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Choriocarcinoma
Classification and external resources
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 far end of the spectrum of gestational trophoblastic disease (GTD), a subset of germ cell tumors.

Contents

[edit] Pathology

Characteristic feature is the identification of intimately related syncytiotrophoblast and cytotrophoblasts without formation of definite placental type villi.

Syncytiotrophoblasts are large cells with bizarre nuclei and an eosinophilic cytoplasm. They often surround the cytotrophoblasts.

Cytotrophoblasts are polyhedral and regular cells. Have a clear/eosinophillic cytoplasm with hyperchromatic nuclei.

[edit] Etiology/Epidemiology

Choriocarcinoma of the placenta during pregnancy is preceded by:

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]

It can also occur in the ovaries.[4][5]

[edit] Symptoms/Signs/Labs

[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 kidneys and/or brain is usually fatal. At present, treatment with single-agent methotrexate or actinomycin D is recommended for low-risk disease, while intense combination regimens including EMACO (etoposide, methotrexate, actinomycin D, cyclosphosphamide and 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 desiring sterilization. It may be required for those with severe infection and uncontrolled bleeding.

[edit] References

  1. ^ choriocarcinoma at Dorland's Medical Dictionary
  2. ^ 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. 
  3. ^ Kufe D (2000). Benedict RC, Holland JF. ed. Cancer medicine (5th ed.). Hamilton, Ont: B.C. Decker. ISBN 1-55009-113-1. OCLC 156944448. 
  4. ^ 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. 
  5. ^ 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. 
  6. ^ 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. 
  7. ^ 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. 
  8. ^ 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. 

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