A RARE CASE OF ABERRANT MIGRATION OF PRIMORDIAL GERM CELLS – UTERINE YOLK SAC TUMOR

October 14, 2014

A RARE CASE OF ABERRANT MIGRATION OF PRIMORDIAL GERM CELLS – UTERINE YOLK SAC TUMOR

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Title:	A RARE CASE OF ABERRANT MIGRATION OF PRIMORDIAL GERM CELLS – UTERINE YOLK SAC TUMOR
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Article_Title:	A RARE CASE OF ABERRANT MIGRATION OF PRIMORDIAL GERM CELLS – UTERINE YOLK SAC TUMOR
Authors:	L. Păiuşan, C. Ülgüt, P. Deme
Affiliation:	“Vasile Goldis” Western University of Arad
Abstract:	Yolk sac tumor of uterus is a very rare tumor that depelops in the uterus as a result of aberrant migration of primordial germ cells. We present a case of 57 years old woman in climax, which presents at gynecological examination after vaginal bleedings. Biopsy report suggested non-keratinized epidermoid carcinoma microcellular with areas of clear cell carcinoma, poorly differentiated G3, with areas of infarction and acute inflammation associated. The mass was excised and sent to our pathology department for histopathological examination. We reported Yolk sac tumor of uterus with hepatoid pattern T2aN0M0. The section from the uterin cervix and ovary did not show any remarkable pathology.
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References:	1. Blaunstein’s Pathology of the Female Genital Tract, 5th Edition, Kurman J. Robert, Springer, New-York, 2001 2. Sternberg’s Diagnostic Surgical Pathology, 4th Edition, Stacey E. Mills, Carter J. Greenson, 2004 3. Rosai and Ackerman’s surgical pathology, th Edition, vol-2, 2004 4. Spatz A., Bouron D., et all – „Primary yolk sac tumor of the endometrium: a case report and review of the literature” Gynecologic Oncology 5. Joseph MG, Fellows FG, Hearn (1990) Primary endodermal sinus tumor of the endometrium. A clinicopathologic, immunocytochemical and ultrastructural study. Cancer (Philadelphia)
Read_full_article:	pdf/vol16/iss1-4/9 JMA 2013 Paiusan Lucian.pdf
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Article Title:	A RARE CASE OF ABERRANT MIGRATION OF PRIMORDIAL GERM CELLS – UTERINE YOLK SAC TUMOR
Authors:	L. Păiuşan, C. Ülgüt, P. Deme
Affiliation:	“Vasile Goldis” Western University of Arad
Abstract:	Yolk sac tumor of uterus is a very rare tumor that depelops in the uterus as a result of aberrant migration of primordial germ cells. We present a case of 57 years old woman in climax, which presents at gynecological examination after vaginal bleedings. Biopsy report suggested non-keratinized epidermoid carcinoma microcellular with areas of clear cell carcinoma, poorly differentiated G3, with areas of infarction and acute inflammation associated. The mass was excised and sent to our pathology department for histopathological examination. We reported Yolk sac tumor of uterus with hepatoid pattern T2aN0M0. The section from the uterin cervix and ovary did not show any remarkable pathology.
Keywords:
References:	1. Blaunstein’s Pathology of the Female Genital Tract, 5th Edition, Kurman J. Robert, Springer, New-York, 2001 2. Sternberg’s Diagnostic Surgical Pathology, 4th Edition, Stacey E. Mills, Carter J. Greenson, 2004 3. Rosai and Ackerman’s surgical pathology, th Edition, vol-2, 2004 4. Spatz A., Bouron D., et all – „Primary yolk sac tumor of the endometrium: a case report and review of the literature” Gynecologic Oncology 5. Joseph MG, Fellows FG, Hearn (1990) Primary endodermal sinus tumor of the endometrium. A clinicopathologic, immunocytochemical and ultrastructural study. Cancer (Philadelphia)
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