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A 64-year-old man with widely invasive thymoma (WHO B1). (a) Contrast-enhanced axial CT image shows an irregular mass (asterisk) in the right anterior mediastinum with infiltration of the mediastinal fat (white arrow). The mass (asterisk) is isointense on the axial T1W image (b), heterogeneously hyperintense on the T2W image (c) and shows delayed heterogeneous enhancement on the post-gadolinium T1W-fat saturated MR images (d).

A 64-year-old man with widely invasive thymoma (WHO B1). (a) Contrast-enhanced axial CT image shows an irregular mass (asterisk) in the right anterior mediastinum with infiltration of the mediastinal fat (white arrow). The mass (asterisk) is isointense on the axial T1W image (b), heterogeneously hyperintense on the T2W image (c) and shows delayed heterogeneous enhancement on the post-gadolinium T1W-fat saturated MR images (d).

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Anterior mediastinal tumours include primary and secondary tumours. Patients may be asymptomatic or present with symptoms related to local tumour invasion or systemic symptoms due to release of hormones/cytokines or antibodies. The most common symptoms at presentation include chest pain, dyspnoea, cough, fever and chills. Despite rapid developments...

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... thymomas usually have smooth contours, sep- tation, complete or near-complete capsules and homoge- neous enhancement [16] . High-risk thymomas and thymic carcinomas commonly have lobulated contours, mediast- inal fat and great vessel invasion. Heterogeneous signal on T2W images are more common in invasive forms (Fig. 3) [3] . Irregular contour, necrotic or cystic compo- nents, heterogeneous enhancement, lymphadenopathy and great vessel invasion suggest thymic carcinomas [16] . Findings associated with more frequent recurrences and metastases include lobulated/irregular contours, oval shape, mediastinal fat or great vessel invasion and pleural seeding ...

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... Many anatomists further divide it into posterior, anterior, and middle compartments. About 50% of all mediastinal masses, including teratoma, thymoma, lymphoma, and thyroid illness, are anterior mediastinal tumors [2,3]. Thymoma, lymphoma, and germ cell cancers like seminoma, teratoma, and yolk sac tumors all can cause a mass in the anterior mediastinum. ...
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... Study variables were collected from medical records, including age, sex, the presence of myasthenia gravis, and the results of clinical and pathological staging. According to the TNM staging system, clinical T stages were determined based on the morphology of TET derived from T2WI, non-contrast, and contrast-enhanced T1WI imaging as previously described [17]. Three classification systems of TET were used to determine pathological stages, including the 2015 WHO classification, the 1994 Masaoka-Koga staging system, and the 8 th edition of the TNM staging system as previously described [9]. ...
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... Anterior mediastinal tumors account for 50% of all mediastinal masses, including thymoma, teratoma, thyroid disease, and lymphoma. 1 Masses of the middle mediastinum are typically congenital cysts, while those arising in the posterior mediastinum are often neurogenic tumors. Although conventional radiography may allow detection of or suggest the presence of a mediastinal mass, in most cases it is of limited use in determining the exact nature and extent of a lesion. ...
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... Germ cell tumors (GCTs) arise along the midline across from the pineal gland to the presacral area [1,2]. They form due to the incomplete migration of primitive germ cells during the early stage of embryonic development [1]. ...
... Germ cell tumors (GCTs) arise along the midline across from the pineal gland to the presacral area [1,2]. They form due to the incomplete migration of primitive germ cells during the early stage of embryonic development [1]. Most GCTs arise in a gonadal tissue; however, 50-70% of extragonadal GCTs occur in the mediastinum [1,3]. ...
... They form due to the incomplete migration of primitive germ cells during the early stage of embryonic development [1]. Most GCTs arise in a gonadal tissue; however, 50-70% of extragonadal GCTs occur in the mediastinum [1,3]. GCTs are broadly classified as either the teratomatous or nonteratomatous type [1]. ...
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Germ cell tumors (GCTs) arise along the midline, in which 50-70% of extragonadal GCTs occur in the mediastinum. Malignant GCTs are more common in males, while benign GCTs occur equally in both males and females. This report presents a case of a giant primary mediastinal nonseminomatous GCT resected from a 35-year-old male who presented with dyspnoea and tightness in the chest. Thorough investigations including a chest MRI were done. It showed a 21 × 19 × 15 cm tumor. Thus, surgical resection of the tumor through a midline sternotomy was done. Histopathological analysis diagnosed the tumor as a primary mediastinal teratocarcinoma with a sarcomatous component. Eighteen-month follow-up showed no tumor recurrence. Mediastinal teratocarcinoma is a rare and life-threatening germ cell tumor. Studies recommend the use of chemotherapy prior to resection as an important step in its management. Close and regular follow-up postsurgical resection is advised.
... Low-risk thymomas commonly have smooth contours, septation, complete or near-complete capsules, and homogeneous enhancement. [6] High-risk thymomas and thymic carcinomas usually have lobulated contours, mediastinal fat and great vessel invasion. [4,6] CT features associated with more frequent recurrences and metastases include lobulated or irregular contours, oval shape, mediastinal fat or great vessel invasion, and pleural seeding. ...
... [6] High-risk thymomas and thymic carcinomas usually have lobulated contours, mediastinal fat and great vessel invasion. [4,6] CT features associated with more frequent recurrences and metastases include lobulated or irregular contours, oval shape, mediastinal fat or great vessel invasion, and pleural seeding. [6] The main differential diagnosis of thymoma in pediatric patients includes thymic hyperplasia, T-cell lymphoblastic lymphoma, and thymic carcinoma. ...
... [4,6] CT features associated with more frequent recurrences and metastases include lobulated or irregular contours, oval shape, mediastinal fat or great vessel invasion, and pleural seeding. [6] The main differential diagnosis of thymoma in pediatric patients includes thymic hyperplasia, T-cell lymphoblastic lymphoma, and thymic carcinoma. [2] Diffuse symmetric enlargement of the gland is the key imaging feature of thymic hyperplasia, whereas thymoma tends to manifest as a focal mass. ...
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Thymoma is an uncommon neoplasm that derived from thymic epithelial cells. Clinically, it is slow-growing and most patients are over 40 years old. Thymoma corresponds to 30% of anterior mediastinal tumors in adults but