巨大的大腿血纤维瘤/动脉瘤性皮纤维瘤:病例报告与放射学病理学相关性

Eva Manuela Pena-Burgos , Carolina D’Angelo , María Cristina Díez-Corral , Elena Sánchez Villanueva , Mar Tapia-Viñe , Jose Juan Pozo-Kreilinger , Dolores Vélez Velázquez
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引用次数: 0

摘要

皮纤维瘤(DF)的血纤维化/动脉瘤变异型并不常见,可能会被误诊为恶性病变。我们报告了一例 53 岁女性患者的大腿皮下巨大(7.6 厘米)血纤维化/动脉瘤性 DF(H/ADF)病例。频谱多普勒超声显示其内部动静脉血管扩张。磁共振成像显示,T1加权成像(WI)和T2-WI肿块呈离散均质低密度,脂肪抑制T2-WI呈高密度区。组织学显示为单调的纺锤形增生,无不典型性,CD163、XIIIa因子和CD10均呈阳性。血色素色素广泛分布,有两个充血的假血管间隙,缺乏内皮衬里。诊断为 H/ADF。肿块被切除,但手术边缘受到影响。患者没有出现局部复发或远处转移。H/ADF 是一种不常见的皮肤软组织肿瘤,在临床、放射学和组织病理学上可与黑色素瘤、血管病变或肉瘤等恶性病变相混淆,尤其是在巨大病例中。
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Giant thigh hemosiderotic/aneurysmal dermatofibroma: Case report with radiologic–pathologic correlation

Hemosiderotic/aneurysmal variant of dermatofibroma (DF) is infrequent and may be misdiagnosed with malignant lesions. We report the case of a giant (7.6 cm) subcutaneous hemosiderotic/aneurysmal DF (H/ADF) of the thigh in a 53-year-old female patient. Internal arterial and venous hypervascularity was seen by spectral Doppler ultrasound. Magnetic resonance image showed a discrete homogeneous hypointense in T1-weighted images (WI) and T2-WI mass, with hyperintense areas in fat-suppressed T2-WI. The histology revealed a monotonous fusocelular proliferation without atypia, positive for CD163, factor XIIIa and CD10. Widely distributed hemosiderin pigment and two blood-filled pseudovascular spaces lacking endothelial lining were present. H/ADF was diagnosed. The mass was removed but surgical margins were affected. The patient did not present local relapse or distant metastasis. H/ADF are unusual cutaneous soft tissue tumours that can be clinically, radiologically and histopathologically confused with malignant lesions such as melanomas, vascular lesions or sarcomas, especially in giant cases.

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来源期刊
Revista Espanola de Patologia
Revista Espanola de Patologia Medicine-Pathology and Forensic Medicine
CiteScore
0.90
自引率
0.00%
发文量
53
审稿时长
34 days
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