中华病理学杂志
中華病理學雜誌
중화병이학잡지
Chinese Journal of Pathology
2013年
10期
675-678
,共4页
沈旭霞%孔蕴毅%戴波%蔡旭%王丽薇%孔今城
瀋旭霞%孔蘊毅%戴波%蔡旭%王麗薇%孔今城
침욱하%공온의%대파%채욱%왕려미%공금성
恶性黑色素瘤%皮肤%消退%预后
噁性黑色素瘤%皮膚%消退%預後
악성흑색소류%피부%소퇴%예후
Malignant melanoma%Cutaneous%Regression%Prognosis
目的 探讨原发皮肤“消退性”恶性黑色素瘤的临床病理特点、预后和鉴别诊断.方法 收集2009至2012年间原发皮肤“消退性”恶性黑色素瘤8例,总结临床病理、治疗和随访资料.常规HE染色和免疫组织化学EnVision法染色行组织病理形态学观察.结果 患者年龄40 ~ 69岁(平均58岁),男女比3∶1,发生部位分别为背部4例,足底2例,足趾腹面1例,上臂1例.临床上,6例初始表现为逐渐增大的皮肤黑斑,随后出现局部区域皮损颜色变浅并扩大,最终可呈瘢痕样.2例表现为散在簇状分布多灶黑点黑斑.组织学上,完全消退型3例,其中1例表现为肿瘤样黑变病.广泛消退型5例,消退比例达75% ~ 90%,大部分区域示完全消退期图像,局部区域呈消退进行期改变,Breslow厚度0.5 ~1.0 mm.免疫组织化学标记显示淋巴结内转移灶和广泛消退型原发灶内残留的少量黑色素瘤细胞均弥漫强阳性表达S-100蛋白、HMB45和Melan A.吞噬黑色素的组织细胞CD68阳性.8例均获得随访,随访时间8~ 27个月(中位时间13个月),5例无瘤生存;3例发生远处转移,其中1例带瘤生存,2例死亡.结论 消退性恶性黑色素瘤是一种好发于中老年人罕见的特殊类型的黑色素瘤,诊断时应综合临床病史和病理学改变.消退≥75%是T1期(Breslow厚度≤1 mm)恶性黑色素瘤预后的一个不利因素,建议行病灶局部广泛切除术同时予以前哨淋巴结活检.
目的 探討原髮皮膚“消退性”噁性黑色素瘤的臨床病理特點、預後和鑒彆診斷.方法 收集2009至2012年間原髮皮膚“消退性”噁性黑色素瘤8例,總結臨床病理、治療和隨訪資料.常規HE染色和免疫組織化學EnVision法染色行組織病理形態學觀察.結果 患者年齡40 ~ 69歲(平均58歲),男女比3∶1,髮生部位分彆為揹部4例,足底2例,足趾腹麵1例,上臂1例.臨床上,6例初始錶現為逐漸增大的皮膚黑斑,隨後齣現跼部區域皮損顏色變淺併擴大,最終可呈瘢痕樣.2例錶現為散在簇狀分佈多竈黑點黑斑.組織學上,完全消退型3例,其中1例錶現為腫瘤樣黑變病.廣汎消退型5例,消退比例達75% ~ 90%,大部分區域示完全消退期圖像,跼部區域呈消退進行期改變,Breslow厚度0.5 ~1.0 mm.免疫組織化學標記顯示淋巴結內轉移竈和廣汎消退型原髮竈內殘留的少量黑色素瘤細胞均瀰漫彊暘性錶達S-100蛋白、HMB45和Melan A.吞噬黑色素的組織細胞CD68暘性.8例均穫得隨訪,隨訪時間8~ 27箇月(中位時間13箇月),5例無瘤生存;3例髮生遠處轉移,其中1例帶瘤生存,2例死亡.結論 消退性噁性黑色素瘤是一種好髮于中老年人罕見的特殊類型的黑色素瘤,診斷時應綜閤臨床病史和病理學改變.消退≥75%是T1期(Breslow厚度≤1 mm)噁性黑色素瘤預後的一箇不利因素,建議行病竈跼部廣汎切除術同時予以前哨淋巴結活檢.
목적 탐토원발피부“소퇴성”악성흑색소류적림상병리특점、예후화감별진단.방법 수집2009지2012년간원발피부“소퇴성”악성흑색소류8례,총결림상병리、치료화수방자료.상규HE염색화면역조직화학EnVision법염색행조직병리형태학관찰.결과 환자년령40 ~ 69세(평균58세),남녀비3∶1,발생부위분별위배부4례,족저2례,족지복면1례,상비1례.림상상,6례초시표현위축점증대적피부흑반,수후출현국부구역피손안색변천병확대,최종가정반흔양.2례표현위산재족상분포다조흑점흑반.조직학상,완전소퇴형3례,기중1례표현위종류양흑변병.엄범소퇴형5례,소퇴비례체75% ~ 90%,대부분구역시완전소퇴기도상,국부구역정소퇴진행기개변,Breslow후도0.5 ~1.0 mm.면역조직화학표기현시림파결내전이조화엄범소퇴형원발조내잔류적소량흑색소류세포균미만강양성표체S-100단백、HMB45화Melan A.탄서흑색소적조직세포CD68양성.8례균획득수방,수방시간8~ 27개월(중위시간13개월),5례무류생존;3례발생원처전이,기중1례대류생존,2례사망.결론 소퇴성악성흑색소류시일충호발우중노년인한견적특수류형적흑색소류,진단시응종합림상병사화병이학개변.소퇴≥75%시T1기(Breslow후도≤1 mm)악성흑색소류예후적일개불리인소,건의행병조국부엄범절제술동시여이전초림파결활검.
Objective To study the clinicopathologic features and differential diagnosis of cutaneous regressing/regressed melanoma.Methods Histopathologic evaluation and immunohistochemical study by EnVision method were performed in 8 cases of cutaneous regressing/regressed melanoma.The clinical presentation,treatment and follow-up data were analyzed.Results The age of the patients ranged from 40 to 69 years (mean 58 years).The male-to-female ratio was 3∶ 1.Tumors were located on the back (4 cases),sole of the foot (2 cases),ventral aspect of the toes (1 case),and the forearm (1 case).Clinically,6 patients presented with progressive black mole of the skin,followed by subsequent focal hypopigmentation,even scarring.Two patients presented with multiple foci of dark-brown pigmentation.Microscopically,3 cases were completely regressed malignant melanoma.Tumoral melanosis was found in 1 of 3 cases.The other 5 cases were melanoma with severe regression.The extent of regression ranged from 75% to 90%.The Breslow depth of the tumors ranged from 0.5 to 1.0 mm.Immunohistochemically,both metastatic and primary tumor cells were diffusely positive for S-100,HMB45 and Melan A,while melanophages were positive for CD68.Follow-up data were available in 8 patients,ranging from 8 to 27 months.Five patients were alive with no evidence of disease,1 patient was alive with stable disease and 2 patients died of metastatic melanoma.Conclusions Correlation between clinical presentation and pathologic features is important for diagnosis of cutaneous regressing/regressed melanoma.Thin melanoma with extensive regression (≥75%) should not been regarded as low metastatic risk and wide excision combined with sentinel lymph node biopsy is recommended.