PLACENTAL MESENCHYMAL DYSPLASIA
- 作者: PAVLOV KA1, DUBOVA EA1, ShchEGOLEV AI1, Pavlov KA2, Dubova EA2, Shchegolev AI2
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隶属关系:
- Academician V. I. Kulakov Research Center of Obstetrics, Gynecology, and Perinatology, Ministry of Health and Social Development ofthe Russian Federation, Moscow
- 期: 编号 5 (2010)
- 页面: 15-20
- 栏目: Articles
- URL: https://journals.eco-vector.com/0300-9092/article/view/246335
- ID: 246335
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作者简介
K PAVLOV
E DUBOVA
A ShchEGOLEV
K Pavlov
Academician V. I. Kulakov Research Center of Obstetrics, Gynecology, and Perinatology, Ministry of Health and Social Development ofthe Russian Federation, MoscowAcademician V. I. Kulakov Research Center of Obstetrics, Gynecology, and Perinatology, Ministry of Health and Social Development ofthe Russian Federation, Moscow
E Dubova
Academician V. I. Kulakov Research Center of Obstetrics, Gynecology, and Perinatology, Ministry of Health and Social Development ofthe Russian Federation, MoscowAcademician V. I. Kulakov Research Center of Obstetrics, Gynecology, and Perinatology, Ministry of Health and Social Development ofthe Russian Federation, Moscow
A Shchegolev
Academician V. I. Kulakov Research Center of Obstetrics, Gynecology, and Perinatology, Ministry of Health and Social Development ofthe Russian Federation, MoscowAcademician V. I. Kulakov Research Center of Obstetrics, Gynecology, and Perinatology, Ministry of Health and Social Development ofthe Russian Federation, Moscow
参考
- Allias F., Lebreton F., Collardeau-Frachon S. et al. Immunohistochemical expression of p57 in placental vascular proliferative disorders of preterm and term placentas // Fetal. Pediatr. Pathol. - 2009. - Vol. 28, № 1. - P. 9-23.
- Arizawa M., Nakayama M. Suspected involvement of the X chromosome in placental mesenchymal dysplasia // Cong. Anomal. - 2002. - Vol. 42, № 4. - P. 309-317.
- Astner A., Schwinger E., Caliebe A. et al. Sonographically detected fetal and placental abnormalities associated with trisomy 16 confined to the placenta: a case report and review of the literature // Prenat. Diagn. - 1998. - Vol. 18. - P. 1308-1315.
- Benirschke K., Kaufmann P. Pathology of the Human Placenta. 4th ed. - NY: Springer Verlag, 2000.
- Bhuiyan Z.A., Yatsuki H., Sasaguri T. et al. Functional analysis of the p57KIP2 gene mutation in Beckwith- Wiedemann syndrome // Hum. Genet. - 1999. - Vol. 104, № 3. - P. 205-210.
- Carta M., Maresi E., Giuffre M. et al. Congenital hepatic mesenchymal hamartoma associated with mesenchymal stem villous hyperplasia of the placenta: case report // J. Pediatr. Surg. - 2005. - Vol. 40, № 5. - P. e37-e39.
- Castrillon D.H., Sun D., Weremowicz S. et al. Discrimination of complete hydatidiform mole from its mimics by immunohistochemistry of the paternally imprinted gene product p57KIP2 // Am. J. Surg. Pathol. - 2001. -Vol. 25, № 10. - P. 1225-1230.
- Chan Y.F., Sampson A. Placental mesenchymal dysplasia: a report of four cases with differentiation from partial hydatidiform mole // Aust. N. Z. J. Obstet. Gynaecol. - 2003. - Vol. 43, № 6. - P. 475-479.
- Chen C.P. Syndromes and disorders associated with omphalocele (I): Beckwith-Wiedemann syndrome // Taiwan J. Obstet. Gynecol. - 2007. - Vol. 46, № 2. - P. 96-102.
- Chen C.P., Chern S.R., Wang T.Y. et al. Pregnancy with concomitant chorangioma and placental vascular malformation with mesenchymal hyperplasia // Hum. Reprod. - 1997. - Vol. 12, № 11. - P. 2553-2556.
- Chilosi M., Piazzola E., Lestani M. et al. Differential expression of p57Kip2, a maternally imprinted cdk inhibitor, in normal human placenta and gestational trophoblastic disease // Lab. Invest. - 1998. - Vol. 78, № 3. - P. 269-276.
- Cohen M.C., Roper E.C., Sebire N.J. et al. Placental mesenchymal dysplasia associated with fetal aneuploidy // Prenat. Diagn. - 2005. - Vol. 25, № 3. - P. 187-192.
- Cohen M.M .Jr. Beckwith-Wiedemann syndrome: historical, clinicopathological, and etiopathogenetic perspectives // Pediatr. Dev. Pathol. - 2005. - Vol. 8, № 3. - P. 287-304.
- DeChiara T.M., Robertson E.J., Efstratiadis A. Parental imprinting of the mouse insulin-like growth factor II gene // Cell. - 1991. - Vol. 64, № 4. - P. 849-859.
- H'mida D., Gribaa M., Yacoubi T. et al. Placental mesenchymal dysplasia with Beckwith-Wiedemann syndrome fetus in the context of biparental and androgenic cell lines // Placenta. - 2008. - Vol. 29, № 5. - P. 454-460.
- Jauniaux E., Nicolaides K.H., Hustin J. Perinatal features associated with placental mesenchymal dysplasia // Placenta. - 1997. - Vol. 18, № 8. - P. 701-706.
- Joukov V., Pajusola K., Kaipainen A. et al. A novel vascular endothelial growth factor, VEGF-C, is a ligand for the Flt4 (VEGFR-3) and KDR (VEGFR- 2) receptor tyrosine kinases // EMBO J. - 1996. - Vol. 15, № 7. - P. 290-298.
- Kaiser-Rogers K.A., McFadden D.E., Livasy CA. et al. Androgenetic/biparental mosaicism causes placental mesenchymal dysplasia // J. Med. Genet. - 2006. - Vol. 43, № 2. - P. 187-192.
- Katz V.L., Blanchard G.F., Watson W.J. et al. The clinical implications of subchorionic placental lucencies // Am. J. Obstet. Gynecol. - 1991. - Vol. 164, № 1, pt 1. - P. 99-100.
- Khong T.Y. Placental vascular development and neonatal outcome // Semin. Neonatol. - 2004. - Vol. 9, № 4. - P. 255-263.
- Kuwabara Y., Shima Y., Araki T., Shin S. Mesenchymal stem villous hyperplasia of the placenta and fetal growth restriction // Obstet. Gynecol. - 2001. - Vol. 98, № 5, pt 2. - P. 940-943.
- Laberge J.M., Patenaude Y., Desilets V. et al. Large hepatic mesenchymal hamartoma leading to mid- trimester fetal demise // Fetal. Diagn. Ther. - 2005. - Vol. 20, № 2. - P. 141-145.
- Lau M.M.H., Stewart C.E.H., Liu Z. et al. Loss of the imprinted Igf2/cation-independent mannose 6-phosphate receptor results in fetal overgrowth and perinatal lethality // Genes Dev. - 1994. - Vol. 8. - P. 2953-2963.
- Lokan J., Chan Y.F. Placental mesenchymal dysplasia // Pathology. - 2002. - Vol. 34, № 4. - P.~375-383.
- Maher E.R., Reik W. Beckwith-Wiedemann syndrome: imprinting in clusters revisited // J. Clin. Invest. - 2000. - Vol. 105, № 3. - P. 247-252.
- Matsui H., Iitsuka Y., Yamazawa K. et al. Placental mesenchymal dysplasia initially diagnosed as partial mole // Pathol. Int. - 2003. - Vol. 53, № 11. - P. 810-813.
- Matsuoka S., Thompson J.S., Edwards M.C. et al. Imprinting of the gene encoding a human cyclin- dependent kinase inhibitor, p57KIP2, on chromosome 11p15 // Proc. Natl. Acad. Sci. USA. - 1996. - Vol. 93, № 7. - P. 3026-3030.
- Moscoso G., Jauniaux E., Hustin J. Placental vascular anomaly with diffuse mesenchymal stem villous hyperplasia: a new clinico-pathological entity? // Pathol. Res. Pract. - 1991. - Vol. 187, № 2-3. - P. 324-328.
- Ohyama M., Kojyo T., Gotoda H. et al. Mesenchymal dysplasia of the placenta // Pathol. Int. - 2000. - Vol. 50, № 9. - P. 759-764.
- Paradinas F.J., Sebire N.J., Fisher R.A. et al. Pseudo- partial moles: placental stem vessel hydrops and the association with Beckwith-Wiedemann syndrome and complete moles // Histopathology. - 2001. - Vol. 39, № 5. - P. 447-454.
- Parveen Z., Tongson-Ignacio J.E., Fraser C.R. et al. Placental Mesenchymal Dysplasia. // Arch. Pathol. Lab. Med. - 2007. - Vol.131. - P. 131-137.
- Pham T., Steele J., Stayboldt C. et al. Placental mes- enchymal dysplasia is associated with high rates of intrauterine growth restriction and fetal demise // Am. J. Clin. Pathol. - 2006. - Vol. 126, № 1. - P. 67-78.
- Ping A.J., Reeve A.E., Law D.J. et al. Genetic linkage of Beckwith-Wiedemann syndrome to 11p15 // Am. J. Hum. Genet. - 1989. - Vol. 44, № 5. - P. 720-723.
- Sander C.M. Angiomatous malformation of placental chorionic stem vessels and pseudo-partial molar placentas: report of five cases // Pediatr. Pathol. - 1993. - Vol. 13, № 5. - P. 621-633.
- Yamada Y., Nezu J., Shimane M., Hirata Y. Molecular cloning of a novel vascular endothelial growth factor, VEGF-D // Genomics. - 1997. - Vol. 42, № 3. - P. 483-488.
- Zhang P., Liegeois N.J., Wong C. et al. Altered cell differentiation and proliferation in mice lacking p57KIP2 indicates a role in Beckwith-Wiedemann syndrome // Nature. - 1997. - Vol. 387, № 6629. - P. 151-158.
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