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大多数发生于腹膜后的恶性纤维组织细胞瘤为去分化脂肪肉瘤:25例最初诊断为恶性纤维组织细胞瘤的病例回顾

Most malignant fibrous histiocytomas developed in the retroperitoneum are dedifferentiated liposarcomas: a review of 25 cases initially diagnosed as malignant fibrous histiocytoma.

作者信息

Coindre Jean-Michel, Mariani Odette, Chibon Frédéric, Mairal Aline, De Saint Aubain Somerhausen Nicolas, Favre-Guillevin Elizabeth, Bui Nguyen Binh, Stoeckle Eberhard, Hostein Isabelle, Aurias Alain

机构信息

Department of Pathology, Institut Bergonié, Bordeaux, France.

出版信息

Mod Pathol. 2003 Mar;16(3):256-62. doi: 10.1097/01.MP.0000056983.78547.77.

Abstract

Forty-four samples from 25 cases of retroperitoneal sarcoma initially diagnosed as malignant fibrous histiocytoma were histologically reviewed. Immunohistochemistry for mdm2 and cdk4 was performed on 20 cases. Comparative genomic hybridization was performed on 18 samples from 13 patients. Seventeen cases were reclassified as dedifferentiated liposarcoma. Twenty-one of 32 samples from these patients showed areas of well-differentiated liposarcoma, allowing the diagnosis of dedifferentiated liposarcoma. Immunohistochemistry performed in 15 of these cases showed positivity for mdm2 and cdk4. Comparative genomic hybridization analysis performed on 15 samples from 11 of these patients showed an amplification of the 12q13-15 region. Eight cases were reclassified as poorly differentiated sarcoma. Twelve samples from these patients showed no area of well-differentiated liposarcoma. Immunohistochemistry showed positivity for mdm2 and cdk4 in one of six of these patients and showed positivity for CD34 in another one. Comparative genomic hybridization analysis performed on three samples from two of these patients showed no amplification of the 12q13-15 region but showed complex profiles. This study shows that most so-called malignant fibrous histiocytomas developed in the retroperitoneum are dedifferentiated liposarcoma and that a poorly differentiated sarcoma in this area should prompt extensive sampling to demonstrate a well-differentiated liposarcoma component, immunohistochemistry for mdm2 and cdk4, and if possible, a cytogenetic or a molecular biology analysis.

摘要

对最初诊断为恶性纤维组织细胞瘤的25例腹膜后肉瘤的44份样本进行了组织学复查。对其中20例进行了mdm2和cdk4的免疫组织化学检测。对13例患者的18份样本进行了比较基因组杂交分析。17例被重新分类为去分化脂肪肉瘤。这些患者的32份样本中有21份显示出高分化脂肪肉瘤区域,从而得以诊断去分化脂肪肉瘤。对其中15例进行的免疫组织化学检测显示mdm2和cdk4呈阳性。对这些患者中11例的15份样本进行的比较基因组杂交分析显示12q13 - 15区域扩增。8例被重新分类为低分化肉瘤。这些患者的12份样本未显示高分化脂肪肉瘤区域。免疫组织化学检测显示,这些患者中有6例中的1例mdm2和cdk4呈阳性,另有1例CD34呈阳性。对这些患者中2例的3份样本进行的比较基因组杂交分析未显示12q13 - 15区域扩增,但显示出复杂的图谱。本研究表明,大多数发生于腹膜后的所谓恶性纤维组织细胞瘤是去分化脂肪肉瘤,该区域的低分化肉瘤应促使进行广泛取材以显示高分化脂肪肉瘤成分、进行mdm2和cdk4的免疫组织化学检测,以及在可能的情况下进行细胞遗传学或分子生物学分析。

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