Speisky Daniela, Villarroel Mariano, Vigovich Félix, Iotti Alejandro, García Teresa Adriana, Quero Luciana Bella, Bregante Mariano, de Dávila Maria Teresa García
Department of Histopathology, Hospital Británico, Buenos Aires C1280AEB, Argentina.
Department of Gastroenterology, Digestive Endoscopy Section, Hospital Británico, Buenos Aires C1280AEB, Argentina.
Ecancermedicalscience. 2020 Jul 17;14:1072. doi: 10.3332/ecancer.2020.1072. eCollection 2020.
Undifferentiated pancreatic carcinoma with osteoclast-like giant cells is a rare tumour that has been published under a wide variety of names, including pleomorphic carcinoma, giant cell carcinoma, sarcomatoid carcinoma and carcinosarcoma, among others. For these reasons and its low frequency, the reports of these tumours are scarce and frequently lead to confusion with other entities which present with giant cells. We present the case of a patient with obstructive jaundice and a mixed cystic and solid pancreatic mass, accompanied by multiple hepatic lesions. The histological study of the material obtained by endoscopic ultrasound guided biopsy demonstrated a proliferation of atypical epithelioid cells, accompanied by a spindle cell component with marked pleomorphism and numerous osteoclast-like giant cells. The epithelioid component showed positive immunostaining with cytokeratin cocktail and cytokeratin 7. The spindle cell component showed coexpression of cytokeratins and vimentin. The osteoclast-like giant cells were positive for CD68. Protein p53 was overexpressed in both epithelial and spindle cell neoplastic components, and was negative in the giant cells. These findings permitted the diagnosis of undifferentiated carcinoma of the pancreas with osteoclast-like giant cells. This case outlines the effectiveness of endoscopic ultrasound-guided biopsy and the importance of morphological and immunohistochemical examination in the diagnosis of different types of pancreatic tumours, especially when they are in advanced stages and are not suitable for surgical treatment.
伴有破骨细胞样巨细胞的未分化胰腺癌是一种罕见肿瘤,曾以多种名称发表,包括多形性癌、巨细胞癌、肉瘤样癌和癌肉瘤等。由于这些原因及其低发病率,关于这些肿瘤的报道很少,并且常常导致与其他伴有巨细胞的实体混淆。我们报告一例伴有梗阻性黄疸和胰腺混合性囊实性肿块并伴有多个肝脏病变的患者。经内镜超声引导活检获取材料的组织学研究显示非典型上皮样细胞增生,伴有梭形细胞成分,具有明显的多形性和大量破骨细胞样巨细胞。上皮样成分对细胞角蛋白混合物和细胞角蛋白7免疫染色呈阳性。梭形细胞成分显示细胞角蛋白和波形蛋白共表达。破骨细胞样巨细胞CD68呈阳性。蛋白p53在上皮和梭形细胞肿瘤成分中均过度表达,在巨细胞中呈阴性。这些发现支持伴有破骨细胞样巨细胞的胰腺未分化癌的诊断。该病例概述了内镜超声引导活检的有效性以及形态学和免疫组化检查在不同类型胰腺肿瘤诊断中的重要性,尤其是当它们处于晚期且不适合手术治疗时。