INTRA ABDOMINAL LYMPHANGIOMAS IN CHILDREN AND ADULTS - ASSESSMENT OF PROLIFERATIVE ACTIVITY

Citation
C. Mahle et al., INTRA ABDOMINAL LYMPHANGIOMAS IN CHILDREN AND ADULTS - ASSESSMENT OF PROLIFERATIVE ACTIVITY, Archives of pathology and laboratory medicine, 121(10), 1997, pp. 1055-1062
Citations number
42
Categorie Soggetti
Pathology,"Medical Laboratory Technology","Medicine, Research & Experimental
Journal title
Archives of pathology and laboratory medicine
ISSN journal
00039985 → ACNP
Volume
121
Issue
10
Year of publication
1997
Pages
1055 - 1062
Database
ISI
SICI code
0003-9985(1997)121:10<1055:IALICA>2.0.ZU;2-J
Abstract
Objective.-Intra-abdominal lymphangiomas are rare in children and even more exceptional in adults. Because these lesions occasionally progre ssively enlarge, we analyzed seven adult and four pediatric cases for evidence of proliferative activity. Design.-Immunohistochemical analys is was performed retrospectively on representative tissue sections usi ng antibodies to the following antigens: Ki-67, proliferating cell nuc lear antigen,and p53 gene product (eight cases). DNA ploidy was examin ed in five cases. Patients.-The study group consisted of seven adult w omen (aged 24 to 73 years), a 3.5-year-old girl, and two boys, aged 3. 5 and 9 years, the last with a recurrence at age 15. The lymphangiomas ranged from 1.7 to 23 cm in maximum size.Results.-Ranges of percentag es of cells staining for proliferating cell nuclear antigen, Ki-67, an d p53 were similar between the pediatric and adult cases. Antibody to Ki-67 stained from 0.5% to 17% of the stromal and endothelial componen ts of the lymphangiomas. Proliferating cell nuclear antigen activity w as noted in 16% to 52% of lesional cells. Reactivity was noted almost exclusively in areas of inflammation and fibroplasia. For comparison, 10% to 50% of intermixed lymphocytes stained for Ki-67 and proliferati ng cell nuclear antigen. There was no labeling with p53. DNA content w as uniformly diploid. Conclusions.-The scant staining for Ki-67 in the majority of the lesions, combined with proliferative rates that were only focally elevated, suggests that lymphangiomas in children and adu lts are quiescent lesions whose enlargement is due to engorgement by c hyle and localized secondary inflammation rather than primary tumoral growth.