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A Curious Case of Hemolytic Anemia with Pseudoreticulopenia
Scott Mayer1, Nikhilesh Srinivasan1, Jenny Nguyen2
1HCA HealthONE, Lone Tree, CO, USA.
Case Reports in Hematology
|May 2, 2022
Summary
A rare Coombs-negative, steroid-refractory autoimmune hemolytic anemia (AIHA) presented with pseudoreticulopenia. This case highlights diagnostic challenges and the impact of coexisting pernicious anemia.
Area of Science:
- Hematology
- Immunology
- Internal Medicine
Background:
- Coombs-negative, steroid-refractory autoimmune hemolytic anemia (AIHA) is rare, accounting for <1% of AIHA cases.
- Diagnosis is challenging due to negative Coombs tests, often delaying treatment and increasing morbidity.
Observation:
- This study details a unique case of AIHA complicated by pseudoreticulopenia.
- The patient exhibited normal bone marrow function, complicating the diagnosis of reticulopenia.
- Pseudoreticulopenia was attributed to erythroid maturation defects caused by coexisting pernicious anemia.
Findings:
- The super-Coombs test can aid in diagnosing AIHA when traditional tests are negative.
- Rituximab is an effective second-line therapy for many AIHA cases.
- This is the first reported instance of pseudoreticulopenia in AIHA secondary to pernicious anemia.
Implications:
- Increased physician awareness of rare AIHA subtypes and pseudoreticulopenia is crucial for timely diagnosis.
- Recognizing the interplay between AIHA and pernicious anemia can improve patient outcomes.
- Prompt diagnosis and treatment of AIHA, even in complex cases, are vital to reduce morbidity.
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