Am Fam Physician. 2005 Jun 1;71(11).
to the editor: A 68-year-old white woman presented to her family physician's office with a four-day history of diffuse bilateral pain and swelling in her wrists, hands, and lower extremities, and a temperature of 101·F (38.3·C). The patient did not have chest pain, palpitations, shortness of breath, a history of injury, or a rash. She was started on 500 mg of naproxen twice daily and was asked to follow up when her laboratory data became available. Laboratory analysis revealed a normal complete blood count, a slightly elevated erythrocyte sedimentation rate of 26 mm per hour, a C-reactive protein level of 23.0 mg per L (219.1 nmol per L), negative rheumatoid factor, and positive antinuclear antibodies (ANA) with a titer of 1:160 in a nucleolar pattern.
The patient returned five days later with a decrease in pain and swelling. Although naproxen had helped alleviate some discomfort, she had developed diarrhea and discontinued its use. At this visit, the patient reported that she had been in close contact with her grandson, whose school recently had experienced an outbreak of parvovirus B19. Subsequent testing for parvovirus B19 antibodies 12 days after the initial presentation revealed an IgG titer of 5.6 and an IgM titer of 8.1. The reference range for both IgM and IgG titer is less than 0.9, negative titer; 0.9 to 1.1, equivocal titer; and greater than 1.1, positive titer. A positive IgG and IgM titer indicates an infection within the last 7 to 120 days. This patient's titers are consistent with her clinical presentation representing an acute infection. The patient was restarted on naproxen, and a decrease in swelling and pain was noted one week later.
Parvovirus B19 infection can have a variety of clinical presentations but is most frequently an asymptomatic infection. Erythema infectiosum, also called fifth disease, causes a classic "slapped cheek" appearance. It is a parvovirus B19 infection most commonly found in children; infected patients present with a low-grade fever, malaise, and a rash. Parvovirus B19 is also known to cause an erythrocyte aplasia, transient aplastic crisis, and in the unborn, hydrops fetalis.1 Arthralgia and arthritis can be symptoms of parvovirus B19, most commonly as acute onset symmetric polyarticular arthritis in the hands. Joint pain and arthritis occur more frequently in infected adult women than in children and adult men. These symptoms often can remain for more than two months. Common laboratory abnormalities include a positive ANA or rheumatoid factor. Forty to 60 percent of adults have antibodies to parvovirus B19.2 There is a steep increase in children older than five years with IgG antibodies, probably indicating that infection is associated with beginning school.3 Treatment of arthropathy from parvovirus B19 is primarily symptom management with nonsteroidal anti-inflammatory drugs.
The differential diagnosis for polyarticular joint pain encompasses many diverse conditions.4 This case of acute arthropathy resulting from parvovirus B19 infection serves as a reminder to consider exposure to parvovirus B19 when a patient presents with an acute transient arthropathy.
REFERENCESshow all references
1. Sabella C, Goldfarb J. Parvovirus B19 infections. Am Fam Physician 1999;60:1455-60. ...
2. Moore TL. Parvovirus-associated arthritis. Curr Opin Rheumatol 2000;12:289-94.
3. Gillespie SM, Cartter ML, Asch S, Rokos JB, Gary GW, Tsou CJ, et al. Occupational risk of human parvovirus B19 infection for school and day-care personnel during an outbreak of erythema infectiosum. JAMA 1990;263:2061-5.
4. Mies Richie A, Francis ML. Diagnostic approach to polyarticular joint pain. Am Fam Physician 2003;68:1151-60.
Send letters to Kenneth W. Lin, MD, MPH, Associate Deputy Editor for AFP Online, e-mail: email@example.com, or 11400 Tomahawk Creek Pkwy., Leawood, KS 66211-2680.
Please include your complete address, e-mail address, and telephone number. Letters should be fewer than 400 words and limited to six references, one table or figure, and three authors.
Letters submitted for publication in AFP must not be submitted to any other publication. Possible conflicts of interest must be disclosed at time of submission. Submission of a letter will be construed as granting the American Academy of Family Physicians permission to publish the letter in any of its publications in any form. The editors may edit letters to meet style and space requirements.
Copyright © 2005 by the American Academy of Family Physicians.
This content is owned by the AAFP. A person viewing it online may make one printout of the material and may use that printout only for his or her personal, non-commercial reference. This material may not otherwise be downloaded, copied, printed, stored, transmitted or reproduced in any medium, whether now known or later invented, except as authorized in writing by the AAFP. Contact firstname.lastname@example.org for copyright questions and/or permission requests.
Want to use this article elsewhere? Get Permissions