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无皮肤外累及的非典型皮肤朗格汉斯细胞肉瘤。

Unusual cutaneous Langerhans cell sarcoma without extracutaneous involvement.

机构信息

Department of Pathology, The First Affiliated Hospital, Sun Yat-sen University, 58, Zhongshan Road II, Guangzhou, 510080, China.

出版信息

Diagn Pathol. 2013 Feb 6;8:20. doi: 10.1186/1746-1596-8-20.

Abstract

UNLABELLED

Langerhans cell sarcoma (LCS) typically presents as cytologic atypia and clinical aggressiveness and may involve multiple organs during the progression of the disease. Primary skin LCS without any extra-cutaneous site association is extremely rare and only a few such cases have been described in the literature. We present a case of unusual primary LCS in skin occurring in a middle-aged male patient. Physical examination revealed a large ulcerated cutaneous lesion and a smaller nodular lesion were located in the skin of the extensor side of his right knee. There was no regional lymph node or any other extra-cutaneous organ involvement. Histologically, typical large and pleomorphological tumor cells with epithelioid appearance and significantly malignant cytological features were observed to infiltrate in dermis and subcutaneous tissue. By immunohistochemistry, the tumor cells were positive for CD1a, S-100 protein and largerin strongly and diffusely. However, these cells were negative for CD3, CD20, CD21, pan-cytokeratin, HMB-45, Melan-A, and MPO. A diagnosis of primary cutaneous LCS was made. The patient received systemic chemotherapy of CHOP regimen, and was on a regular follow-up period for 12 months. There was no sign of relapse of tumor or any other extra-cutaneous organ involvement by whole body positron emission tomography/computed tomography (PET/CT) study. Because LCS is a high-grade malignancy with poor prognosis, it suggests that strict histological analysis and thorough radiographic examination are necessary for accurately diagnosing this tumor even if cutaneous involvement presented only.

VIRTUAL SLIDES

http://www.diagnosticpathology.diagnomx.eu/vs/6527428618381393.

摘要

未标注

朗格汉斯细胞肉瘤(LCS)通常表现为细胞异型性和临床侵袭性,并且在疾病进展过程中可能涉及多个器官。无任何皮肤外部位关联的原发性皮肤 LCS 极为罕见,文献中仅描述了少数此类病例。我们报告了一例罕见的皮肤原发性 LCS,发生于中年男性患者。体格检查显示右膝伸展侧皮肤有一个大的溃疡性皮肤病变和一个较小的结节性病变。无区域性淋巴结或任何其他皮肤外器官受累。组织学上,观察到典型的大而多形性肿瘤细胞呈上皮样外观,并具有明显的恶性细胞学特征,浸润真皮和皮下组织。通过免疫组织化学,肿瘤细胞对 CD1a、S-100 蛋白和 largerin 呈阳性,强烈且弥漫性表达。然而,这些细胞对 CD3、CD20、CD21、泛细胞角蛋白、HMB-45、Melan-A 和 MPO 呈阴性。诊断为原发性皮肤 LCS。患者接受 CHOP 方案的全身化疗,并在 12 个月的定期随访期间进行全身正电子发射断层扫描/计算机断层扫描(PET/CT)研究,未发现肿瘤复发或任何其他皮肤外器官受累的迹象。由于 LCS 是一种高度恶性且预后不良的肿瘤,因此即使仅出现皮肤受累,也建议进行严格的组织学分析和彻底的影像学检查,以准确诊断这种肿瘤。

幻灯片

http://www.diagnosticpathology.diagnomx.eu/vs/6527428618381393.

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6228/3570402/ba08b2b37283/1746-1596-8-20-1.jpg

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