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表现为布加综合征的下腔静脉平滑肌肉瘤伴心脏内延伸:1例罕见病例报告

Leiomyosarcoma of inferior vena cava with intracardiac extension presenting as Budd-Chiari syndrome: Report of a rare case.

作者信息

Nambiyar Kaniyappan, Ahuja Arvind, Bhardwaj Minakshi

机构信息

Department of Pathology, Postgraduate Institute of Medical Education and Research, Dr. Ram Manohar Lohia Hospital, New Delhi, India.

出版信息

Indian J Pathol Microbiol. 2017 Apr-Jun;60(2):256-258. doi: 10.4103/IJPM.IJPM_782_15.

Abstract

Primary leiomyosarcoma of vascular origin is a rare malignant smooth muscle tumor. This report describes a case of primary leiomyosarcoma of the inferior vena cava (IVC) in a 52-year-old male who presented with complaints of abdominal pain, chest pain, and bilateral lower limb swelling for 4 months. Imaging of the chest and abdomen revealed a mass in the IVC extending into right atrium, heterogeneous enhancement of liver, hepatosplenomegaly, and ascites. Histopathological examination showed a malignant spindle cell tumor with cells arranged in fascicular and hemangiopericytomatous pattern. Immunohistochemistry for smooth muscle actin and desmin confirmed smooth muscle origin of the tumor. Recognition of this tumor in this rare location and Budd-Chiari syndrome-like presentation is imperative for proper management of the patient.

摘要

原发性血管源性平滑肌肉瘤是一种罕见的恶性平滑肌肿瘤。本报告描述了一例52岁男性下腔静脉原发性平滑肌肉瘤病例,该患者主诉腹痛、胸痛及双侧下肢肿胀4个月。胸部和腹部影像学检查显示下腔静脉有一肿块延伸至右心房,肝脏不均匀强化、肝脾肿大及腹水。组织病理学检查显示为恶性梭形细胞瘤,细胞呈束状和血管外皮细胞瘤样排列。平滑肌肌动蛋白和结蛋白免疫组化证实肿瘤起源于平滑肌。认识到这种罕见部位的肿瘤及布加综合征样表现对于患者的正确治疗至关重要。

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