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Yolk sac tumour

{{{Name|Yolk sac tumour}}}
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ICD-10 (ICD-O9071/3)
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Yolk sac tumours are members of the germ cell tumourgroup of ovarian neoplasms. Almost all ovarianyolk sactumoursoccur in womenunder the age of 30. Patients usually present with sudden onset painand a large pelvic mass. Serum alpha-fetoprotein(AFP) is elevated in virtually all cases and is the prototypic serum marker for ovarian tumours in young patients. At laparotomy, there is spread to the peritoneumor lymph nodesin 30-70% of cases.

The tumours are soft and friable with a smooth external surface and a cystic and perhaps solid variegated yellow or gray sectioned surface. Extensive hemorrhageand necrosisis usual.

Microscopically, there is a wide variety of patterns and several histologic subtypes. Typical features are Schiller-Duval bodiesand eosinophilichyalineglobules. Before contemporary chemotherapy, this type of neoplasm was highly lethal, but the prognosis has significantly improved since.




This article is licensed under the GNU Free Documentation License.
It uses material from the http://en.wikipedia.org/wiki/Yolk+sac+tumour Wikipedia article Yolk sac tumour.

 
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