Types Of Hyperplasia

There are two forms of thymic hyperplasia: 
1- True thymic hyperplasia (or rebound hyperplasia), in which there are normal proportions of glandular/ lymphoid elements in an enlarged gland secondary to rebound following stress-related atrophy, illness, or immune suppression (following chemotherapy or discontinuation of corticosteroid administration) [15,19]. When the body is exposed to stress the thymus may shrink to as little as 40% of its original volume (depending on the severity and duration of the stress) [20]. Once the body recovers, the thymus can usually grows back to its original size within 9 months, but it can grow to be as much as 50% larger [20]. Approximately 10-25% of patient who undergo chemotherapy may develop rebound hyperplasia [20].  Most cases of thymic hyperplasia secondary to chemotherapy occur within a year or two and the gland typically returns to normal size [8,20]. Because of bolstered cell-mediated immunity, thymic hyperplasia has been associated with a good prognosis in post-chemotherapy patients [19]. Thymic hyperplasia has also been described in patients with endocrine abnormalities such as Graves' disease, acromegaly, and thyrotoxicosis [8], as well as during recovery from burn injuries, in patients with infections, and after cardiovascular surgery [19]. On CT the gland may be normal sized or there may be symmetric enlargement of the gland with preservation of its normal shape and no discrete mass. The borders of the enlarged thymus are most often concave, but occasionally the gland may have a convex margin and appear oval. Streaks of fat should be identified and the gland should maintain a bilobed appearance.
2- Thymic lymphoid follicular hyperplasia: 
Thymic lymphoid follicular hyperplasia is characterized by the presence of an increased number of hyperplastic lymphoid follicles and germinal centers in the thymic medulla that is associated with lymphocytic and plasma cell infiltration [20,22]. It is more common than true hyperplasia and is associated with myasthenia gravis [20]. In fact, lymphoid hyperplasia is seen in 65-85% of patients with myasthenia. About 10-15% of myasthenia patients are discovered to have a thymoma, and about 20% have a normal or involuted thymus. Following thymectomy, a clinical remission occurs in 35% of myasthenia patients with lymphoid follicular hyperplasia, and 30-50% will demonstrate clinical improvement [8]. However, even myasthenia patients with a normal thymus may improve clinically following thymectomy (up to two-thirds of such patients). Thymic lymphoid hyperplasia is also associated with collagen vascular disorders such as scleroderma, rheumatoid arthritis, and SLE [15]; as well as endocrinopathies such as Graves disease [15], Addisons disease, acromegaly, and the early stages of human immunodeficiency virus infection [20]. 
On CT scan, thymic lymphoid hyperplasia can appear as an anterior mediastinal mass (20%), as a diffusely enlarged thymic gland (35%), or as a normal thymus (45%) [20]. It has been suggested that the non-contrast attenuation of the thymus is significantly higher in patients with lymphoid hyperplasia than in true hyperplasia (HU greater than 41.2) [22]. Note: The use of iodinated contrast agents in patients with myasthenia gravis has been reported to cause increased weakness. Although not contraindicated, intravenous contrast agents should not be used routinely in the assessment of these patients. [1] 
Thallium may be beneficial in differentiating thymic hyperplasia from other thymic lesions. Normally, no thallium uptake should be seen in the mediastinum which appears photon deficient against the normal faint pulmonary activity. Therefore- the normal thymus is usually gallium avid, but will be negative on the thallium scan. 
MR chemical shift imaging can also be used to differentiate thymic hyperplasia from other thymic lesions [18,24]. Signal loss on out-of-phase images compare to in-phase images suggests the presence of fat and thymic hyperplasia [18,22,24]. However, it should be noted that the amount of fat tissue within the thymus increases with age [24].
FDG PET imaging is not useful for evaluation of thymic hyperplasia as the condition can be associated with FDG accumulation and there is considerable overlap with other thymic lesions [18].
REFERENCES: 
(3) J Thorac Imag 1996; Abnormalities of the thymus.11:58-65 (No abstract available) 
(5) RadioGraphics 1998; Ros PR, et al. Image interpretation session: 1997. 18: 195-228 (Case1- pages 196-199) (No abstract available) 
(6) AJR 1992; Fox MA, et al. Thymoma with hypogammaglobulinemia (Good's syndrome): An unusual cause of bronchiectasis. 158: 1229-1230 (No abstract available) 
(7) Radiographics 1999; Rosado de Christenson ML, et al. Thoracic carcinoids: Radiologic-Pathologic correlation. From the archives of the AFIP. 19: 707-736 
(8) J Thoracic Imag 1999; Strollo DC, et al. Tumors of the thymus. 14: 152-171 
(9) AJR 2001; Jung KJ, et al. Malignant thymic epithelial tumors: CT-Pathologic correlation. 176: 433-439
(10) Radiographics 2002; Gaerte SC, et al. Fat-containing lesions of the chest. 22: S61-S78
(11) Radiographics 2002; Jeung MY, et al. Imaging of cystic masses of the mediastinum. 22: S79-S93
(12) Radiographics 2002; Santana L, et al. Best cases from the AFIP: Thymoma. 22: S95-S102
(13) AJR 2003; Takahashi K, et al. Characterization of the normal and hyperplastic thymus on chemical-shift MR imaging. 180: 1265-1269
(14) Radiol Clin N Am 2005; Franco A, et al. Imaging evaluation of pediatric mediastinal masses. 43: 325-353
(15) Radiographics 2006; Nishino M, et al. The thymus: a comprehensive review. 26: 335-348
(16) J Nucl Med 2006; Sung YM, et al. 18F-FDG PET/CT of thymic epithelial tumors: usefulness for distinguishing and staging tumor subgroups. 47: 1628-1634
(17) Radiographics 2007; Scarsbrook AF, et al. Anatomic and functional imaging of metastatic carcinoid tumors. 27: 455-476
(18) Radiology 2007; Inaoka T, et al. Thymic hyperplasia and thymus gland tumors: differentiation with chemical shift MR imaging. 243: 869-876
(19) J Nucl Med 2009; Jerushalmi J, et al. Physiologic thymic uptake of 18F-FDG in chidlren and young adults: a PET/CT evaluation of incidence, patterns, and relationship to treatment. 50: 849-853
(20) Radiographics 2010; Nasseri F, Eftekhari F. Clinical and radiologic review of the normal and abnormal thymus: pearls and pitfalls. 30: 413-428
(21) Radiographics 2011; Benveniste MFK, et al. Role of imaging n the diagnosis, staging, and treatment of thymoma. 31: 1847-1861
(22) AJR 2014; Araki T, et al. Imaging characteristics of pathologically proven thymic hyperplasia: identifying features that can differentiate true from lymphoid hyperplasia. 202: 471-478
(23) Radiographics 2014; Chou SHS, et al. Thoracic diseases associated with HIV infection in the era of anti-retroviral therapy: clinical and imaging findings. 34: 895-911
(24) Radiology 2015; Priola AM, et al. Differentiation of rebound and lymphoid thymic hyperplasia from anterior mediastinal tumors with dual-echo chemical-shift MR imaging in adulthood: reliability of the chemical-shift ratio and signal intensity index. 274: 238-249

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