肿瘤研究与临床
腫瘤研究與臨床
종류연구여림상
CANCER RESEARCH AND CLINIC
2009年
10期
692-694
,共3页
张伟%唐仁泉%郭静%刘媛媛
張偉%唐仁泉%郭靜%劉媛媛
장위%당인천%곽정%류원원
血管球瘤%病理学%临床%免疫组织化学
血管毬瘤%病理學%臨床%免疫組織化學
혈관구류%병이학%림상%면역조직화학
Glomus tumor%Pathology%clinical%Immunohistoehemistry
目的 探讨血管球瘤(GT)的临床病理学特征和鉴别诊断.方法 对11例GT的临床特征、组织学形态和免疫学表型进行观察.结果 7例肿瘤发生于手指甲下,2例发生于前臂皮下,1例发生于膝关节皮下,1例发生于胃窦后壁.临床主要表现为局部疼痛.9例诊断为实体性球瘤,2例诊断为球血管瘤,其组织学特点为肿瘤细胞小、圆形、大小一致,呈巢状、小簇状围绕于毛细血管、扩张的小静脉周围,间质玻璃样变性及黏液变性.免疫组织化学:11例肿瘤细胞SMA、Vimentin均为(+);而CK、CD117、CD34、CgA、Syn、Desmin、S-100、HMB45均为(-).11例患者术后随访12~30个月,均无复发或转移.结论 GT非常少见,确诊依赖组织学和免疫组织化学检测.该肿瘤发生于内脏时极易误诊,需要和其他肿瘤鉴别.
目的 探討血管毬瘤(GT)的臨床病理學特徵和鑒彆診斷.方法 對11例GT的臨床特徵、組織學形態和免疫學錶型進行觀察.結果 7例腫瘤髮生于手指甲下,2例髮生于前臂皮下,1例髮生于膝關節皮下,1例髮生于胃竇後壁.臨床主要錶現為跼部疼痛.9例診斷為實體性毬瘤,2例診斷為毬血管瘤,其組織學特點為腫瘤細胞小、圓形、大小一緻,呈巢狀、小簇狀圍繞于毛細血管、擴張的小靜脈週圍,間質玻璃樣變性及黏液變性.免疫組織化學:11例腫瘤細胞SMA、Vimentin均為(+);而CK、CD117、CD34、CgA、Syn、Desmin、S-100、HMB45均為(-).11例患者術後隨訪12~30箇月,均無複髮或轉移.結論 GT非常少見,確診依賴組織學和免疫組織化學檢測.該腫瘤髮生于內髒時極易誤診,需要和其他腫瘤鑒彆.
목적 탐토혈관구류(GT)적림상병이학특정화감별진단.방법 대11례GT적림상특정、조직학형태화면역학표형진행관찰.결과 7례종류발생우수지갑하,2례발생우전비피하,1례발생우슬관절피하,1례발생우위두후벽.림상주요표현위국부동통.9례진단위실체성구류,2례진단위구혈관류,기조직학특점위종류세포소、원형、대소일치,정소상、소족상위요우모세혈관、확장적소정맥주위,간질파리양변성급점액변성.면역조직화학:11례종류세포SMA、Vimentin균위(+);이CK、CD117、CD34、CgA、Syn、Desmin、S-100、HMB45균위(-).11례환자술후수방12~30개월,균무복발혹전이.결론 GT비상소견,학진의뢰조직학화면역조직화학검측.해종류발생우내장시겁역오진,수요화기타종류감별.
Objective To investigate the clinicopathological features of glomus tumor and its differential diagnosis. Methods Clinical, morphologie and immunohistoehemical representations were described in 11 cases of glomus tumor. Results The tumors were located at the hyponychial in 7 cases, forearm subcutaneous in 2 cases, knee subcutaneous in 1 case, gastric antrum forewall in 1 cases. Localized pain was the primary symptom. 9 giomus tumors were histopathologically classified as solid type, and 2 glomangiomatous type. The prominent morphologic features of glomus tumor were as follows: the tumor cells were small, round, uniform, the tumor cells arranged around capillary vessel or expansion of the small vein showing nest pattern,some tumor cells in fasciation pattern; focally myxoid change in the stroma were seen. Immunohistochemistry: 11 cases were positive for SMA and Vimentin; while other markers including CK, CD117, CD34, CgA, Syn, Desmin, S-100 and HMB45, were all negative. All 11 cases were without any evidence of recurrence or metastasis in followed-up for 12-30 months. Conclusion Glomus tumor is extremely rare. The diagnosis depends on the histology and immunohistochemistry. Glomus tumor is rare in visceral sites. It may be misdiagnosed and needs to he differentiated from other tumors.