hydatidiform mole

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Related to Complete mole: choriocarcinoma, vesicular mole, Partial mole

Hydatidiform Mole



A hydatidiform mole is a relatively rare condition in which tissue around a fertilized egg that normally would have developed into the placenta instead develops as an abnormal cluster of cells. (This is also called a molar pregnancy.) This grapelike mass forms inside of the uterus after fertilization instead of a normal embryo. A hydatidiform mole triggers a positive pregnancy test and in some cases can become cancerous.


A hydatidiform mole ("hydatid" means "drop of water" and "mole" means "spot") occurs in about 1 out of every 1,500 (1/1,500) pregnancies in the United States. In some parts of Asia, however, the incidence may be as high as 1 in 200 (1/200). Molar pregnancies are most likely to occur in younger and older women (especially over age 45) than in those between ages 20-40. About 1-2% of the time a woman who has had a molar pregnancy will have a second one.
A molar pregnancy occurs when cells of the chorionic villi (tiny projections that attach the placenta to the lining of the uterus) don't develop correctly. Instead, they turn into watery clusters that can't support a growing baby. A partial molar pregnancy includes an abnormal embryo (a fertilized egg that has begun to grow) that does not survive. In a compete molar pregnancy there is a small cluster of clear blisters or pouches that don't contain an embryo.
If not removed, about 15% of moles can become cancerous. They burrow into the wall of the uterus and cause serious bleeding. Another 5% will develop into fast-growing cancers called choriocarcinomas. Some of these tumors spread very quickly outside the uterus in other parts of the body. Fortunately, cancer developing from these moles is rare and highly curable.

Causes and symptoms

The cause of hydatidiform mole is unclear; some experts believe it is caused by problems with the chromosomes (the structures inside cells that contain genetic information) in either the egg or sperm, or both. It may be associated with poor nutrition, or a problem with the ovaries or the uterus. A mole sometimes can develop from placental tissue that is left behind in the uterus after a miscarriage or childbirth.
Women with a hydatidiform mole will have a positive pregnancy test and often believe they have a normal pregnancy for the first three or four months. However, in these cases the uterus will grow abnormally fast. By the end of the third month, if not earlier, the woman will experience vaginal bleeding ranging from scant spotting to excessive bleeding. She may have hyperthyroidism (overproduction of thyroid hormones causing symptoms such as weight loss, increased appetite, and intolerance to heat). Sometimes, the grapelike cluster of cells itself will be shed with the blood during this time. Other symptoms may include severe nausea and vomiting and high blood pressure. As the pregnancy progresses, the fetus will not move and there will be no fetal heartbeat.


The physician may not suspect a molar pregnancy until after the third month or later, when the absence of a fetal heartbeat together with bleeding and severe nausea and vomiting indicates something is amiss.
First, the physician will examine the woman's abdomen, feeling for any strange lumps or abnormalities in the uterus. A tubal pregnancy, which can be life threatening if not treated, will be ruled out. Then the physician will check the levels of human chorionic gonadotropin (hCG), a hormone that is normally produced by a placenta or a mole. Abnormally high levels of hCG together with the symptoms of vaginal bleeding, lack of fetal heartbeat, and an unusually large uterus all indicate a molar pregnancy. An ultrasound of the uterus to make sure there is no living fetus will confirm the diagnosis.


It is extremely important to make sure that all of the mole is removed from the uterus, since it is possible that the tissue is potentially cancerous. Often, the tissue is naturally expelled by the fourth month of pregnancy. In some instances, the physician will give the woman a drug called oxytocin to trigger the release of the mole that is not spontaneously aborted.
If this does not happen, however, a vacuum aspiration can be performed to remove the mole. In a procedure similar to a dilatation and curettage (D & C), a woman is given an anesthetic (to deaden feeling during the procedure), her cervix (the structure at the bottom of the uterus) is dilated and the contents of the uterus is gently suctioned out. After the mole has been mostly removed, gentle scraping of the uterus lining is usually performed.
If the woman is older and does not want any more children, the uterus can be surgically removed (hysterectomy) instead of a vacuum aspiration because of the higher risk of cancerous moles in this age group.
Because of the cancer risk, the physician will continue to monitor the patient for at least two months after the end of a molar pregnancy. Since invasive disease is usually signaled by high levels of hCG that don't go down after the pregnancy has ended, the woman's hCG levels will be checked every two weeks. If the levels don't return to normal by that time, the mole may have become cancerous.
If the hCG level is normal, the woman's hCG will be tested each month for six months, and then every two months for a year.
If the mole has become cancerous, treatment includes removal of the cancerous issue and chemotherapy. If the cancer has spread to other parts of the body, radiation will be added. Specific treatment depends on how advanced the cancer is.
Women should make sure not to become pregnant within a year after hCG levels have returned to normal. If a woman were to become pregnant sooner than that, it would be difficult to tell whether the resulting high levels of hCG were caused by the pregnancy or a cancer from the mole.


A woman with a molar pregnancy often goes through the same emotions and sense of loss as does a woman who has a miscarriage. Most of the time, she truly believed she was pregnant and now has suffered a loss of the baby she thought she was carrying. In addition, there is the added worry that the tissue left behind could become cancerous.
In the unlikely case that the mole is cancerous the cure rate is almost 100%. As long as the uterus was not removed, it would still be possible to have a child at a later time.



Carlson, Karen J., Stephanie A. Eisenstat, and Terra Ziporyn. The Harvard Guide to Women's Health. Cambridge, MA: Harvard University Press, 1996.

Key terms

Dilatation and curettage (D & C) — Dilating the cervix and scraping the lining of the uterus with an instrument called a curette.
Placenta — The circular, flat organ that connects the fetus via the umbilical cord to the uterus for oxygen, food, and elimination of wastes.
Gale Encyclopedia of Medicine. Copyright 2008 The Gale Group, Inc. All rights reserved.

hy·da·tid·i·form mole

, hydatid mole [MIM*231090]
a vesicular or polycystic mass resulting from the proliferation of the trophoblast, with hydropic degeneration and avascularity of the chorionic villi; the abnormal tissue typically results from expression of paternally derived chromosomes and a loss of maternal chromosomes.
Farlex Partner Medical Dictionary © Farlex 2012

hydatidiform mole

Hydatid mole Obstetrics A pathologic product of pregnancy or trophoblastic tumor, which occurs in 1:2000 pregnancies in the US; it is a benign neoplasm or 'allograft' of trophoblastic tissue, characterized by edematous chorionic villi with proliferative trophoblastic tissue Lab Marked ↑ in hCG
Hydatidiform moles
Complete mole The chorionic villi are swollen, often accompanied by trophoblastic proliferation but not fetal tissue; CMs are 10-20 times more common in Southeast Asia, and demonstrate innumerable grape-like avascular chorionic villi, the usual fate is passage of the product; most CMs have a 46 XX genotype, of which both X chromosomes are of paternal origin; in 10-15% of the complete moles that are 46 XY, both the X and Y chromosomes are of paternal origin; CMs may be due to abnormal gametogenesis and fertilization, while in 46 XX moles, there is fertilization of an empty ovum with no effective genome by a haploid sperm that duplicates without cytokinesis; in the 46 XY complete moles, there may be fertilization of an empty ovum by 2 haploid sperm with subsequent fusion and replication
Partial mole A mass characterized by a mixture of fetal tissue with normal edematous villi and/or hydropic degeneration; most partial moles are triploid–47 XXY > 47 XXX, > 47 XYY, rarely also trisomy 16, and may be the result of unsuccessful dual fertilization of a single ovum; the conceptus does not die, but remains as a proliferating 'tumor'
Invasive mole A trophoblastic proliferation that penetrates the myometrium, and may undergo malignant degeneration into a choriocarcinoma  
McGraw-Hill Concise Dictionary of Modern Medicine. © 2002 by The McGraw-Hill Companies, Inc.

hy·da·tid·i·form mole

, hydatid mole (hī'dă-tid'i-fōrm mōl, hī'dă-tid)
A vesicular or polycystic mass resulting from the proliferation of the trophoblast, with hydropic degeneration and avascularity of the chorionic villi.
Medical Dictionary for the Health Professions and Nursing © Farlex 2012

hydatidiform mole

A tumour arising from the part of the embryo that normally forms the PLACENTA. A normal pregnancy is assumed but, instead of containing a fetus, the womb fills with a mass of grape-like cystic bodies of various size. Often, all the chromosomal material comes from the father. There is usually vaginal bleeding and the woman is often ill. Early diagnosis and removal is important as some hydatidiform moles change into the highly malignant CHORION EPITHELIOMA.
Collins Dictionary of Medicine © Robert M. Youngson 2004, 2005
References in periodicals archive ?
(30-32) Antecedent complete mole and missed abortion were seen in 16% and 13% of the cases, respectively.
They reported 20/180 (11.1%) as partial mole and 3/180 (1.7%) as complete mole. The diagnosis of partial hydatidiform mole based solely on histopathology is difficult even for experienced pathologists [8].
The karyotype of complete moles is usually 46,XX; the chromosomes derive completely from the father as a complete mole likely results from the fertilization of anuclear empty ovum by a haploid sperm that duplicates its own chromosomes after meiosis [6, 7].
Prenatal diagnosis of a complete mole coexisting with a dichorionic twin pregnancy: case report.
In our hospital, report of sample pathology given from first and second curettage was complete mole. After molar evacuation, the patient was not monitored for weekly determination of [beta]HCG level.
A dizygotic diploid twin pregnancy coexistent with a complete mole can be differentiated from a triploid partial mole on ultrasound by identifying a separate normal placenta in the former [1, 2, 6].
In about 20% of complete moles and 2% of partial moles, there is some molar tissue left inside of the uterus, which can continue growing and lead to abnormal vaginal bleeding and risk of infection.
A number of environmental factors might contribute to the incidence of complete mole. For example, a low-carotene diet and vitamin A deficiency, age of mothers, parity, history of previous molar pregnancy, history of OCP intake, pregnancies due to ovulation induction and type A blood group may account for the incidence (4).
Cytogenetic analyses performed on G-bands with trypsin-Giemsa-banded chromosomes showed a 46,XY complete mole and a normal 46,XX fetus.
Rest 50 cases (50%) includes cases which are complete abortion12 cases (12%), incomplete abortion 5cases (5%), inevitable abortion 2 cases (2%), missed abortion 19 cases (19%) blighted ovum 8 cases (8%), ectopic gestation 3 cases (3%) and complete Mole 1 cases (1%).
Histologically, GTD includes complete mole, partial mole, invasive mole, placental site trophoblastic tumor and choriocarcinoma.
The most likely entity to be confused with PMD is a partial mole; however, a twin pregnancy with 1 normal fetus and 1 complete mole could also mimic PMD.

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