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年轻女性心脏肿瘤;韦格纳肉芽肿病的罕见表现。

Tumor of the heart in a young woman; a rare manifestation of Wegener granulomatosis.

机构信息

Department of Pathology, Beth Israel Deaconess Medical Center, Boston, MA 02215, USA.

出版信息

Hum Pathol. 2012 Feb;43(2):289-92. doi: 10.1016/j.humpath.2011.04.020. Epub 2011 Jul 30.

Abstract

Wegener granulomatosis may rarely present with tumor masses that are in areas not typically involved by the disease. Although some cases have an associated positive anti-neutrophilic cytoplasmic antibodies, other cases do not, especially those of the limited form. To prevent misdiagnosis and ensure prompt treatment, it is extremely important to consider Wegener granulomatosis even in cases without the classic clinical findings. We report a case of a 19-year-old woman with no prior significant medical history who presented with persistent ventricular tachycardia and a papillary muscle mass in her left ventricle which upon excision and tissue evaluation demonstrated histologic changes of Wegener granulomatosis.

摘要

韦格纳肉芽肿病罕见情况下可能以肿瘤的形式出现,且这些肿瘤通常不在疾病的典型累及部位。虽然有些病例与抗中性粒细胞胞质抗体阳性相关,但其他病例并非如此,尤其是局限性病例。为了避免误诊并确保及时治疗,即使在没有典型临床发现的情况下,也必须考虑韦格纳肉芽肿病。我们报告了一例 19 岁女性病例,无既往重大病史,表现为持续性室性心动过速和左心室乳头肌肿块,切除并进行组织评估后显示韦格纳肉芽肿病的组织学改变。

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