Teratoma classification
Teratoma Microchapters |
Diagnosis |
---|
Treatment |
Case Studies |
Teratoma classification On the Web |
American Roentgen Ray Society Images of Teratoma classification |
Risk calculators and risk factors for Teratoma classification |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Monalisa Dmello, M.B,B.S., M.D. [2]
Classification
- 1. World Health Organization classification of CNS Germ Cell Tumors[1]
- Germinomas
- Nongerminomatous germ cell tumor (NGGCT) groups
- Choriocarcinoma.
- Embryonal carcinoma.
- Mixed germ cell tumor.
- Teratoma.
- Immature.
- Mature.
- Teratoma with malignant transformation.
- Yolk sac tumor.
- 2. Childhood Extracranial Germ Cell Tumors classification
- 2.1 GCTs arise from primordial germ cells, which migrate during embryogenesis from the yolk sac through the mesentery to the gonads.[2][3] Childhood extracranial GCTs can be divided into the following two types:
- Gonadal.
- Extragonadal.
- 2.2 Most childhood extragonadal GCTs arise in midline sites (i.e., sacrococcygeal, mediastinal, and retroperitoneal); the midline location may represent aberrant embryonic migration of the primordial germ cells.Childhood extracranial GCTs are broadly classified as the following:
- Mature teratomas.
- Immature teratomas.
- Malignant GCTs.
- 2.3 GCTs comprise a variety of histologic diagnoses and can also be divided into the following histologic types:
- Germinoma.
- Germinoma.
- Dysgerminoma (ovary).
- Seminoma (testis).
- Nongerminoma.
- Teratoma (mature and immature).
- Yolk sac tumor (endodermal sinus tumor).
- Choriocarcinoma.
- Embryonal carcinoma.
- Gonadoblastoma.
- Mixed GCT
- 2.4 Pediatric GCT Biology
- The following biologically distinct subtypes of GCTs are found in children and adolescents:
- Testicular GCTs.
- Ovarian GCTs.
- Extragonadal extracranial GCTs.
- Cellular Classification of Ovarian Germ Cell Tumors
- The following histologic subtypes have been described.[1, [4]
- Dysgerminoma.
- Other germ cell tumors:
- Endodermal sinus tumor (rare subtypes are hepatoid and intestinal).[1]
- Embryonal carcinoma.
- Polyembryoma.
- Choriocarcinoma.
- Teratoma:
- Immature.
- Mature:
- Solid.
- Cystic:
- Dermoid cyst (mature cystic teratoma).
- Dermoid cyst with malignant transformation.
- Monodermal and highly specialized:
- Struma ovarii.
- Carcinoid.
- Struma ovarii and carcinoid.
- Others (e.g., malignant neuroectodermal and ependymoma).
- Mixed forms.
References
- ↑ Matsutani M, Sano K, Takakura K, Fujimaki T, Nakamura O, Funata N; et al. (1997). "Primary intracranial germ cell tumors: a clinical analysis of 153 histologically verified cases". J Neurosurg. 86 (3): 446–55. doi:10.3171/jns.1997.86.3.0446. PMID 9046301.
- ↑ Dehner LP (1983). "Gonadal and extragonadal germ cell neoplasia of childhood". Hum Pathol. 14 (6): 493–511. PMID 6343221.
- ↑ McIntyre A, Gilbert D, Goddard N, Looijenga L, Shipley J (2008). "Genes, chromosomes and the development of testicular germ cell tumors of adolescents and adults". Genes Chromosomes Cancer. 47 (7): 547–57. doi:10.1002/gcc.20562. PMID 18381640.
- ↑ Serov SF, Scully RE, Robin IH: International Histologic Classification of Tumours: No. 9. Histological Typing of Ovarian Tumours. Geneva: World Health Organization, 1973.