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伴有反应性小汗腺导管纤维腺瘤的未分化多形性肉瘤:一例报告

Undifferentiated Pleomorphic Sarcoma with Reactive Eccrine Syringofibroadenoma: A Case Report.

作者信息

Donsakul Navinda, Jerasutus Suthep, Tubtieng Ittipon, Assavanatenapa Ravion, Vejjabhinanta Voraphol

机构信息

Southern Regional Hospital of Tropical Dermatology-Trang Province, Department of Medical Services, Ministry of Public Health, Trang 92000, Thailand.

Division of Dermatology, Department of Medicine, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok 10400, Thailand.

出版信息

Dermatopathology (Basel). 2024 Oct 20;11(4):286-292. doi: 10.3390/dermatopathology11040030.

Abstract

Undifferentiated pleomorphic sarcoma (UPS) is an aggressive soft tissue sarcoma with a poor prognosis. The patients are usually found to have metastasis when the primary tumor is diagnosed. Eccrine syringofibroadenoma (ESFA) is a rare cutaneous adnexal lesion of eccrine duct origin. There are five subtypes, one of which is reactive ESFA, known to occur in reaction to an inflammatory or neoplastic process. In this article, we report a case of the co-existence of both UPS and ESFA in a 70-year-old male patient, presenting with a painless, erythematous, irregular surface nodule with a peripherally extended brownish hyperkeratotic plaque on the right palm. The histologic findings revealed an ill-defined dermal tumor of atypical epithelioid and spindle-shaped cells with large pleomorphic hyperchromatic nuclei and abundant eosinophilic cytoplasm. Some of those cells were multinucleated giant cells in the stroma with vascular proliferation and mixed inflammatory cell infiltrate. The tumor cells, which were only positive for vimentin, supported the diagnosis of undifferentiated pleomorphic sarcoma (UPS). Meanwhile, the overlying epidermis demonstrated hyperkeratosis, papillated epidermal hyperplasia, and proliferation of anastomosing slender cords and strands of cuboid cells within loose fibrovascular stroma. These findings are the characteristics of eccrine syringofibroadenoma (ESFA). We describe here a patient in whom reactive ESFA occurred on and surrounded the UPS tumor.

摘要

未分化多形性肉瘤(UPS)是一种侵袭性软组织肉瘤,预后较差。患者通常在原发性肿瘤被诊断时就已出现转移。小汗腺导管纤维腺瘤(ESFA)是一种罕见的起源于小汗腺导管的皮肤附属器病变。它有五种亚型,其中一种是反应性ESFA,已知其发生与炎症或肿瘤性过程有关。在本文中,我们报告了一例70岁男性患者同时存在UPS和ESFA的病例,该患者右手掌出现一个无痛性、红斑性、表面不规则的结节,周围有褐色角化过度斑块延伸。组织学检查结果显示,真皮内有一个边界不清的肿瘤,由非典型上皮样和梭形细胞组成,细胞核大、多形性、深染,细胞质丰富嗜酸性。其中一些细胞是间质中的多核巨细胞,伴有血管增生和混合性炎症细胞浸润。肿瘤细胞仅波形蛋白阳性,支持未分化多形性肉瘤(UPS)的诊断。同时,上方表皮显示角化过度、乳头样表皮增生,以及在疏松纤维血管间质内出现相互吻合的细长索状和束状立方体细胞增生。这些表现是小汗腺导管纤维腺瘤(ESFA)的特征。我们在此描述了一例反应性ESFA发生在UPS肿瘤上并围绕该肿瘤的患者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f93/11503294/5abaa55300ca/dermatopathology-11-00030-g001.jpg

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