Mekheal Erinie, Veeraballi Sindhusha, Kania Brooke E, Bondili Leena, Maroules Michael
Internal Medicine, St. Joseph's University Medical Center, Paterson, USA.
Internal Medicine, Saint Michael's Medical Center, Newark, USA.
Cureus. 2022 Jul 7;14(7):e26632. doi: 10.7759/cureus.26632. eCollection 2022 Jul.
Spindle cell carcinoma (SpCC)/sarcomatoid carcinoma is a biphasic tumor with molecular and histopathological properties of both epithelial and mesenchymal tumors. SpCC usually occurs either in sun-exposed areas like the head, neck, upper extremities, and chest or in the areas of skin with prior radiation exposure or in immuno-suppressed individuals. Cutaneous SpCC is a very rare disease, with only a handful of reported cases so far. SpCC differs from conventional squamous cell carcinoma (SCC) with dermal infiltration of atypical keratinocytes as single cells with hyperchromatic eosinophilic cytoplasm and elongated, pleomorphic nuclei with multiple nucleoli, in contrast to cohesive nests or islands in SCC. The objective of this study is to complete a review of the current literature and present a rare manifestation of malignant SpCC which developed from a localized basal cell carcinoma following excision and radiation therapy (RT) in a 79-year-old female. We plan to elucidate the importance of a timely and accurate diagnosis of this disease in order to maximize treatment options and improve survival outcomes.
梭形细胞癌(SpCC)/肉瘤样癌是一种具有上皮性和间叶性肿瘤分子及组织病理学特征的双相肿瘤。SpCC通常发生于头部、颈部、上肢和胸部等阳光暴露部位,或既往有放疗史的皮肤区域,或免疫抑制个体。皮肤SpCC是一种非常罕见的疾病,迄今为止仅有少数病例报道。SpCC与传统鳞状细胞癌(SCC)不同,其真皮浸润的非典型角质形成细胞为单个细胞,细胞质嗜酸性、核深染,核呈细长形、多形性且有多个核仁,而SCC表现为细胞巢或细胞岛。本研究的目的是全面回顾当前文献,并呈现1例79岁女性在局部基底细胞癌切除及放疗(RT)后发生恶性SpCC的罕见表现。我们计划阐明及时、准确诊断该疾病的重要性,以最大化治疗选择并改善生存结局。