J Med Life Sci > Volume 11(1); 2014 > Article
Journal of Medicine and Life Science 2014;11(1):33-39.
DOI: https://doi.org/10.22730/jmls.2014.11.1.33    Published online December 18, 2018.
혈철소피부섬유종: 다양한 피부섬유종 변종 및 간엽 기원 섬유조직구 종양들과의 조직학적 감별
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Hemosiderotic Dermatofibroma: Histopathologic Differential Diagnosis from Other Variants of Dermatofibroma and a Variety of Fibrohistiocytic Tumors of Mesenchymal Origin
Minsu Kim, Minseok Cheon, Jae-Wang Kim
Correspondence:  Jae-Wang Kim,
Abstract
Dermatofibroma(benign fibrous histiocytoma) is a relatively common fibrohistiocytic tumor. It has a variety of histologic variants and the diagnosis may be difficult in atypical or rare cases. Hemosiderotic dermatofibroma is an uncommon pathologic subtype of dermatofibroma. Histopathologically, it is characterized by widespread deposition of intra- and extracellular hemosiderin, numerous small vessels and extravasated erythrocytes, in addition to the typical features of classic dermatofibroma. It has been recognized as a precursor lesion for the development of aneurysmal dermatofibroma. This tumor should be differentiated from other histologic variants of dermatofibroma and fibrohistiocytic tumors with variable grade of malignancy. Herein, we represent a case of hemosiderotic dermatofibroma occurring in a 32-year-old male.
Key Words: Hemosiderotic Dermatofibroma
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