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Perivascular epithelioid cell neoplasm

ORPHA:595133疾病暂无中文名

定义 英文原文(暂无中文)

A rare soft tissue tumor characterized by distinctive perivascular epitheloid cells, often arranged radially around a vascular lumen, as well as spindled cells in variable proportion. Melanocytic and muscle markers are typically positive. The tumors have been reported in the uterus, falciform ligament, and large and small intestine, among others. Depending on their location, they may present as a painful or painless mass, or with vaginal bleeding. Tumors displaying infiltrative growth, marked hypercellularity, nuclear enlargement and hyperchromasia, high mitotic activity, atypical mitotic figures, and/or coagulative necrosis should be regarded as malignant.

别名

PEComa、Perivascular epithelioid tumour

基本事实

遗传方式
不适用
发病年龄
青少年期、成年期、儿童期、老年期

相关基因 2来自下位疾病

Orphanet 未在本条目上直接标注致病基因。下表由本组所属的下位疾病汇总而来,「来源条目」列给出基因实际标注在哪一个 ORPHA 条目上。

基因名称来源条目
TSC1TSC complex subunit 1ORPHA:538
TSC2TSC complex subunit 2ORPHA:538

外部标识与链接

OrphanetMONDO:0006359ICD-10 D21.9ICD-11 2F7C、XH4CC6、XH9WD1ClinicalTrials.gov 检索

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本页数据来源

  • 疾病定义、同义词、基因、表型、流行病学:Orphanet(CC BY 4.0)
  • 中文病名:Orphanet 中文包,冻结于 2020-06-01;本条目在该版本中无中文名
  • 表型中文标签:HPO 简体中文翻译(CHPO 上游成果)