0
We're unable to sign you in at this time. Please try again in a few minutes.
Retry
We were able to sign you in, but your subscription(s) could not be found. Please try again in a few minutes.
Retry
There may be a problem with your account. Please contact the AMA Service Center to resolve this issue.
Contact the AMA Service Center:
Telephone: 1 (800) 262-2350 or 1 (312) 670-7827  *   Email: subscriptions@jamanetwork.com
Error Message ......
Special Feature |

Pathological Case of the Month FREE

[+] Author Affiliations

Section Editor: Enid Gilbert-barness, MD

More Author Information
Arch Pediatr Adolesc Med. 2001;155(1):92. doi:10.1001/archpedi.155.1.91.
Text Size: A A A
Published online

DIAGNOSIS AND DISCUSSION: BLASTOMYCES DERMATITIDIS

Figure 1. Blastomycosis of the skin.

Figure 2. Goiter from blastomycosis of the thyroid.

Figure 3. Extension to the skin from osteomyelitis of the radius.

Figure 4. Pneumonia due to blastomycosis.

Figure 5. Osteomyelitis of the radius due to blastomycosis.

Figure 6. Broad-based budding (hematoxylin-eosin, original magnification ×400).

Microscopic examination of skin, bone biopsy specimens, and bronchoalveolar lavage specimens revealed Blastomyces dermatitidis. He was treated with 250 mg/kg of liposomal amphotericin and 400 mg daily of itraconazole for 8 weeks with resolution of pneumonia, goiter, and systemic symptoms. Surgeries of his left wrist included multiple incision and debridements, external fixator placement, split-thickness skin graft placement, and wrist fusion.

Blastomyces dermatitidis, a primary pathogen, is a dimorphic fungus that exists as a thick-walled yeast cell with broad-based budding daughter cells in tissues and in the mycelial form in its environmental reservoir.1,2 The US endemic area includes the Ohio and Mississippi River valleys as well as the south-central and southeastern portions of the United States.1,3 Most patients are between age 20 and 70 years with an estimated 3% to 11% of cases occurring in patients younger than age 20 years.1,4,5 The primary site of infection is the lungs after inhalation of spores from soil.2,6 The larger spores are more resistant to phagocytosis and can succeed in transitioning to the yeast phase.5 Over the next 4 to 8 weeks, the yeast forms proliferate, leading to an influenzalike illness.5 Roughly 50% of infected children will develop symptomatic illness.5

Chronic pneumonia usually precedes definitive diagnosis by 2 to 6 months.1 This pneumonia can resolve or progress to localized pulmonary involvement or extrapulmonary disease.4 Most patients progressing to adult respiratory distress syndrome die soon thereafter.1 The most common finding on chest radiography is an alveolar or masslike infiltrate.1 There may also be interstitial disease with reticulonodular, nodular, or miliary opacities and cavitation.2 Diagnosis may be delayed because these various patterns can mimic other disease processes such as tuberculosis, bacterial pneumonia, malignant tumors, and sarcoidosis.5 Hilar and mediastinal adenopathy are rare, however, in contrast to histoplasmosis.2

Dissemination occurs months to years after pulmonary infection, and almost any organ site can be involved, including skin, bone, male genitourinary system, and the central nervous system.2 Findings from skin lesions reveal papillomatosis and downward proliferation of the epidermis with intraepidermal abscesses.1 Hyperplasia and acanthosis suggest a diagnosis of cancer.1 Osteomyelitis occurs in up to 25% of extrapulmonary cases with involvement of the vertebrae, pelvis, sacrum, skull, ribs, and long bones.1 Radiographs of osteomyelitis are nonspecific and cannot be differentiated from other forms of osteomyelitis.1 Prostatitis and epididymo-orchitis are the most common genitourinary manifestations.1 Meningitis and epidural or cranial abscesses are the forms of central nervous system involvement.1 Other areas of involvement include the liver, spleen, heart, lymph nodes, psoas muscle, kidney, middle ear, and adrenal and thyroid glands.5,6

Diagnosis is easily established by recovery of the organism from clinical specimens.1,4 Examination of bronchoalveolar fluid microscopically in addition to culture is an effective method for diagnosis in adults.4 In children and adolescents, failure to identify organisms in sputum or bronchoalveolar fluid is common.4 It is recommended that children and adolescents suspected of having blastomycosis undergo lung biopsy if sputum and bronchoscopy examination are nondiagnostic.4 Other techniques such as complement fixation, immunodiffusion, or delayed hypersensitivity of skin to blastomycin are unreliable for diagnosis.1

The decision to treat requires balancing the severity of illness with the toxic effects of antifungals. Observation should be limited to cases of mild pulmonary blastomycosis.1 If therapy is withheld, patients must be followed carefully for evidence of reactivation or dissemination.6 Pleural disease or extrapulmonary manifestations require antifungal therapy.1 Amphotericin has the greatest proven efficacy, but it is associated with toxic effects.2 Oral ketoconazole and itraconazole are only slightly less effective but have lower toxic effects and easier administration.2 Itraconazole has replaced amphotericin as the agent of choice to treat less than life-threatening blastomycosis in adults.4 Amphotericin is warranted if patients do not clinically respond within 2 to 4 weeks, if serum levels are not adequate, if clinical deterioration is documented, if osteomyelitis or central nervous system involvement is present, or if life-threatening blastomycosis exists.1,4 A high index of suspicion for blastomycosis is essential. Its symptoms are nonspecific and can mimic other diseases. When there is a persistent pulmonary infiltrate, skin lesions, bone involvement, and a suspicious travel history, blastomycosis must be considered.

Accepted for publication January 1, 1999.

Reprints: Mary Ann DeLeon, MD, Children's Memorial Hospital, 2300 Children's Plaza, Chicago, IL 60614.

Bradsher  RW Histoplasmosis and blastomycosis. Clin Infect Dis. 1996;22 ((suppl 2)) S102- S111
Link to Article
Kuzo  RSGoodman  LR Blastomycosis. Semin Roentgenol. 1996;3145- 51
Link to Article
Lowry  PWKelso  KYMcFarland  LM Blastomycosis in Washington Parish, Louisiana, 1976-1985. Am J Epidemiol. 1989;130151- 159
Schutze  GEHickerson  SLFortin  EM  et al.  Blastomycosis in children. Clin Infect Dis. 1996;22496- 502
Link to Article
Bradsher  RW Blastomycosis. Clin Infect Dis. 1996;14 ((suppl 1)) S82- S90
Link to Article
Schutze  GE Blastomycosis. Feigin  RDCherry  JDeds.Textbook of Pediatric Infectious Diseases Philadelphia, Pa WB Saunders Co1998;

Tables

References

Bradsher  RW Histoplasmosis and blastomycosis. Clin Infect Dis. 1996;22 ((suppl 2)) S102- S111
Link to Article
Kuzo  RSGoodman  LR Blastomycosis. Semin Roentgenol. 1996;3145- 51
Link to Article
Lowry  PWKelso  KYMcFarland  LM Blastomycosis in Washington Parish, Louisiana, 1976-1985. Am J Epidemiol. 1989;130151- 159
Schutze  GEHickerson  SLFortin  EM  et al.  Blastomycosis in children. Clin Infect Dis. 1996;22496- 502
Link to Article
Bradsher  RW Blastomycosis. Clin Infect Dis. 1996;14 ((suppl 1)) S82- S90
Link to Article
Schutze  GE Blastomycosis. Feigin  RDCherry  JDeds.Textbook of Pediatric Infectious Diseases Philadelphia, Pa WB Saunders Co1998;

Correspondence

CME
Meets CME requirements for:
Browse CME for all U.S. States
Accreditation Information
The American Medical Association is accredited by the Accreditation Council for Continuing Medical Education to provide continuing medical education for physicians. The AMA designates this journal-based CME activity for a maximum of 1 AMA PRA Category 1 CreditTM per course. Physicians should claim only the credit commensurate with the extent of their participation in the activity. Physicians who complete the CME course and score at least 80% correct on the quiz are eligible for AMA PRA Category 1 CreditTM.
Note: You must get at least of the answers correct to pass this quiz.
You have not filled in all the answers to complete this quiz
The following questions were not answered:
Sorry, you have unsuccessfully completed this CME quiz with a score of
The following questions were not answered correctly:
Commitment to Change (optional):
Indicate what change(s) you will implement in your practice, if any, based on this CME course.
Your quiz results:
The filled radio buttons indicate your responses. The preferred responses are highlighted
For CME Course: A Proposed Model for Initial Assessment and Management of Acute Heart Failure Syndromes
Indicate what changes(s) you will implement in your practice, if any, based on this CME course.
Submit a Comment

Multimedia

Some tools below are only available to our subscribers or users with an online account.

Related Content

Customize your page view by dragging & repositioning the boxes below.

Articles Related By Topic
Related Collections
PubMed Articles