Dey Biswajit, Srinivas Bheemanathi Hanuman, Badhe Bhawana, Nachiappa Ganesh Rajesh, Gochhait Debasis, Toi Pampa C, Jinkala Sreerekha
Pathology, North Eastern Indira Gandhi Regional Institute of Health and Medical Sciences, Shillong, IND.
Pathology, Jawaharlal Institute of Postgraduate Medical Education and Research, Puducherry, IND.
Cureus. 2020 Dec 24;12(12):e12263. doi: 10.7759/cureus.12263.
Background Soft tissue tumours with epithelioid morphology have many differential diagnoses, which include epithelioid sarcoma, malignant extrarenal rhabdoid tumour, epithelioid malignant peripheral nerve sheath tumour, epithelioid leiomyosarcoma, epithelioid angiosarcoma and sclerosing epithelioid fibrosarcoma. There are other rare entities also. They often express characteristic patterns of immunohistochemical markers that can be used to identify these tumours. Materials and methods This retrospective study comprises 22 cases of malignant soft tissue tumours with epithelioid differentiation diagnosed over a period of four years. Findings regarding clinical presentation, cytological findings, histopathological findings and immunohistochemical profile of the tumours were noted and analyzed. Results A total of 22 cases were included in the study including five cases of epithelioid sarcoma (conventional and proximal), three cases of epithelioid angiosarcoma and epithelioid myxofibrosarcoma, two cases of epithelioid malignant peripheral nerve sheath tumour, epithelioid gastrointestinal stromal tumour and clear cell sarcoma each, one case of epithelioid leiomyosarcoma, sclerosing epithelioid fibrosarcoma, malignant extrarenal rhabdoid tumour, monophasic synovial sarcoma and malignant and malignant perivascular epithelioid cell tumour each. Conclusion Pathologists should be aware of the various differential diagnoses of soft tissue tumours with epithelioid morphology. Over and above the clinical findings and morphological features, ancillary methods like immunohistochemistry help to arrive at a definitive diagnosis in most cases.
背景 具有上皮样形态的软组织肿瘤有多种鉴别诊断,包括上皮样肉瘤、恶性肾外横纹肌样肿瘤、上皮样恶性外周神经鞘瘤、上皮样平滑肌肉瘤、上皮样血管肉瘤和硬化性上皮样纤维肉瘤。还有其他一些罕见的实体。它们通常表达可用于识别这些肿瘤的免疫组化标志物特征模式。
材料与方法 这项回顾性研究包括4年间诊断的22例具有上皮样分化的恶性软组织肿瘤。记录并分析了肿瘤的临床表现、细胞学表现、组织病理学表现和免疫组化特征。
结果 该研究共纳入22例病例,包括5例上皮样肉瘤(经典型和近端型)、3例上皮样血管肉瘤和上皮样黏液纤维肉瘤、2例上皮样恶性外周神经鞘瘤、上皮样胃肠道间质瘤和透明细胞肉瘤各2例、1例上皮样平滑肌肉瘤、硬化性上皮样纤维肉瘤、恶性肾外横纹肌样肿瘤、单相滑膜肉瘤以及恶性和恶性血管周上皮样细胞瘤各1例。
结论 病理学家应了解具有上皮样形态的软组织肿瘤的各种鉴别诊断。除了临床表现和形态学特征外,免疫组化等辅助方法有助于在大多数情况下做出明确诊断。