Results 1 to 10 of about 12,098 (117)

Incidental placental choriocarcinoma in a term pregnancy: a case report

open access: yesJournal of Medical Case Reports, 2008
Introduction Gestational choriocarcinoma occurs in 1 in 40,000 pregnancies. Of all forms of gestational choriocarcinoma, placental choriocarcinoma is the most rare.
Chung Christopher   +2 more
doaj   +1 more source

Uterine choriocarcinoma coexistence with endometroid adenocacinoma: a case report and literature review

open access: yesBMC Women's Health, 2023
Background Choriocarcinoma coexisting with endometrial carcinoma is rare. To the best of our knowledge, only one case of choriocarcinoma coexisting with endometrial carcinoma has been reported.
Liping Bai   +4 more
doaj   +1 more source

Ultra-high-risk choriocarcinoma with atraumatic splenic rupture: a rare case report

open access: yesJournal of International Medical Research, 2021
Choriocarcinoma is a malignant tumor associated with early vascular invasion and a high mortality. Ultra-high-risk choriocarcinoma, which was proposed in the International Federation of Gynecology and Obstetrics cancer report of 2018, has a higher risk ...
Jun Zhang   +3 more
doaj   +1 more source

Case Report: 18F-FDG PET/CT and Laparoscopic Nephron Sparing Surgery in the Management of Bleeding From Renal Metastases of Choriocarcinoma

open access: yesFrontiers in Oncology, 2022
Choriocarcinoma is a cancer that usually occurs in the uterus during pregnancy. Although choriocarcinoma with renal metastasis and spontaneous renal hemorrhage is very rare, it can occur. We describe a rare case of metastatic choriocarcinoma, wherein the
Yuancheng Du   +11 more
doaj   +1 more source

Cutaneous Manifestation of Metastatic Infantile Choriocarcinoma

open access: yesCase Reports in Pediatrics, 2014
Infantile choriocarcinoma is a highly malignant rare germ cell tumor that arises from the placenta. Simultaneous intraplacental choriocarcinoma involving both mother and infant is extremely rare.
Timothy Brooks, Laura Nolting
doaj   +1 more source

Delayed diagnosis of intraplacental choriocarcinoma in a term healthy neonate—A case report and literature review

open access: yesClinical Case Reports, 2022
Gestational choriocarcinoma is rare. The intraplacental formation of choriocarcinoma is much rarer. We present a diagnosis of choriocarcinoma, 4 months postpartum, in a 28‐year‐old, presenting with vaginal bleeding.
Mahdokht Azizi   +3 more
doaj   +1 more source

Drug library screening identifies histone deacetylase inhibition as a novel therapeutic strategy for choriocarcinoma

open access: yesCancer Medicine, 2023
Background Choriocarcinoma is a rare and aggressive gynecological malignancy. The standard treatment is systemic chemotherapy as choriocarcinoma exhibits high chemosensitivity.
Eri Watanabe   +9 more
doaj   +1 more source

A case of complete remission of intractable gestational choriocarcinoma with subsequent chemotherapy after pembrolizumab

open access: yesTaiwanese Journal of Obstetrics & Gynecology, 2023
Objective: Gestational choriocarcinoma is a gestational trophoblastic neoplasia (GTN) that originates from abnormal trophoblast proliferation. Although chemotherapy is effective for choriocarcinoma, personalized treatment becomes essential when patients ...
Kaoru Niimi   +6 more
doaj   +1 more source

Male choriocarcinoma presenting with intracerebral hemorrhage: a case report and literature review

open access: yesFrontiers in Oncology
Male choriocarcinoma is an extremely rare malignant tumor. It has the characteristics of hidden onset, easy invasion and metastasis. Clinically, when choriocarcinoma is found in a patient, most of the tumor cells have metastasized to distant organs. This
Jie Chen   +6 more
doaj   +1 more source

Intra-operative cytodiagnosis of primary ovarian choriocarcinoma with Ki67 immunoexpression

open access: yesJournal of Cytology, 2015
Primary ovarian choriocarcinoma is a rare neoplasm that can be gestational and non-gestational in origin. It accounts for one in 369 million pregnancies. Both types present with similar clinical, histomorphological and ultrastructural findings.
Asaranti Kar   +3 more
doaj   +1 more source

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