Evidence map›Paper›PMID 37733410›Full record

ArticleActa medica Lituanic2022

Incidentally Diagnosed Extraluminal Leiomyosarcoma of Infrarenal Inferior Vena Cava: A Case Report and Literature Review from a Radiologist's Perspective.

A Ebinesh, Aanchal Ashta, Satyam, Gaurav Shanker Pradhan, Rohin Sharma, Prince Das

Abstract readCase Reports
In one paragraph

Article in Acta medica Lituanic, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

What it found

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

A EbineshDepartment of Radiodiagnosis, Maulana Azad Medical College and associated hospitals, Jawahar Lal Nehru Marg, New Delhi, India.
Aanchal AshtaDepartment of Radiology, Maulana Azad Medical College and associated hospitals, Jawahar Lal Nehru Marg, New Delhi, India.
SatyamDepartment of Radiodiagnosis, Maulana Azad Medical College and associated hospitals, Jawahar Lal Nehru Marg, New Delhi, India.
Gaurav Shanker PradhanDepartment of Radiodiagnosis, Maulana Azad Medical College and associated hospitals, Jawahar Lal Nehru Marg, New Delhi, India.
Rohin SharmaDepartment of Radiodiagnosis, Maulana Azad Medical College and associated hospitals, Jawahar Lal Nehru Marg, New Delhi, India.
Prince DasDepartment of Radiology, Maulana Azad Medical College and associated hospitals, Jawahar Lal Nehru Marg, New Delhi-110002, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

imaging featuresinferior vena cavaLeiomyosarcomaretroperitoneal tumor

Identifiers

PMID37733410
PMCPMC9799014

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