Gynecomastia in type-1 neurofibromatosis with features of pseudoangiomatous stromal hyperplasia with giant cells. Report of two cases

Citation
S. Damiani et V. Eusebi, Gynecomastia in type-1 neurofibromatosis with features of pseudoangiomatous stromal hyperplasia with giant cells. Report of two cases, VIRCHOWS AR, 438(5), 2001, pp. 513-516
Citations number
14
Categorie Soggetti
Medical Research Diagnosis & Treatment
Journal title
VIRCHOWS ARCHIV-AN INTERNATIONAL JOURNAL OF PATHOLOGY
ISSN journal
09456317 → ACNP
Volume
438
Issue
5
Year of publication
2001
Pages
513 - 516
Database
ISI
SICI code
0945-6317(200105)438:5<513:GITNWF>2.0.ZU;2-6
Abstract
We describe the histological finding in two cases of gynecomastia in patien ts with von Recklinghausen's disease. The histological and immunohistochemi cal features of the two cases were reviewed and compared with those of five cases of gynecomastia in men without clinical evidence of neurofibromatosi s. In both patients bearing von Recklinghausen's disease, the breast stroma showed features consistent with pseudoangiomatous stromal hyperplasia (PAS H). It was characterised by anastomosing empty spaces lined by spindle and multinucleated giant cells which were positive with CD34 and anti-vimentin antisera and negative with anti-FVIII and CD31 antisera, In two of five of the control cases without neurofibromatosis, the mammary stroma showed foca l areas with features of PASH, but no multinucleated giant cells were prese nt in any case. PASH with giant cells should be recognised as a feature of gynecomastia in von Recklinghausen's disease. The presence of multinucleate d giant cells is very unusual and, although more cases have to be studied, these cells seem to be a feature of PASH occurring in patients with von Rec klinghausen's disease.