Teratocarcinosarcoma: A rare malignant tumor of sinonasal tract

Preetham Raj T S, Nirmala C
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Abstract

Sinonasal teratocarcinosarcoma is an extremely rare malignant tumor arising in the sinonasal tract, having combined histological features of teratoma and carcinosarcoma. Here, we are presenting a case of sinonasal teratocarcinosarcoma in a 44 year‑old male patient. 44 year old male presented to us with complains of nasal obstruction and intermittent epistaxis since 1 month. On examination polypoidal mass was noted in left nasal cavity which bleeds on touch. On MRI, well defined heterogeneously enhancing lesion completely filling the left nasal cavity was noted. Histopathological examination of resected specimen revealed, malignant epithelial components being adenocarcinoma and squamous cell carcinoma, mesenchymal component composed of spindle cells, along with primitive mesenchymal and blastemal components. Immunohistochemistry showed epithelial and stromal markers positive for Cytokeratin and Vimentin respectively. Sinonasal teratocarcinosarcoma (TCS) is a rare and aggressive malignant neoplasm characterized by the combination of malignant teratoma and carcinosarcoma. Most common presentation being nasal obstruction and epistaxis with male preponderance. The tumor shows heterogeneous morphology with varying proportions of benign and malignant epithelial, mesenchymal, and blastemal components. Less than 100 cases have been reported in literature. Teratocarcinosarcoma is a rare aggressive sinonasal tumor. Total excision of the tumor and aggressive sampling for histopathological examination is necessary to avoid misdiagnosis of olfactory neuroblastoma and carcinosarcoma.
畸胎肉瘤:一种罕见的鼻窦恶性肿瘤
鼻窦畸胎肉瘤是一种极为罕见的鼻窦恶性肿瘤,具有畸胎瘤和癌肉瘤的综合组织学特征。在此,我们将介绍一例 44 岁男性患者的鼻窦畸胎肉瘤病例。44 岁男性患者主诉鼻塞和间歇性鼻衄 1 个月。检查发现左侧鼻腔有息肉样肿块,一碰就出血。核磁共振检查发现,清晰的异质性增强病变完全充满了左鼻腔。切除标本的组织病理学检查显示,恶性上皮成分为腺癌和鳞癌,间质成分由纺锤形细胞组成,还有原始间质和胚芽成分。免疫组化显示,上皮和基质标记物细胞角蛋白和波形蛋白分别呈阳性。鼻窦畸胎肉瘤(TCS)是一种罕见的侵袭性恶性肿瘤,其特点是恶性畸胎瘤和癌肉瘤的结合。最常见的表现是鼻塞和鼻衄,男性居多。该肿瘤形态不一,良性和恶性上皮、间质和胚芽成分比例各异。文献报道的病例不足 100 例。畸胎肉瘤是一种罕见的侵袭性鼻窦肿瘤。为避免误诊为嗅神经母细胞瘤和癌肉瘤,有必要对肿瘤进行全切除,并积极取样进行组织病理学检查。
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