转移性上皮样血管内皮细胞瘤病例，来源于未知原发灶，与膜性肾病和高凝状态相关。
Case of metastatic epithelioid haemangioendothelioma from an unknown primary site associated with membranous nephropathy and hypercoagulable state.
机构信息
Surgery, Saint Barnabas Medical Center, Livingston, New Jersey, USA
Surgery, Saint Barnabas Medical Center, Livingston, New Jersey, USA.
出版信息
BMJ Case Rep. 2022 Aug 22;15(8):e247253. doi: 10.1136/bcr-2021-247253.
Abstract
We report a rare case of metastatic epithelioid haemangioendothelioma from an unknown primary site presenting with axillary lymph node metastases. The patient also had a new-onset membranous glomerulonephritis and thromboembolism, which we postulate were paraneoplastic. The pathogenesis of this rare cancer, the risk of misdiagnosis and membranous glomerulonephritis as a paraneoplastic syndrome are discussed.
摘要
我们报告了一例罕见的转移性上皮样血管内皮细胞瘤，该肿瘤来源于未知原发灶，伴腋窝淋巴结转移。患者还伴有新发膜性肾小球肾炎和血栓栓塞，我们推测这是副肿瘤性的。讨论了这种罕见癌症的发病机制、误诊风险以及膜性肾小球肾炎作为副肿瘤综合征的可能性。
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Case of metastatic epithelioid haemangioendothelioma from an unknown primary site associated with membranous nephropathy and hypercoagulable state.转移性上皮样血管内皮细胞瘤病例，来源于未知原发灶，与膜性肾病和高凝状态相关。
BMJ Case Rep. 2022 Aug 22;15(8):e247253. doi: 10.1136/bcr-2021-247253.
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