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分化良好的梭形细胞脂肪肉瘤(“非典型梭形细胞脂肪瘤性肿瘤”)不属于非典型脂肪瘤性肿瘤范畴,而与梭形细胞脂肪瘤密切相关:六例病例的临床病理、免疫组织化学和分子分析。

Well-differentiated spindle cell liposarcoma ('atypical spindle cell lipomatous tumor') does not belong to the spectrum of atypical lipomatous tumor but has a close relationship to spindle cell lipoma: clinicopathologic, immunohistochemical, and molecular analysis of six cases.

机构信息

Dermatopathologie, Friedrichshafen, Germany.

出版信息

Mod Pathol. 2010 May;23(5):729-36. doi: 10.1038/modpathol.2010.66. Epub 2010 Mar 12.

Abstract

Well-differentiated spindle cell liposarcoma represents a rare atypical/low-grade malignant lipogenic neoplasm that has been regarded as a variant of atypical lipomatous tumor. However, well-differentiated spindle cell liposarcoma tends to occur in subcutaneous tissue of the extremities, the trunk, and the head and neck region, contains slightly atypical spindled tumor cells often staining positively for CD34, and lacks an amplification of MDM2 and/or CDK4 in most of the cases analyzed. We studied a series of well-differentiated spindle cell liposarcomas arising in two female and four male patients (age of the patients ranged from 59 to 85 years). The neoplasms arose on the shoulder, the chest wall, the thigh, the lower leg, the back of the hand, and in paratesticular location. The size of the neoplasms ranged from 1.5 to 10 cm (mean: 6.0 cm). All neoplasms were completely excised. The neoplasms were confined to the subcutis in three cases, and in three cases, an infiltration of skeletal muscle was seen. Histologically, the variably cellular neoplasms were composed of atypical lipogenic cells showing variations in size and shape, and spindled tumor cells with slightly enlarged, often hyperchromatic nuclei. Multivacuolated lipoblasts were present in three neoplasms. Focal myxoid stromal changes were seen in three cases. Immunohistochemically, CD34 was at least focally positive in all cases, whereas scattered tumor cells only showed a nuclear expression of MDM2 in two neoplasms. FISH analysis revealed a deletion of the Rb-1 gene in all six cases, whereas no MDM2/CDK4 amplification was identified in all cases tested. Follow-up information was available in four cases (range from 4 to 24 months), and revealed a local recurrence in one case. Although well-differentiated spindle cell liposarcoma and atypical lipomatous tumor behave clinically similar, it can be speculated on the basis of clinicopathologic and molecular findings that well-differentiated spindle cell liposarcoma may constitute an independent entity rather than a morphologic variant of atypical lipomatous tumor, and may represent the atypical/low-grade counterpart of spindle cell lipoma.

摘要

高分化梭形细胞脂肪肉瘤是一种罕见的非典型/低度恶性的脂肪源性肿瘤,被认为是非典型性脂肪肿瘤的一种变体。然而,高分化梭形细胞脂肪肉瘤倾向于发生在四肢、躯干和头颈部的皮下组织中,含有轻度非典型的梭形肿瘤细胞,通常 CD34 染色阳性,并且在大多数分析的病例中缺乏 MDM2 和/或 CDK4 的扩增。我们研究了一系列发生在两名女性和四名男性患者(患者年龄 59 岁至 85 岁)中的高分化梭形细胞脂肪肉瘤。肿瘤发生在肩部、胸壁、大腿、小腿、手背和附睾丸部位。肿瘤大小从 1.5 厘米至 10 厘米不等(平均:6.0 厘米)。所有肿瘤均完全切除。在三个病例中,肿瘤局限于皮下组织,在三个病例中,可见骨骼肌浸润。组织学上,形态可变的肿瘤由大小和形状不同的非典型脂肪细胞组成,梭形肿瘤细胞具有稍大的、常染色质深的核。三个肿瘤中均存在多泡性脂肪母细胞。三个病例中可见局灶性黏液样基质变化。免疫组化染色显示,所有病例 CD34 至少局灶性阳性,而两个肿瘤中仅散在肿瘤细胞表现出 MDM2 的核表达。FISH 分析显示,所有六个病例均存在 Rb-1 基因缺失,而所有检测的病例均未发现 MDM2/CDK4 扩增。在四个病例(4 至 24 个月)中可获得随访信息,一个病例出现局部复发。虽然高分化梭形细胞脂肪肉瘤和非典型性脂肪肿瘤在临床行为上相似,但根据临床病理和分子研究结果可以推测,高分化梭形细胞脂肪肉瘤可能构成一个独立的实体,而不是非典型性脂肪肿瘤的形态学变体,并且可能代表梭形细胞脂肪瘤的非典型/低度恶性对应物。

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