Smith Stephen M, Schmitt Alessandra C, Carrau Ricardo L, Iwenofu O Hans
Department of Pathology and Laboratory Medicine, Wexner Medical Center at The Ohio State University, 410 West 10th Avenue, Columbus, OH, 43210, USA.
Head Neck Pathol. 2015 Mar;9(1):165-71. doi: 10.1007/s12105-014-0553-5. Epub 2014 Jun 29.
The broad morphologic spectrum, inherent immunophenotypic heterogeneity of malignant melanoma and its rarity in the sinonasal tract are major challenges in eliciting the correct diagnosis, which may lead to misclassification and inadequate medical management. Herein, we describe a single case of a 70 year-old male with sinonasal mucosal melanoma, exhibiting varying histologic phenotypes including small round blue cell morphology, epithelioid and focal rhabdoid morphology and strong, diffuse desmin immunoreactivity. These constellation of features initially prompted the diagnosis of rhabdomyosarcoma. The differential diagnosis in this anatomic area includes other malignant small round blue cell tumors of the sinonasal mucosa such as rhabdomyosarcoma, olfactory neuroblastoma, sinonasal undifferentiated carcinoma, and lymphoma. We reviewed precedent literature and further discuss the potential pitfalls to which pathologists may be prone.
恶性黑色素瘤广泛的形态学谱、固有的免疫表型异质性及其在鼻窦区域的罕见性是做出正确诊断的主要挑战,这可能导致错误分类和不充分的医疗管理。在此,我们描述一例70岁男性鼻窦黏膜黑色素瘤病例,其呈现出多种组织学表型,包括小圆形蓝细胞形态、上皮样和局灶性横纹肌样形态以及强烈弥漫的结蛋白免疫反应性。这些特征组合最初促使诊断为横纹肌肉瘤。该解剖区域的鉴别诊断包括鼻窦黏膜的其他恶性小圆形蓝细胞肿瘤,如横纹肌肉瘤、嗅神经母细胞瘤、鼻窦未分化癌和淋巴瘤。我们回顾了先前的文献,并进一步讨论了病理学家可能容易出现的潜在陷阱。