Choriocarcinoma
| Choriocarcinoma | |
|---|---|
| Classification and external resources | |
 Micrograph of choriocarcinoma showing both of the components necessary for the diagnosis - cytotrophoblasts and syncytiotrophoblasts. The syncytiotrophoblasts are multinucleated and have a dark staining cytoplasm. The cytotrophoblasts are mononuclear and have a pale staining cytoplasm. H&E stain. |
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| ICD-10 | C58 |
| ICD-9 | 181 |
| ICD-O: | M9100/3-9101 |
| DiseasesDB | 2602 |
| MeSH | D002822 |
Choriocarcinoma is a malignant, trophoblastic[1] and aggressive cancer, usually of the placenta. It is characterized by early hematogenous spread to the lungs. It belongs to the malignant end of the spectrum in gestational trophoblastic disease (GTD). It is also classified as a germ cell tumor and may arise in the testis or ovary.
Contents |
[edit] Pathology
Characteristic feature is the identification of intimately related syncytiotrophoblasts and cytotrophoblasts without formation of definite placental type villi.
Syncytiotrophoblasts are large multi-nucleated cells with eosinophilic cytoplasm. They often surround the cytotrophoblasts, reminiscent of their normal anatomical relationship in chorionic villi. Cytotrophoblasts are polyhedral, mononuclear cells with hyperchromatic nuclei and a clear or pale cytoplasm. Extensive hemorrhage is a common finding.
[edit] Etiology/Epidemiology
Choriocarcinoma of the placenta during pregnancy is preceded by:
- hydatidiform mole (50% of cases)
- spontaneous abortion (20% of cases)
- ectopic pregnancy (2% of cases)
- normal term pregnancy (20-30% of cases)
Rarely, choriocarcinoma occurs in primary locations other than the placenta; very rarely, it occurs in testicles. Although trophoblastic components are common components of mixed germ cell tumors, pure choriocarcinoma of the adult testis is rare. Pure choriocarcinoma of the testis represents the most aggressive pathologic variant of germ cell tumors in adults, characteristically with early hematogenous and lymphatic metastatic spread. Because of early spread and inherent resistance to anticancer drugs, patients have poor prognosis. Elements of choriocarcinoma in a mixed testicular tumor have no prognostic importance.[2][3]
Choriocarcinomas can also occur in the ovaries.[4][5]
[edit] Symptoms/Signs/Labs
- increased quantitative β-hCG levels
- vaginal bleeding
- shortness of breath
- hemoptysis (coughing up blood)
- chest pain
- chest X-ray shows multiple infiltrates of various shapes in both lungs
- presents in males as a testicular neoplasm, sometimes with skin hyperpigmentation (from excess beta hCG cross reacting with the alpha MSH receptor), gynecomastia, and weight loss (from excess beta hCG cross reacting with the TSH receptor) in males
- can present with increased TSH
[edit] Treatment
Choriocarcinoma is one of the tumors that is most sensitive to chemotherapy. The cure rate, even for metastatic choriocarcinoma, is around 90-95%. Virtually everyone without metastases can be cured; however, metastatic disease to the liver and/or brain is usually fatal. At present, treatment with single-agent methotrexate is recommended for low-risk disease, while intense combination regimens including EMACO (etoposide, methotrexate, actinomycin D, cyclosphosphamide and vincristine (Oncovin)) are recommended for intermediate or high-risk disease.[6][7]
Hysterectomy (surgical removal of the uterus) can also be offered[8] to patients > 40 years of age or those for whom sterilisation is not an obstacle. It may be required for those with severe infection and uncontrolled bleeding.
[edit] Additional images
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High mag.
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Very high mag.
[edit] References
- ^ "choriocarcinoma" at Dorland's Medical Dictionary
- ^ Rosenberg S, DePinho RA, Weinberg RE, DeVita VT, Lawrence TS (2008). DeVita, Hellman, and Rosenberg's Cancer: Principles & Practice of Oncology. Hagerstwon, MD: Lippincott Williams & Wilkins. ISBN 0-7817-7207-9. OCLC 192027662.
- ^ Kufe D (2000). Benedict RC, Holland JF. ed. Cancer medicine (5th ed.). Hamilton, Ont: B.C. Decker. ISBN 1-55009-113-1. OCLC 156944448.
- ^ Gerson RF, Lee EY, Gorman E (November 2007). "Primary extrauterine ovarian choriocarcinoma mistaken for ectopic pregnancy: sonographic imaging findings". AJR Am J Roentgenol 189 (5): W280–3. doi:10.2214/AJR.05.0814. PMID 17954626. http://www.ajronline.org/cgi/pmidlookup?view=long&pmid=17954626.
- ^ Ozdemir I, Demirci F, Yucel O, Demirci E, Alper M (May 2004). "Pure ovarian choriocarcinoma: a difficult diagnosis of an unusual tumor presenting with acute abdomen in a 13-year-old girl". Acta Obstet Gynecol Scand 83 (5): 504–5. doi:10.1111/j.0001-6349.2004.00092a.x. PMID 15059168. http://www3.interscience.wiley.com/resolve/openurl?genre=article&sid=nlm:pubmed&issn=0001-6349&date=2004&volume=83&issue=5&spage=504.
- ^ Rustin GJ, Newlands ES, Begent RH, Dent J, Bagshawe KD (1989). "Weekly alternating etoposide, methotrexate, and actinomycin/vincristine and cyclophosphamide chemotherapy for the treatment of CNS metastases of choriocarcinoma". J. Clin. Oncol. 7 (7): 900–3. PMID 2472471.
- ^ Katzung, Bertram G. (2006). "Cancer Chemotherapy". Basic and clinical pharmacology (10th ed.). New York: McGraw-Hill Medical Publishing Division. ISBN 0-07-145153-6. OCLC 157011367.
- ^ Lurain JR, Singh DK, Schink JC (2006). "Role of surgery in the management of high-risk gestational trophoblastic neoplasia". The Journal of reproductive medicine 51 (10): 773–6. PMID 17086805.
[edit] External links
- MyMolarPregnancy.com Information about molar pregnancy and choriocarcinoma
- 00976 at CHORUS
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