Ciąża poroniona
Etiologia i przyczyny

Ciąża poroniona, zwana również zaśniadem groniastym lub hydatidiform mole, jest patologicznym stanem wynikającym z aberracji genetycznych podczas zapłodnienia, prowadzącym do nieprawidłowego rozwoju trofoblastu i charakterystycznej proliferacji tkanki łożyskowej. Wyróżnia się dwa typy: całkowitą ciążę poronioną, gdzie kariotyp najczęściej wynosi 46,XX (90%) lub 46,XY (10%) i brak jest tkanki płodowej, oraz częściową ciążę poronioną z kariotypem triploidalnym (69,XXY 70%, 69,XXX 27%, 69,XYY 3%), w której może występować niedorozwinięty zarodek. Histopatologicznie całkowita ciąża poroniona charakteryzuje się obrzękiem kosmków, brakiem naczyń krwionośnych i proliferacją trofoblastu, natomiast w częściowej obserwuje się obecność tkanki płodowej z wadami genetycznymi. Etiologia obejmuje mutacje w genach NLRP7 i KHDC3L, zwłaszcza w przypadkach nawracających ciąż poronionych, dziedziczonych autosomalnie recesywnie.

Do czynników ryzyka należą wiek matki (z istotnym wzrostem ryzyka u kobiet >35 lat, a szczególnie 7-krotnym wzrostem po 40. roku życia), wcześniejsze poronienia (ryzyko 1-2% po jednym, 15-20% po dwóch lub więcej), pochodzenie etniczne (wyższe u kobiet azjatyckich) oraz czynniki środowiskowe, takie jak ekspozycja na pył i glebę. Związek z niedoborem karotenu (witamina A) oraz ekspozycją na wysokie wysokości wymaga dalszych badań. Zrozumienie molekularnych i klinicznych aspektów ciąży poronionej jest kluczowe dla diagnostyki, monitorowania i leczenia, zwłaszcza u pacjentek z nawracającymi epizodami, podkreślając, że jest to stan wynikający z losowych nieprawidłowości genetycznych, a nie efekt działań pacjentki lub partnera.

Etiologia ciąży poronionej

Ciąża poroniona (określana również jako zaśniad groniasty lub hydatidiform mole) jest rzadkim powikłaniem ciąży, które powstaje w wyniku nieprawidłowego rozwoju komórek trofoblastu, które w normalnej ciąży tworzą łożysko. Zamiast prawidłowego rozwoju zarodka, dochodzi do powstawania nieprawidłowej tkanki o charakterystycznym wyglądzie przypominającym grona winogron.12

Podłoże genetyczne ciąży poronionej

Ciąża poroniona jest wynikiem nieprawidłowości genetycznych, które zachodzą podczas zapłodnienia. W normalnej sytuacji komórki ludzkie posiadają 23 pary chromosomów, gdzie jeden chromosom z każdej pary pochodzi od matki, a drugi od ojca. W przypadku ciąży poronionej dochodzi do zaburzenia tego procesu.13

Wyróżniamy dwa podstawowe typy ciąży poronionej:4

  1. Całkowita ciąża poroniona – powstaje, gdy pustą komórkę jajową (pozbawioną materiału genetycznego matki) zapładnia jeden lub dwa plemniki. Chromosomy matczyne są nieobecne lub nie funkcjonują, a chromosomy ojcowskie ulegają duplikacji. W efekcie cały materiał genetyczny pochodzi od ojca. Kariotyp najczęściej wynosi 46,XX (90% przypadków) lub rzadziej 46,XY (10% przypadków).425
  2. Częściowa ciąża poroniona – powstaje, gdy prawidłowa komórka jajowa zostaje zapłodniona przez dwa plemniki lub jeden plemnik z podwojonym materiałem genetycznym. W rezultacie zarodek posiada 69 chromosomów zamiast normalnych 46. Najczęstsze kariotypy to 69,XXY (70%), 69,XXX (27%) lub 69,XYY (3%).67

W całkowitej ciąży poronionej nie rozwija się tkanka płodowa, zamiast tego tworzy się masa nieprawidłowej tkanki tropoblastycznej. W częściowej ciąży poronionej może rozwinąć się zarodek, jednak ma on poważne wady genetyczne i nie jest zdolny do przeżycia.89

Mechanizmy molekularne nieprawidłowej implantacji i rozwoju

W całkowitej ciąży poronionej, badania morfologiczne wykazały, że zaśniad groniasty powstaje w wyniku transformacji wewnętrznej masy komórek zarodkowych przed różnicowaniem się w tkankę zarodkową. Bez prawidłowego różnicowania się w endodermę i ektodermę zarodkową, wewnętrzna masa komórkowa wytwarza mezodermę pozazarodkową i pęcherzyki zaśniadowe, prowadząc do powstania zaśniadu groniastego.6

Zarówno w całkowitej, jak i częściowej ciąży poronionej dochodzi do nieprawidłowej proliferacji trofoblastu, co prowadzi do charakterystycznego obrazu histopatologicznego. W całkowitej ciąży poronionej obserwuje się trzy klasyczne cechy histologiczne: obrzęk kosmków kosmówkowych spowodowany napływem wody, kosmki bez naczyń krwionośnych oraz proliferację trofoblastu otaczającego obrzmiałe kosmki. Tkanka płodowa jest nieobecna.6

Czynniki ryzyka ciąży poronionej

Chociaż dokładna przyczyna ciąży poronionej nie jest w pełni poznana, zidentyfikowano kilka czynników ryzyka, które mogą zwiększać prawdopodobieństwo jej wystąpienia:310

  • Wiek matki – ryzyko jest wyższe u kobiet poniżej 20. roku życia oraz znacząco wzrasta u kobiet powyżej 35. roku życia. U kobiet po 40. roku życia ryzyko jest 7-krotnie większe w porównaniu do kobiet w wieku optymalnym.1112
  • Poprzednia ciąża poroniona – jeśli kobieta miała już jedną ciążę poronioną, ryzyko wystąpienia kolejnej wynosi około 1-2%. Po dwóch lub więcej ciążach poronionych ryzyko wzrasta do 15-20%.313
  • Pochodzenie etniczne – ciąża poroniona występuje prawie dwukrotnie częściej u kobiet pochodzenia azjatyckiego w porównaniu do kobiet nie-azjatyckich.312
  • Historia poronień – kobiety z historią wcześniejszych poronień mogą mieć zwiększone ryzyko ciąży poronionej.1014
  • Czynniki dietetyczne – niektóre badania sugerują związek między niskim poziomem karotenu (forma witaminy A) a zwiększonym ryzykiem ciąży poronionej.1015

Genetyczne predyspozycje do nawracających ciąż poronionych

Badania wykazały, że nawracające ciąże poronione mogą mieć podłoże genetyczne związane z mutacjami w określonych genach. Zidentyfikowano mutacje w genach NLRP7 i KHDC3L, które mogą predysponować kobiety do nawracających ciąż poronionych.1617

Opisano również rodzinną, nawracającą formę zaśniadu dwurodzicielskiego (biparental mole), która wydaje się być dziedziczona jako cecha autosomalna recesywna. W szczególności, homozygotyczne i złożone heterozygotyczne recesywne mutacje w genach NLRP7 i KHDC3L są związane ze zwiększonym ryzykiem nawrotów ciąży poronionej.1618

Czynniki środowiskowe i związek z ekspozycją na czynniki zewnętrzne

Niektóre badania sugerują potencjalny związek między ciążą poronioną a czynnikami środowiskowymi. W badaniu kliniczno-kontrolnym zaobserwowano, że mężowie kobiet z ciążą poronioną częściej wykonywali prace fizyczne związane z ekspozycją na glebę i pył w porównaniu do grupy kontrolnej.1920

Istnieją również hipotezy łączące ciążę poronioną z ekspozycją na wysokie wysokości oraz nieodpowiednim żywieniem, jednak wymagają one dalszych badań w celu ustalenia jednoznacznych wniosków.21

Podsumowanie etiologii ciąży poronionej

Ciąża poroniona jest wynikiem genetycznych nieprawidłowości zachodzących podczas zapłodnienia, które prowadzą do nieprawidłowego rozwoju trofoblastu. Choć dokładna przyczyna tych nieprawidłowości nie jest w pełni poznana, zidentyfikowano szereg czynników ryzyka, takich jak wiek matki, pochodzenie etniczne oraz historia poprzednich ciąż poronionych. Badania genetyczne wykazały również potencjalny związek z mutacjami w genach NLRP7 i KHDC3L w przypadku nawracających ciąż poronionych.1621

Ważne jest, aby podkreślić, że ciąża poroniona nie jest spowodowana niczym, co kobieta lub jej partner zrobili lub czego nie zrobili – jest to zdarzenie losowe wynikające z nieprawidłowości genetycznych podczas zapłodnienia.1222

Zrozumienie etiologii ciąży poronionej jest kluczowe dla właściwego zarządzania tym stanem oraz opracowania skutecznych strategii monitorowania i leczenia, szczególnie w przypadku kobiet z czynnikami ryzyka lub historią nawracających ciąż poronionych.23

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  1. 11.04.2026
  2. www.leksykon.com.pl

Materiały źródłowe

  • #1 Molar pregnancy – Symptoms and causes – Mayo Clinic
    https://www.mayoclinic.org/diseases-conditions/molar-pregnancy/symptoms-causes/syc-20375175
    A molar pregnancy is a rare complication of pregnancy. It involves unusual growth of cells called trophoblasts. These cells typically become the organ that feeds a growing fetus. That organ also is known as the placenta. […] An egg fertilized atypically causes a molar pregnancy. Human cells usually have 23 pairs of chromosomes. In a typical fertilization, one chromosome in each pair comes from the father, the other from the mother. […] In a complete molar pregnancy, one or two sperm fertilize an egg. The chromosomes from the mother’s egg are missing or don’t work. The father’s chromosomes are copied. There’s none from the mother. […] In a partial or incomplete molar pregnancy, the mother’s chromosomes are present, but the father supplies two sets of chromosomes. The embryo then has 69 chromosomes instead of 46. This most often occurs when two sperm fertilize an egg, resulting in an extra copy of the father’s genes.
  • #2 Molar Pregnancy: Types, Symptoms, Causes & Treatments
    https://my.clevelandclinic.org/health/diseases/17889-molar-pregnancy
    A molar pregnancy occurs when an egg and sperm join incorrectly at fertilization and create a noncancerous tumor. […] Molar pregnancies are caused by genetic errors that occur during the fertilization of an egg by a sperm. […] Molar pregnancies contain an imbalance of chromosomes. In a complete molar pregnancy, the egg contains no chromosomes. The embryo gets 23 chromosomes from the sperm. In a partial molar pregnancy, an egg is fertilized by two sperm. This results in the embryo having 69 chromosomes. […] This genetic error leads to an unsuccessful pregnancy.
  • #3 Risks and causes of molar pregnancy | Gestational trophoblastic disease (GTD) | Cancer Research UK
    https://www.cancerresearchuk.org/about-cancer/gestational-trophoblastic-disease-gtd/molar-pregnancy/risks-causes
    Molar pregnancies are caused by an imbalance in genetic material (chromosomes) in the pregnancy. […] Researchers haven’t yet been able to identify what causes molar pregnancies. […] Complete molar pregnancies are more common in women over the age of 45. […] Molar pregnancy is almost twice as common in Asian women compared to non-Asian women. […] If you’ve already had one molar pregnancy, you have about a 1 in 100 chance (1%) of having another one. […] If you have had two or more molar pregnancies your risk of having another is higher, at about 15 to 20 out of 100 (15 to 20%).
  • #4 Hydatidiform Mole – StatPearls – NCBI Bookshelf
    https://www.ncbi.nlm.nih.gov/books/NBK459155/
    Hydatidiform moles originate from aberrantly proliferated placental tissue. A complete mole results from the fertilization of an empty ovum by 1 or 2 sperms, resulting in paternally-derived haploid genetic material. Therefore, a complete mole comprises solely maternally derived mitochondrial DNA, while all its nuclear DNA originates paternally. The haploid paternal genetic material undergoes duplication, resulting in a diploid 46,XX or 46,XY molar pregnancy; 46,XX is the more common karyotype. […] Conversely, a partial mole arises when a viable ovum is fertilized by 2 or more sperms, with resultant karyotype 69,XXY. Partial molar pregnancies, therefore, feature a triploid diandrous monogynic genome, typically resulting from the fertilization of an ovum by 2 or more sperms or rarely from reduplications of a single sperm’s genetic material post-fertilization, resulting in a triploid 69,XXY; 69,XXX; or 69,XYY karyotypes.
  • #5 Molar pregnancy | Radiology Reference Article | Radiopaedia.org
    https://radiopaedia.org/articles/molar-pregnancy-2?lang=us
    Molar pregnancies, also called hydatidiform moles, are one of the most common forms of gestational trophoblastic disease. […] Molar pregnancies are one of the common complications of gestation, estimated to occur in one of every 1000-2000 pregnancies. […] These moles can occur in a pregnant woman of any age, but the rate of occurrence is higher in pregnant women in their teens or between the ages of 40-50 years. […] Ninety percent of complete hydatidiform moles have a 46XX diploid chromosomal pattern. […] All the chromosomes are derived from a single sperm in 90% or less likely two sperms, suggesting fertilization of a single egg that has lost its chromosomes. […] With partial moles, the karyotype is usually triploid (69XXY), the result of fertilization of a normal egg by two sperm, one bearing a 23X chromosomal pattern and the other a 23Y chromosomal pattern.
  • #6 Educational Case: Hydatidiform Molar Pregnancy
    https://pmc.ncbi.nlm.nih.gov/articles/PMC7863141/
    A molar pregnancy arises from aberrant fertilization. In a complete mole, genetic material is completely supplied by the paternal chromosome, with either 2 spermatozoa or a diploid sperm fertilizing an empty ovum that lacks maternal chromosomes. In approximately 90% of cases, the fertilized ovum is 46, XX. Morphologic studies of hysterectomy specimens provides evidence that hydatidiform moles arise from a transformation of the inner embryonic cell mass prior to differentiation into embryonic tissue. Without normal differentiation into the embryonic endoderm and ectoderm, the inner cell mass produces extraembryonic mesoderm and molar vesicles leading to the hydatidiform mole. […] A partial mole is an abnormal pregnancy that has a triploid karyotype with rare exceptions, caused by fertilization of a 23X ovum with 2 haploid sperm or a duplicate sperm. The most common karyotype is 69, XXY (70%), followed by 69, XXX (27%) and 69, XYY (3%). Complete moles have 3 classic histological findings: edema of the chorionic villi due to influx of water, avascular villi, and trophoblast proliferation surrounding the edematous villous circumference. Fetal tissue is absent.
  • #7 Gestational trophoblastic disease – Knowledge @ AMBOSS
    https://www.amboss.com/us/knowledge/gestational-trophoblastic-disease/
    Gestational trophoblastic disease (GTD) is a class of neoplastic conditions characterized by abnormal trophoblast-cell growth in the uterus. […] Hydatidiform moles are typically treated via suction evacuation and curettage, whereas GTN treatment typically starts with chemotherapy. […] A type of GTD resulting from abnormal fertilization of an egg that can invade the uterus and metastasize. […] Complete mole: a type of hydatidiform mole typically resulting from fertilization by a single sperm of an abnormal egg that lacks maternal chromosomes. […] Partial mole: a type of hydatidiform mole typically resulting from fertilization of an egg by two sperm or a diploid sperm. […] Etiology: Fertilization of an egg containing a haploid set of chromosomes with two sperms. […] Fertilization of a normal (haploid) egg by two sperm.
  • #8 Molar pregnancy | Pregnancy Birth and Baby
    https://www.pregnancybirthbaby.org.au/molar-pregnancy
    A molar pregnancy happens when the cells that normally form the placenta grow into abnormal cells instead. […] A molar pregnancy occurs when the cells that normally form a placenta grow into a clump of abnormal cells instead. […] In a complete molar pregnancy, an embryo does not develop at all. It usually occurs when an egg that does not contain any genetic material is fertilised by a sperm. […] In a partial molar pregnancy, a fetus can develop, but it will be abnormal and cannot survive. A partial molar pregnancy usually develops when a normal egg is fertilised by 2 sperm. […] If you have a molar pregnancy, it wasn’t caused by anything you did or didn’t do.
  • #9 Molar pregnancy | March of Dimes
    https://www.marchofdimes.org/find-support/topics/miscarriage-loss-grief/molar-pregnancy
    A molar pregnancy is caused when theres a problem with an embryos chromosomes. […] Molar pregnancy happens when there are two sets of chromosomes from the father. […] Complete molar pregnancy happens when chromosomes from the mothers egg are missing or not working, and chromosomes from the father are copied, so all 46 chromosomes come from the father. […] Partial molar pregnancy happens when the mother’s chromosomes are present, but the father provides two sets of chromosomes, giving the embryo 69 chromosomes instead of 46.
  • #10
    https://myhealth.alberta.ca/Health/pages/conditions.aspx?hwid=hw165877
    A molar pregnancy is thought to be caused by a problem with the genetic information of an egg or sperm. […] Things that may increase your risk of having a molar pregnancy include: Age. The risk for complete molar pregnancy is higher if you are 15 or younger or 35 or older. […] A history of molar pregnancy, especially if you’ve had two or more. […] A history of miscarriage. […] A diet low in carotene. Carotene is a form of vitamin A.
  • #11 Educational Case: Hydatidiform Molar Pregnancy
    https://pmc.ncbi.nlm.nih.gov/articles/PMC7863141/
    Several risk factors are associated with molar pregnancies. A history of prior molar pregnancy increases the risk of a repeat molar pregnancy to 1%, which is approximately 10 times the risk for the general population. The risk of a complete mole is the highest at extremes of maternal age (15 years and 35 years), and data suggest that ova from older women are more susceptible to abnormal fertilizations. The risk for a complete mole is twice as likely in women 35 years and 7 times as likely in women 40 years. The association with maternal age is mostly correlated with risk of complete molar pregnancy, while the risk of partial molar pregnancy varies very little with age. […] Molar pregnancy is treated with suction curettage in patients who wish to preserve fertility and patients are monitored with weekly -hCG measurements until undetectable.
  • #12 Molar pregnancy
    https://www.nhs.uk/conditions/molar-pregnancy/
    A molar pregnancy happens by chance. It’s not caused by either parent doing something wrong. […] You may be more likely to have a molar pregnancy if: you’re a young teenager or over 45 years old when you get pregnant; you’ve had a molar pregnancy before; you have an Asian background.
  • #13 Understanding Molar Pregnancy
    https://www.natera.com/resource-library/anora/understanding-molar-pregnancy/
    A molar pregnancy is a rare but serious condition that occurs in approximately 1 in 1,000 pregnancies. […] A molar pregnancy occurs when an error happens during fertilization, leading to an additional set of chromosomes from the father. […] In all cases, the resulting fertilized egg will have chromosomal abnormalities related to an extra set of chromosomes from the father. […] A molar pregnancy cannot be prevented and is not caused by anything a mother does or doesn’t do. […] Unfortunately, having one molar pregnancy increases the risk of a future molar pregnancy by 1-2%.
  • #14 Molar Pregnancy Information & Treatment
    https://www.columbiadoctors.org/health-library/condition/molar-pregnancy/
    A molar pregnancy means that tissue that normally becomes a fetus instead becomes a mass of abnormal tissue in your uterus. It is also called a hydatidiform mole. This abnormal tissue causes symptoms of pregnancy. […] Molar pregnancy is thought to be caused by a problem with the genetic information of an egg or sperm. There are two types of molar pregnancy: complete and partial. […] Complete molar pregnancy. An egg with no genetic information is fertilized by a sperm. It does not develop into a fetus. It continues to grow as a lump of abnormal tissue that looks a bit like a cluster of grapes and can fill the uterus. […] Partial molar pregnancy. An egg is fertilized by two sperm. The placenta develops into abnormal tissue. Any fetal tissue that forms is likely to have severe defects. […] Things that may increase your risk of having a molar pregnancy include: Age. The risk for complete molar pregnancy is higher if you are 15 or younger or 35 or older. […] A history of molar pregnancy, especially if you’ve had two or more. […] A history of miscarriage. […] A diet low in carotene. Carotene is a form of vitamin A.
  • #15 Molar Pregnancy: Signs, Symptoms & Treatment | Live Science
    https://www.livescience.com/55508-molar-pregnancy.html
    A molar pregnancy, also called hydatidiform mole, is an abnormal growth of placental tissue in a woman’s uterus. […] There doesn’t seem to be a reason why it occurs aside from a woman’s age, he said. Becoming pregnant before age 20 or after age 40 increases a woman’s risk of having a molar pregnancy, Schorge said. […] Both types are caused by an abnormally fertilized egg. […] In a complete molar pregnancy, the embryo does not develop but placental tissue grows rapidly into an abnormal mass. […] In a partial molar pregnancy, a woman releases a normal egg, but two sperm fertilize the egg instead of one. […] For the most part, doctors don’t truly know what causes a molar pregnancy, Schorge said. Some dietary theories, such as a deficiency of carotene, a plant pigment found in some red and orange fruits and vegetables that is converted by the body into vitamin A, have been proposed as one possible reason, he explained.
  • #16 Azthena logo with the word Azthena
    https://www.news-medical.net/health/Causes-of-Molar-Pregnancy.aspx
    A pregnancy that results in the formation of a hydatidiform mole is referred to as a molar pregnancy. A hydatidiform mole is produced by an abnormal conception, resulting from a chromosomal anomaly. […] Both types of molar pregnancy fail to produce a healthy living baby due to the chromosomal anomaly. […] Women who have had one molar pregnancy already have a 6-fold increased risk of having a recurrence, and those who have had more than two previous molar pregnancies have a 120-fold increased risk. Certain genes are associated with this recurrence risk, namely, maternal homozygous and compound heterozygous recessive, such as NLRP7 and KHDC3L. […] The tissue in the complete hydatidiform mole is usually diploid, but the entire DNA comes from the father. […] In the case of a partial mole, the tissue is triploid. Two copies of the DNA come from the father (diandric) and one from the mother. The mechanism is either dispermic fertilization or fertilization by a sperm whose chromosomes were not reduced.
  • #17 Hydatidiform Mole: Practice Essentials, Background, Pathophysiology
    https://emedicine.medscape.com/article/254657-overview
    A hydatidiform mole (molar pregnancy) is a gestational trophoblastic disease. […] A diet deficient in animal fat and carotene may be a risk factor. […] More recently, Japanese investigators identified a novel homozygous nonsense mutation in the NLRP7 gene (c.584GA; p.W195X) in a patient that appears to be associated with recurrent hydatidiform mole. […] Germ line mutations in NLRP7 and KhDCL3 have been identified as causative in recurrent molar pregnancies. […] A recurrent form of biparental mole, which is familial and appears to be inherited as an autosomal recessive trait, has been described. […] With a partial mole, fetal tissue is often present. […] The chromosomal complement is usually 69,XXX or 69,XXY. […] This results from fertilization of a haploid ovum and duplication of the paternal haploid chromosomes or from dispermy.
  • #18 Molar pregnancy – Wikipedia
    https://en.wikipedia.org/wiki/Molar_pregnancy
    A molar pregnancy, also known as a hydatidiform mole, is an abnormal form of pregnancy in which a non-viable fertilized egg implants in the uterus. […] The occurrence of a molar pregnancy can be attributed to the fertilized egg lacking an original maternal nucleus. […] A complete mole is caused by either a single sperm (90% of the time) or two sperm (10% of the time) combining with an egg that has lost its DNA. […] The cause of this condition is not completely understood. Potential risk factors may include defects in the egg, abnormalities within the uterus, or nutritional deficiencies. […] The diploid set of sperm-only DNA means that all chromosomes have sperm-patterned methylation suppression of genes. […] Most partial moles are triploid (three chromosome sets). […] A small percentage of hydatidiform moles have biparental diploid genomes, as in normal living persons; they have two sets of chromosomes, one inherited from each biological parent. […] Some of these moles occur in women who carry mutations in the gene NLRP7, predisposing them towards molar pregnancy.
  • #19 WHO EMRO | Short communication: Molar pregnancy and husband’s occupation: do soil and dust have any role? | Volume 14, issue 1 | EMHJ volume 14, 2008
    https://www.emro.who.int/emhj-volume-14-2008/volume-14-issue-1/article21.html
    This casecontrol study investigated the association between molar pregnancy and husbands work. […] The husbands of cases were more likely to have occupations involving physical work than non-physical work and this physical work more usually involved exposure to soil and dust. […] Among all occupations, the husbands of cases were more likely to have occupations which had exposure to soil and dust (P 0.01). […] Comparing all occupations that had exposure to soil and dust with all those who did not have this exposure (physical and non-physical) resulted in a statistically significant difference in the occurrence of molar pregnancy (P 0.001). […] Molar pregnancy (hydatidiform mole) is a pathological condition and has adverse effects on womens health. […] Although age, geographic location, ethnicity, low socioeconomic status, history of previous mole or abortion, history of oral contraceptive or intrauterine device use, blood group, radiation and artificial insemination have been suggested as risk factors, little is known about its etiology.
  • #20 WHO EMRO | Short communication: Molar pregnancy and husband’s occupation: do soil and dust have any role? | Volume 14, issue 1 | EMHJ volume 14, 2008
    https://www.emro.who.int/emhj-volume-14-2008/volume-14-issue-1/article21.html
    The aim of the present study was to evaluate the relationship between molar pregnancy and husbands occupation and the role of soil and dust. […] The results indicate that such a relationship exists. […] Therefore it is possible that a husbands occupation can influence gonads and germ cells, through exposure to some environmental factors, which may in turn lead to abnormal fertilization as occurs in molar pregnancy. […] Further research into the association between occupation and molar pregnancy is recommended with larger samples and investigation of the spermatogenesis and fertilization processes.
  • #21 Molar Pregnancy: Expert Explains Symptoms, Risk Factors, And Treatment Of This Rare Pregnancy Complication | OnlyMyHealth
    https://www.onlymyhealth.com/molar-pregnancy-symptoms-causes-risk-factors-diagnosis-treatment-and-post-follow-up-1715061755
    Molar pregnancy occurs when a fertilised egg does not develop normally. […] It is a rare complication that occurs when a fertilised egg doesn’t develop normally. Instead of a healthy embryo and placenta, abnormal tissue forms inside the uterus. […] Hydatidiform moles occur due to abnormal proliferation of trophoblasts and are of two subtypes – complete and partial, based on genetic and biopsy features, highlighted Dr Agarwal. […] According to a 2023 study, there is speculation that environmental elements, such as inadequate nutrition and high-altitude exposure may contribute to the onset of molar pregnancy, although further investigation is necessary to establish definitive findings. […] Dr Agarwal concluded, Molar pregnancies, while serious, are treatable. Molar pregnancies result from genetic problems that occur during conception that are beyond your control.
  • #22 Molar pregnancy – The Miscarriage Association
    https://www.miscarriageassociation.org.uk/information/molar-pregnancy/
    Molar pregnancy is a chance event. Doctors understand how it happens but there are no obvious underlying causes or risk factors, except a previous molar pregnancy. It just happens.
  • #23 Molar Pregnancy – Women’s Health Issues – Merck Manual Consumer Version
    https://www.merckmanuals.com/home/women-s-health-issues/cancers-of-the-female-reproductive-system/molar-pregnancy
    Most often, a molar pregnancy is an abnormal fertilized egg that develops into a hydatidiform mole rather than a fetus. A molar pregnancy may also develop from cells that remain in the uterus after a miscarriage, a full-term pregnancy, or a mislocated pregnancy (ectopic pregnancy). Rarely, a molar pregnancy develops when there is a living fetus. In such cases, the fetus typically dies, and a miscarriage often occurs. […] Molar pregnancies are a type of gestational trophoblastic disease. […] An abnormal fertilized egg or abnormal placental tissue can overgrow, causing symptoms similar to those of pregnancy, but the abdomen becomes larger more rapidly. […] Approximately 80% of cases of gestational trophoblastic disease are not cancerous. […] The rest tend to persist and start to invade surrounding tissue. Approximately 2 to 3% of hydatidiform moles develop into choriocarcinomas. Choriocarcinomas can spread quickly through the lymphatic vessels or bloodstream. […] If a molar pregnancy or another type of gestational trophoblastic disease is present, the level is usually very high because these tumors produce a large amount of this hormone. […] If the molar pregnancy tissue has spread widely and is considered high risk, doctors refer women to a specialist.