Histopathological and Immunohistochemical Appearance of Pleomorphic Dermal Sarcoma

A. Tinca, R. Niculescu, O. Cotoi
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Abstract

Pleomorphic dermal sarcoma is a rare and aggressive entity that originates in the skin’s dermis. This poorly defined tumor usually appears on the sun exposed skin of the elderly and involves the male gender more often. We describe the case of a 54 year old male patient who presented to the Surgery Department with a tumor located on the scalp. Surgery was performed and the sample was sent to the Pathology Department of Mures Clinical County Hospital for further analysis. Histological analysis showed a tumor with solid architecture and nesting phenomenon, composed of pleomorphic epithelioid cells with high atypia. Typical and atypical mitoses were observed. Immunohistochemistry showed positivity for the following markers: vimentin, CD68 and ki67- proliferation value of 90%. The cells were negative to CK AE1/AE3, S100, SOX10, HMB45, MelanA, CD31, Desmin and SMA. In conclusion, pleomorphic dermal sarcoma represents a challenging diagnosis. The case highlights the histological and immunohistochemistry appearance of the neoplasm. Due to the local aggressivity, difficulty in providing negative resection margins and uncertain prognosis, it’s important to take this entity into consideration each time we encounter a cutaneous pleomorphic tumor.
多形性真皮肉瘤的组织病理学和免疫组织化学表现
多形性真皮肉瘤是一种罕见的侵袭性肉瘤,起源于皮肤真皮层。这种不明确的肿瘤通常出现在老年人暴露在阳光下的皮肤上,并且更多地涉及男性。我们描述的情况下,54岁的男性患者谁提出了外科部门与肿瘤位于头皮。手术后将标本送往Mures临床县医院病理科进一步分析。组织学分析显示肿瘤结构坚固,有巢状现象,由高度异型性的多形性上皮样细胞组成。观察到典型和非典型有丝分裂。免疫组化示vimentin、CD68、ki67阳性,增殖值90%。细胞CK AE1/AE3、S100、SOX10、HMB45、MelanA、CD31、Desmin、SMA均阴性。总之,多形性真皮肉瘤是一个具有挑战性的诊断。该病例突出了肿瘤的组织学和免疫组织化学外观。由于局部侵袭性,难以提供阴性切除边缘和预后不确定,每次遇到皮肤多形性肿瘤时都要考虑到这一实体。
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