Harris GE Siemens
CTisUS Sponsers
Chest

Mediastinal Masses

  • Lymphoma: Facts
    - Hodgkins is most common in the anterior mediastinum
    - Nodes rarely calcify unless the patient has undergone radiation therapy or occasionally chemotherapy
    - Parenchymal involvement at time of presentation is rare (under 10%)
    - Non-Hodgkin’s disease more commonly involves the lung parenchyma
  • Anterior Mediastinal Mass: Differential Diagnosis
    - Lymphoma
    - Germ cell tumor
    - Thymoma
    - Thyroid goiter
    - Inflammatory nodes like TB or Sarcoidosis
  • "CT and MR imaging of the thorax are helpful to characterize lesions initially identified at plain radiography. This characterization helps narrow the differential diagnosis when a lesion is detected in this location."

    Lesions of the Cardiophrenic Space: Findings at Cross Sectional Imaging
    Pineda V et al.
    RadioGraphics 2007; 27:19-32

  • Pericardial Cyst: Facts
    - More common in right cardiophrenic space (77%)
    - Congenital in origin
    - Always asymptomatic
    - Attenuation usually 0-20 HU
    - No enhancement on contrast enhanced studies
  • Lesions of the Cardiophrenic Space: Differential Diagnosis
    - Prominent cardiac fat pad
    - Diaphragmatic hernia (Morgagni hernia)
    - Pericardial fat necrosis
    - Pericardial cysts
    - Thymic tumors
    - Lymphoma
    - Adenopathy
  • Paraganglioma: Facts

    Paragangliomas are found predominantly in the abdomen (85%) and the thorax (12%), and only 3% are found in the head and neck region. Most occur as single tumors. When they occur in multiple sites they are usually found as a part of a heritable syndrome such as multiple endocrine neoplasia types II-A and II-B and SDH-related mutations.
  • Paraganglioma: Facts

    - Rare neuroendocrine tumors of chromaffin cell origin
    - When they arise outside the adrenal glands in extraadrenal neuroendocrine tissue they are called paragangliomas
    - May arise in the chest from the aortic body
  • Paraganglioma: Facts

    - Patients may have mutations in the mitochondrial II genes SDHB, SDHC and SDHD
    - 15% of these tumors are extra-adrenal, 85% adrenal in origin (pheochromocytoma)
  • Paragangliomas: CT Findings

    - Vasular lesions especially well enhanced on arterial phase imaging
    - Multiple lesions at multiple sites may be seen in select cases and may be part of a familial disorder as well
    - Carney syndrome- paraganglioma, pulmonary chondroma, and GI stromal tumor
  • Paragangliomas

    "Paragangliomas of the aortic body and the great vessels have a characteristic imaging appearance. They originate from known sites of the branchiomeric paraganglia such as the aortic body."

    Cross-Sectional Imaging of Paragangliomas of the Aortic Body and Other Thoracic Branchiomeric Paraganglia Balcombe J et al.
    AJR 2007; 188:1054-1058
  • Paragangliomas

    "Aortic body paragangliomas are accompanied by other synchronous paragangliomas in 10% of cases."

    Cross-Sectional Imaging of Paragangliomas of the Aortic Body and Other Thoracic Branchiomeric Paraganglia Balcombe J et al.
    AJR 2007; 188:1054-1058
  • Paragangliomas and Syndromes

    - Carney’s triad Paraganglioma, pulmonary chondroma, and GIST tumor
    - Hereditary Paraganglioma (J Med Genet 2002; 39:617-622)
  • Branchiomeric Paraganglia: Some Sites

    - Carotid body
    - Coronary paraganglia
    - Pulmonary paraganglia
    - Jugulotympanic paraganglia
    - Subclavian paraganglia
    - Laryngeal paraganglia
  • Extraadrenal Paragangliomas: CT Findings

    - Homogeneous or heterogeneous hyperenhancing mass
    - Range in size from 1 cm to over 20 cm
    - Common locations are carotid body, jugular foramen, aorticopulmonary region, posterior mediastinum, abdominal paraaortic region including Organ of Zuckerkandl, and pelvis
  • Paraganglioma: Facts

    - Neuroendocrine tumor which arises from the paraganglionic cells
    - Pheochromocytoma is a paraganglioma of the adrenal gland
    - Usually 4th and 5th decades of life
    - 10% are clinically silent and picked up incidentally
  • Paraganglioma: Facts

    - Familial Paragangliomas are 10% of cases
    - 35-50% of familial cases are multicentric
    - Occur with MEN IIA and IIB, tuberous sclerosis, neurofibromatosis, and von Hippel Lindau disease. Also part of Carney’s triad with gastric leiomyosarcoma, chondroma and extraadrenal paraganglioma
  • Paraganglioma: Facts

    "Although paragangliomas can occur in a variety of anatomic locations, the majority are seen in relatively predictable regions of the body."

    Extraadrenal Paragangliomas of the Body: imaging Features
    Lee KY et al.
    AJR 2006; 187:492-504
  • "Paragangliomas of the aortic body and the great vessels have a characteristic imaging appearance. They originate from known sites of the branchiomeric paraganglia such as in the aortic body."

    Cross-Sectional Imaging of Paragangliomas of the Aortic Body and Other Thoracic Branchiomeric Paraganglia
    Balcombe J et al.
    AJR 2007; 188:1054-1058
  • "Aortic body paragangliomas are accompanied by other synchronous paragangliomas in about 10% of cases."

    Cross-Sectional Imaging of Paragangliomas of the Aortic Body and Other Thoracic Branchiomeric Paraganglia
    Balcombe J et al.
    AJR 2007; 188:1054-1058