Incidentally Diagnosed Extraluminal Leiomyosarcoma of Infrarenal Inferior Vena Cava: A Case Report and Literature Review from a Radiologist’s Perspective
Case studies
Ebinesh A
Department of Radiodiagnosis, Maulana Azad Medical College and associated hospitals, Jawahar Lal Nehru Marg, New Delhi, India
https://orcid.org/0000-0001-8778-9902
Aanchal Ashta
Department of Radiology, Maulana Azad Medical College and associated hospitals, Jawahar Lal Nehru Marg, New Delhi, India
Satyam Satyam
Department of Radiodiagnosis, Maulana Azad Medical College and associated hospitals, Jawahar Lal Nehru Marg, New Delhi, India
Gaurav Shanker Pradhan
Department of Radiodiagnosis, Maulana Azad Medical College and associated hospitals, Jawahar Lal Nehru Marg, New Delhi, India
Rohin Sharma
Department of Radiodiagnosis, Maulana Azad Medical College and associated hospitals, Jawahar Lal Nehru Marg, New Delhi, India
Prince Das
Department of Radiology, Maulana Azad Medical College and associated hospitals, Jawahar Lal Nehru Marg, New Delhi-110002, India
Published 2022-10-26
https://doi.org/10.15388/Amed.2022.29.2.12
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Keywords

Leiomyosarcoma
inferior vena cava
retroperitoneal tumor
imaging features

How to Cite

1.
A E, Ashta A, Satyam S, Shanker Pradhan G, Sharma R, Das P. Incidentally Diagnosed Extraluminal Leiomyosarcoma of Infrarenal Inferior Vena Cava: A Case Report and Literature Review from a Radiologist’s Perspective. AML [Internet]. 2022 Oct. 26 [cited 2024 Nov. 21];29(2):325–337. Available from: https://www.journals.vu.lt/AML/article/view/29025

Abstract

Background: Vascular leiomyosarcoma is a rare but most common vascular tumor of the inferior vena cava.
Case presentation: We present the case of an incidentally diagnosed extraluminal leiomyosarcoma of the inferior vena cava in a 62 year old patient who presented with abdominal pain following blunt trauma. Ultrasonography showed a lobulated hypoechoic lesion in the upper abdomen. Computed tomography (CT) and magnetic resonance imaging (MRI) showed a circumscribed lobulated near homogeneously enhancing retroperitoneal lesion in anterior relation to the infrarenal inferior vena cava, right paramedian in location with imperceptible vena caval lumen at the site of maximum contact. In positron emission tomography (PET) CT the lesion showed mild fluorodeoxyglucose (FDG) uptake with no distant metastases. CT guided biopsy with immunohistochemical analysis showed leiomyosarcoma. Patient underwent surgical resection with inferior vena cava reconstruction.
Conclusions: Leiomyosarcoma of the inferior vena cava is a rare tumor of vascular origin. Imaging plays an imperative role in the diagnosis and preoperative evaluation. This article also provides a comprehensive literature review of the radiological features of inferior vena caval leiomyosarcoma that would aid in optimal preoperative characterization and evaluation.

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