MULTINUCLEATE CELL ANGIOHISTIOCYTOMA - RE PORT OF 6 CASES

Citation
C. Lecamsavin et al., MULTINUCLEATE CELL ANGIOHISTIOCYTOMA - RE PORT OF 6 CASES, Annales de pathologie, 16(6), 1996, pp. 435-438
Citations number
7
Categorie Soggetti
Pathology
Journal title
ISSN journal
02426498
Volume
16
Issue
6
Year of publication
1996
Pages
435 - 438
Database
ISI
SICI code
0242-6498(1996)16:6<435:MCA-RP>2.0.ZU;2-X
Abstract
Multinucleate cell angiohistiocytoma is a recently described entity. I t is a benign vascular proliferation. Clinically, it is characterized by violaceous red papules, often mimicking Kaposi's salcoma. Acral sit es and face were the commonest sires. The six patient's age tvas betwe en 41 and 64 years and sex ratio tvas equal. Microscopic features were an increased number of blood vessels together with mononucleated and multinucleated histiocyte-like cells with scalloped borders. Staining of mononucleated cells with CD68, anti vimentin and anti factor XIIIa antibodies emphasized a fibrohistiocytic origin. Loss of factor XIIIa expression in multinucleate cells gets clue to think thar these cells are dedifferenciated.