is a known aggressive variant of urothelial carcinoma. However, the reasons for its aggressiveness remain unclear.Objective.-To investigate the frequency of lymphovascular invasion in 22 cases of MPUC.Design.-Consecutive tissue sections were stained with D2-40 and CD34 to highlight lymphovascular channels associated with MPUC. Spaces containing tumor cells were scored as positive for lymphovascular invasion if the staining pattern on immunohistochemistry was distinct and circumferential.Results.-Of 22 cases, 21 (95%) had lymphovascular invasion on immunohistochemical staining, with 91% lymphatic invasion and 4% vascular invasion. Interestingly, 8 cases were originally signed out as negative for lymphovascular invasion on the basis of hematoxylineosin-stained sections; of these, 7 (88%) had focal lymphovascular invasion evident on immunohistochemical staining.Conclusions.-Our results confirm that micropapillary lacunae are not lymphovascular channels. However, nearly all MPUC tumors (95% in this series) have evidence of lymphovascular invasion by immunohistochemical analysis. Our data support the use of micropapillary features as a morphologic marker for lymphovascular invasion and MPUC as an adverse histologic type of urothelial carcinoma.(Arch Pathol Lab Med. 2012;136:635-639; doi: 10.5858/ arpa.2011-0463-OA) M icropapillary urothelial carcinoma (MPUC) is a rare, clinically aggressive histologic variant of urothelial carcinoma (UC). It was first described by Amin et al 1 in 1994 and is characterized by small, infiltrating clusters of neoplastic cells that appear to float within clear lacunar spaces and that lack a fibrovascular core (Figure 1). Micropapillary urothelial carcinoma occurs almost exclusively in the setting of conventional UC, 2,3 and the proportion of MPUC predicts high pathologic stage and lymph node metastasis. 4,5 The overall prognosis is poor; the 5-year and 10-year survival in the largest study were 51% and 24%, respectively.
6Multiple investigators have examined vascular invasion in MPUC by using immunohistochemistry for factor VIII, Ulex europaeus, CD31, and CD34, 1,7-10 as summarized in Table 1. Together, these studies demonstrate vascular invasion in 23 of 33 cases (70%). But these studies are hampered by exclusive use of vascular endothelial markers, and the rate of lymphovascular invasion in MPUC may be even higher.