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      Intraplacental Choriocarcinoma: Rare or Underdiagnosed? Report of 2 Cases Diagnosed after an Incomplete Miscarriage and a Preterm Spontaneous Vaginal Delivery

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          Abstract

          Intraplacental choriocarcinoma is a rare malignant tumor diagnosed after an abortion, an ectopic pregnancy, or a term or preterm pregnancy or following the diagnosis of a hydatidiform mole. During pregnancy, it may be more common than reported, as most patients are asymptomatic and placental choriocarcinomas are usually inconspicuous macroscopically and are often mistaken for an infarct. Based upon a case study methodology, we describe 2 cases of intraplacental choriocarcinoma: the first case was identified in the product of a uterine curettage following an incomplete miscarriage and the second in one of the placentas of a bichorionic twin pregnancy. Maternal investigation did not reveal evidence of metastatic disease and neither did the infants' one in the second case. The two cases underwent maternal surveillance with serum hCG and remained disease-free until the present. In conclusion, intraplacental choriocarcinoma is easily underdiagnosed but with current treatment, even in the presence of metastasis, the prognosis is excellent. A routine microscopic examination of all the placentas and products of miscarriage can increase the real incidence of this entity and consequently improve its management.

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          Most cited references19

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          Intraplacental choriocarcinoma: Systematic review and management guidance.

          Intraplacental choriocarcinoma (IC) is a rare form of malignant gestational trophoblastic disease (GTD). We present a review of 62 cases, including four previously unreported, and a suggested management algorithm.
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            Transplacental Hemorrhage Associated with Placental Neoplasms

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              Intraplacental choriocarcinoma in a term placenta with both maternal and infantile metastases: a case report and review of the literature.

              Intraplacental choriocarcinoma is rare, and usually results in maternal metastasis at the time of diagnosis. Intraplacental choriocarcinoma involves both mother and infant is extremely rare. There was only one case report of intraplacental choriocarcinoma with confirmed metastases involving both the mother and the infant. We describe a second case of intraplacental choriocarcinoma in a term placenta with both maternal and infantile metastases. Grossly, the primary lesion of the placenta resembled an old infarct. Microscopically, clusters of malignant trophoblasts arose from residual normal chorionic villi and infiltrated into the intervillous spaces. Both the mother and the infant received chemotherapy and were alive without disease after one year's follow-up. The optimal treatment for intraplacental choriocarcinoma is controversial. However, aggressive chemotherapy is suggested for patients with metastatic disease.
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                Author and article information

                Journal
                Case Rep Med
                Case Rep Med
                CRIM
                Case Reports in Medicine
                Hindawi
                1687-9627
                1687-9635
                2017
                16 April 2017
                : 2017
                : 7892980
                Affiliations
                1Department of Obstetrics and Gynecology, Centro Hospitalar de Entre o Douro e Vouga, Santa Maria da Feira, Portugal
                2Department of Anatomic Pathology Lab Albino Oliveira, Centro Hospitalar de Entre o Douro e Vouga, Santa Maria da Feira, Portugal
                3Department of Anatomic, Cytopathology and Thanatology, Escola Superior de Saúde, Instituto Politécnico do Porto, Porto, Portugal
                4Department of Fetal Pathology and Anatomic Pathology Lab, CGC Genetics, Porto, Portugal
                5Life and Health Sciences Research Institute (ICVS), School of Medicine, ICVS/3B's-PT Government Associate Laboratory, Campus of Gualtar, University of Minho, Guimarães, Braga, Portugal
                Author notes
                *Rita Ferraz Caldas: ritafcaldas@ 123456gmail.com

                Academic Editor: Raoul Orvieto

                Author information
                http://orcid.org/0000-0003-3970-1595
                http://orcid.org/0000-0003-3639-3419
                http://orcid.org/0000-0001-8703-4622
                Article
                10.1155/2017/7892980
                5439247
                28567059
                835a514b-6e61-45d6-a557-60c55a522bcf
                Copyright © 2017 Rita Ferraz Caldas et al.

                This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 19 January 2017
                : 15 March 2017
                Categories
                Case Report

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