THE FEMALE GENITAL TRACT AND BREAST - PowerPoint PPT Presentation

1 / 114
About This Presentation
Title:

THE FEMALE GENITAL TRACT AND BREAST

Description:

THE FEMALE GENITAL TRACT AND BREAST Li chun Genital Tract Anatomy Cervix Uterus Fallopian tubes Ovaries HISTOLOGY Ovary cortex, follicles in varying stages of ... – PowerPoint PPT presentation

Number of Views:805
Avg rating:3.0/5.0
Slides: 115
Provided by: Cyl9
Category:
Tags: and | breast | female | genital | the | tract | ring | vaginal

less

Transcript and Presenter's Notes

Title: THE FEMALE GENITAL TRACT AND BREAST


1
THE FEMALE GENITAL TRACT AND BREAST
  • Li chun
  • ??

2
Genital Tract Anatomy
  • Cervix
  • Uterus
  • Fallopian tubes
  • Ovaries

3
HISTOLOGY
  • Ovary
  • cortex, follicles in varying stages of maturation
    are found within the outer cortex
  • medulla, made up of a more loosely arranged
    mesenchymal tissue and may contain small clusters
    of round to polygonal, epithelial-appearing cells
    around vessels and nerves

4
  • Cervix
  • Divided into the vaginal portion and the
    endocervix. The vaginal portion is covered by a
    stratified nonkeratinizing squamous epithelium
    continuous with the vaginal vault. Endocervix is
    lined by columnar, mucus-secreting epithelium
    that dips down into the underlying stroma to
    produce crypts.
  • Transformation zone a combination of ingrowth of
    the squamous epithelium portion are intrinsic
    squamous differentiation of subcolumnar reserve
    cells(squamous metaplasia) transforms this area
    into squamous epithelium

5
Slide 24.2
6
Slide 24.3
7
  • During reproductive life, the squamocolumnar
    junction migrates cephalad on the leading edge of
    the transformation zone and may be invisible to
    the naked eye after menopause.
  • The uterus endometrial changes that occur during
    the menstrual cycle are keyed to the rise and
    fall in the levels of ovarian hormones

8
Cervix
  • Inflammations
  • Acute and Chronic Cervicitis
  • Some degree of cervical inflammation may be
    found in virtually all multiparous and in many
    nulliparous adult women, and it is usually of
    little clinical consequence

9
  • Morphology The pathologic correlates of acute
    and chronic cervicitis include intercellular
    edema, submucosal edema, and a combination of
    epithelial and stromal changes. Acute cervicitis
    includes acute inflammatory cells, erosion, and
    reactive or reparative epithelial change. Chronic
    cervicitis includes inflammation, usually
    mononuclear, with lymphocytes, macrophages, and
    plasma cells

10
Slide 24.15
11
Slide 24.16
12
  • Endocervical Polyps
  • Most polyps arise within the endocervical
    canal and vary from small and sessile to large,
    5-cm masses that may protrude through the
    cervical os. All are soft, almost mucoid, and are
    composed of a loose fibromyxomatous stroma
    harboring dilated, mucus-secreting endocervical
    glands often accompanied by inflammation and
    squamous metaplasia. In almost all instances,
    simple curettage or surgical excision effects a
    cure

13
Slide 24.17
14
  • Intraepithelial and invasive squamous neoplasia
  • Pathogenesis
  • Sexually transmitted agent
  • Early age at first intercourse
  • Multiple sexual partners
  • A male partner with multiple previous
  • sexual partners
  • Papillomaviruses(HPV) There is mounting
    evidence linding HPV to cancer in general and
    cervical cancer in particular. But the evidence
    does not implicate HPV as the only factor. A high
    percentage of young women are infected with one
    or more HPV types during their reproductive
    years, and only a few develop cancer.

15
  • Cervical Intraepithelial Neoplasia (precancerous
    changes)
  • (1) they represent a continuum of morphologic
    change with relatively indistinct boundaries
  • (2) they will not invariably progress to
    cancer and may spontaneously regress, with the
    risk of persisting or progressing to cancer
    increasing with the severity of the precancerous
    change
  • (3) they are associated with papillomaviruses,
    and high-risk HPV types are found in increasing
    frequency in the higher grade precursors

16
  • Morphology
  • CIN(cervical intraepithelial neoplasia)
    classification
  • CIN? atypical cells in the lower layers of
    the squamous epithelium, involved less than 1/3
    layers
  • CIN ? the range of atypical cells involved
    less than 2/3 squamous epithelium layers, but
    more than 1/3 layers
  • CIN ? atypical cells involved more and more
    layers of the epithelium, until it is totally
    replaced by immature atypical cells ( carcinoma
    in situ)

17
  • Atypical cell show changes in nucleocytoplasmic
    ratio varation in nuclear size loss of
    polarity increased mitotic figures, including
    abnormal mitoses and hyperchromasiain other
    words, they take on some of the characteristics
    of malignant cells

18
Normal
CIN I
CIN II
CIN III
Slide 24.21
19
Squamous Cell Carcinoma
  • may occur at any age from the second decade of
    life to senility. The peak incidence in occurring
    at an increasingly younger age 40 to 45 years

20
  • Morphology
  • Invasive cervical carcinoma manifests in three
    somewhat distinctive patterns
  • fungating (or exophytic)
  • ulcerating
  • infiltrative cancer

21
  • On histologic examination
  • (1) large cell, either keratinizing(well-differ
    entiated) or nonkeratinizing (moderately
    diffferentiated), about 95
  • (2) small cell undifferentiated carcinomas
    (neuroendocrine or oat cell carcinomas)
  • Ten per cent to 25 of cercical carcinomas
    constitute adenocarcinomas, adenosquamous
    carcinomas, undifferentiated carcinomas. They
    look grossly and behave like the squamous cell
    lesions, but arise in a slightly older age group

22
Slide 24.26
23
  • Cervical cancer is staged as follows
  • stage0 Carcinoma in situ(CIN )
  • stage? Carcinoma confined to the cervix
  • stage? Carcinoma extends beyond the cervix
    but not onto the pelvic wall. Carcinoma involves
    the vagina but not the lower third.
  • stage? Carcinoma has extended onto pelvic
    wall. On rectal examination, there is no
    cancer-free space between the tumor and the
    pelvic wall. The tumor involves the lower third
    of the vagina
  • stage? Carcinoma has extended beyond the
    true pelvis or has involved the mucosa of the
    bladder or rectum. This stage obviously includes
    those with metastatic dissemination

24
  • Spread(1)direct extension into contiguous
    tissues, including the peritoneum, urinary
    bladder, uterus, rectum, and vagina.
  • (2)spread through lymphatics
  • (3)spread through blood vessel

25
  • Clinical Course
  • Diagnosis cytologic examination merely detects
    the possible presence of a cervical precancer or
    cancer it does not make an absolute diagnosis,
    which requires histologic evaluation of
    appropriate biopsy specimens
  • Ultimately, when these cancers become clinically
    overt, they usually produce irregular vaginal
    bleeding, leukorrhea, bleeding or pain on coitus,
    and dysuria

26
  • Treatment
  • Precarcinoma cryotherapy, laser, wire loop
    excision, and cone biopsy
  • Invasive cancers usually result in hysterectomy
    and, for advanced lesions, radiation
  • with current methods of treatment, there is a
    5-year survival rate of about 80 to 90 with
    stage?, 75 with stage?, 35 with stage?, and 10
    to 15 with stage?

27
Endometrial Hyperplasia
  • Endometrial histology in the menstrual cycle

28
  • Endometrial hyperplasia is related to an
    abnormally high, prolonged level of estrogenic
    stimulation with diminution or absence of
    progestational activity. Thus, hyperplasia occurs
    most commonly around menopause or in association
    with persistent anovulation in younger women.

29
  • Morphology
  • Gross appearance endometrium thicken polyp
  • Histologic appearance
  • Simple hyperplasia, also known as cystic or
    mild hyperplasia, is characterized by the
    presence of architectural alterations in glands
    of various sizes, producing irregularity in gland
    shape with cystic alterations. The epithelial
    growth pattern and cytology are similar to
    proliferative endometrium. The stroma between
    glands is also frequently increased.

30
  • Complex hyperplasia, also known as adenomatous
    hyperplasia without atypia, exhibits an increase
    in the number and size of endometrial glands,
    with gland crowding and a disparity in their size
    and irregularity in their shape
  • Atypical hyperplasia, or adenomatous hyperplasia
    with atypia. In addition to glandular crowding
    and complexity, epithelial lining is irregular,
    characterized by stratification, scalloping and
    tufting, most cells are atypia. In one study, 23
    of patients with atypical hyperplasias eventually
    developed adenocarcinoma.

31
Slide 24.35
32
Slide 24.36
33
Carcinoma of The Endometrium
  • Endometrial carcinoma is the most common invasive
    cancer of the female genital tract. endometrial
    cancers arise mainly in postmenopausal women,
    causing abnormal bleeding.

34
  • Morphology
  • gross apearance
  • localized polypoid tumor
  • diffuse tumor (involving the entire
  • endometrial surface)

35
  • Histologic appearance most endometrial
    carcinomas(about 85) are adenocarcinomas. Tow
    per cent to 20 of endometrioid carcinomas
    contain foci of squamous differentiation.
    Squamous elements most commonly are
    histologically benign in appearance(called
    adenoacanthoma).less commonly, poorly
    differentiated endometrioid carcinomas contain
    squamous elements that appear frankly malignant.
    Such tumors have also been termed adenosquamous
    carcinomas

36
Slide 24.38
37
Leiomyomas
  • Morphology
  • In gross appearance, leiomyomas are sharply
    circumscribed, discrete, round, firm, gray-white
    tumors varying in size from small, barely visible
    nodules to massive tumors that fill the pelvis.
    They can occur within the myometrium(intramural),
    just beneath the endometrium (submucosal), or
    beneath the serosa (subserosal). The cut section
    usually makes characteristic pattern of smooth
    muscle bundles.

38
  • On histologic examination, the leiomyoma is
    composed of whorled bundles of smooth muscle
    cells that resemble the architecture of the
    uninvolved myometrium.mitotic figures are scarce
  • Clinical courseLeiomyomas of the uterus, even
    when they are extensive, may be asymptomatic. The
    most important symptoms are produced by
    submucosal leiomyomas (abnormal bleeding),
    compression of the bladder, sudden pain if
    disruption of blood supply occurs, and impaired
    fertility

39
Slide 24.39
40
Overian Tumors
41
Tumors of Surface (Coelomic) Epithelium
  • Serous Tumors
  • These common cystic neoplasms are lined by
    tall, columnar, ciliated epithelial cells and are
    filled with clear serous fluid. Together the
    benign, borderline, and malignant types account
    for about 30 of all ovarian tumors. About 75
    are benign or of borderline malignancy, and 25
    are malignant. Serous cystadenocarcinomas account
    for approximately 40 of all cancers of the ovary
    and are the most common malignant ovarian tumors

42
  • Morphology
  • Gross appearance
  • Serous tumor has one or a few fibrous walled
    cysts averaging 10 to 15 cm in diameter and
    occasionally up to 40 cm.
  • Benign tumors contain a smooth glistening cyst
    wall with no epithelial thickening or small
    papillary projections

43
  • . Borderline tumors contain an increasing amount
    of papillary projections. Larger amounts of solid
    or papillary tumor mass, irregularity in the
    tumormass, and fixation or nondularity of the
    capsule are all important indicators of probable
    malignancy. Bilaterality is common, occurring in
    20 of benign cystadenomas, 30 of borderline
    tumors, and approximately 66 of
    cystadenocarcinomas.

44
Slide 24.43
45
Slide 24.47
46
  • Histologic appearance the lining epithelium is
    composed of columnar epithelium with abundant
    cilia in benign tumors. Borderline malignancy
    contain increased complexity of the stromal
    papillae with stratification of the epithelium
    and nuclear atypia, but destructive infiltrative
    growth into the stroma is not seen.

47
  • Cystadenocarcinomas exhibit even more complex
    growth with infiltration or frank effacement of
    the underlying stroma by solid growth. Concentric
    calcifications (psammoma bodies) characterize
    serous tumors.

48
Slide 24.44
49
Slide 24.45
50
Slide 24.46
51
  • Clinical course the biologic behavior of serous
    tumors depends on both degree of differentiation
    and distribution. Most benign tumor is no
    symptoms. Borderline tumors are no symptoms, or
    slowly spread, producing intestinal obstruction
    or other complications after many years. Frank
    carcinomas infiltrate the soft tissue and form
    large intra-abdominal masses and rapid
    deterioration.

52
  • Mucinous Tumors
  • These tumors are less common, accounting for
    about 25 of all ovarian neoplasms. They occur
    principally in middle adult life and are rare
    before puberty and after menopause

53
  • Morphology
  • Gross appearance characterized by more cysts of
    variable size and a rarity of surface involvement
    and are less frequently bilateral. They appear
    grossly as multiloculated tumors filled with
    sticky, gelatinous fluid rich in glycoproteins

54
  • Histologic appearance benign mucinous tumors
    are characterized by a lining of tall columnar
    epithelial cells with apical mucin and the
    absence of cilia, akin to benign cervical or
    intestinal epithelia.

55
  • Borderline tumors exhibit abundant glandlike or
    papillary growth with nuclear atypia and
    stratification and are strikingly similar to
    tubular adenomas or villous adenomas of the
    intestine.

56
  • Cystadenocarcinomas contain more solid growth
    with conspicuous epithelial cell atypia and
    stratification, loss of gland architecture, and
    necrosis and are similar to colinic cancer in
    appearance.

57
Slide 24.48
58
Teratomas
  • Teratomas are divided into three categories
  • (1)mature (benign)
  • (2) immature (malignant)
  • (3) monodermal or highly specialized

59
  • Mature Teratomas
  • Most benign teratomas are cystic and are better
    known in clinical parlance as dermoid cysts.
    These neoplasms are presumably derived from the
    ectodermal differentiation of totipotential
    cells. Cystic teratomas are usually found in
    young women during the active reproductive year.

60
  • Morphology
  • In gross appearance, benign teratomas are
    bilateral in 10 to 15 of cases.
    Characteristically, they are unilocular cysts
    containing hair and cheesy sebaceous material. On
    section, they reveal a thin wall lined by an
    opaque, gray-white wrinkled, apparent epidermis.
    From this epidermis hair shafts frequently
    protrude. Within the wall, it is common to find
    tooth structures and areas of calcification

61
Slide 24.52
62
  • On histologic examination, the cyst wall is
    composed of stratified squamous epithelium with
    underlying sebaceous glands, hair shafts, and
    other skin adnexal structures. In most cases,
    structure from other germ layers can be
    identified, such as cartilage, bone, thyroid
    tissue, and other organoid formations

63
Slide 24.53
64
  • Immature malignant teratomas
  • These are rare tumors that differ from benign
    teratomas in that the component tissue resembles
    that observed in the fetus or embryo rather than
    the adult. The tumor is found chiefly in
    prepubertal adolescents and young women, the mean
    age being 18 years

65
  • Morphology
  • In gross appearance, the tumors are bulky and
    have a smooth external surface. On section, they
    have a solid or predominantly solid structure.
    There are areas of necrosis and hemorrhage. Hair,
    grumous material, cartilage, bone, and
    calcification may be present

66
  • On microscopic examination, there are varying
    amounts of immature tissue differentiation toward
    cartilage, glands, bone, muscle, nerve, and
    others. An important risk for subsequent
    extraovarian spread is the histologic grade of
    tumor, which is based on the proportion of tissue
    containing immature neutoepithelium

67
Slide 24.54
68
  • Immature teratomas grow rapidly and frquently
    penetrate the capsule with spread or metastases

69
Gestational and Placental Disorders
  • Hydatidiform Mole (Complete and Partial)
  • Pathogenesis Cytogenetic studies of these moles
    show

70
Slide 24.68
71
  • Morphology
  • Gross appearance In most instances, moles
    develop within the uterus, but they may occur in
    any ectopic site of pregnancy. The uterine cavity
    is filled with a delicate, friable mass of
    thin-walled, translucent, cystic, grapelike
    structures. Fetal parts are frequently seen in
    partial moles but are never found in complete
    moles.

72
Slide 24.70
73
  • On microscopic examination, the complete mole
    shows hydropic swelling of most chorionicvilli
    and virtual absence or inadequate development of
    vascularization of villi. The central substance
    of the villi is a loose, myxomatous, edematous
    stroma, and they may be covered by a layer of
    chorionic epithelium, both cytotrophoblast and
    syncytiotrophoblast. In partial moles, the
    villous edema involves only a proportion of
    villi, and the trophoblastic proliferation is
    focal and slight.

74
Slide 24.71
75
  • Clinical Course
  • Most patients have abnormal uterine bleeding
    uterine enlargement more rapid than anticipated.
    Ultrasound examination permits a definitive
    diagnosis in most cases. Once the diagnosis is
    made, the mole must be removed by thorough
    curettage. From many studies, it is clear that
    80 to 90 of these moles remain benign and give
    no further difficulty. Ten per cent develop into
    invasive moles and 2.5 into choriocarcinoma

76
  • Invasive Mole
  • Defined as a mole that penetrates and may even
    perforate the uterine wall. There is invasion of
    the myometrium by hydropic chorionic villi,
    accompanied by proliferation of both
    cytotrophoblast and syncytiotrophoblast.

77
  • The tumor is locally destructive and may invade
    parametrial tissue and blood vessels. Hydropic
    villi may embolize to distant sites, such as
    lungs and brain, but do not grow in these organs
    as true metastases, and even before the advent of
    chemotherapy, they eventually regressed unless
    fatal hemorrhage occurred. The tumor is
    manifested clinically by vaginal bleeding and
    irregular uterine enlargement, persisting
    elevated human chorionic gonadotropin level. The
    tumor responds well to chemotherapy.

78
Slide 24.72
79
  • Choriocarcinoma
  • These is an epithelial malignant neoplasm of
    trophoblastic cells. Choriocarcinoma is a rapidly
    invasive, widely metastasizing malignant
    neoplasm, but once it is identified, it responds
    well to chemotherapy

80
  • Morphology
  • Gross appearance a soft, fleshy, yellow-white
    tumor with a marked tendency to form large pale
    areas of ischemic necrosis, foci of cystic
    softening, and extensive hemorrhage

81
  • Histologic appearance a purely epithelial
    cellular malignancy that does not produce
    chorionic villi and that grows by the abnormal
    proliferation of both cytotrophoblast and
    syncytiotrophoblast. The tumor invades
    myometrium, frequently penetrates blood vessels
    and lymphatics, and in some cases extends out
    onto the uterine serosa and adjacent structure.
    In its rapid growth, it is subject to hemorrhage,
    ischemic necrosis, and secondary inflammatory
    infiltration.

82
Slide 24.73
83
  • In fatal cases, metastases are found in the
    lungs, brain, bone marrow, liver, and other
    organs. On occasion, metastatic choriocarcinoma
    is discovered without a detectable primary in the
    uterus, presumably because the primary has
    undergone total necrosis

84
The Female Breast
85
Slide 25.2
86
Slide 25.5
87
  • Fibrocystic Changes
  • These are common disease disorder of the breast,
    and it is found frequently between the ages of 20
    to 40 years. There are three principal patterns
    of morphologic change (1) cyst formation, often
    with apocrine metaplasia (2) fibrosis and (3)
    adenosis

88
  • Morphology
  • Cysts in gross appearance, there are numerous
    small cysts within one or bilateral breast. On
    microscopic examination, cysts are lined by
    columnar epithelium (in larger cysts, lining
    cells may be flattened or may be totally
    atrophic). Frequently, cysts are lined by large
    polygonal cells resembling the apocrine
    epithelium of sweat glands(apocrine metaplasia)

89
Slide 25.10
90
  • Fibrosis cysts frequently rupture with release
    of secretory material into the adjacent stroma.
    The resulting chronic inflammation and scarring
    fibrosis contribute to the palpable formness of
    the breast.

91
  • Adenosis Adenosis is recognized as an increase
    in the number of acinar units per lobule. The
    gland lumens are often enlarged (blunt duct
    adenosis) and are not distorted as is seen in the
    distinctly proliferative lesion. Calcifications
    are occasionally present within lumens.

92
Proliferative breast disease
  • Epithelial hyperplasia
  • Morphology Epithelial hyperplasia is usually not
    grossly evident. The proliferating epithelium
    takes the form of solid masses extending and
    encroaching into the duct lumen, partially
    obliterating into the duct lumens (fenestrations)
    can usually be discerned at the periphery of the
    cellular masses. Various degrees of cellular and
    architectural atypia may be present (atypical
    hyperplasia)

93
Slide 25.11
94
  • Sclerosing Adenosis
  • Morphology
  • On gross inspection, areas of sclerosing adenosis
    sometimes have a hard cartilaginous consistency
    that begins to approximate that found in breast
    cancer. On section, the involved area is not well
    localized and does not have the chalky
    yellow-white foci and streaks that identify
    breast carcinoma, an important gross differential
    feature.

95
  • On histologic examination, the number of acine
    per terminal duct is increased. The lobuar
    arrangement is maintained. The acini are
    compressed and distorted in the central portions
    of the lesion but characteristically dilated at
    the periphery. Myoepithelial cells are often
    prominent. On occasion, stromal fibrosis may
    totally compress the lumens to create the
    appearance of solid cords or double strands of
    cells lying with dense stroma

96
Slide 25.12
97
  • Current evidence suggests that the increased risk
    of cancer is proportional to the type of
    proliferative breast disease and to the presence
    of atypia. Fortunately, among women undergoing
    breast biopsies for benign disease, about 50
    with proliferative changes, only 5 to 10 will
    have atypical hyperplasia. Of the latter, less
    than 15 will develop cancer.

98
Cancinoma of The Breast
  • Among breast carcinomas small enough for their
    general areas of origin to be identified,
    approximately 50 arise in the upper outer
    quadrant 10 in each of the remaining quadrants
    and about 20 in the central or subareolar
    region. Carcinoma is divided into noninvaseve or
    in situ carcinomas and invasive carcinomas.

99
In Situ Carcinoma
  • Ductal Carcinoma In Situ (DCIS)
  • DCIS are divided into comedocarcinoma and
    noncomedo DCIS
  • Comedocarcinoma is characterized by solid sheets
    of high-grade malignant cells and central
    necrosis. The necrosis commonly calcifies.
    Punctate areas of necrotic material
    (comedone-like) can be seen grossly.

100
Slide 25.18
101
  • Noncomedo DCIS can have nuclear grades ranging
    from low to high. Calcifications are seen
    associated with central necrosis, but more
    commonly when there are intraluminal secretions.
    The cells appear monomorphic. In cribriform DCIS,
    intraepithelial spaces are evenly distributed and
    regular in shape. Papillary DCIS typically lacks
    the normal myoepithelial cell layer.
    Micropapillary DCIS is recognized by bulbous
    protrusions without a fibrovascular core, often
    forming complex intraductal patterns.

102
Slide 25.19
103
  • Lobular Carcinoma In Situ (LCIS)
  • LCIS is manifested by proliferation, in one or
    more terminal ducts or ductules (acini), of a
    monomorphic population of cells that are loosely
    cohesive, are somewhat larger than normal, and
    have oval or round nuclei with small nucleoli.
    Signet-ring cells containing mucin are commonly
    present. LCIS rarely distorts the underlying
    architecture, and the involved lobules remain
    recognizable. LCIS is an incidental finding in
    biopsies performed for other reasons because it
    is only rarely associated with calcifications and
    never forms a mass

104
Slide 25.21
105
Invasive Carcinoma
  • Invasive Ductal Cafrcinoma, No Special type (NST)
  • On palpation, they may have an infiltrative
    attachment to the surrounding structures with
    fixation to the underlying chest wall, dimpling
    of the skin, and retraction of the nipple. The
    mass is characteristic on cut section. It is
    retracted below the cut surface, has a hard
    cartilaginous consistency, and produces a grating
    sound when scraped. Within the central focus,
    there are small pinpoint foci or streaks of
    chalky white elastotic stroma and occasionally
    small foci of calcification

106
Slide 25.22
107
  • On histologic examination, the tumor consists of
    malignant cells disposed in cords, solid cell
    nests, tubules, anastomosing masses, and mixtures
    of all these invading into stroma. The cytologic
    detail of tumor cells varies from small cells
    with moderately hyperchromatic regular nuclei to
    huge cells with large irregular and
    hyperchromatic nuclei. Frequently, invasion of
    lymphatic and perineural spaces is readily
    evident.

108
Slide 25.23
109
  • Medullary carcinoma
  • Morphology
  • Grossly soft, fleshy consistency and well
    circumscribed
  • Histology
  • solid, syncytium-like sheets of large cells
    frequent mitoses
  • A moderate to marked lymphoplasmacytic infitrate
  • A pushing (noninfiltrative border)

110
  • Invasive Lobular Carcinoma
  • Although making up only 5 to 10 of breast
    carcinomas, invasive lobular carcinomas are of
    particular interest for the following reasons
  • (1) they tend to be bilateral (about 20) far
    more frequently than other subtypes.
  • (2) they tend to be multicentric within the same
    breast.
  • (3) they more frequently metastasize to
    cerebrospinal fluid, serosal surfaces, ovary and
    uterus, and bone marrow compared with other
    subtypes

111
  • Morphology
  • On gross appearance, the tumor is rubbery and
    poorly circumscribed but sometimes appears as a
    typical scirrhous type.

112
  • On histologic examination, strands of
    infiltrating tumor cells, often only one cell in
    width (in the form of a single file), are loosely
    dispersed throughout the fibrous matrix. The
    cells have the same cytologic features of LCIS
    and lack cohesion without formation of tubules or
    papilae. Signet-ring cells are common.
    Irregularly shaped, solid nests may also occur in
    continuity with the single-file pattern.

113
Slide 25.24
114
  • A number of factors influence the prognosis of
    women with breast cancer without distant
    metastases
  • (1) lymph node metastases (2) locally
    advanced disease (3) tumor size (4) histologic
    subtypes (5) tumor grade (6) estrogen and
    progesterone receptors Seventy per cent of
    tumors with estrogen receptors regress after
    hormonal manipulation. Cancers with high levels
    of hormone receptors have a slightly better
    prognosis than those without receptors. (7)
    lymphovascular invasion
Write a Comment
User Comments (0)
About PowerShow.com