Teratoma classification: Difference between revisions
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::::* Ovarian GCTs. | ::::* Ovarian GCTs. | ||
::::* Extragonadal extracranial GCTs. | ::::* Extragonadal extracranial GCTs. | ||
Cellular Classification of Ovarian Germ Cell Tumors | |||
The following histologic subtypes have been described.[1,2] <ref>Serov SF, Scully RE, Robin IH: International Histologic Classification of Tumours: No. 9. Histological Typing of Ovarian Tumours. Geneva: World Health Organization, 1973.</ref> | |||
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== | ==References== | ||
{{reflist|2}} | {{reflist|2}} |
Revision as of 19:36, 19 August 2015
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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.[1,2] [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.