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具有淋巴道和血行转移的毛母质癌(“恶性毛母细胞瘤”)

Trichoblastic carcinoma ("malignant trichoblastoma") with lymphatic and hematogenous metastases.

作者信息

Regauer S, Beham-Schmid C, Okcu M, Hartner E, Mannweiler S

机构信息

Institute of Pathology, University of Graz Medical School, Austria.

出版信息

Mod Pathol. 2000 Jun;13(6):673-8. doi: 10.1038/modpathol.3880118.

Abstract

We report an aggressively behaving malignant trichogenic tumor arising in a trichoblastoma (TB) with widespread lymphatic and hematogenous metastases in a 55-year-old man with a concomitant B-cell chronic lymphocytic leukemia. The primary tumor had been present and unchanged for as long as 40 years before excision. Typical trichogenic TB with dystrophic calcification and even ossification was still present peripheral to the malignant transformation. The malignant neoplasm consisted of basaloid cells, spindle cells arranged in fascicles and densely packed rounded nests or "cell balls." The metastases consisted of immature basaloid cells and cell balls, and the recurrences became successively more undifferentiated. The residual TB reacted with antibodies to cytokeratin (CK) 6, 8, 14, and 17 and focally to S-100; the malignant primary tumor reacted uniformly with antibodies to vimentin and only focally with antibodies to CK and S-100. The metastatic tumor had lost epidermal CK expression but maintained expression of S-100 in paraffin-embedded tissues. Trichoblastic differentiation was confirmed in frozen tissues with antibodies to hair keratins. No expression of p53 or bcl-2 was identified, but p-glycoprotein (MDR-1 gene related) was expressed by primary and metastatic tumor cells. We believe that this neoplasm is best classified as a trichoblastic carcinoma arising in a TB in association with a B-cell chronic lymphocytic leukemia. This case illustrates that TBs have the potential for malignant transformation and aggressive behavior.

摘要

我们报告了一例侵袭性生长的恶性毛囊源性肿瘤,该肿瘤发生于成毛细胞瘤(TB),一名55岁男性患者伴有B细胞慢性淋巴细胞白血病,出现广泛的淋巴和血行转移。在切除肿瘤前,原发性肿瘤已存在长达40年且无变化。在恶性转化区域周围仍存在典型的伴有营养不良性钙化甚至骨化的毛囊源性TB。恶性肿瘤由基底样细胞、呈束状排列的梭形细胞以及密集排列的圆形巢状或“细胞球”组成。转移灶由未成熟的基底样细胞和细胞球组成,复发灶的分化程度逐渐降低。残留的TB对细胞角蛋白(CK)6、8、14和17抗体有反应,局部对S-100有反应;恶性原发性肿瘤对波形蛋白抗体呈均匀反应,仅局部对CK和S-100抗体有反应。在石蜡包埋组织中,转移瘤失去了表皮CK表达,但维持了S-100的表达。在冰冻组织中用毛发角蛋白抗体证实了毛囊母细胞分化。未检测到p53或bcl-2的表达,但原发性和转移性肿瘤细胞均表达了P-糖蛋白(与MDR-1基因相关)。我们认为,该肿瘤最好归类为与B细胞慢性淋巴细胞白血病相关的TB中发生的毛囊母细胞癌。该病例表明,TB具有恶性转化和侵袭性行为的潜能。

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