Types A and B thymomas are epithelial neoplasms showing thymus-like (organotypic) differentiation. The number of non-neoplastic lymphocytes is variable.
They may occur at any age, with a peak incidence at 55-65 years. Cases in the first two decades of life are extremely rare. There is an association of thymomas with the MEN1 syndrome.
Classification
Various histological classifications of thymoma have been proposed:
WHO0 |
Muller-Hermelink |
Kuo3 |
||
Medullary |
Spindle cell |
|||
Mixed |
Small polygonal cell |
|||
Mixed |
||||
Predominantly cortical |
Organoid |
|||
Cortical |
Large polygonal cell |
|||
Well-differentiated thymic carcinoma |
Squamoid |
|||
Prevalences of subtypes0,4
5-10% |
|||
20-35% |
|||
5-10% |
|||
20-35% |
|||
10-25% |
|||
10-25% |
|||
Rare types |
2.5%4 |
||
Correlation of type with stage7
Type |
I |
II |
III |
IVA |
IVB |
Invasive |
subsequent recurrence |
20 year survival |
|
A |
7 |
|
1 |
|
|
13%, 11%8 |
0% (0/8) |
100%8 |
|
AB |
27 |
15 |
1 |
|
1 |
39%, 42%8 |
2% (1/44) |
87% |
|
B1 |
15 |
5 |
4 |
1 |
|
40%, 47%8 |
9% (2/25) |
91% |
|
B2 |
11 |
10 |
12 |
2 |
1 |
69%, 69%8 |
19% (7/36) |
59%8 |
|
B3 |
2 |
2 |
6 |
|
|
80%, 85%8 |
20% (2/10) |
36%8 |
|
C |
|
1 |
8 |
|
5 |
100% |
- |
|
Incidence of myasthenia gravis7
Type |
Incidence of myasthenia gravis |
|
A |
24%0 |
|
AB |
14%0 |
|
B1 |
18%-56%0 |
|
B2 |
30%-82%0 |
|
B3 |
30%-70%0 |
|
C |
0%0 |
Cytogenetic abnormalities:
|
chromosomal gains |
chromosomal losses |
||
|
homogenous -6p6 |
|||
|
-5q21-22, -6q, -12p, -16q |
|||
|
|
|||
|
aberrations of multiple chromosomes6 |
|||
+1q |
aberrations of multiple chromosomes6, including -6, -13q |
|||
+1q, +17q, +18 |
aberrations of multiple chromosomes6, including -3p, -6, -13q, -16q, -17p, |
|||
The various WHO-defined histological thymoma types, including the lymphocyte-rich AB and B2, exhibit different profiles of genetic aberrations6.
Some of the lymphocyte-poor type B3 thymomas are genetically closely related to the lymphocyte-rich B2 thymomas and may arise from them by gain of genetic aberrations6.
Only WHO type A thymomas exhibit a generally homogeneous profile of genetic abnormalities mainly involving chromosome 6, in contrast with the heterogeneity in the other thymoma types6. Loss of heterozygocity at 6q25 may be common to tumourogenesis across the spectrum of thymomas6.
Metastatic behavior shows a significant correlation with allelic imbalances at 8p11.21 and 16q22.16.
Some type A and AB thymomas share apparently similar profiles of genetic aberrations with type B or C thymomas but maintain their distinctive morphology and benign clinical behavior6.
Immunohistochemistry
In type B thymomas, the T-lymphocytes are immature, as evidenced by their positivity for CD1a and CD99. Positivity for CD79a may also be common1.
The cytokeratin staining pattern is distinctively dendritic in thymomas but not in thymic carcinomas9.
CD205 and Foxn1 have been proposed as specific markers for thymoma (benign and malignant), and CD5 and CD117 as markers for thymic carcinomas9:
|
CD205 |
|
Foxn1 |
|
CD5 |
|
CD117 |
||||||||||||||||||
0 |
0 |
0 |
0 |
||||||||||||||||||||||
Thymoma type |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|||||
A |
1/9 |
2/9 |
|
|
6/9 |
1/9 |
|
|
4/9 |
4/9 |
8/9 |
1/9 |
|
|
|
9/9 |
|
|
|
|
|||||
AB: component A |
1/18 |
8/18 |
3/18 |
2/18 |
4/18 |
0/18 |
1/18 |
3/18 |
6/18 |
8/18 |
16/16 |
|
|
|
|
16/16 |
|
|
|
|
|||||
AB: component B |
|
|
1/19 |
11/19 |
7/19 |
|
|
1/19 |
3/19 |
15/19 |
18/19 |
1/19 |
|
|
|
19/19 |
|
|
|
|
|||||
B1 |
|
|
|
1/7 |
6/7 |
|
|
|
|
7/7 |
7/7 |
|
|
|
|
7/7 |
|
|
|
|
|||||
B2 |
|
|
1/16 |
3/16 |
12/16 |
|
|
2/16 |
4/16 |
10/16 |
15/15 |
|
|
|
|
15/15 |
|
|
|
|
|||||
B3 |
|
1/7 |
1/7 |
1/7 |
4/7 |
|
|
|
1/7 |
6/7 |
5/7 |
2/7 |
|
|
|
7/7 |
|
|
|
|
|||||
C |
7/17 |
4/17 |
3/17 |
2/17 |
1/17 |
4/17 |
7/17 |
2/17 |
2/17 |
2/17 |
5/16 |
2/16 |
|
4/16 |
5/16 |
6/17 |
1/17 |
1/17 |
4/17 |
5/17 |
|||||
Neuroendocrine carcinoma |
3/3 |
|
|
|
|
3/3 |
|
|
|
|
3/3 |
|
|
|
|
3/3 |
|
|
|
|
|||||
Steroid receptor positivity for oestrogen receptor ERa and progesterone receptor PR-B has been demonstrated in the epithelial cells of thymomas.
|
cases positive |
|||
87/1322 |
86±802 |
|||
9/1322 |
7±92 |
|||
5/1322 |
3±52 |
|||
65/1322 |
56±682 |
|||
Androgen receptor |
20/1322 |
14±122 |
||
There is a progressive reduction in immunoreactivity for both ERa and PR-B from Type A, through types AB, B1 and B2 to Type B32.
Survival
Histological type correlates with stage, but is also an independent predictor of survival for stage I and II tumours4,8.
|
5 years |
|||
100%4 |
||||
100%4 |
||||
94%4 |
||||
75%4 |
||||
70%4 |
||||
48%4 |
||||
Smaller studies have perhaps lacked the power to show differences in survival other than between thymoma (types A and B) and thymic carcinoma (type C)5.
References
0 Tumours of the Lung, Pleura, Thymus and Heart. WHO Classification of Tumours. IARC Press 2004.
6 Inoue M, Starostik P, Zettl A, et al. Correlating genetic aberrations with World Health Organization-defined histology and stage across the spectrum of thymomas. Cancer Res 2003; 63:3708-15 FULL TEXT
This page last revised 11.11.2007.
©SMUHT/PW Bishop