(Intravascular) papillary endothelial hyperplasia or Masson's tumour of the axilla in a patient with a history of breast cancer.

IF 0.6 Q3 MEDICINE, GENERAL & INTERNAL BMJ Case Reports Pub Date : 2024-11-11 DOI:10.1136/bcr-2024-261765
Maxime Van Houdt, Tom Fidlers, Patrick Neven, Sileny Han
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Abstract

Intravascular papillary endothelial hyperplasia, or Masson's tumour, is a benign lesion of the subcutaneous tissue and skin, characterised by a reactive proliferation of endothelial cells within a vessel. Although this pathology can occur at various sites, it is generally rare. Differential diagnosis with other benign lesions or malignancies can be challenging, and since its circumscribed nature is impossible to recognise with a biopsy, excision is frequently required.We present the case of a female patient with a history of bilateral breast cancer, treated with surgery, chemotherapy and radiotherapy, who developed a slowly growing, large bulging mass in the right axilla. Biopsies were benign, and the positron emission tomography-CT showed no hypermetabolism of the mass. However, due to the debilitating bleeding from the fragile mass and uncertainty about its biological behaviour, excision was performed. Pathological examination revealed an intravascular lesion with a central thrombus, characteristic of intravascular papillary endothelial hyperplasia.

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(有乳腺癌病史的患者的腋窝(血管内)乳头状内皮增生症或马森氏瘤。
血管内乳头状内皮增生症或马森氏瘤是皮下组织和皮肤的一种良性病变,其特征是血管内皮细胞的反应性增生。虽然这种病变可发生在不同部位,但一般很少见。与其他良性病变或恶性肿瘤的鉴别诊断具有挑战性,而且由于其周缘性无法通过活组织检查识别,因此经常需要进行切除手术。本病例是一名女性患者,曾患双侧乳腺癌,接受过手术、化疗和放疗治疗,右侧腋窝出现缓慢生长的巨大隆起性肿块。活检结果为良性,正电子发射计算机断层扫描(Positron emission tomography-CT)显示肿块没有高代谢现象。然而,由于脆弱的肿块引起的出血使人虚弱,而且无法确定其生物学行为,因此对其进行了切除。病理检查显示,这是一种血管内病变,中央有血栓,具有血管内乳头状内皮增生症的特征。
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来源期刊
BMJ Case Reports
BMJ Case Reports Medicine-Medicine (all)
CiteScore
1.40
自引率
0.00%
发文量
1588
期刊介绍: BMJ Case Reports is an important educational resource offering a high volume of cases in all disciplines so that healthcare professionals, researchers and others can easily find clinically important information on common and rare conditions. All articles are peer reviewed and copy edited before publication. BMJ Case Reports is not an edition or supplement of the BMJ.
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