Blood film examination for vacuolated lymphocytes in the diagnosis of metabolic disorders; retrospective experience of more than 2,500 cases from a single centre
- PMID: 16311352
- PMCID: PMC1770783
- DOI: 10.1136/jcp.2005.027045
Blood film examination for vacuolated lymphocytes in the diagnosis of metabolic disorders; retrospective experience of more than 2,500 cases from a single centre
Abstract
Background: A range of metabolic diseases can result in abnormal accumulation of metabolic byproducts, resulting in abnormal lymphocyte cytoplasmic vacuolation, identifiable on routine blood film examination.
Aims: This study retrospectively examines the usefulness of blood film examination for vacuolated lymphocytes in a specialist paediatric pathology department in relation to patient's age and presentation. It also describes specific diagnostic features in relation to specific classes of metabolic disease.
Methods: Retrospective review of a histopathology database to identify all blood films examined for the detection of vacuolated lymphocytes during a 15 year period (1989-2004).
Results: In total, 2,550 blood films were investigated. The median age at submission was 2 years (range, birth to 88), and>90% of samples were from children<18 years. The most common indications were developmental delay/regression, ataxia, seizures, and cardiomyopathy. Vacuolated lymphocytes were identified in 156 films (6.1%). The frequency of vacuolated lymphocytes varied with clinical presentation, with ophthalmic indications having the highest positive rate (40%). In cases with vacuolated lymphocytes, a wide range of underlying metabolic diagnoses was apparent, the most common being juvenile neuronal ceroid lipofuscinosis and acid maltase deficiency, which accounted for more than half of the diagnoses.
Conclusions: The examination of blood films for lymphocyte vacuolation is clinically useful in patients with a history suggestive of metabolic disease. The test is cheap, rapid, minimally invasive, and provides first line screening, with some findings indicating clues to a specific underlying diagnosis.
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References
-
- Lake BD. Blood, bone marrow, spleen and lymph nodes in metabolic disorders. In: Lake BD, Filipe MI, eds. Histochemistry in pathology. London: Churchill-Livingstone, 1990:303–18.
-
- Derwort A, Detering K. Vacuolated lymphocytes in familial amaurotic idiocy and their diagnostic significance. Nervenarzt 1959;30:442–8. - PubMed
-
- Baumann RJ, Markesbery WR. Juvenile amaurotic idiocy (neuronal ceroid lipofuscinosis) and lymphocyte fingerprint profiles. Ann Neurol 1978;4:531–6. - PubMed
-
- Lake BD, Cavanagh NP. Early-juvenile Batten’s disease—a recognisable sub-group distinct from other forms of Batten’s disease. Analysis of 5 patients. J Neurol Sci 1978;36:265–71. - PubMed
-
- Aula P, Autio S, Raivio KO, et al. “Salla disease”: a new lysosomal storage disorder. Arch Neurol 1979;36:88–94. - PubMed
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