More common than you think: common variable immune deficiency
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Updated: May 4, 2026

Author Spotlight: Advancing Immune Monitoring in Critical Care Patients Using Whole Blood Assays
Published on: September 20, 2024
Abimbola Aderinto1, Vibav Mouli1, Danielle F Resar1
1Department of Medicine, The Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA ; Hematology Division, The Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Abstract:
We report a challenging case of a 16-year-old male who presented with thrombocytopenia and eluded a definitive diagnosis for over 2 years. He was initially diagnosed with a viral illness, although he later developed adenopathy and splenomegaly. An evaluation by an oncologist was unrevealing. He worked on a farm with livestock exposure and was later diagnosed with an atypical, zoonotic infection. Despite appropriate antibiotic therapy, the thrombocytopenia and splenomegaly persisted. Further evaluation revealed that he has a relatively common immunologic disorder. He is currently doing well on appropriate therapy for this disorder.
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