Fischer Edgar G, Bocklage Thèrése J, Rabinowitz Ian, Smith Harriet O, Viswanatha David S
Department of Pathology, University of New Mexico Health Sciences Center, Albuquerque 87131-5301, USA.
Arch Pathol Lab Med. 2003 Jan;127(1):e28-31. doi: 10.5858/2003-127-e28-PPAIAE.
Primary plasmacytomas of the female genital tract are extremely rare and present a substantial diagnostic challenge. Five cases morphologically representing plasmacytomas and localized to the uterine cervix have been reported previously; however, only 1 was shown to be monotypic for immunoglobulin light-chain expression. We report the case of a 37-year-old woman who had highly atypical plasma cells on her Papanicolaou test. A clinically detected endocervical polyp was removed and revealed a plasmacytoma, the diagnosis of which was substantiated by demonstrating monotypic lambda-light-chain restriction and a clonal immunoglobulin heavy-chain gene rearrangement. The cytologic and histopathologic findings of plasmacytomas of the uterine cervix are discussed, including the utility of immunophenotypic and molecular techniques to confirm the neoplastic diagnosis.
女性生殖道原发性浆细胞瘤极为罕见,诊断颇具挑战。此前已有5例形态学表现为浆细胞瘤且局限于子宫颈的病例报告;然而,仅有1例显示免疫球蛋白轻链表达为单型。我们报告1例37岁女性,其巴氏涂片检查发现高度非典型浆细胞。临床检测到的宫颈息肉切除后显示为浆细胞瘤,通过证实单型λ轻链限制和克隆性免疫球蛋白重链基因重排确诊。本文讨论了子宫颈浆细胞瘤的细胞学和组织病理学表现,包括免疫表型和分子技术在确诊肿瘤方面的应用。