白血病·淋巴瘤
白血病·淋巴瘤
백혈병·림파류
JOURNAL OF LEUKEMIA & LYMPHOMA
2009年
10期
619-621
,共3页
陈燕坪%陈刚%林晋%许磊%力超%郑雄伟
陳燕坪%陳剛%林晉%許磊%力超%鄭雄偉
진연평%진강%림진%허뢰%력초%정웅위
滤泡树突细胞肉瘤%免疫组织化学%诊断%鉴别%原位杂交
濾泡樹突細胞肉瘤%免疫組織化學%診斷%鑒彆%原位雜交
려포수돌세포육류%면역조직화학%진단%감별%원위잡교
Follicular dendritic cell sarcoma%lmmunohistochemistry%Diagnosis,differential%Insitu hybridization
目的 探讨并分析结外滤泡树突细胞肉瘤(FDCS)的临床病理特征.方法 应用组织学、免疫组织化学(EnVision)及EBV原位杂交检测技术,对4例FDCS进行临床和组织病理学分析,并结合文献进行探讨.结果 镜下观察肿瘤细胞旱梭形、卵圆形,胞质丰富淡染、颗粒状,核早泡状、有清晰的小核仁,排列呈束状,席纹状及漩涡状,瘤细胞间穿行大量的小淋巴细胞并有小淋巴细胞围绕小血管形成血管周围套现象,散在多核巨细胞,病理性核分裂少见.肿瘤细胞特异性表达一个或多个树突细胞标志CD21、CD23和CD35,CD68、Vimentin、LCA和S-100表达不定,CD20、CD3和CD1α阴性,Ki-67指数10%~20%,EBV原位杂交阴性.结论 FDCS是罕见的低度恶性肿瘤,有一定的特征性,确诊需要结合病理形态和免疫表型,应与胃肠道间质瘤、炎性假瘤、指突树突细胞肉瘤、恶性纤维组织细胞瘤、弥漫性大B细胞淋巴瘤、未分化癌、恶性黑色素细胞瘤等鉴别.
目的 探討併分析結外濾泡樹突細胞肉瘤(FDCS)的臨床病理特徵.方法 應用組織學、免疫組織化學(EnVision)及EBV原位雜交檢測技術,對4例FDCS進行臨床和組織病理學分析,併結閤文獻進行探討.結果 鏡下觀察腫瘤細胞旱梭形、卵圓形,胞質豐富淡染、顆粒狀,覈早泡狀、有清晰的小覈仁,排列呈束狀,席紋狀及漩渦狀,瘤細胞間穿行大量的小淋巴細胞併有小淋巴細胞圍繞小血管形成血管週圍套現象,散在多覈巨細胞,病理性覈分裂少見.腫瘤細胞特異性錶達一箇或多箇樹突細胞標誌CD21、CD23和CD35,CD68、Vimentin、LCA和S-100錶達不定,CD20、CD3和CD1α陰性,Ki-67指數10%~20%,EBV原位雜交陰性.結論 FDCS是罕見的低度噁性腫瘤,有一定的特徵性,確診需要結閤病理形態和免疫錶型,應與胃腸道間質瘤、炎性假瘤、指突樹突細胞肉瘤、噁性纖維組織細胞瘤、瀰漫性大B細胞淋巴瘤、未分化癌、噁性黑色素細胞瘤等鑒彆.
목적 탐토병분석결외려포수돌세포육류(FDCS)적림상병리특정.방법 응용조직학、면역조직화학(EnVision)급EBV원위잡교검측기술,대4례FDCS진행림상화조직병이학분석,병결합문헌진행탐토.결과 경하관찰종류세포한사형、란원형,포질봉부담염、과립상,핵조포상、유청석적소핵인,배렬정속상,석문상급선와상,류세포간천행대량적소림파세포병유소림파세포위요소혈관형성혈관주위투현상,산재다핵거세포,병이성핵분렬소견.종류세포특이성표체일개혹다개수돌세포표지CD21、CD23화CD35,CD68、Vimentin、LCA화S-100표체불정,CD20、CD3화CD1α음성,Ki-67지수10%~20%,EBV원위잡교음성.결론 FDCS시한견적저도악성종류,유일정적특정성,학진수요결합병리형태화면역표형,응여위장도간질류、염성가류、지돌수돌세포육류、악성섬유조직세포류、미만성대B세포림파류、미분화암、악성흑색소세포류등감별.
Objective To study the clinicopathoiogic features of four cases of extranodal follicular dendritic cell sarcoma(FDCS). Methods Four cases of FDCS were examined by histological and immunohistochemistry and in situ hybridization for Epstein-Barr virus (EBV)-encoded RNA, and the related literatures were reviewed. Results Microscopically, the neoplastic cells were spindle-shaped or ovoid with pale-stained cytoplasm, indistinct cell borders, granular chromatin, distinct small nucleoli. There were varied growth patterns in the tumour, such as fascicular, circular whorls and storiform, and abundant with intermixed small lymphocytes. There scattered multinucleated giant cells and perivascular cuffing phenomenon. There were rare mitoses. The neoplastic cells were positive for one or more of the follicular dendritic markers such as CD21, CD23 and CD35. It was variably positive for CD68, Vimentin, LCA and S-100. Staining for CD20, CD3 and CD1α were negative. Ki-67 labeling ranged from 10 %-20 %. The neoplastic cells were negative for Epstein-Barrvirus (EBV)-encoded RNA. Conclusion FDCS is a rare low-grade malignant tumor with varied growth pattern. The diagnosis should be confirmed by immunohistochemical staining. It is important to recognize its morphological characteristics to avoid confusion with other similar lesions, such as gastrointestinal stromal tumour, inflammatory pseudotumor, interdigitaing dendtritic cell sarcoma, malignant histiocytoma, lymphoepithelial carcinoma, diffuse large B-cell lymphoma, and malignant melanoma.