Volume 4 No. 2, April 2009

Kaposi’s sarcoma: Role of Diagnostic and Prognostic Immunohistochemical Markers

Abdel-Ghani A Selim & Omnia MK Rizk

Department of Pathology, Faculty of Medicine, Tanta University, Egypt
Tanta Med. Sc. J 2009; 4(2):112-120

Abstract provided by Publisher   
 

Background/Aim: Kaposi sarcoma, a tumor of uncertain histogenesis, has long been considered to be caused by a transmissible infectious agent. Human herpes virus 8 (HHV8) or Kaposi sarcoma associated herpes virus (KSHV) is generally accepted to be the most likely candidate agent, and this is supported by its strong association with all subtypes of Kaposi. On the other hand, down-regulation of p27Kip1 expression seems to facilitate metastatic dissemination in a variety of human neoplasms. Although the neoplastic nature of KS remains controversial, it has been repeatedly demonstrated that in some patients KS may behave as a malignant neoplasm and follow an ominous course. The aim of this study was to differentiate between KS and its mimickers, then to use prognostic markers and study their relation to progression of KS. Patients & Methods, this study included nine cases of KS and 12 cases of KS mimickers. These cases were examined by routine staining with H&E, then they were immunostained for CD31, CD34, HHV-8 LNA-1(Diagnostic markers), Bcl-2, p53, p27Kip1, and Ki-67 (Prognostic markers). Results, the included cases of KS and its mimickers showed positive expression of the vascular markers CD31 and/or CD34. The nine cases of KS were immunopositive for HHV-8 LNA- but all the mimickers were negative. An increase in the expression of p53, bcl-2, Ki-67 was detected in relation with progression of KS. On the other hand down regulation of p27Kip1 was reported with the progression of KS. Conclusion positive immunostaining for HHV-8 LNA-1 exhibits high sensitivity and specificity for the diagnosis of KS and was, thus, useful for distinguishing it from the mimickers. The use of the prognostic markers was useful in detection the progression of macular form to tumor form of KS.

ICID 889689