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1. BFH was obvious similar with MFH at the cellular changes of histology, imaging diagnostic indexes, recurrence rate, age of onset and disease focus. BFH was different from NOF and MFD significantly.

BFH瘤灶与周围正常组织之间的微细变化的组织病理学与影像诊断学指标,复发性、年龄、病灶范围等临床指标,与MFH有明显的同一趋向性,而与NOF、MFD则有明显的差异性。

2. A 37-year-old female patient presented with malignant fibrous histiocytoma (MFH) of the right axilla, occurring 7.8 years after radiation treatment for infiltrating duct carcinoma of right breast.

一位37岁妇女于7.8年前因乳癌接受放射线治疗后，于右侧腋下发生恶性纤维组织细胞瘤。

3. Different from cases with single or multiple MFH of pleura reported in the literature, this case of diffuse myxoid MFH had an abrupt onset, and progressed aggressively.

与文献报道的非弥漫性胸膜MFH相比，本例为胸膜弥漫性多灶性MFH，起病急，病情进展快。

4. From 1984 to 1988, 26 patients with pathologically proven malignant fibrous histiocytoma (MFH) were collected and their radiologic findings were reviewed.

从1984年到1988年，共收集26个已由病理证实为恶性纤维组织细胞瘤(MFH)的病例。

5. We reported a case of MFH of the lung in a 28-year-old youth who was evaluated by computed tomography (CT) preoperatively.

以往的病例报告绝大部份都发生于老年人。本文提出一发生于28岁青年男性之病性。

6. Primary MFH may arise in the renal parenchyma or in the renal capsule.

原发性肾恶性纤维组织细胞瘤可发生于肾实质或肾包膜。

7. MFH in the soft tissue appeared as a nonspecific mass, adjacent bone was normal or involved.

发生于软组织者表现为非特异性肿块，邻近骨正常或受累。

8. MFH of the retroperitoneum, head and neck were large, invasive tumors with destruction of adjacent structures.

后腹膜及头颈部之MFH为巨大，有侵袭性之肿瘤，且常侵犯邻近器官。

9. Most of these non-lipogenic elements appear like fibrosarcoma or MFH, and often display features of high grade sarcoma.

大部分非脂肪肉瘤成分镜下很像纤维肉瘤或恶性纤维组织细胞瘤，并且通常显示的是高级别肉瘤的特征。

10. MFH is one of the most common soft tissue tumors of adults.

它是成人的软组织瘤中最常见的一种。

11. MFH is an aggressive, deep-seated pleomorphic sarcoma with a high local recurrence rate and significant metastatic rate usually associated with a poor prognosis.

恶性纤维组织瘤是一种富侵犯性且深部多形性肉瘤，经常合并有代表不良预后的高复发率及远处转移机率。

12. Primary malignant fibrous histiocytoma (MFH) of the lung is a very rare pulmonary malignancy.

摘要原发性肺部恶性纤维组织瘤为一类极罕见之肺癌。

13. Malignant fibrous histiocytoma (MFH) is rare in the larynx.The tumor is aggressive as it tends to both recur and metastasize to distant organs.

摘要喉部恶性纤维组织细胞瘤，是极为罕见的肿瘤，其具有侵犯性、高复发性及高转移性。

14. Malignant fibrous histiocytoma (MFH) was introduced in the early 1960s to describe a group of soft tissue tumors.

摘要恶性纤维组织细胞瘤是在1960年代被提出，用来描述一群软组织瘤。

15. Malignant fibrous histiocytoma (MFH) is the most common soft tissue sarcoma of adulthood with a male preponderance, and it often involves the extremities and retroperitoneum.

摘要恶性纤维组织细胞瘤是成年人最常见的恶性软组织肉瘤，以男性居多，好发于四肢及后腹腔。

16. Objective: To study the prognosis of surgical treatment of primary pulmonary malignant fibrous histocytoma (MFH).

摘要目的：研究经外科手术治疗的肺原发恶性纤维组织细胞瘤的临床特点及其预后。

17. Primary malignant fibrous histiocytoma (MFH) of the lung is rare and most reported cases are in late adulthood.

摘要肺原发性恶性纤维组织细胞瘤是非常罕有的肿瘤。

18. Methods Clinical data of 21 cases of MFH were retrospectively analyzed.

方法回顾性分析21例恶性纤维组织细胞瘤患者的临床资料。

19. METHODS: A retrospectie analysis of 5 patients operated on for primary MFH in the Department of Thoracic Surgery of the Medical Uniersity in Gdansk between 1990 and 2000 was performed.

方法：回顾性分析1990-2000年间在格但斯克的医科大学胸外科的5例手术的原发性MFH患者。

20. Final diagnosis of MFH was achieved based on histopathology and immunohistochemical stains.

最后的确定诊断有赖于组织病理切片以及免疫萤光染色等检查。

21. they have a male preponderance, and often involve the extremities and retroperitoneum, but a primary MFH of the urinary tract is extremely rare.

本例为62岁男性，在左侧输尿管患有恶性纤维组织细胞瘤，病人接受肾脏输尿管及膀胱袖口切除。

22. Most of MFH arising in the kidney are storiform-pleomorphic type as seen here. Distinction from sarcomatoid renal cell carcinoma may be difficult in some cases.

本肿瘤瘤体大并向周围浸润生长，常为多形性、编织型及炎症型。前者较难与肉瘤样肾细胞癌区别。

23. Materials and Methods:in 5 cases of primary MFH, radiography (X-ray, CT and MRI) were retrospectively reviewed and diagosis was established by pathology.

材料和方法：回顾性分析5例原发性恶性纤维组织细胞瘤的X线、CT或MRI影像表现特点。

24. We believe that most of the MFH cannot be diagnosed pre-operatively.

由于MFH可发生于任何部位而放射续表现多变，手术前准确之诊断十分困难。

25. Objective: To probe into the diagnosis and treatment of malignant fibrous histiocytoma (MFH) of the prostate.

目的:探讨前列腺恶性纤维组织细胞瘤(MFH)的诊断和治疗。

26. Objective To explore the clinical characteristics,diagnosis and treatment of malignant fibrous histocytoma (MFH).

目的探讨恶性纤维组织细胞瘤的临床特点及诊断、治疗方法。

27. Objective To investigate the changes of bone benign fibrous histiocytom (BFH) and its biological behavior and to identify it from malignant fibrous histiocytoma (MFH), nonossifying fibroma (NOF) and metaphyseal fibrous defect.

目的探讨骨BFH的特殊变化与生物学行为的关系,以与MFH、NOF、MFD鉴别。

28. Purpose: To study the radiological features of primary malignant fibrous histiocytoma(MFH).

目的：探讨原发性恶性纤维组织细胞瘤影像学特征。

29. Magnetic Fluid Hyperthermia(MFH)

磁流体热疗

30. Results 21 patients with MFH consisted of 16 cases of body wall,2 of lung,1 of pleura,1 of bile duct,and 1 of bone.

结果21例患者中肿瘤位于体壁16例,肺2例,胸膜1例,胆管1例,骨1例,均行手术治疗。

31. Combined utilization of plain X-ray, CT, and MRI is helpful for the diagnosis and differential diagnosis of MFH.

结论MFH影像学表现具有一定特征性，X线平片、CT和MRI结合有助于本病的诊断和鉴别诊断。

32. Conclusion Diffuse myxoid MFH of pleura is a very rare high-grade malignant tumor with very poor prognosis.

结论胸膜弥漫性黏液性MFH是非常罕见的胸膜原发性肿瘤，恶性程度高，预后极差。

33. Recurrence occurred in 4 cases and distal metastasis in 2 cases.Conclusion The aspiration cytology is helpful to the diagnosis of MFH.The main treatment of MFH resorts to surgery an...

结论针吸细胞学检查对恶性纤维组织细胞瘤的诊断有很大帮助,治疗以手术为主,彻底切除是治愈的关键。

34. CONCLUSION: Although surgical resection of MFH is the treatment of choice in MFH, the results are unsatisfactory.

结论：虽然MFH进行手术切除是该病治疗的首选，但结果并不令人满意。

35. Keywords Liver;Malignant fibrous histiocytoma （MFH）;Prognosis;metastasis;Immunohistochemistry;Vimentin;

肝脏;恶性纤维组织细胞瘤;预后;转移;免疫组化;波形蛋白;

36. In the mesenteric MFH, only mass effect on terminal ileum was shown in barium enema.

肠系膜MFH却只有在钡灌肠中表现出对迴肠有外在压迫。

37. A large, well-defined mass density with eccentric amorphous calcifications was seen in the pulmonary MFH.

肺原性MFH表现为一边绿清晰，有离心性钙化之大肿块。

38. The tumor origin was the surrounding soft tissue.Pathology showed storiform type of MFH.

肿瘤起源为周围软组织，病理切片显示为恶性纤维组织细胞瘤中的贮藏形成型。

39. The clinical features, diagnosis and treatment of MFH of the prostate were reviewed and presented.

行前列腺肿瘤根治术+直肠切除术+乙状结肠造瘘术。