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Cytologic aspects of T-cell acute lymphoblastic leukemia presenting as a massive pericardial effusion: a case report
Debdatta Basu1, Neelaiah Siddaraju, Paari Murugan
1Department of Pathology, Jawaharlal Institute of Postgraduate Medical Education and Research, Pondicherry, India.
Insights
Acute lymphoblastic leukemia (ALL) can rarely present as cardiac tamponade with leukemia cells in pericardial fluid. Cytopathologists must carefully examine lymphoid-rich effusions to avoid misdiagnosis of this critical condition.
Area of Science:
- Hematology
- Cytopathology
- Oncology
Background:
- Acute lymphoblastic leukemia (ALL) presenting with cardiac tamponade and pericardial effusion is rare.
- Cytopathologists must exercise caution with lymphoid-rich pericardial effusions to prevent false-negative diagnoses.
Observation:
- A 27-year-old male presented with symptoms of cardiac tamponade and a pericardial effusion.
- Pericardial fluid cytology revealed atypical lymphoid cells with blastoid morphology, initially resembling mature lymphocytes.
- Hematologic workup confirmed T-cell acute lymphoblastic leukemia (FAB L1) with 90% lymphoblasts in the bone marrow.
Findings:
- The case highlights the uncommon presentation of ALL with cardiac tamponade and malignant cells in pericardial fluid.
- Morphological analysis of pericardial fluid cytology is crucial for early detection of ALL.
- Immunophenotyping confirmed T-cell lineage and blast characteristics.
Implications:
- Clinicians and cytopathologists must recognize the potential for ALL to manifest initially as pericardial effusion and cardiac tamponade.
- Prompt and accurate diagnosis of lymphoid cells in pericardial fluid is critical for patient management and prognosis.
- This emphasizes the importance of integrating clinical, cytologic, and hematologic findings in diagnosing rare oncologic emergencies.
Background:
Acute lymphoblastic leukemia (ALL) with a clinical presentation of cardiac tamponade and the presence of blasts in the pericardial fluid is an uncommon event. A cytopathologist needs to adopt a cautious interpretive approach while dealing with a lymphoid-rich pericardial effusion in order to prevent a false negative diagnosis.
Case:
A 27-year-old male presented with breathlessness, ascites, bilateral pedal edema and fever. He had mild hepatomegaly. On detailed clinical examination, a diagnosis of anemia with cardiac tamponade was made. Cytology of pericardial fluid revealed a large number of lymphoid cells in a hemorrhagic background that, under low magnification, closely resembled mature lymphocytes. However, a careful examination of May-Grünwald-Giemsa-stained cytologic smears, under an oil immersion objective (x 1,000), showed atypical lymphoid cells having blastoid morphology. Rare lymphoid cells displayed a "hand mirror" appearance. A hematologic workup was carried out to exclude leukemia/lymphoma. Complete blood count revealed pancytopenia with abnormal lymphoid cells. Bone marrow showed replacement by 90% lymphoblasts exhibiting periodic acid-Schiff stain, CD3 and terminal deoxynucleotidyl transferase positivity. A diagnosis of T-cell acute lymphoblastic leukemia (FAB L1) was offered, and the patient was started on a remission and induction regimen. However, he had a rapid downhill course and died of cardiorespiratory arrest.
Conclusion:
Both clinicians and cytopathologists need to be aware of rare instances in which ALL may present with a pericardial effusion as an initial manifestation. The abnormal lymphoid cells found in the pericardial fluid in such situations need to be interpreted cautiously, as their presence is of clinical significance.
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