Abstract | OBJECTIVE: METHODS: This report describes two cases that arose in patients with documented complete hydatidiform moles and summarizes the antecedent prenatal histories of PSTTs based on a detailed Medline literature analysis. CASES: A 28-year-old, G(2) P(2) female had a live, 12-week gestation fetus and a coexisting molar pregnancy. Her hCG levels dropped promptly from 1.5 million to 23,273 IU/ml after termination, but rose shortly thereafter together with the onset of recurrent vaginal bleeding. Curettage revealed persistent mole. Persistently elevated hCG led to hysterectomy disclosing a fundal PSTT. The second case was that of a 48-year-old, G(2) woman who presented with symptoms of preeclampsia, hyperthyroidism, and elevated hCG. Curettage yielded a complete hydatidiform mole. Although the hCG level decreased for a short period, it soon increased despite treatment with methotrexate. A second curettage revealed a PSTT. DISCUSSION: CONCLUSIONS:
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Authors | Crystal A Moore-Maxwell, Stanley J Robboy |
Journal | Gynecologic oncology
(Gynecol Oncol)
Vol. 92
Issue 2
Pg. 708-12
(Feb 2004)
ISSN: 0090-8258 [Print] United States |
PMID | 14766272
(Publication Type: Case Reports, Journal Article, Review)
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Topics |
- Adult
- Female
- Humans
- Hydatidiform Mole
(complications, pathology)
- Middle Aged
- Pregnancy
- Trophoblastic Tumor, Placental Site
(etiology, pathology)
- Uterine Neoplasms
(etiology, pathology)
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