Wiriosuparto Sony, Krassilnik Nina, Gologan Adrian, Cohen Jean-Marc, Wenig Bruce
Department of Pathology and Laboratory Medicine, University of California-Los Angeles Medical Center, CHS A7-149, 10833 LeConte Avenue, Los Angeles, California 90095-1732, USA.
Acta Cytol. 2003 Jul-Aug;47(4):673-8. doi: 10.1159/000326587.
We report a case of malignant fibrous histiocytoma, giant cell type (MFHGC), of the breast. A review of the literature failed to reveal cytology-based reports on this entity. The cytologic similarity of breast MFHGC on fine needle aspiration biopsy (FNAB) to other malignant breast neoplasms, including carcinoma with osteoclastlike giant cells, metaplastic carcinoma and breast sarcomas, as well as benign reactive processes, makes the recognition of this tumor challenging.
A 72-year-old woman presented with a 5-month history of an enlarging breast mass. FNAB of the mass showed a hypercellular smear composed of cohesive, branching clusters of spindle cells with ovoid, focally hyperchromatic nuclei and inconspicuous nucleoli. Interspersed osteoclastlike giant cells, some associated with clusters of spindle cells, were uniformly seen throughout the smear. The background was hemorrhagic, with cellular debris and occasional spindle cells and lymphocytes. No ductal epithelial or myoepithelial cells were seen. An incisional biopsy was performed, followed by radical mastectomy. The histologic examination was diagnostic of MFHGC. The diagnosis was supported by immunohistochemical and electron microscopic studies.
MFHGC, also called primary giant cell tumor of soft tissues, is composed of a mixture of histiocytes, fibroblasts and bland-appearing osteoclastlike giant cells with a multinodular growth pattern. Although MFHGC rarely occurs in the breast and the definitive diagnosis is difficult based on cytology alone, the diagnosis can be considered when a cytologic examination reveals a hypercellular, spindle cell smear with osteoclastlike giant cells in the absence of ductal epithelial or myoepithelial cells.
我们报告一例乳腺巨细胞型恶性纤维组织细胞瘤(MFHGC)。文献回顾未发现基于细胞学的关于该实体的报道。乳腺MFHGC在细针穿刺活检(FNAB)时的细胞学表现与其他恶性乳腺肿瘤相似,包括伴有破骨细胞样巨细胞的癌、化生性癌和乳腺肉瘤,以及良性反应性病变,这使得识别该肿瘤具有挑战性。
一名72岁女性,有乳腺肿块增大5个月的病史。肿块的FNAB显示涂片细胞丰富,由相互黏附的梭形细胞分支簇组成,细胞核呈卵圆形,局部染色质增多,核仁不明显。整个涂片中均可见散在的破骨细胞样巨细胞,有些与梭形细胞簇相关。背景为出血性,有细胞碎片,偶尔可见梭形细胞和淋巴细胞。未见导管上皮或肌上皮细胞。进行了切开活检,随后行根治性乳房切除术。组织学检查诊断为MFHGC。免疫组化和电子显微镜研究支持该诊断。
MFHGC,也称为软组织原发性巨细胞瘤,由组织细胞、成纤维细胞和外观温和的破骨细胞样巨细胞混合组成,呈多结节生长模式。虽然MFHGC很少发生于乳腺,仅依靠细胞学难以做出明确诊断,但当细胞学检查显示细胞丰富的梭形细胞涂片且伴有破骨细胞样巨细胞,同时无导管上皮或肌上皮细胞时,可考虑该诊断。