Massive Hemorrhage Following Spontaneous Mediastinal Inflammatory Myofibroblastic Tumor Rupture: A Case Report

被引:0
作者
Bellegarde, Sophia B. [1 ,2 ]
Gibson, Vanessa [3 ]
Andaz, Shahriyour [3 ]
Huang, Lillian [2 ]
Robinson, Eric [4 ]
Turi, George [4 ]
Tofuah, Donald [4 ,5 ]
Ekhator, Chukwuyem [6 ]
Bardarov, Svetoslav [7 ]
机构
[1] Amer Univ Antigua, Pathol & Lab Med, St Johns, Antigua & Barbu
[2] Mt Sinai South Nassau, Cardiothorac Surg, Mt Sinai South Nassau, Oceanside, NY USA
[3] Mt Sinai South Nassau, Thorac Surg, Oceanside, NY USA
[4] Mt Sinai South Nassau, Surg, Oceanside, NY USA
[5] Amer Univ Antigua, Cardiothorac Surg, St Johns, Antigua & Barbu
[6] New York Inst Technol, Coll Osteopath Med, Neurooncol, Old Westbury, NY 10023 USA
[7] Richmond Univ, Med Ctr, Pathol & Lab Med, Staten Isl, NY USA
关键词
pathology; thoracotomy procedure; hemothorax; inflammatory myofibroblastic tumor; hypertensive emergency; mediastinal mass;
D O I
10.7759/cureus.45833
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
A 45-year-old male in a hypertensive emergency was admitted with complaints of frontal headache, progressive chest discomfort, shortness of breath, dysphagia, and right upper quadrant abdominal pain radiating across the epigastrium and to the back that increases in intensity with deep inspiration. He denied any history of abdominal pain, vomiting, dyspnea, nausea, and weight loss. A computed tomography (CT) scan of the chest showed a posterior mediastinal mass between the esophagus and descending aorta. A magnetic resonance imaging (MRI) scan revealed a non-enhancing posterior mediastinal mass possibly compressing both the esophagus and the airway. A 30-degree thoracoscope was inserted in the chest cavity revealing a large hemothorax from a possibly ruptured inflammatory myofibroblastic tumor (IMT) encompassing nearly the entire pleural space with both fresh and clotted blood. Two liters of fresh blood was removed via a right thoracotomy procedure. Once removed, a large fibrinous clot-filled mass was resected entirely and sent to pathology. Postoperative recovery was uneventful; dysphagia and shortness of breath resolved. The patient gradually resumed his regular diet.
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页数:6
相关论文
共 5 条
  • [1] Rare monophasic mediastinal pleural synovial sarcoma diagnosed via endobronchial ultrasound-transbronchial needle aspiration
    Aung, Hnin
    Tsaknis, George
    Walter, David
    [J]. BMJ CASE REPORTS, 2020, 13 (08)
  • [2] Griffin CA, 1999, CANCER RES, V59, P2776
  • [3] Successful surgical management of a rare esophageal inflammatory myofibroblastic tumour: a case report
    Khakural, Prabhat
    Sapkota, Ranjan
    Shrestha, Uttam K.
    Sayami, Prakash
    [J]. JOURNAL OF CARDIOTHORACIC SURGERY, 2015, 10
  • [4] Mediastinal synovial sarcoma: Report of two cases with molecular genetic analysis
    Trupiano, JK
    Rice, TW
    Herzog, K
    Barr, FG
    Shipley, J
    Fisher, C
    Goldblum, JR
    [J]. ANNALS OF THORACIC SURGERY, 2002, 73 (02) : 628 - 630
  • [5] Inflammatory myofibroblastic tumor of the mediastinum presenting as superior vena cava syndrome
    Yamaguchi, M
    Yoshino, I
    Osoegawa, A
    Kameyama, T
    Tagawa, T
    Fukuyama, S
    Oda, Y
    Tsuneyoshi, M
    Maehara, Y
    [J]. JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY, 2003, 126 (03) : 870 - 872