Germ cell tumor
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Overview
| Germ cell tumor Classification and external resources | |
| ICD-10 | C56., C62., D27., D29.2 |
|---|---|
| ICD-9 | 183, 186, 220, 222.0 |
| ICD-O: | 9060-9100 |
| eMedicine | med/863 |
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Germ cell tumor (GCT) is a tumor (neoplasm) derived from germ cells. (Germ cells themselves are not pathogenic; i.e., they are not the viral and bacterial "germs" that cause illness.) Germ cell tumors can occur both inside and outside of the gonads (ovary and testis).
Etiology
Some investigators suggest that this distribution arises as a consequence of abnormal migration of germ cells during embryogenesis. Others hypothesize a widespread distribution of germ cells to multiple sites during normal embryogenesis, with these cells conveying genetic information or providing regulatory functions at somatic sites.
Extragonadal germ cell tumors were thought initially to be isolated metastases from an undetected primary tumor in a gonad, but it is now known that many germ cell tumors are congenital and originate outside the gonads. The most notable of these is sacrococcygeal teratoma, the single most common tumor diagnosed in babies at birth.
Classification
Germ cell tumors are classified by their histology,[1] regardless of location in the body.
| Tumor | ICD-O | Peak Age (yr) | Benign or malignant | Histology | Tumor marker |
|---|---|---|---|---|---|
| Germinoma including dysgerminoma and seminoma | 9060/3 | 40-50 | Malignant | Sheets of uniform polygonal cells with cleared cytoplasm; lymphocytes in the stroma | 10% have elevated hCG |
| Embryonal carcinoma | 9070/3 | 20-30 | Malignant | Poorly differentiated, pleomorphic cells in cords, sheets, or papillary formation | Pure tumors do not secrete hCG, AFP |
| Endodermal sinus tumor, also known as yolk sac tumor (EST, YST) | 9071/3 | 3 | Malignant | Poorly differentiated endothelium-like, cuboidal, or columnar cells | 100% secrete AFP |
| Choriocarcinoma | 9100/3 | 20-30 | Malignant | Cytotrophoblast and syncytiotrophoblast without villus formation | 100% secrete hCG |
| Teratoma including mature teratoma, dermoid cyst, immature teratoma, teratoma with malignant transformation | 9080/0-9080/3 | 0-3, 15-30 | Mature teratoma, dermoid cyst usually benign (but follow-up required); others usually malignant | Very variable, but "normal" tissues are common | Pure tumors do not secrete hCG, AFP |
| Polyembryoma | 9072/3 | 15-25 | ? | ? | ? |
| Gonadoblastoma | 9073/1 | ? | ? | ? | ? |
| Mixed | 15-30 | Malignant | Depends on elements present | Depends on elements present |
Germ cell tumors are broadly divided in two classes:[1]
- The germinomatous or seminomatous germ cell tumors (GGCT, SGCT) include only germinoma and its synonyms dysgerminoma and seminoma.
- The nongerminomatous or nonseminomatous germ cell tumors (NGGCT, NSGCT) include all other germ cell tumors, pure and mixed.
The two classes reflect an important clinical difference. Compared to germinomatous tumors, nongerminomatous tumors tend to grow faster, have an earlier mean age at time of diagnosis (~25 years versus ~35 years, in the case of testicular cancers), and have a lower 5 year survival rate. The survival rate for germinomatous tumors is higher in part because these tumors are exquisitely sensitive to radiation, and they also respond well to chemotherapy. The prognosis for nongerminomatous has improved dramatically, however, due to the use of platinum-based chemotherapy regimens.[1]
Teratocarcinoma is an old name for a germ cell tumor that is a mixture of teratoma and embryonal carcinoma. In more modern usage, this kind of mixed germ cell tumor may be known as a teratoma with elements of embryonal carcinoma, or simply as an embryonal carcinoma.
Location
Despite their name, germ cell tumors occur both within and outside the ovary and testis.
- head
- neck
- 1% to 5% in the mediastinum (mediastinal germ cell tumor)
- pelvis, particularly sacrococcygeal teratoma
In females, germ cell tumors account for 30% of ovarian tumors, but only 1 to 3% of ovarian cancers in North America. In younger women germ cell tumors are more common, thus in patients under the age of 21, 60% of ovarian tumors are of the germ cell type, and up to one-third are malignant. In males, germ cell tumors of the testis occur typically after puberty and are malignant (testicular cancer). In neonates, infants, and children younger than 4 years, the majority of germ cell tumors are sacrococcygeal teratomas.
Persons with Klinefelter's syndrome have a 50 times greater risk of germ cell tumors (GSTs)[1]. In these persons, GSTs usually contain nonseminomatous elements, present at an earlier age, and seldom are gonadal in location.
Prognosis
The 1997 International Germ Cell Consensus Classification[1] is a tool for estimating the risk of relapse after treatment of malignant germ cell tumor.
A small study of ovarian tumors in girls[1] reports a correlation between cystic and benign tumors and, conversely, solid and malignant tumors. Because the cystic extent of a tumor can be estimated by ultrasound, MRI, or CT scan before surgery, this permits selection of the most appropriate surgical plan to minimize risk of spillage of a malignant tumor.
Research
Germ cell tumors of children are the subject of clinical research by the worldwide Children's Oncology Group (COG), in a number of studies coordinated by Dr. John Cullen, MD.[1]
Intracranial Germ Cell Tumors have been studied through the International CNS GCT Study Group. Under the direction of Jonathan Finlay, the program director, three international treatment studies have been initiated since 1990 with the goal to maintain a high rate of cure while minimizing the late effects of treatment.
References
See also
External links
- Childhood Extracranial Germ Cell Tumors
- Extragonadal Germ Cell Tumors
- Ovarian Germ Cell Tumors
- Primary Germ Cell Tumors of the Thorax
- Malignant Mediastinal Germ Cell Tumors
- Intracranial Germ Cell Tumors The Oncologist, Vol. 5, No. 4, 312-320, August 2000
Acknowledgement and Attribution Regarding Sources of Content
Some of the initial content on this page may be incorporated in part from copyleft sources in the public domain including wikis such as Wikipedia and AskDrWiki. Drug information for patients came from the The National Library of Medicine. Infectious disease information may have come from the Centers for Disease Control (CDC). Differential Diagnoses are drawn from clinicians as well as an amalgamation of 3 sources: 1.The Disease Database; 2. Kahan, Scott, Smith, Ellen G. In A Page: Signs and Symptoms. Malden, Massachusetts: Blackwell Publishing, 2004:3; 3. Sailer, Christian, Wasner, Susanne. Differential Diagnosis Pocket. Hermosa Beach, CA: Borm Bruckmeir Publishing LLC, 2002:7 .
