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肝原发性血管肉瘤临床病理分析 被引量:1

Clinicopathological study on primary hepatic angiosarcoma
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摘要 目的探讨肝原发性血管肉瘤(PHA)的临床病理学与免疫组织化学特点。方法采用HE和免疫组织化学SP法染色对3例PHA进行研究,观察PHA的临床病理学、免疫组织化学特点。结果患者年龄2.68岁,男:女为2:1;临床症状和实验室检查无特异性。1例为多个结节,2例为单个结节;肿瘤直径平均大小为7.2(5—11-3)cm,有出血和坏死。病理学特征:肿瘤细胞呈梭形和不规则形,大小不一。胞质较少,嗜酸性,淡染,边界不清,核较大,卵圆形或梭形,染色深,核仁大小不一,可见少数核分裂象,瘤细胞部分排列成索状,片状,较密集,与周围肝组织界线不清,部分区域可见大而不规则的血管腔隙,局部肿瘤细胞集聚成团,呈乳头状突入血管腔内,相互吻合,内衬不典型性细胞。不规则血管腔样结构广泛弥漫分布于肝实质内,伴局部出血。免疫组化因子Ⅷ和(或)CD34阳性。结论PHA极少见,为高度恶性,预后差。临床和病理上均易误诊为肝血管瘤、肝上皮样血管内皮瘤、肝细胞癌等;根据PHA的组织学和免疫组化特点,可作出明确的病理诊断。 Objective To study the clinicopathological and immunohistochemical features of Primary Hepatic Angiosarcoma(PHA). Method H-E and immunohistochemistry were used to study 3 cases of PHA. Results The patients were 2-68 years old, with male to female ratio being 2/1, and presented with nonspecific symptoms. The lesion was muhinodular in 1 case and uninodular in 2 cases. The median size was 7.2 cm (5-11.3 cm), accompanied by hemorrhage and necrosis. Histological, there was a wide morphologic spectrum among cases. 3 cases of PHA included areas similar to cavernous and capillary hemangioma,spindle cell and epithelioid sarcoma. The spindle, rounded or irregular tumor cells of relatively high nuclear grade were arranged in sheets, small nests, cords or rudimentary vascular channels, and displayed mitotic activity. The vascular channels were irregular in shape, freely intercommunicate with one another in a sinusoidal fashion, and infiltrated adjacent hepatic tissues in a destructive fashion. In some areas the vascular channels were lined by a surfeit of neoplastic endothelium forming intraluminal buds, projections or papillae. Immunohistochemically, tumor cells were positive for factor Ⅷ-related antigen and CD34. Conclusions PHA is an extremely rare, highly malignant hepatic tumor with poor outcome. Surgical resection can obtain prolonged survival. PHA may be clinically or histological misdiagnosed as hepatic hemangioma, hepatic epithelioid hemangioendothelioma or hepatic cell carcinoma. The diagnosis can be made based on histological and immunohistochemical features of the tumor.
出处 《肿瘤研究与临床》 CAS 2007年第1期35-36,42,共3页 Cancer Research and Clinic
关键词 肝肿瘤 血管肉瘤 临床病理学 Liver neoplasm Hemangiosarcoma Clinical pathology
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参考文献11

  • 1武忠弼 杨光华主编.中华外科病理学[M].北京:人民卫生出版社,2002.646.
  • 2Neshiwat L F, Friedland M L, Schorr-Lesnick B, et al. Hepatic angiosarcoma[J]. Am J Med, 1992, 93(2): 219-222.
  • 3Molina E, Hernandez A. Clinical manifestations of primary hepaticangiosarcoma[J]. Dig Dis Sci, 2003, 48(4): 677-682.
  • 4Koyama T, Fletcher J G, Johnson C D, et al. Primary hepatic angiosarcoma: findings at CT and MR imaging[J]. Radiology, 2002,222(3): 667-673.
  • 5Dimashkieh H H, Mo J Q, Wyatt-Ashmead J, et al. Pediatric hepatic angiosarcoma: case report and review of the literature[J]. Pediatr Dev Pathol, 2004, 7(5): 527-532.
  • 6回允中主译.诊断外科病理学[M](第3版)[M].北京:北京大学医学出版社,2003.1498.
  • 7Ohsawa M, Naka N, Tomita Y, et al. Use of immunohistochemicalprocedures in diagnosing angiosarcoma. Evaluation of 98 cases[J].Cancer, 1995, 75(12): 2867-2874.
  • 8Basten O, Bandorski D, Langner C. Hemangiosarcoma of the liverwith unusual expression of neuron-specific enolase(NSE)[J]. Gastroenterol, 2002, 40(8): 577-580.
  • 9Ishak K G. Malignant mesenchymal tumor and some other nnnhepatocellular tumor of the liver. Liver cancer[M]. New York: ChurchillLivingstone, 1997: 291-314.
  • 10Kirchstein T, Aeberli D, Zimmermann A, et al. Metastatic angiosarcoma of the liver preoperatively presenting as giant hemangioma[J].Digestion, 2000, 62(4): 280-283.

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  • 1邓晓,侯英勇,陈颖,侯君,谭云山,宿杰.阿克苏.肝原发性恶性血管肿瘤临床病理分析[J].临床与实验病理学杂志,2006,22(2):141-145. 被引量:3
  • 2张海增,董书晓,邵永孚.原发性肝脏恶性间质瘤的临床病理特征及诊治分析[J].中国实用外科杂志,2006,26(7):517-519. 被引量:4
  • 3王健,李强,崔云龙,孙燕,肖建宇.肝血管肉瘤:16例回顾[J].中华肝胆外科杂志,2006,12(8):532-535. 被引量:28
  • 4Falk H, Herbert J, Crowleg S, et al. Epidemiology of hepatic angiosarcom in the United States: 1964 -1974[ J]. Environ Health Perspect, 1981, 41 (1) : 107 - 113.
  • 5Locker GY, Doroshow JH, Zwelling LA, et al. The clinical features of hepatic angiosarcoma : a report of four cases and a review of the English literature [ J ]. Medicine ( Baltimore ) , 1979, 58 (1) : 48 - 64.
  • 6Hamihor SR, Aaltonen LA. World Health Organization classification of tumors. Pathology and genetics of tumors of the digestive system [ M ] . Lyon : IARC Press, 2000 : 237 - 238.
  • 7回允中.外科病理学下卷[M].北京:北京大学医学出版社,2006:1009-1010.
  • 8Timaran CH, Grandas OH, Bell JL. Hepatic angiosarcoma: long-teml survival after complete surgical removal [ J ]. Am Surg,2000,66(12) :1153 - 1157.
  • 9Kim HR, Rha SY, Cheon SH. Clinical features and treatment outcomes of advanced stage primary hepatic angiosarcoma [J]. Ann Oncal, 2009,20(4) :780 -787.
  • 10Molina E, Hernandz A. Clinical manifestations of primary hepatic angiosarcoma[J]. Dig Dis Sci, 2003,48(4) :677 -682.

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