scholarly journals Case Report of An Unusual Mediastinal Mass - Thymolipoma

2020 ◽  
Vol 7 (11) ◽  
pp. C169-171
Author(s):  
Sreeja Raju ◽  
Divya S ◽  
M C Savithri ◽  
Ajaykumar KK ◽  
Gayathri G Nair
Keyword(s):  
Case Report ◽  
World Literature ◽  
Mediastinal Mass ◽  
Anterior Mediastinal Mass ◽  
Chest Discomfort ◽  
Mediastinal Neoplasms ◽  
Slow Growing

Thymolipomas are rare, slow-growing, benign anterior mediastinal neoplasms which are very often detected incidentally. Here we present a case of a 47 year old female who presented with chest discomfort and radiology revealed an anterior mediastinal mass. Total thymectomy was done and histopathology showed features consistent with thymolipoma. Very few cases of thymolipomas have been reported in Indian and world literature.

Primary Mucinous Adenocarcinoma of the Thymus: A Case Report and Review of the Literature

2006 ◽  
Vol 130 (2) ◽  
pp. 201-204 ◽  
Author(s):  
Payal Kapur ◽  
Dinesh Rakheja ◽  
Michael Bastasch ◽  
Kyle H. Molberg ◽  
Venetia R. Sarode
Keyword(s):  
Case Report ◽  
Gastrointestinal Tract ◽  
Mucinous Adenocarcinoma ◽  
Mediastinal Mass ◽  
The Body ◽  
Anterior Mediastinal Mass ◽  
Review Of The Literature ◽  
Specific Identification ◽  
Biopsy Specimens ◽  
Thymic Neoplasm

Abstract Primary thymic mucinous adenocarcinoma is extremely rare; to our knowledge, only 2 cases have been reported to date. We describe a third case of primary mucinous adenocarcinoma of the thymus in a 41-year-old man who presented with an anterior mediastinal mass with subsequent metastasis to the lung. The initial diagnosis was of metastatic mucinous adenocarcinoma, but extensive clinical workup of the patient failed to reveal a primary tumor elsewhere in the body. The specific identification of mucinous adenocarcinoma as a primary thymic neoplasm can be difficult or impossible. Morphologic and immunophenotypic similarities to mucinous adenocarcinomas of the gastrointestinal tract can pose diagnostic challenges for surgical pathologists, especially in small biopsy specimens.

An unusual case of thymolipoma as an anterior mediastinal mass in a 17-year-old girl—case report

2016 ◽  
Vol 32 (2) ◽  
pp. 146-148
Author(s):  
Chandan Kumar Ray Mohapatra ◽  
Ranjitsinh Bapusaheb Jadhav ◽  
Abdul Majeed Mulla ◽  
Jayant Vasant Khandekar ◽  
Ganesh Kumar Ammannaya
Keyword(s):  
Case Report ◽  
Unusual Case ◽  
Mediastinal Mass ◽  
Anterior Mediastinal Mass

scholarly journals Anterior Mediastinal Mass Causing Intermittent Atrial Fibrillation

2021 ◽  
Author(s):  
Adam M Spanier ◽  
Garrett R Evans ◽  
Hugh M Hiller
Keyword(s):  
Atrial Fibrillation ◽  
Emergency Department ◽  
Mediastinal Mass ◽  
Mass Effect ◽  
Metabolic Effects ◽  
Anterior Mediastinal Mass ◽  
Chest Discomfort ◽  
Rare Finding ◽  
Ventricular Response ◽  
History Of

ABSTRACT Mediastinal masses are a rare finding in the emergency department and typically present with vague chest complaints such as chest discomfort, chest pain, or dyspnea. Rarely do these tumors present with dysrhythmias, and when dysrhythmias are present, they typically arise secondary to endocrine or metabolic effects exerted by the tumor. Here we report a case of a patient who presented to the emergency department with atrial fibrillation with rapid ventricular response, concomitant with a history of recurrent palpitations that were previously aborted with self-induced vagal maneuvers. Upon further investigation, the patient had an anterior mediastinal mass, diagnosed as a thymoma, suspected to be contributing to his presenting dysrhythmia through mass effect.

scholarly journals Pulmonary blastoma: a case report of a rare lung tumour

2017 ◽  
Vol 4 (2) ◽  
pp. 823
Author(s):  
Bishal Gautam ◽  
Sanjeev Devgarha ◽  
R. M. Mathur ◽  
Anula Sisodiya
Keyword(s):  
Case Report ◽  
Ct Scan ◽  
Male Patient ◽  
Lung Tissue ◽  
Mediastinal Mass ◽  
Anterior Mediastinal Mass ◽  
Lung Tumour ◽  
Pulmonary Blastoma ◽  
Lung Tumours ◽  
Foetal Lung

Pulmonary blastomas are a rare aggressive neoplasm comprising 0.25-0.5% of all primary lung tumours. Morphologically they mimic foetal lung tissue before 4 months gestation. Study reports a case of 23-year-old male patient who came with heaviness in chest and breathing difficulty since one and a half months. On CT scan of chest, findings are suggestive of anterior mediastinal mass extending till right hila with cardiac displacement and compression. Histopathology confirmed the presence of pulmonary blastoma.

scholarly journals Anterior Mediastinal Leiomyosarcoma: A Case Report and Literature Review

2021 ◽  
pp. 101-106
Author(s):  
Akira Ishikawa ◽  
Kazuya Kuraoka ◽  
Junichi Zaitsu ◽  
Akihisa Saito ◽  
Atsushi Kamigaichi ◽  
...  
Keyword(s):  
Smooth Muscle ◽  
Case Report ◽  
Literature Review ◽  
Tumor Cells ◽  
Growth Pattern ◽  
Mediastinal Mass ◽  
Smooth Muscle Actin ◽  
Anterior Mediastinum ◽  
Anterior Mediastinal Mass ◽  
Muscle Actin

Primary mediastinal sarcomas are extremely rare. Additionally, mediastinal leiomyosarcomas account for approximately 9% of mediastinal sarcoma cases. Until date, only few cases of anterior mediastinal leiomyosarcomas have been reported. Herein, we report a case of an 85-year-old female with an anterior mediastinal mass of 15 mm. Histological examination revealed spindle tumor cells showing a fascicular growth pattern. Immunohistochemically, the tumor cells were focal positive for desmin, calponin, and α-smooth muscle actin. The pathological diagnosis was leiomyosarcoma. In conclusion, we encountered a case of a very rare leiomyosarcoma that occurred in the anterior mediastinum, and our report may contribute to the understanding of this disease.

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