scholarly journals OP21.02: Dichorionic diamniotic twin pregnancy after single blastocyst embryo transfer may not be a rare finding: a single center experience

2013 ◽  
Vol 42 (s1) ◽  
pp. 108-108 ◽  
Author(s):  
T. Murakoshi ◽  
T. Mishima ◽  
K. Miura ◽  
M. Ohashi ◽  
S. Shiojima ◽  
...  
Keyword(s):  
Embryo Transfer ◽  
Twin Pregnancy ◽  
Single Center ◽  
Rare Finding ◽  
Single Center Experience

scholarly journals Coexistence of Myeloid and Lymphoid Neoplasms: A Single-Center Experience

2019 ◽  
Vol 2019 ◽  
pp. 1-5 ◽  
Author(s):  
Anthi Bouchla ◽  
Thomas Thomopoulos ◽  
Sotirios Papageorgiou ◽  
Panagiotis Tsirigotis ◽  
Efthymia Bazani ◽  
...  
Keyword(s):  
Internal Medicine ◽  
Multiple Myeloma ◽  
Clinical Practice ◽  
B Cell ◽  
Clinical Course ◽  
Jak2 V617f ◽  
Single Center ◽  
Everyday Clinical Practice ◽  
Rare Finding ◽  
Single Center Experience

The coexistence of a myeloid and a lymphoid neoplasm in the same patient is a rare finding. We retrospectively searched the records of the Hematology Division of the Second Department of Internal Medicine and Research Institute at Attikon University General Hospital of Athens from 2003 to 2018. Nine cases have been identified in a total of 244 BCR-/ABL1- negative MPN and 25 MDS/MPN patients and 1062 LPD patients referred to our institution between 2003 and 2018. Each case is distinct in the diversity of myeloid and lymphoid entities, the chronological occurrence of the two neoplasms, and the patient clinical course. All of them exhibit myeloproliferative (6 JAK2 V617F-positive cases) and lymphoproliferative features, with 1 monoclonal B-cell lymphocytosis (MBL), 3 B-chronic lymphocytic leukemias (B-CLL), 3 B-non-Hodgkin lymphomas (B-NHL), 1 multiple myeloma (MM), and 1 light and heavy deposition disease (LHCDD), while in three cases myelodysplasia is also present. The challenges in identifying and dealing with these rare situations in everyday clinical practice are depicted in this article.

scholarly journals The Incidence of Dichorionic Diamniotic Twin Pregnancy After Single Blastocyst Embryo Transfer and Zygosity: 8 Years of Single-Center Experience

2020 ◽  
Vol 23 (1) ◽  
pp. 51-54 ◽  
Author(s):  
Hiroko Konno ◽  
Takeshi Murakoshi ◽  
Kiyonori Miura ◽  
Hideaki Masuzaki
Keyword(s):  
Embryo Transfer ◽  
Twin Pregnancy ◽  
Hormone Replacement ◽  
First Trimester ◽  
Frozen Embryo Transfer ◽  
The Other ◽  
Placental Pathology ◽  
Monochorionic Twin ◽  
Single Center Experience ◽  
Twin Pregnancies

AbstractDichorionic diamniotic (DCDA) twin pregnancies after single blastocyst embryo transfer have been reported recently, although a blastocyst ovum is generally believed to divide into monochorionic twin pregnancy. We investigated the incidence of DCDA twin pregnancy after single blastocyst embryo transfer and their zygosity. This prospective cohort study included 655 consecutive twin pregnancies that were managed from 2006 to 2014 at our institution. Chorionicity and amnionicity were determined using first-trimester ultrasonography and/or placental pathology. Zygosity was analyzed if the cases were DCDA twins after single blastocyst embryo transfer. Among 655 twin pregnancies, there were 348 DCDA cases, 295 monochorionic diamniotic (MCDA) cases and 12 monochorionic monoamniotic cases. Single blastocyst embryo transfer was performed in 43 cases. Six out of the 43 (14%) cases involved DCDA twin pregnancies and the other 37 cases involved MCDA twin pregnancies. Three DCDA twins born after single blastocyst embryo transfer, wherein frozen embryo transfer (FET) was performed in the natural cycle, were dizygotic, and the other three cases, wherein FET with hormone replacement therapy was performed, were monozygotic. DCDA twin pregnancy occurred in 14% (7% for monozygotic and 7% for dizygotic) of twin pregnancies after single blastocyst embryo transfer cases.

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