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Table 3 Clinical and radiological features of the most common mediastinal masses

From: A diagnostic approach to the mediastinal masses

 

Anatomical location

Imaging features (CT)

Imaging features (MRI)

Manifestations

Lipoma

anterior mediastinum

encapsulated homogeneous fat attenuation (-40 to -120 HU)

homogeneous hyperintensity on T1-WI

asymptomatic (occasionally local compression of surrounding structures)

Liposarcoma

posterior mediastinum

- inhomogeneous fat attenuation

inhomogeneous appearance

symptomatic at presentation

- irregular areas of soft-tissue appearance

- locally aggressive tumours

Thymolipoma

cardiophrenic angle

- fat-containing lesions (up to 90% fat content)

- homogeneous hyperintensity on T1-WI

- asymptomatic (occasionally local compression of surrounding structures)

- variable component of soft-tissue elements

- small amounts of solid areas and fibrous septa

- a/w myasthenia gravis, Graves disease and haematological disorders

Bronchogenic cyst

middle/posterior mediastinum

- well-defined homogeneous fluid attenuation (0–20 HU)

- homogeneous hyperintensity on T2-WI

40% symptomatic at presentation

Duplication cyst

- variable composition of fluid if complication or presence of protein or mucoid material

- variable patterns of signal intensity on T1-WI because of variable cyst contents

asymptomatic

Pericardial cyst

cardiophrenic angle

  

asymptomatic

Neuroenteric cyst

posterior mediastinum

- well-defined homogeneous low-attenuation paravertebral mass

homogeneous hyperintensity on T2-WI

a/w neurofibromatosis, vertebral and rib anomalies or scoliosis

- enlargement of intervertebral foramina

Thymic cyst

anterior mediastinum

CONGENITAL THYMIC CYST: unilocular well-defined fluid attenuation mass

homogeneous hyperintensity on T2-WI

asymptomatic

ACQUIRED THYMIC CYST: multilocular well-defined fluid attenuation mass with a clearly seen wall

homogeneous hyperintensity on T2-WI with fibrous septa

a/w thymic tumours, after thoracotomy or radiation therapy for HD or as sequelae of inflamatory processes

Mediastinal goitre

anterior mediastinum

- spontaneous hyperattenuation

- heterogeneous appearance on T2-WI

asymptomatic or airway/oesophageal compression

- inhomogeneous density with cystic areas and calcifications

- relatively hypointensity on T1-WI as compared with normal gland tissue, except foci of haemorrhage and cysts

- markedly contrast-enhancement

Thymic hyperplasia

anterior mediastinum

TRUE THYMIC HYPERPLASIA: enlargement of the thymus which remains normally organised

- similar MR signals to those of normal thymus

after chemotherapy, corticosteroid therapy, irradiation or thermal burns

LYMPHOID HYPERPLASIA: normal, enlarged or as a focal thymic mass

- apparent decrease in the signal intensity of the thymus at opposed-phase images in contrast to in-phase images

a/w myasthenia gravis, rheumatoid arthritis, scleroderma, Graves disease

Thymoma

anterior mediastinum

- soft-tissue attenuation

- low signal intensity on T1-WI

- patients older than 40 years-old

- mild to moderate contrast enhancement

- relatively high signal intensity on T2-WI

- asymptomatic vs pressure-induced symptoms

- occasionally, focal haemorrhage, necrosis, cyst formation and linear or ring-like calcifications

- complete obliteration of the adjacent fat planes highly suggests mediastinal invasion

- a/w myasthenia gravis (30-50%), hypogammaglobulinaemia (10%) and pure red cells apasia (5%)

- pleural nodules

  

Thymic carcinoma

anterior mediastinum

- ill-defined soft-tissue mass

- similar features on CT

- mean age of 50 years

- necrotic or cystic component

- absence of tumour capsule

- symptomatic at presentation

- heterogeneous contrast enhancement

- lymphadenopathy and great vessel invasion

- 50–65% distant metastases at presentation

Lymphoma

anterior mediastinum

- homogeneous soft-tissue mass

various signal patterns on T1- and T2-WI

- the most common cause of masses in the paediatric mediastinum

- mild to moderate contrast enhancement

- HD: bimodal distribution of incidence. Constitutional symptoms

- cystic and necrotic changes

- TCLL: children and adolescents. Pressure-induced symptoms

- absence of vascular involvement

- DLBCL: mean age of 30 years

- mediastinal lymphadenopathy

- pleural and pericardial effusions

Teratoma

anterior mediastinum

- well-defined unilocular or multilocular cystic lesion containing fluid, soft tissue, and fat attenuation. Calcifications may be present

- heterogeneous signal intensity

usually asymptomatic

- 15% as nonspecific cystic lesion

- fat-fluid levels within the lesion are virtually diagnostic of teratoma

NTGCT

anterior mediastinum

- heterogeneous ill-circumscribed large mass

heterogeneous signal intensity

- symptomatic young males

- pericardial and pleural effusion

- tumour markers ß–hCG and AFP

- involvement of great vessels

- distant metastases

Schwannoma

posterior mediastinum

- markedly convex mass

homogeneous or heterogeneous high signal intensity on T2-WI

- patients from 20 to 30 years old

- “dumbbell” or “hourglass” configuration

- a/w neurofibromatosis type 2 when multiple

- cystic, haemorrhage and calcification elements are common

SGT

posterior mediastinum

- well-defined or ill-defined mass oriented along the anterolateral surface of several vertebrae

heterogeneous high signal intensity on T2-WI

children and young adults

- “whorled appearance”

Paraganglioma

APP: along great vessels

hypervascular tumours

“salt and pepper” appearance

APP: asymptomatic patients older than 40 years

ASP: posterior mediastinum

ASP: younger adults. Half of them present symptoms

  1. NTGCT non-teratomatous germ cell tumours, SGT sympathetic ganglion tumours, AFP alpha-fetoprotein, ß–hCG beta human chorionic gonadotropin, HD Hodgkin disease, TCLL T-cell lymphoblastic lymphoma, DLBCL diffuse large B-cell lymphoma, APP aortopulmonary paraganglioma, ASP aortosympathetic paraganglioma, a/w association with, WI weighted imaging