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老年人心包源性肌纤维母细胞瘤,罕见但并非不可能:一例报告。

Thoracic myopericytoma in an older adult, rare but possible: A case report.

机构信息

Department of Experimental, Diagnostic, and Specialty Medicine, S.Orsola-Malpighi University Hospital, University of Bologna, Bologna, Italy.

Pathology Unit, S.Orsola-Malpighi University Hospital, Bologna, Italy.

出版信息

Thorac Cancer. 2022 Sep;13(17):2532-2535. doi: 10.1111/1759-7714.14535. Epub 2022 Jul 27.

Abstract

Myopericytoma is a rare tumor generally arising from skin and soft tissues of extremities, trunk, head, and neck regions, rarely from visceral sites. An intrathoracic visceral localization may carry a broad differential diagnosis including primary lung, pleura and chest wall lesions, or metastatic lesions. To date, any radiological features have been recognized and diagnosis of myopericytoma with intrathoracic localization remains still challenging. Here, we describe the case of a subpleural lesion incidentally diagnosed in an older adult affected by gastric cancer. Radiological features did not allow a differential diagnosis between a benign lesion, a primary tumor, or a metastasis. After resection, the histological examination showed histopathological features congruent with the diagnosis of myopericytoma. This unusual presentation reflects the need to share clinical, radiological, and histopathological data about this uncommon but frequently misdiagnosed disease.

摘要

血管外皮细胞瘤是一种罕见的肿瘤,通常起源于四肢、躯干、头部和颈部的皮肤和软组织,很少来源于内脏部位。胸腔内脏器的定位可能需要广泛的鉴别诊断,包括原发性肺、胸膜和胸壁病变,或转移性病变。迄今为止,已经认识到任何影像学特征,并且胸腔内定位的血管外皮细胞瘤的诊断仍然具有挑战性。在这里,我们描述了一例偶然诊断的老年患者的胸膜下病变,该患者患有胃癌。影像学特征不允许对良性病变、原发性肿瘤或转移瘤进行鉴别诊断。切除后,组织学检查显示与血管外皮细胞瘤的诊断一致的组织病理学特征。这种不常见的表现反映了需要分享关于这种罕见但经常误诊的疾病的临床、放射学和组织病理学数据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c595/9436698/c064ab516f97/TCA-13-2532-g002.jpg

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