients with chronic pulmonary histoplasmosis.

Procedures

  • Lumbar puncture: If CNS involvement is suspected, consider performing a lumbar puncture to evaluate for other possible CNS infections or lesions. Always perform CT scanning prior to lumbar puncture to evaluate for masses or bleeding that may complicate the lumbar procedure.
  • Lavage: Lavage may be required for histiologic evaluation and to obtain cultures to make the diagnosis.
  • Thoracentesis: This procedure may be required if the presence of pleural fluid is causing respiratory distress.
  • Tissue biopsy: Obtaining tissue from pulmonary lesions and lymph nodes by bronchoscopy, percutaneous needle biopsies, or rarely, thoracoscopy may be required to make the diagnosis. Results of biopsy of oropharyngeal ulcers are usually diagnostic.
  • Pericardiocentesis: Cultures of pericardial fluid are rarely diagnostic.

Histologic Findings

Tissue biopsy results may reveal the presence of yeast forms in tissue through hematoxylin and eosin staining. Using the Grocott-Gomori methenamine-silver procedure, yeast may be detected in areas of caseation necrosis from histoplasmomas and calcified lymph nodes. Yeast forms in circulating neutrophils and monocytes are rarely detected using Wright-Giemsa staining. Most biopsies do not reveal organisms.

More on Histoplasmosis

Overview: Histoplasmosis
Differential Diagnoses & Workup: Histoplasmosis
Treatment & Medication: Histoplasmosis
Follow-up: Histoplasmosis
References
Further Reading

References

  1. Outbreak of histoplasmosis among travelers returning from El Salvador--Pennsylvania and Virginia, 2008. MMWR Morb Mortal Wkly Rep. Dec 19 2008;57(50):1349-53. [Medline].

  2. Lowell JR. Diagnosis of histoplasmosis. Ann Intern Med. Feb 1983;98(2):260. [Medline].

  3. Kauffman CA. Histoplasmosis: a clinical and laboratory update. Clin Microbiol Rev. Jan 2007;20(1):115-32. [Medline].

  4. Kauffman CA. Histoplasmosis. Clin Chest Med. Jun 2009;30(2):217-25, v. [Medline].

  5. Hage CA, Wheat LJ, Loyd J, Allen SD, Blue D, Knox KS. Pulmonary histoplasmosis. Semin Respir Crit Care Med. Apr 2008;29(2):151-65. [Medline].

  6. Picardi JL, Kauffman CA, Schwarz J, Holmes JC, Phair JP, Fowler NO. Pericarditis caused by Histoplasma capsulatum. Am J Cardiol. Jan 1976;37(1):82-8. [Medline].

  7. Wheat LJ. Improvements in diagnosis of histoplasmosis. Expert Opin Biol Ther. Nov 2006;6(11):1207-21. [Medline].

  8. Corcoran GR, Al-Abdely H, Flanders CD, Geimer J, Patterson TF. Markedly elevated serum lactate dehydrogenase levels are a clue to the diagnosis of disseminated histoplasmosis in patients with AIDS. Clin Infect Dis. May 1997;24(5):942-4. [Medline].

  9. Wheat LJ, Kohler RB, Tewari RP. Diagnosis of disseminated histoplasmosis by detection of Histoplasma capsulatum antigen in serum and urine specimens. N Engl J Med. Jan 9 1986;314(2):83-8. [Medline].

  10. Davies SF, Rohrbach MS, Thelen V, et al. Elevated serum angiotensin-converting enzyme (SACE) activity in acute pulmonary histoplasmosis. Chest. Mar 1984;85(3):307-10. [Medline].

  11. [Guideline] Wheat LJ, Freifeld AG, Kleiman MB, et al. Clinical practice guidelines for the management of patients with histoplasmosis: 2007 update by the Infectious Diseases Society of America. Clin Infect Dis. 2007;45:807-825.

  12. Bennish M, Radkowski MA, Ripon JW. Cavitation in acute histoplasmosis. Chest. Oct 1983;84(4):496-7. [Medline].

  13. Wheat J, Hafner R, Wulfsohn M, et al. Prevention of relapse of histoplasmosis with itraconazole in patients with the acquired immunodeficiency syndrome. Ann Intern Med. Apr 15 1993;118(8):610-6. [Medline].

  14. Davies SF, Khan M, Sarosi GA. Disseminated histoplasmosis in immunologically suppressed patients. Occurrence in a nonendemic area. Am J Med. Jan 1978;64(1):94-100. [Medline].

  15. Goldman M, Johnson PC, Sarosi GA. Fungal pneumonias. The endemic mycoses. Clin Chest Med. Sep 1999;20(3):507-19. [Medline].

  16. Goodwin RA, Alcorn GL. Histoplasmosis with symptomatic lymphadenopathy. Chest. Feb 1980;77(2):213-5. [Medline].

  17. Goodwin RA, Loyd JE, Des Prez RM. Histoplasmosis in normal hosts. Medicine (Baltimore). Jul 1981;60(4):231-66. [Medline].

  18. Newman SL, Gootee L, Bucher C, Bullock WE. Inhibition of intracellular growth of Histoplasma capsulatum yeast cells by cytokine-activated human monocytes and macrophages. Infect Immun. Feb 1991;59(2):737-41. [Medline].

  19. Paya CV, Roberts GD, Cockerill FR 3rd. Transient fungemia in acute pulmonary histoplasmosis: detection by new blood-culturing techniques. J Infect Dis. Aug 1987;156(2):313-5. [Medline].

  20. Salzman SH, Schindel ML, Aranda CP, Smith RL, Lewis ML. The role of bronchoscopy in the diagnosis of pulmonary tuberculosis in patients at risk for HIV infection. Chest. Jul 1992;102(1):143-6. [Medline].

  21. Salzman SH, Smith RL, Aranda CP. Histoplasmosis in patients at risk for the acquired immunodeficiency syndrome in a nonendemic setting. Chest. May 1988;93(5):916-21. [Medline].

  22. Wheat J. Histoplasmosis. Experience during outbreaks in Indianapolis and review of the literature. Medicine (Baltimore). Sep 1997;76(5):339-54. [Medline].

  23. Wheat LJ. Systemic fungal infections: diagnosis and treatment. I. Histoplasmosis. Infect Dis Clin North Am. Dec 1988;2(4):841-59. [Medline].

  24. Wheat LJ, Batteiger BE, Sathapatayavongs B. Histoplasma capsulatum infections of the central nervous system. A clinical review. Medicine (Baltimore). Jul 1990;69(4):244-60. [Medline].

  25. Wheat LJ, Conces D, Allen SD, Blue-Hnidy D, Loyd J. Pulmonary histoplasmosis syndromes: recognition, diagnosis, and management. Semin Respir Crit Care Med. Apr 2004;25(2):129-44. [Medline].

  26. Wheat LJ, Wass J, Norton J, Kohler RB, French ML. Cavitary histoplasmosis occurring during two large urban outbreaks. Analysis of clinical, epidemiologic, roentgenographic, and laboratory features. Medicine (Baltimore). Jul 1984;63(4):201-9. [Medline].

Further Reading

Murray & Nadel's Textbook of Respiratory Medicine. 4th ed. 2005. WB Saunders; Philadelphia, Pa. Chapter 34.

Keywords

histoplasmosis, Histoplasma capsulatum, H capsulatum, Histoplasma species, dimorphic fungus, yeast, bat droppings, bird droppings, acute pulmonary histoplasmosis, pleural effusion, pericarditis, chronic pulmonary histoplasmosis, pulmonary fibrosis, mycelium, macroconidia, microconidia, progressive disseminated histoplasmosis, ocular histoplasmosis syndrome, chronic progressive disseminated histoplasmosis, subacute progressive disseminated histoplasmosis, acute progressive disseminated histoplasmosis

Contributor Information and Disclosures

Author

Jazeela Fayyaz, DO, Senior Fellow, Department of Pulmonology, Lenox Hill Hospital
Jazeela Fayyaz, DO is a member of the following medical societies: American College of Physicians and American Thoracic Society
Disclosure: Nothing to disclose.

Coauthor(s)

Klaus-Dieter Lessnau, MD, FCCP, Clinical Associate Professor of Medicine, New York University School of Medicine; Medical Director, Pulmonary Physiology Laboratory; Director of Research in Pulmonary Medicine, Department of Medicine, Section of Pulmonary Medicine, Lenox Hill Hospital
Klaus-Dieter Lessnau, MD, FCCP is a member of the following medical societies: American College of Chest Physicians, American College of Physicians, American Medical Association, American Society for Artificial Internal Organs, American Thoracic Society, Physicians for Social Responsibility, and Society of Critical Care Medicine
Disclosure: sepracor Ownership interest None

Medical Editor

Michael Peterson, MD, Chief of Medicine, Vice-Chair of Medicine, University of California at San Francisco; Endowed Professor of Medicine, University of California at San Francisco-Fresno
Michael Peterson, MD is a member of the following medical societies: American College of Chest Physicians, American College of Physicians, and American Thoracic Society
Disclosure: Nothing to disclose.

Pharmacy Editor

Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine
Disclosure: eMedicine Salary Employment

Managing Editor

Om Prakash Sharma, MD, FRCP, FCCP, DTM&H, Professor, Department of Medicine, Division of Pulmonary and Critical Care Medicine, University of Southern California Keck School of Medicine
Om Prakash Sharma, MD, FRCP, FCCP, DTM&H is a member of the following medical societies: American Academy of Allergy Asthma and Immunology, American College of Chest Physicians, American College of Physicians, American Federation for Medical Research, American Osler Society, American Thoracic Society, New York Academy of Medicine, and Royal Society of Medicine
Disclosure: Keck School of Medicine, USC None None

CME Editor

Timothy D Rice, MD, Associate Professor, Departments of Internal Medicine and Pediatrics and Adolescent Medicine, Saint Louis University School of Medicine
Timothy D Rice, MD is a member of the following medical societies: American Academy of Pediatrics and American College of Physicians
Disclosure: Nothing to disclose.

Chief Editor

Burke A Cunha, MD, Professor of Medicine, State University of New York School of Medicine at Stony Brook; Chief, Infectious Disease Division, Winthrop-University Hospital
Burke A Cunha, MD is a member of the following medical societies: American College of Chest Physicians, American College of Physicians, and Infectious Diseases Society of America
Disclosure: Nothing to disclose.

 
 
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