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Dysfunctional Uterine Bleeding Clinical Presentation


Author: Millie A Behera, MD; Chief Editor: Richard Scott Lucidi, MD, FACOG more...
Updated: Sep 29, 2014

History

Suspect dysfunctional uterine bleeding (DUB) when a patient presents with


unpredictable or episodic heavy or light bleeding despite a normal pelvic
examination.
Note the following:

Typically, the usual moliminal symptoms that accompany ovulatory cycles will
not precede bleeding episodes.
Exclude the diagnosis of pregnancy first.
Address the presence of local and systemic disease. Rule out the presence
of signs or symptoms indicative of bleeding disorders. Screening for personal
and family history of easy bruising, bleeding gums, epistaxis, and excessive
bleeding episodes during childbirth, surgery, or dental procedures may be
useful.
Rule out iatrogenic causes of bleeding, including bleeding secondary to
steroid hormone contraception, hormone replacement therapy, or other
hormone treatments, which are common causes.
Most patients are adolescents or are older than 40 years.

Patients who report irregular menses since menarche may have polycystic ovarian
syndrome (PCOS). PCOS is characterized by anovulation or oligo-ovulation and
hyperandrogenism. These patients often present with unpredictable cycles and/or
infertility, hirsutism with or without hyperinsulinemia, and obesity.

Patients with adrenal enzyme defects, hyperprolactinemia, thyroid disease, or other


metabolic disorders also might present with anovulatory bleeding.

Physical

The physical examination can elicit several anatomic and organic causes of
abnormal uterine bleeding.

A complete physical examination should begin with assessment of hemodynamic


stability (vital signs) and proceed with evaluation of the following:

Obesity (BMI)
Signs of androgen excess (hirsutism, acne)
Thyroid enlargement or manifestations of hyperthyroidism or hypothyroidism.
Galactorrhea (may suggest hyperprolactinemia)
Visual field deficits (raise suspicion of intracranial/pituitary lesion)
Ecchymosis, purpura (signs of bleeding disorder)
Signs of anemia or chronic blood loss
A careful gynecologic examination, including Papanicolaou test (Pap smear)
and sexually transmitted disease (STD) screening, is warranted.
The hallmark of DUB is a negative pelvic examination despite the clinical
history. In such cases, management might rest on a clinical diagnosis. Rule
out the presence of uterine fibroids or polyps, as well as rule out endometrial
hyperplasia or carcinoma.

Causes

In ovulatory cycles, progesterone production from the corpus luteum converts


estrogen primed proliferative endometrium to secretory endometrium, which sloughs
predictably in a cyclic fashion if pregnancy does not occur. Heavy but regular uterine
bleeding implies ovulatory bleeding and should not be diagnosed as DUB. Subtle
disturbances in endometrial tissue mechanisms, other forms of uterine pathology, or
systemic causes might be implicated.
Anovulatory cycles are associated with a variety of bleeding manifestations.
Estrogen withdrawal bleeding and estrogen breakthrough bleeding are the most
common spontaneous patterns encountered in clinical practice. Iatrogenically
induced anovulatory uterine bleeding might occur during treatment with oral
contraceptives, progestin-only preparations, or postmenopausal steroid replacement
therapy.
Estrogen breakthrough bleeding\\ Anovulatory cycles have no corpus luteal
formation. Progesterone is not produced. The endometrium continues to proliferate
under the influence of unopposed estrogen.

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Eventually, this out-of-phase endometrium is shed in an irregular manner that might


be prolonged and heavy. This pattern is known as estrogen breakthrough bleeding
and occurs in the absence of estrogen decline.

Estrogen withdrawal bleeding

This frequently occurs in women approaching the end of reproductive life. In older
women, the mean length of menstrual cycle is shortened significantly due to
aberrant follicular recruitment, resulting in a shortened proliferative phase. Ovarian
follicles in these women secrete less estradiol. Fluctuating estradiol levels might
lead to insufficient endometrial proliferation with irregular menstrual shedding. This
bleeding might be experienced as light, irregular spotting.
Eventually, the duration of the luteal phase shortens, and, finally, ovulation stops.
Dyssynchronous endometrial histology with irregular menstrual shedding and
eventual amenorrhea result.

Oral contraceptives, progestin-only preparations, or


postmenopausal steroid replacement therapy

Treatment with oral contraceptives, progestin-only preparations, or postmenopausal


steroid replacement therapy might be associated with iatrogenically induced uterine
bleeding.
Progesterone breakthrough bleeding occurs in the presence of an unfavorably high
ratio of progestin to estrogen.
Intermittent bleeding of variable duration can occur with progestin-only oral
contraceptives, depo-medroxyprogesterone, and depo-levonorgestrel.

rogesterone withdrawal bleeding can occur if the endometrium initially has been
primed with endogenous or exogenous estrogen, exposed to progestin, and then
withdrawn from progestin. Such a pattern is seen in cyclic hormonal replacement
therapy.

Adolescents

The primary defect in the anovulatory bleeding of adolescents is failure to mount an


ovulatory luteinizing hormone (LH) surge in response to rising estradiol levels.
Failure occurs secondary to delayed maturation of the hypothalamic-pituitary axis.
Because a corpus luteum is not formed, progesterone levels remain low.

The existing estrogen primed endometrium does not become secretory. Instead, the
endometrium continues to proliferate under the influence of unopposed estrogen.
Eventually, this out-of-phase endometrium is shed in an irregular manner that might
be prolonged and heavy, such as that seen in estrogen breakthrough bleeding.

Climacteric

Anovulatory bleeding in menopausal transition is related to declining ovarian


follicular function.

Estradiol levels will vary with the quality and state of follicular recruitment and
growth. Bleeding might be light or heavy depending on the individual cycle
response.

Bleeding disorders

An international expert panel including obstetrician/gynecologists and hematologists


has issued guidelines to assist physicians in better recognizing bleeding disorders,
such as von Willebrand disease, as a cause of menorrhagia and postpartum
hemorrhage and to provide disease-specific therapy for the bleeding disorder.[2]
Historically, a lack of awareness of underlying bleeding disorders has led to
underdiagnosis in women with abnormal reproductive tract bleeding. The panel
provided expert consensus recommendations on how to identify, confirm, and
manage a bleeding disorder.

An underlying bleeding disorder should be considered when a patient has any of the
following:
Menorrhagia since menarche
Family history of bleeding disorders
Personal history of 1 or more of the following: (1) Notable bruising without
known injury; (2) bleeding of the oral cavity or gastrointestinal tract without
obvious lesion; or (3) epistaxis greater than 10 minutes duration (possibly
necessitating packing or cautery)

If a bleeding disorder is suspected, consultation with a hematologist is suggested.


Differential Diagnoses

Contributor Information and Disclosures

Author
Millie A Behera, MD Assistant Professor (Adjunct), Division of Reproductive Endocrinology and Fertility,

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Dysfunctional Uterine Bleeding Clinical Presentation: History, Physical,...

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Department of Obstetrics and Gynecology, Duke University Medical Center; Medical Director, Bloom Reproductive
Institute
Millie A Behera, MD is a member of the following medical societies: American College of Obstetricians and
Gynecologists, American Society for Reproductive Medicine, AAGL
Disclosure: Nothing to disclose.

Coauthor(s)
Thomas Michael Price, MD Associate Professor, Division of Reproductive Endocrinology and Infertility,
Department of Obstetrics and Gynecology, Director of Reproductive Endocrinology and Infertility Fellowship
Program, Duke University Medical Center
Thomas Michael Price, MD is a member of the following medical societies: Alpha Omega Alpha, American
College of Obstetricians and Gynecologists, Phi Beta Kappa, Society for Reproductive Investigation, Society for
Reproductive Endocrinology and Infertility, American Society for Reproductive Medicine
Disclosure: Received research grant from: Insigtec Inc<br/>Received consulting fee from Clinical Advisors Group
for consulting; Received consulting fee from MEDA Corp Consulting for consulting; Received consulting fee from
Gerson Lehrman Group Advisor for consulting; Received honoraria from ABOG for board membership.
Specialty Editor Board
Francisco Talavera, PharmD, PhD Adjunct Assistant Professor, University of Nebraska Medical Center College
of Pharmacy; Editor-in-Chief, Medscape Drug Reference
Disclosure: Received salary from Medscape for employment. for: Medscape.

Frances E Casey, MD, MPH Director of Family Planning Services, Department of Obstetrics and Gynecology,
VCU Medical Center
Frances E Casey, MD, MPH is a member of the following medical societies: American College of Obstetricians
and Gynecologists, Association of Reproductive Health Professionals, Society of Family Planning, National
Abortion Federation, Physicians for Reproductive Health
Disclosure: Nothing to disclose.

Chief Editor
Richard Scott Lucidi, MD, FACOG Associate Professor of Reproductive Endocrinology and Infertility,
Department of Obstetrics and Gynecology, Virginia Commonwealth University School of Medicine
Richard Scott Lucidi, MD, FACOG is a member of the following medical societies: American College of
Obstetricians and Gynecologists, American Society for Reproductive Medicine
Disclosure: Nothing to disclose.

Additional Contributors
Anthony Charles Sciscione, DO Professor, Department of Obstetrics and Gynecology, Drexel University College
of Medicine; Director, Maternal and Fetal Medicine, Christiana Care Health System; Director, Delaware Center for
Maternal and Fetal Medicine
Anthony Charles Sciscione, DO is a member of the following medical societies: American College of Obstetricians
and Gynecologists, American Medical Association
Disclosure: Nothing to disclose.

Acknowledgements
The authors and editors of Medscape Drugs & Diseases gratefully acknowledge the contributions of previous
author John T Queenan, Jr, MD, to the development and writing of this article.

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