A Rare Solitary Fibrous Tumor Originating From the Distal Aortic Arch.


Journal

The Annals of thoracic surgery
ISSN: 1552-6259
Titre abrégé: Ann Thorac Surg
Pays: Netherlands
ID NLM: 15030100R

Informations de publication

Date de publication:
03 2019
Historique:
received: 16 03 2018
revised: 11 07 2018
accepted: 11 07 2018
pubmed: 30 9 2018
medline: 12 11 2019
entrez: 30 9 2018
Statut: ppublish

Résumé

We report a 68-year-old man who presented with a well-circumscribed 6.9 × 6.5 × 3.6-cm tumor with a feeding vessel from the thyrocervical trunk in his left pleural cavity. The tumor was attached to the distal aortic arch, so he underwent a tumor resection with prosthetic graft replacement of the distal aortic arch. Pathological examination revealed a solitary fibrous tumor with potentially malignant features. To our knowledge, this is the first case of a solitary fibrous tumor arising from the aortic adventitia reported in the literature.

Identifiants

pubmed: 30266616
pii: S0003-4975(18)31312-2
doi: 10.1016/j.athoracsur.2018.07.063
pii:
doi:

Types de publication

Case Reports Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e195-e197

Informations de copyright

Copyright © 2019 The Society of Thoracic Surgeons. Published by Elsevier Inc. All rights reserved.

Auteurs

Sohsyu Kotani (S)

Division of Cardiovascular Surgery, Hiratsuka City Hospital, Hiratsuka, Japan. Electronic address: sohsyu_k@yahoo.co.jp.

Yoshito Inoue (Y)

Division of Cardiovascular Surgery, Hiratsuka City Hospital, Hiratsuka, Japan.

Hirofumi Haida (H)

Division of Cardiovascular Surgery, Hiratsuka City Hospital, Hiratsuka, Japan.

Reiko Dehari (R)

Division of Pathology, Hiratsuka City Hospital, Hiratsuka, Japan.

Ikuma Kato (I)

Department of Molecular Pathology, Yokohama City University School of Medicine, Yokohama, Japan.

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