Composition of the Inflammatory Infiltrate in Pediatric Penile Lichen Sclerosus Et Atrophicus (Balanitis Xerotica Obliterans): A Prospective, Comparative Immunophenotyping Study

Dermatopathological evaluation of pediatric preputial inflammatory disease rarely allows for specific diagnosis other than pediatric penile lichen sclerosus et atrophicus (balanitis xerotica obliterans, LSA/BXO). A prospective immunopathological study was performed on 20 consecutive, unselected, cli...

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Veröffentlicht in:Fetal and pediatric pathology 1994, Vol.14 (2), p.223-233
Hauptverfasser: Hinchliffe, S. A., Ciftci, A. O., Khine, M. M., Rickwood, A. M. K., Ashwood, J., McGill, F., Clapham, E. M., van Velzen, D.
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Sprache:eng
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Zusammenfassung:Dermatopathological evaluation of pediatric preputial inflammatory disease rarely allows for specific diagnosis other than pediatric penile lichen sclerosus et atrophicus (balanitis xerotica obliterans, LSA/BXO). A prospective immunopathological study was performed on 20 consecutive, unselected, clinically and histopathologically confirmed LSA/BXO cases to determine the relative presence of T and B lymphocytes. There were seven cases with early stages of disease, eight with florid disease, and five with later stages of disease. Two ritual circumcision specimens and 12 specimens with non-LSA/BXO balanitis, collected during the same period, were used as controls. The infiltrate in LSA/BXO patients was wholly composed of T cells (positive with UCLH-1 antibody) in all cases. B cells (positive with L-26 antibody) were found only focally in small, discreet, easily recognizable (follicular or early follicle-like) aggregates, positioned slightly deeper than the band-like infiltrate of T cells. T cells were inconspicuous in 9 of the 12 control specimens. In the three other controls, T cells were much more obvious and these patients showed clinical features possibly suggestive of LSA/BXO in early, fiediagnosable phases of development. We conclude that limited immunophenotyping may be a useful adjunct to diagnosis in pediatric cases in which onb limited tissue is available 07 the disease may be m e difficult to classify with confidence.
ISSN:1551-3815
0277-0938
1551-3823
DOI:10.3109/15513819409024256