Uterus Pathology Study Guide

Infections of the Female Genital System
Summary of current evidences supporting the existence of stem cells in the female reproductive system. The existence of stem/progenitor cells is indicated in primary functional parts of the reproductive system, including ovary, uterus and cervix. Abbreviations: CD = Cluster of differentiation, MSC = Mesenchymal stem cell, SP = Side population. Normal and cancer stem cells of the human female reproductive system. López J, Valdez-Morales FJ, Benítez-Bribiesca L, Cerbón M, Carrancá AG - Reproductive biology and endocrinology : RB&E (2013). Not Altered. CC.

Uterus Pathology Video

Uterus

The uterus is responsible for incubating human life.

The mucosal lining of the uterus is called endometrium.

The endometrium is supported by a smooth muscular wall called the myometrium.

Hormonal sensitivity exists in the endometrium.

Estrogen drives the endometrium’s growth (proliferative phase).

Progesterone is responsible for preparing the endometrium for implantation (secretory phase).

Shedding happens when progesterone support is lost (menstrual phase).

  • Uterus
    Uterus. Different regions of Uterus displayed & labelled using a 3D medical animation still shot. Not altered. CC BY-SA 4.0

Asherman Syndrome

Asherman syndrome is secondary amenorrhea caused by the loss of the basal layer of the endometrium and scarring.

Asherman syndrome can be a complication of overaggressive dilation and curettage (D&C).

  • Asherman Syndrome
    Asherman Syndrome. Hysteroscopic view Floranerolia - Not altered. CC BY-SA 4.0

Anovulatory Cycle

An anovulatory cycle is a lack of ovulation.

An anovulatory cycle results in a proliferative phase driven by estrogen without a following secretory phase driven by progesterone.

Uterine bleeding results from the breakdown and shedding of proliferative glands.

Anovulatory cycle is a frequent reason for abnormal uterine bleeding, particularly around menarche and menopause.

  • Anovulatory Cycle
    Continuum of menstrual cycle disturbances.Notes: On the far left of the continuum is optimal menstrual health, which is characterized by regular ovulatory menstrual cycles that are 26–35 days in length. The subclinical/subtle menstrual cycle disturbances include luteal phase defects and anovulation, which represent the least severe disturbances. Menstrual cycles with a luteal phase defect are ovulatory but characterized by a short luteal phase and/or insufficient progesterone production during the luteal phase. Menstrual cycles in which ovulation does not occur and progesterone concentrations are notably low are called anovulatory cycles. It must be noted that cycles that have a luteal phase defect or are anovulatory frequently appear to be regular cycles due to intermenstrual intervals of normal length. The clinical/severe menstrual cycle disturbances include oligomenorrhea which is characterized by long, inconsistent intermenstrual intervals and amenorrhea, the most severe menstrual cycle disturbance, which is characterized by the absence of menses for at least 3 months. Current perspectives on the etiology and manifestation of the "silent" component of the Female Athlete Triad. Mallinson RJ, De Souza MJ - International journal of women's health (2014). Not Altered. CC.

Acute Endometritis

Acute endometritis is typically secondary to bacterial infection of the endometrium.

After baby delivery or miscarriage there may be retained fetal products.

Retained fetal products serve as an infection nidus.

Symptoms of acute endometritis include:

  • Fever
  • Abnormal uterine bleeding (AUB)
  • Pelvic pain
  • Acute Endometritis
    Acute Endometritis. Very high magnification micrograph of endometritis. H&E stain. Images show endometrium with abundant plasma cells (diagnostic for chronic endometritis) and scattered neutrophils. Related images High mag. Very high mag. High mag. Very high mag. Very high mag. Nephron Not altered. CC BY-SA 3.0

Chronic Endometritis

Chronic endometritis is inflammation of the endometrium.

Chronic endometritis is characterized by the presence of lymphocytes and plasma cells.

Given that lymphocytes are typically detected in the endometrium, plasma cells are required for the diagnosis of chronic endometritis.

Cause of chronic endometritis include:

  • Retained fetal products of conception
  • Chronic pelvic inflammatory illness
  • Intrauterine device presence

Chronic endometritis presents as:

  • Unusual uterine bleeding
  • Pain
  • Infertility
  • Chronic Endometritis
    (a) Plasma cells are not readily seen in H and E slide with mucosal odema of stroma H and E ×100; (b) Syndecan-1 showed numerous plasma cells in stroma. ×100; (c) H and E slide showing prominent spindle cell component. ×100; (d) Plasma cells easily identified in spindle cell component. ×100. Evaluation of endometrium for chronic endometritis by using syndecan-1 in abnormal uterine bleeding. Kannar V, Lingaiah HK, Sunita V - Journal of laboratory physicians (2012). Not Altered. CC.

Endometrial Polyp

An endometrial polyp is a hyperplastic protrusion of endometrium.

Endometrium polyps presents as unusual uterine bleeding.

Endometrial polyps may develop from adverse side effects of medications such as tamoxifen, which has mild pro-estrogenic effects on the endometrium but anti-estrogenic effects on the breast.

  • Endometrial Polyp
    Endometrial Polyp. Uterine polyps BruceBlaus - Not altered, CC BY-SA 4.0

Endometriosis

Endometriosis occurs outside of the uterine cavity endometrial lining.

Endometriosis mostly occurs due to retrograde menstruation with implantation at an ectopic site.

Symptoms of endometriosis include:

  • Pelvic discomfort
  • Dysmenorrhea

Complications of endometriosis include:

  • Infertility
  • Pain while urinating
  • Pain while defecating
  • Scarring increases the risk for ectopic tubal pregnancy

Endometriosis cycles (the same way as normal endometrium).

The ovary is the most frequently affected region by endometriosis, and this typically causes the development of a “chocolate” cyst.

Other sites of endometriosis involvement include:

  • Fallopian tube mucosa
  • Bladder wall
  • Intestine serosa
  • Pouch of Douglas
  • Uterine ligaments

Traditionally, endometriosis implants look like yellow-brown “gun-powder” nodules.

Adenomyosis is the medical term for endometriosis involvement of the uterine myometrium.

At the site of endometriosis, particularly in the ovary, there is an elevated chance of developing endometrial adenocarcinoma.

  • Endometriosis
    Endometriosis. Drawing showing endometriosis.  Bruce Blaus., Not altered. CC BY 3.0

Endometrial Hyperplasia

Endometrial gland hyperplasia is excessive growth of the endometrium.

Endometrial hyperplasia occurs due to increased amounts of estrogen.

Increased estrogen may be present from:

  • Obesity
  • Polycystic ovary syndrome (PCOS)
  • Estrogen replacement therapy

Endometrial hyperplasia typically manifests as uterine hemorrhage after menopause.

Histologically endometrial hyperplasia with cellular atypia is the most significant predictor of development to carcinoma.

Atypical simple hyperplasia frequently develops into cancer (30% of cases). 

Complex hyperplasia without atypia, on the other hand, seldom develops into carcinoma (5% of cases).

  • Endometrial Hyperplasia
    Endometrial Hyperplasia. Histopathology of complex hyperplasia with atypia: Closely packed endometrial glands with sparse intervening stroma and stratification of the lining epithelium. Epithelial cells show cytological atypia with high nucleocytoplasmic ratio, irregular clumping of nuclear chromatin, and mitotic figures. Shalinee Rao, Sandhya Sundaram, Raghavan Narasimhan - Not altered. CC BY 2.0

Endometrial Carcinoma

Endometrial carcinoma is the malignant proliferation of endometrial glands.

Endometrial carcinoma is a female vaginal tract invasive cancer, which is most prevalent.

Endometrial carcinoma presents as bleeding after menopause.

Endometrial carcinoma occurs through two different ways:

  • Sporadic
  • Hyperplastic

Carcinoma may develop from endometrial hyperplasia.

Risk factors for endometrial carcinoma are linked to estrogen exposure such as:

  • Early menarche
  • Late menopause
  • Obesity
  • Nulliparity
  • Infertility with anovulatory cycles

Endometrial carcinoma typically presents around 60-years-old.

Histology of endometrial carcinoma is usually full of abnormal endometrioid cells.

In 25 percent of cases, the sporadic pathway, cancer develops in an atrophic endometrium without any obvious antecedent lesions.

P53 mutation is frequent, and the tumor behaves aggressively.

  • Endometrial Carcinoma
    Endometrial Carcinoma.

Leiomyoma

Leiomyomas are also called fibroids.

Leiomyomas are the most typical female tumor is a benign neoplastic growth of smooth muscle that arises from the myometrium.

Leiomyomas are associated with estrogen exposure.

Leiomyomas are prevalent in premenopausal females.

Leiomyomas may enlarge during pregnancy.

Leiomyomas shrink after menopause.

On a gross examination, leiomyomas have, white, whorled, round masses that could encroach on the pelvic tissues and deform the uterus.

Leiomyomas are typically asymptomatic.

When symptoms from leiomyomas exist they typically include:

  • Abnormal uterine bleed (AUB)
  • Abdominal distension
  • Bloating
  • Infertility
  • Leiomyoma
    Leiomyoma. Leiomyoma From a uterine myomectomy Ed Uthman Not altered. CC By 2.0

Leiomyosarcoma

Leiomyosarcomas are tumors of myometrial smooth muscle that have become malignant.

Leiomyosarcomas arises de novo.

Leiomyosarcomas do not develop from leiomyomas.

Leiomyosarcomas normally occur in postmenopausal females.

Leiomyosarcomas typically show a single lesion with areas of necrosis and bleeding is frequently visible on a gross exam.

Histologic features of leiomyosarcomas include:

  • Necrosis
  • Multiple mitoses
  • Cellular atypia
  • Leiomyosarcoma
    Leiomyosarcoma. Histopathology of leiomyosarcoma shows variable atypia, often with cytoplasmic vacuoles at both ends of nuclei, and frequent mitoses. Eiji Kobayashi, Takuhei Yokoyama, Satoshi Nakagawa, Shinya Matsuzaki, Toshihiro Kimura, Yutaka Ueda, Kiyoshi Yoshino, Masami Fujita, Yumiko Hori, Eiichi Morii and Tadashi Kimura. Not altered. CC BY 4.0