Hurtado-Cordovi Jorge, Pathak Prajwol, Avezbakiyev Boris, Frieri Marianne
Divisions of Hematology and Oncology and Allergy and Immunology, Department of Medicine, Nassau University Medical Center and North Shore- Long Island Jewish Health Care System, 2201 Hempstead Turnpike, East Meadow, NY 11554, USA.
ISRN Oncol. 2012;2012:946019. doi: 10.5402/2012/946019. Epub 2012 Oct 14.
Inflammatory malignant fibrous histiocytoma (IMFH) associated with leukemoid reaction (LR)/leukocytosis is a rare entity. In this paper, we search PubMed for all known cases of IMFH associated with LR/leukocytosis in an attempt to draw conclusions about this variant's response to treatments and its pathophysiology. Medline electronic database was searched using key words such as malignant fibrous histiocytoma, leukemoid reaction, and leukocytosis. A total of 16 patients were found, twelve males (75%) and 4 female (25%), with a mean age of 62.6 years, ranging from 47 to 77. The mean survival was 770 days, ranging from 14 to 6570 days. Four patients were alive at last follow-up: 6570 days, 1095 days, 335 days, and 180 days, respectively. Of the 12 patients that expired, death occurred approximately 92 days after the onset of LR or leukocytosis, ranging from 3 to 334 days. We conclude that IMFH associated with LR/leukocytosis does not completely respond to chemoradiation. Overproduction of growth factors and cytokines by IMFH cells and their interactions with the inflammatory infiltrate seem to promote immunological effector cell's dysfunction and substantiate the development and growth of this neoplasm. A clear understanding of these molecular pathways is crucial in order to identify targets for potential therapy.
伴有类白血病反应(LR)/白细胞增多的炎性恶性纤维组织细胞瘤(IMFH)是一种罕见的疾病。在本文中,我们在PubMed上搜索了所有已知的伴有LR/白细胞增多的IMFH病例,试图得出关于该变体对治疗的反应及其病理生理学的结论。使用恶性纤维组织细胞瘤、类白血病反应和白细胞增多等关键词在Medline电子数据库中进行搜索。共发现16例患者,其中男性12例(75%),女性4例(25%),平均年龄62.6岁,范围为47至77岁。平均生存期为770天,范围为14至6570天。在最后一次随访时有4例患者存活:分别为6570天、1095天、335天和180天。在12例死亡患者中,死亡发生在LR或白细胞增多开始后约92天,范围为3至334天。我们得出结论,伴有LR/白细胞增多的IMFH对放化疗并不完全敏感。IMFH细胞生长因子和细胞因子的过度产生及其与炎性浸润的相互作用似乎促进了免疫效应细胞的功能障碍,并证实了这种肿瘤的发生和发展。清楚了解这些分子途径对于确定潜在治疗靶点至关重要。