Definition
Angiomatoid fibrous histiocytoma (AFH) is a rare lesion of uncertain differentiation, regarded as an intermediate malignant potential (rarely metastasizing), tumor (Enzinger 1979). AFH is not related either with high-grade pleomorphic sarcoma or fibrous histiocytoma of the skin.
Clinical Features
Incidence
AFH is extremely rare, accounting approximately for 0.3% of all mesenchymal tumors (Enzinger 1979; Fanburg-Smith and Miettinen 1999).
Age
A wide age range has been reported but typically occurs in young people with a mean age of 20 years (Enzinger 1979; Fanburg-Smith and Miettinen 1999).
Sex
There is no significant gender predilection (Enzinger 1979; Fanburg-Smith and Miettinen 1999).
Site
AFH occur most often in deep dermis and subcutis of the extremities, followed by the trunk and head and neck region (Enzinger 1979; Fanburg-Smith and Miettinen 1999). The majority of cases involve anatomic sites rich in lymph nodes....
References and Further Reading
Antonescu, C. R., Dal Cin, P., Nafa, K., et al. (2007). EWSR1-CREB1 is the predominant gene fusion in angiomatoid fibrous histiocytoma. Genes, Chromosomes & Cancer, 46, 1051–1060.
Cheah, A. L., Zou, Y., Lanigan, C., et al. (2019). ALK expression in angiomatoid fibrous histiocytoma: A potential diagnostic pitfall. The American Journal of Surgical Pathology, 43, 93–101.
Chen, G., Folpe, A. L., Colby, T. V., et al. (2011). Angiomatoid fibrous histiocytoma: Unusual sites and unusual morphology. Modern Pathology, 24, 1560–1570.
Costa, M. J., & Weiss, S. W. (1990). Angiomatoid malignant fibrous histiocytoma. A follow-up study of 108 cases with evaluation of possible histologic predictors of outcome. The American Journal of Surgical Pathology, 14, 1126–1132.
Enzinger, F. M. (1979). Angiomatoid malignant fibrous histiocytoma: A distinct fibrohistiocytic tumor of children and young adults simulating a vascular neoplasm. Cancer, 44, 2147–2157.
Fanburg-Smith, J. C., & Miettinen, M. (1999). Angiomatoid “malignant” fibrous histiocytoma: A clinicopathologic study of 158 cases and further exploration of the myoid phenotype. Human Pathology, 30, 1336–1343.
Fletcher, C. D. (1991). Angiomatoid “malignant fibrous histiocytoma”: An immunohistochemical study indicative of myoid differentiation. Human Pathology, 22, 563–568.
Hallor, K. H., Mertens, F., Jin, Y., et al. (2005). Fusion of the EWSR1 and ATF1 genes without expression of the MITF-M transcript in angiomatoid fibrous histiocytoma. Genes, Chromosomes & Cancer, 44, 97–102.
Kao, Y. C., Lan, J., Tai, H. C., et al. (2014). Angiomatoid fibrous histiocytoma: Clinicopathological and molecular characterization with emphasis on variant histomorphology. Journal of Clinical Pathology, 67, 210–215.
Raddaoui, E., Donner, L. R., & Panagopoulos, I. (2002). Fusion of the FUS and ATF1 genes in a large, deep-seated angiomatoid fibrous histiocytoma. Diagnostic Molecular Pathology, 11, 157–162.
Rossi, S., Szuhai, K., Ijszenga, M., et al. (2007). EWSR1-CREB1 and EWSR1-ATF1 fusion genes in angiomatoid fibrous histiocytoma. Clinical Cancer Research, 13, 7322–7328.
Schaefer, I. M., & Fletcher, C. D. (2014). Myxoid variant of so-called angiomatoid “malignant fibrous histiocytoma”: Clinicopathologic characterization in a series of 21 cases. The American Journal of Surgical Pathology, 38, 816–823.
Waters, B. L., Panagopoulos, I., & Allen, E. F. (2000). Genetic characterization of angiomatoid fibrous histiocytoma identifies fusion of the FUS and ATF-1 genes induced by a chromosomal translocation involving bands 12q13 and 16p11. Cancer Genetics and Cytogenetics, 121, 109–116.
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Sbaraglia, M. (2020). Angiomatoid Fibrous Histiocytoma. In: van Krieken, J. (eds) Encyclopedia of Pathology. Encyclopedia of Pathology. Springer, Cham. https://doi.org/10.1007/978-3-319-28845-1_5347-1
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DOI: https://doi.org/10.1007/978-3-319-28845-1_5347-1
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