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病例报告:具有非典型基质细胞增殖和恶性潜能的透明血管型Castleman病的富含基质变体:一例发生于纵隔淋巴结的罕见病例。

Case report: The stroma-rich variant of Castleman's disease of hyaline-vascular type with atypical stromal cell proliferation and malignant potential: An exceptional rare case occurred in mediastinal lymph node.

作者信息

Shi Xiaoxin, Liao Mengying, Yin Xiaomin, Chen Yaoli, Huang Chuqiang, Yin Weihua, Li Jian

机构信息

Department of Pathology, Peking University Shenzhen Hospital, Shenzhen, China.

State Key Laboratory of Chemical Oncogenomics, Peking University Shenzhen Graduate School, Shenzhen, China.

出版信息

Front Oncol. 2023 Mar 16;13:1008587. doi: 10.3389/fonc.2023.1008587. eCollection 2023.

DOI:10.3389/fonc.2023.1008587
PMID:37007164
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10061130/
Abstract

The stroma-rich variant of Castleman disease of hyaline-vascular type (SR-HVCD) is characterized by interfollicular proliferation of the fibroblastic, myofibroblastic, and/or histiocytic-derived stromal cells, occurred in a background of Castleman disease of hyaline-vascular type (HVCD). It has been considered as a hyperplastic disorder by far. Herein, we presented a case of a 40-year-old male suffering from an occupation in the right middle mediastinum. Microscopically, the lesion was characterized by atretic lymphoid follicles and overgrowth of the interfollicular spindle-shaped cells. Those spindle cells were histologically bland in some areas, while exhibited notable cellular atypia and focal necrosis in other areas. SMA and CD68 were immunostained with a subset of the spindle cells in both areas, whereas p53 staining was only perceived in areas with markedly cellular atypia. In addition, indolent T-lymphoblastic proliferation (iT-LBP) was present inside the lesion. The patient developed multiple sites metastases 4 months after surgery, and succumbed to the disease at 7 months. Our case demonstrates for the first time that SR-HVCD have a tumorigenesis potential rather than a simple hyperplastic process. Such disorder should be carefully evaluated to avoid underdiagnosis.

摘要

透明血管型Castleman病的富含基质变体(SR-HVCD)的特征是成纤维细胞、肌成纤维细胞和/或组织细胞来源的基质细胞在滤泡间增殖,发生于透明血管型Castleman病(HVCD)的背景中。到目前为止,它一直被认为是一种增生性疾病。在此,我们报告一例40岁男性,病变位于右中纵隔。显微镜下,病变的特征为闭锁性淋巴滤泡和滤泡间梭形细胞过度生长。这些梭形细胞在某些区域组织学表现平淡,但在其他区域表现出明显的细胞异型性和局灶性坏死。SMA和CD68在两个区域均对一部分梭形细胞进行免疫染色,而p53染色仅在细胞异型性明显的区域可见。此外,病变内存在惰性T淋巴细胞增殖(iT-LBP)。患者术后4个月出现多处转移,7个月时死于该疾病。我们的病例首次证明SR-HVCD具有肿瘤发生潜能,而非简单的增生过程。对此类疾病应仔细评估以避免漏诊。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe32/10061130/3e983eb8c43c/fonc-13-1008587-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe32/10061130/96b1fb3ca848/fonc-13-1008587-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe32/10061130/c11e5b782fb0/fonc-13-1008587-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe32/10061130/00283bd42d44/fonc-13-1008587-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe32/10061130/3e8ba83f2c0a/fonc-13-1008587-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe32/10061130/3e983eb8c43c/fonc-13-1008587-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe32/10061130/96b1fb3ca848/fonc-13-1008587-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe32/10061130/c11e5b782fb0/fonc-13-1008587-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe32/10061130/00283bd42d44/fonc-13-1008587-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe32/10061130/3e8ba83f2c0a/fonc-13-1008587-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe32/10061130/3e983eb8c43c/fonc-13-1008587-g005.jpg

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