scholarly journals Micronodular Thymoma with Lymphoid Stroma: A Mediastinal Mass Masquerading as a Pericardial Mass

2021 ◽  
Vol 17 (3) ◽  
pp. 18-23
Author(s):  
Kent Swimley ◽  
Hilda M. Gonzalez-Bonilla ◽  
Alpana Senapati ◽  
Karla M. Kurrelmeyer
2021 ◽  
pp. 106689692110011
Author(s):  
Neha Bakshi ◽  
Shashi Dhawan ◽  
Seema Rao ◽  
Kishan Singh Rawat

Introduction. Micronodular thymoma with lymphoid stroma (MNTLS) is a rare thymoma subtype characterized by distinctive histological appearance, unique clinical profile, and indolent course with good prognosis. In addition to its distinctive morphology, MNTLS may be associated with diverse histological features, such as thymic cysts and conventional thymoma, complicating the diagnostic picture further. Materials and methods. We report herein an account of 3 elderly patients (male—02; female—01), who presented with anterior mediastinal mass, and underwent robotic thymectomy. Microscopic examination revealed MNTLS in all 3 cases. In addition, 2 cases showed associated histological features in the form of a multilocular thymic cyst and conventional (type B2) thymoma, respectively. All 3 patients are doing well without recurrence or metastasis at 34, 28, and 19 months postsurgery. Conclusions. Awareness of this rare thymoma subtype is vital among pathologists to avoid misdiagnosis and ensure appropriate patient management. To date, only a few cases of this rare thymoma subtype have been reported in the literature, mostly as single case reports.


2018 ◽  
Vol 24 ◽  
pp. 15-16
Author(s):  
Lima Lawrence ◽  
Alexandra Mikhael ◽  
Khawla Ali ◽  
Varun Kshettry ◽  
Pablo Recinos ◽  
...  

2012 ◽  
Vol 15 (3) ◽  
pp. 170
Author(s):  
Hee Moon Lee ◽  
Dong Seop Jeong ◽  
Pyo Won Park ◽  
Wook Sung Kim ◽  
Kiick Sung ◽  
...  

A 54-year-old man was referred to our institution with hemoptysis and hoarseness of 1 year's duration. A computed tomography (CT) scan showed an anterior mediastinal mass (2.5 cm x 1.0 cm), which was diagnosed as thymoma. The tumor was resected under a sternotomy. The tumor had invaded the anterior wall of the ascending aorta. With the patient under cardiopulmonary bypass, the aortic wall invaded by the mass was resected, and arterial reconstruction was performed with patch material. The tumor was revealed to be a tumor of neuronal origin. The patient's postoperative course was uneventful. The patient was discharged on postoperative day 9. One year after the operation, a follow-up chest CT evaluation showed no specific complications or recurrence.


2011 ◽  
Vol 9 (1) ◽  
pp. 52 ◽  
Author(s):  
Daniel D Correa de Sa ◽  
Thais Coutinho ◽  
Paul Sorajja ◽  
◽  
◽  
...  

1994 ◽  
Vol 35 (3) ◽  
pp. 255-257
Author(s):  
Rickard Nyman ◽  
W. von Sinner ◽  
T. Mygind ◽  
I. Kagevi
Keyword(s):  

1993 ◽  
Vol 161 (5) ◽  
pp. 1110-1111 ◽  
Author(s):  
M A Picou ◽  
R Antonovic ◽  
W E Holden

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