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Hematology

Exposed to Fifth Disease with Hereditary Spherocytosis?

At a Glance

If a person with hereditary spherocytosis is exposed to Fifth Disease (Parvovirus B19), they must contact their hematologist immediately. The virus halts red blood cell production, causing a dangerous aplastic crisis that may require an emergency blood transfusion. Do not wait for a rash.

If a person with Hereditary Spherocytosis (HS) is exposed to Fifth Disease (also known as Parvovirus B19), they or their parents should contact their hematologist or primary care team immediately [1]. Because this virus temporarily halts red blood cell production, it can cause a rapid, dangerous drop in blood counts [2]. You will need to monitor closely for extreme paleness, severe lethargy, and a rapid heart rate [1][3]. In many cases, patients with HS will need a temporary blood transfusion in the hospital to keep them safe while their body fights off the virus [4][5].

Note for adults: While this guide often refers to children (as Fifth Disease spreads rapidly in schools and daycares), adults with HS who have never had the virus are at the exact same risk for an aplastic crisis and must follow the same emergency steps.

Why Parvovirus B19 Affects HS Differently

In a healthy person, Fifth Disease usually starts with mild cold-like symptoms (like fever or a runny nose) followed by a characteristic “slapped cheek” facial rash. However, Parvovirus B19 has a specific trait: it selectively infects the bone marrow and temporarily shuts down the production of new red blood cells [2][6]. Currently, there is no vaccine available to prevent it.

Normally, red blood cells live for about 120 days, so a brief pause in production goes unnoticed. But in Hereditary Spherocytosis (HS), the fragile, sphere-shaped red blood cells break down much faster than normal [7][8]. Because the body is already working overtime to replace these rapidly dying cells, the sudden halt in production caused by the virus means the red blood cell count plummets [7][9]. This event is called a transient aplastic crisis, and Parvovirus B19 is responsible for the vast majority of these crises in patients with HS [10].

Signs to Watch For

If an exposure occurs, the incubation period before symptoms appear can take up to two weeks. Importantly, the classic “slapped cheek” rash often never appears during an aplastic crisis. Do not wait for a rash. Instead, monitor for signs of severe anemia (low red blood cells). Contact your medical team or seek emergency care immediately if you notice:

  • Extreme paleness (pallor): Check the face, the inside of the lips, and the nail beds [3].
  • Profound lethargy: The person may be unusually exhausted, difficult to wake, or lack the energy to walk or play [1][3].
  • Rapid heart rate (tachycardia): The heart beats faster to pump the remaining limited oxygen around the body [1].
  • Jaundice: Yellowing of the skin or eyes can sometimes become more pronounced during a crisis [1][3].

Research shows that patients who have a more severe baseline of HS—meaning they usually run lower hemoglobin levels and have a higher percentage of new red cells (reticulocytes)—are more likely to have a severe crisis [10].

  • Call the hematologist right away: Do not wait for symptoms. Let the care team know about the exposure to establish a monitoring plan.
  • Call ahead before arriving: People experiencing a Parvovirus B19 aplastic crisis are highly contagious and shed large amounts of the virus [11]. Always call the clinic or emergency room before arriving so they can place the patient in appropriate droplet isolation, protecting pregnant women and immunocompromised individuals in the waiting room [11].
  • Protect pregnant family members: Parvovirus B19 infection during pregnancy carries significant risks to the fetus. Pregnant household members should contact their obstetrician immediately if an exposure occurs in the home [11].
  • Prepare for blood work: The doctor will likely want to check a complete blood count (CBC) and reticulocyte count (a measure of newly produced red blood cells) to confirm if the virus has stopped production [12][3].
  • Expect a potential hospital stay and transfusion: If hemoglobin drops too low, an inpatient hospital admission for a blood transfusion is the standard, highly effective way to stabilize the patient [4][5].
  • Focus on recovery: The word “transient” means temporary. Once the immune system clears the virus, the bone marrow will restart red blood cell production. Patients generally achieve a full hematologic recovery, and the crisis typically resolves within a week or two [10].

Common questions in this guide

What happens if someone with hereditary spherocytosis gets Fifth Disease?
Fifth Disease, or Parvovirus B19, temporarily shuts down red blood cell production in the bone marrow. Because people with hereditary spherocytosis already break down their red blood cells rapidly, this sudden pause causes a dangerous drop in blood counts known as a transient aplastic crisis.
Should I wait for the 'slapped cheek' rash before calling my doctor?
No, you should not wait for a rash to appear. Patients experiencing a severe aplastic crisis from Parvovirus B19 often never develop the classic 'slapped cheek' facial rash associated with Fifth Disease. You should contact your hematologist immediately after you learn of an exposure.
What are the signs of a transient aplastic crisis?
Key warning signs of severe anemia include extreme paleness in the face, inside the lips, and the nail beds. You should also watch for profound lethargy, unusual exhaustion, a rapid heart rate, and an increase in jaundice.
Why do I need to call the clinic or ER before arriving for an aplastic crisis?
People experiencing an aplastic crisis from Parvovirus B19 shed large amounts of the virus and are highly contagious. Calling ahead allows the medical team to place the patient in appropriate droplet isolation, which protects vulnerable people like pregnant women in the waiting room.
How is a transient aplastic crisis treated?
If blood counts drop dangerously low, patients are typically admitted to the hospital for a temporary blood transfusion. This stabilizes the patient and keeps them safe while their immune system clears the virus and the bone marrow naturally restarts red blood cell production.

Questions to Ask Your Doctor

Curated prompts to bring to your next appointment.

  1. 1.What is my child's (or my) baseline hemoglobin and reticulocyte count, and what specific number would trigger the need for a hospital admission during an aplastic crisis?
  2. 2.Can you provide a standing lab order for a complete blood count and reticulocyte count so we can get tested quickly if an exposure occurs at school?
  3. 3.If we suspect an aplastic crisis, should we go directly to the emergency room, or can we be seen in your clinic with isolation precautions?
  4. 4.Can we test my (or my child's) Parvovirus B19 immunity status with a blood test so we know if we remain at risk for a future aplastic crisis?

Questions For You

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References

References (12)
  1. 1

    Hereditary Spherocytosis Unmasked by Human Parvovirus B19 Induced Aplastic Crisis in a Family.

    Alavi S, Arabi N, Yazdi MK, et al.

    Iranian journal of medical sciences 2015; (40(5)):461-4.

    PMID: 26379354
  2. 2

    New Insights of Human Parvovirus B19 in Modulating Erythroid Progenitor Cell Differentiation.

    Feng S, Zeng D, Zheng J, Zhao D

    Viral immunology 2020; (33(8)):539-549 doi:10.1089/vim.2020.0013.

    PMID: 32412895
  3. 3

    Aplastic Crisis Secondary to Parvovirus B19 Infection as the First Manifestation of an Undiagnosed Hereditary Spherocytosis: Report of a Pediatric Series of Spanish Patients.

    Alonso-Saladrigues A, Català A, Berrueco R, et al.

    Journal of pediatric hematology/oncology 2016; (38(1)):81-2 doi:10.1097/MPH.0000000000000481.

    PMID: 26583618
  4. 4

    Significance of parvovirus B19 infection in childhood - collection of demographic data, clinical presentation, diagnostic findings and the impact on patients with hemolytic anemia.

    Lawatsch L, Baier M, Milde T, Gruhn B

    Diagnostic microbiology and infectious disease 2026; (114(4)):117263 doi:10.1016/j.diagmicrobio.2026.117263.

    PMID: 41529596
  5. 5

    Parvovirus B19-induced aplastic crises in children with hereditary spherocytosis in the Czech Republic: multicentre retrospective study.

    Birke P, Fiamoli V, Ludíková B, et al.

    BMC infectious diseases 2026; (26(1)).

    PMID: 42174500
  6. 6

    Parvovirus-Induced Transient Aplastic Crisis in a Patient With Newly Diagnosed Hereditary Spherocytosis.

    Nandu NS, Hafzah H, Patel C

    Cureus 2020; (12(7)):e8995 doi:10.7759/cureus.8995.

    PMID: 32775077
  7. 7

    Leukoerythroblastosis as an Unusual Presentation of Parvovirus B19 Infection in a Sickle Cell Patient.

    Patel PA, Weinzierl EP, Wechsler DS

    Case reports in pediatrics 2020; (2020()):8841607 doi:10.1155/2020/8841607.

    PMID: 33029441
  8. 8

    Aplastic Crisis Triggered by Parvovirus B19 in an Adult Man With Sickle Cell Disease.

    Rahman Z, Watford S, Carlson S, et al.

    Cureus 2026; (18(6)):e110547 doi:10.7759/cureus.110547.

    PMID: 42428213
  9. 9

    Parvovirus b19 infection in children with sickle cell disease, watch out for splenomegaly! A case report.

    de la Hoz JA, Otones LL, Sáenz MH, Martín MJR

    African health sciences 2022; (22(1)):598-601 doi:10.4314/ahs.v22i1.69.

    PMID: 36032454
  10. 10

    Disease severity of children with hereditary spherocytosis predicts the clinical course of aplastic crisis.

    Rubin S, Ben Ami SD, Atia O, et al.

    European journal of pediatrics 2026; (185(7)).

    PMID: 42410007
  11. 11

    Healthcare-Associated Transmission of Parvovirus B19 Arthropathy.

    Rosenstein RK, Rosenstein PK, Kramer N, Rosenstein ED

    Bulletin of the Hospital for Joint Disease (2013) 2020; (78(2)):140-143.

    PMID: 32510300
  12. 12

    Aplastic Crisis in a Woman with Autoimmune Hemolytic Anemia.

    Koduri PR, Joshi S, Vanajakshi S

    Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion 2020; (36(2)):422-423 doi:10.1007/s12288-019-01222-6.

    PMID: 32425406

This page is for informational purposes only and does not replace professional medical advice. If you or your child with hereditary spherocytosis is exposed to Parvovirus B19, contact your hematologist immediately to prevent a medical emergency.

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