Germinoma laboratory tests: Difference between revisions
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==Laboratory Findings== | ==Laboratory Findings== | ||
The following tests are done for intracranial germ cell tumors: | |||
*CSF cytology to detect malignant cells | |||
*Measurement of AFP and beta-hCG in the CSF and serum | |||
**Tumor marker levels are usually higher in CSF than in serum. In patients in whom endoscopic biopsy is not considered possible, detection of elevated tumor markers may be sufficient for diagnosis. | |||
**Measurement of beta-hCG and AFP in the CSF is more sensitive than serum levels in detecting abnormalities. However, due to discordant serum and CSF tumor marker results that were observed, both serum and CSF tumor markers should be obtained in the absence of clinical contraindications. Lumbar CSF is considered more accurate for tumor markers and cytology than ventricular CSF. | |||
**Tumor markers from ventricular CSF can be used , if a lumbar puncture is contradicted. | |||
*Laboratory studies to detect the hormonal dysfunction that may occur in patients with central nervous system (CNS) germinomas are as follows: | |||
**Diabetes insipidus | |||
***Serum sodium, serum osmolality, and urine osmolality | |||
**Hypopituitarism | |||
***Thyroid function tests, growth hormone levels, cortisol levels | |||
**Gonadal dysfunction | |||
***Testosterone level in males; prolactin level in females | |||
Although elevated alpha-fetoprotein levels may be seen in the germ cell tumors; however, AFP levels may be normally elevated both in serum and CSF of neonates and infants. Alpha-fetoprotein (AFP) levels may be elevated in the following tumors: | Although elevated alpha-fetoprotein levels may be seen in the germ cell tumors; however, AFP levels may be normally elevated both in serum and CSF of neonates and infants. Alpha-fetoprotein (AFP) levels may be elevated in the following tumors: | ||
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Other relevant tumor marker findings are as follows: | Other relevant tumor marker findings are as follows: | ||
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! style="background: #4479BA; width: 200px;" | {{fontcolor|#FFF|Level of tumor marker }} | |||
! style="background: #4479BA; width: 400px;" | {{fontcolor|#FFF|interpretation}} | |||
|- | |||
| style="padding: 5px 5px; background: #DCDCDC; font-weight: bold" | | |||
:beta human chorionic gonadotropin (β-hCG) above 50-100 IU/L | |||
| style="padding: 5px 5px; background: #F5F5F5;" | | |||
*choriocarcinoma | |||
|- | |||
| style="padding: 5px 5px; background: #DCDCDC;font-weight: bold" | | |||
:lower levels of β-hCG | |||
| style="padding: 5px 5px; background: #F5F5F5;" | | |||
*pure germinoma that contain syncytotrophoblastic giant cells | |||
|- | |||
| style="padding: 5px 5px; background: #DCDCDC;font-weight: bold" | | |||
:Basal ganglia, thalamus, cerebral hemisphere | |||
| style="padding: 5px 5px; background: #F5F5F5;" | | |||
*5-10% | |||
|- | |||
| style="padding: 5px 5px; background: #DCDCDC;font-weight: bold" | | |||
:Both pineal and suprasellar region | |||
| style="padding: 5px 5px; background: #F5F5F5;" | | |||
*6-13% | |||
|- | |||
|} | |||
Levels of beta human chorionic gonadotropin (β-hCG) above 50-100 IU/L indicate the presence of choriocarcinoma while lower levels may indicate pure germinoma that contain syncytotrophoblastic giant cells. [17, 51, 32, 6] | Levels of beta human chorionic gonadotropin (β-hCG) above 50-100 IU/L indicate the presence of choriocarcinoma while lower levels may indicate pure germinoma that contain syncytotrophoblastic giant cells. [17, 51, 32, 6] | ||
Carcinoembryonic antigen (CEA) levels may be increased in nongerminomatous germ cell tumors (NGGCTs) or their components. | Carcinoembryonic antigen (CEA) levels may be increased in nongerminomatous germ cell tumors (NGGCTs) or their components. | ||
Pure germinomas and mature teratomas typically present with normal levels of AFP and beta-hCG in both serum and CSF. Some histologically confirmed germinomas have elevated beta-hCG levels that are presumed to be due to beta-hCG secreting syncytiotrophoblasts. In such cases, elevations of serum beta-hCG are generally limited (<50 IU/L), although some tumors have levels >100 IU/L [14]. (See 'Beta-HCG secreting germinomas' below.) | Pure germinomas and mature teratomas typically present with normal levels of AFP and beta-hCG in both serum and CSF. Some histologically confirmed germinomas have elevated beta-hCG levels that are presumed to be due to beta-hCG secreting syncytiotrophoblasts. In such cases, elevations of serum beta-hCG are generally limited (<50 IU/L), although some tumors have levels >100 IU/L [14]. (See 'Beta-HCG secreting germinomas' below.) | ||
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Any tumor with an elevated AFP (>10 microg/L or higher than the institutional normal range) can be assumed to contain elements of endodermal sinus tumor and/or immature teratoma. If a histologic diagnosis is not possible because surgery is contraindicated, such a patient should be treated as having a NGGCT. Pure endodermal sinus tumor or pure choriocarcinomas are often associated with dramatic elevations in AFP (>500 microg/L) or beta-hCG (>1000 IU/L), whereas immature teratomas have less dramatic elevations of AFP and/or beta-hCG. A serum AFP >1000 microg/L has recently been identified as a poor prognostic indicator [24,25], but since a significant proportion of these tumors have mixed components, it is not yet feasible to use tumor markers for risk stratification without a tissue diagnosis. | Any tumor with an elevated AFP (>10 microg/L or higher than the institutional normal range) can be assumed to contain elements of endodermal sinus tumor and/or immature teratoma. If a histologic diagnosis is not possible because surgery is contraindicated, such a patient should be treated as having a NGGCT. Pure endodermal sinus tumor or pure choriocarcinomas are often associated with dramatic elevations in AFP (>500 microg/L) or beta-hCG (>1000 IU/L), whereas immature teratomas have less dramatic elevations of AFP and/or beta-hCG. A serum AFP >1000 microg/L has recently been identified as a poor prognostic indicator [24,25], but since a significant proportion of these tumors have mixed components, it is not yet feasible to use tumor markers for risk stratification without a tissue diagnosis. | ||
Revision as of 17:02, 11 February 2016
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Associate Editor(s)-in-Chief: {{Simrat}
Overview
Laboratory Findings
The following tests are done for intracranial germ cell tumors:
- CSF cytology to detect malignant cells
- Measurement of AFP and beta-hCG in the CSF and serum
- Tumor marker levels are usually higher in CSF than in serum. In patients in whom endoscopic biopsy is not considered possible, detection of elevated tumor markers may be sufficient for diagnosis.
- Measurement of beta-hCG and AFP in the CSF is more sensitive than serum levels in detecting abnormalities. However, due to discordant serum and CSF tumor marker results that were observed, both serum and CSF tumor markers should be obtained in the absence of clinical contraindications. Lumbar CSF is considered more accurate for tumor markers and cytology than ventricular CSF.
- Tumor markers from ventricular CSF can be used , if a lumbar puncture is contradicted.
- Laboratory studies to detect the hormonal dysfunction that may occur in patients with central nervous system (CNS) germinomas are as follows:
- Diabetes insipidus
- Serum sodium, serum osmolality, and urine osmolality
- Hypopituitarism
- Thyroid function tests, growth hormone levels, cortisol levels
- Gonadal dysfunction
- Testosterone level in males; prolactin level in females
- Diabetes insipidus
Although elevated alpha-fetoprotein levels may be seen in the germ cell tumors; however, AFP levels may be normally elevated both in serum and CSF of neonates and infants. Alpha-fetoprotein (AFP) levels may be elevated in the following tumors:
- Pure endodermal sinus tumor (yolk sac)
- Embryonal carcinoma
- Malignant teratoma.
Interpretation of the AFP level must take into account the normal variation seen in this age group. The median AFP levels in CSF, in normal infants, are as follows:
Age | AFP levels |
---|---|
|
|
|
|
|
|
Other relevant tumor marker findings are as follows:
Level of tumor marker | interpretation |
---|---|
|
|
|
|
|
|
|
|
Levels of beta human chorionic gonadotropin (β-hCG) above 50-100 IU/L indicate the presence of choriocarcinoma while lower levels may indicate pure germinoma that contain syncytotrophoblastic giant cells. [17, 51, 32, 6] Carcinoembryonic antigen (CEA) levels may be increased in nongerminomatous germ cell tumors (NGGCTs) or their components.
Pure germinomas and mature teratomas typically present with normal levels of AFP and beta-hCG in both serum and CSF. Some histologically confirmed germinomas have elevated beta-hCG levels that are presumed to be due to beta-hCG secreting syncytiotrophoblasts. In such cases, elevations of serum beta-hCG are generally limited (<50 IU/L), although some tumors have levels >100 IU/L [14]. (See 'Beta-HCG secreting germinomas' below.)
Any tumor with an elevated AFP (>10 microg/L or higher than the institutional normal range) can be assumed to contain elements of endodermal sinus tumor and/or immature teratoma. If a histologic diagnosis is not possible because surgery is contraindicated, such a patient should be treated as having a NGGCT. Pure endodermal sinus tumor or pure choriocarcinomas are often associated with dramatic elevations in AFP (>500 microg/L) or beta-hCG (>1000 IU/L), whereas immature teratomas have less dramatic elevations of AFP and/or beta-hCG. A serum AFP >1000 microg/L has recently been identified as a poor prognostic indicator [24,25], but since a significant proportion of these tumors have mixed components, it is not yet feasible to use tumor markers for risk stratification without a tissue diagnosis.