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Title: SKIN and Pregnancy.ppt


1
SKINand PREGNANCY
  • By
  • Dr M. Y.Abd El-Mawla,MD
  • Zagazig Faculty of Medicine,Zagazig ,EGYPT

2
Introduction
  • Changes in the Skin Due to Pregnancy
  • Skin Conditions Influenced by Pregnancy
  • Pregnancy and Immune-Mediated Disorders
  • Skin Conditions Specific to Pregnancy
  • The Use of Drugs for Dermatologic

3
Changes in the Skin Due to Pregnancy
  • Hyperpigmentation
  • Generalized or increase in pigment at specific
    areas such as the areolae, genitals, inner
    thighs, or axillae
  • Melasma In most cases, the hyperpigmentation
    epidermal melanin deposition due to a
    combination of light exposure and elevated
    hormones (estrogen, progesterone, and
    melanocyte-stimulating hormone.

4
Melasma
5
Changes in the Skin Due to Pregnancy
  • Hair Nail Changes
  • Hirsutism frontoparietal thinning of
    male-pattern alopecia increase in androgens
  • Postpartum hirsutism resolves and hair may enter
    the telogen phase, resulting in the diffuse
    shedding of telogen effluvium
  • Nail changes transverse grooving, brittleness,
    distal onycholysis, and subungual hyperkeratosis

6
Telogen effluvium
7
Androgenic aalopecia
8
Vascular Changesin Pregnancy
  • Erythema (most women)
  • Spider telangiectases (66)
  • Vagina (Jacquemier-Chadwick sign)Cervix
    (Goodell's sign -- bluish)PalmsGingiva
  • Chest
  • Legs
  • Face

9
Vascular Changesin Pregnancy
  • Varicosities (40 of women)
  • Purpura
  • Vasomotor instability
  • Non pitting edema (50 of women
  • Pyogenic granuloma
  • Legs Hemorrhoids
  • Lower extremities
  • Facial flushing ,Pallor Cutis marmorata
    ,Raynaud'sphenomena
  • Face,lids extremities
  • Gingiva and other sites

10
Pyogenic granuloma
11
Glandular Changes
  • Increased Eccrine glands function
  • Miliaria ,Hyperhidrosis Dyshidrotic
    eczema
  • Decreased Apocrine function
  • Increased Sebaceous function in third trimester
  • Acne (variant-pruritic folliculitis of
    pregnancy) Sebaceous glands on the areolae
    (Montgomery's glands)

12
Connective Tissue Changes in Pregnancy
  • Striae distensae (90) on the abdomen, on the
    breasts, thighs, and inguinal areas.
  • Mechanical stretch increased hormones
    (adrenocortical, estrogen, and relaxin) are the
    most significant factors in the development of
    striae,

13
Striae distensae
14
Skin Conditions Influenced by Pregnancy
  • Melanomas no increased risk of melanoma in
    pregnancy .When diagnosed during pregnancy may
    be thicker and therefore have a worse prognosis
  • Nevi may develop, enlarge, or darken. show mild
    cytologic atypia.
  • Dermatofibromas Leiomyomas Keloids
    Dermatofibrosarcoma may develop or grow
    rapidly in pregnancy

15
Other Skin Conditions Influenced by Pregnancy
  • Atopic dermatitis
  • More likely to worsen than improve
  • May present for the first time
    during pregnancy with keratosis pilaris
  • Irritant hand dermatitis due to
    washing postpartum nipple dermatitis due to
    nursing

16
Other Skin Conditions Influenced by Pregnancy
  • Psoriasis More likely to improve than worsen
  • Psoriatic arthritis may worsen
  • Impetigo herpetiformis (generalized pustular
    psoriasis) during last trimester, but may
    present earlier persists until delivery or long
    after
  • Associated with decreased calcium and/or
    vitamin D
  • Severe malaise, fever, nausea , vomiting, tetany,
    seizures
  • Grouped pustules at the margins of symmetric
    erythematous patches

17
Impetigo herpetiformis
18
Impetigo herpetiformis 2
19
Pregnancy Autoimmune Disorders
  • Changes in hormones including the increase in
    estrogen affect the course of autoimmune
    diseases.
  • The fetoplacental unit directs maternal immunity
    toward humoral responses by favoring certain
    cytokines and other inflammatory mediators
  • Enhanced humoral immunity weakened cellular
    immunity lead to variable effects that are
    dependent on the specific disease process .

20
Systemic lupus erythematosus
  • SLE may worsen and may flare postpartum.
  • Lupus patients are advised to avoid trying to
    conceive when their disease is active
  • Underlying lupus renal disease may worsen during
    pregnancy.
  • There is a significant risk of eclampsia
  • Active disease in the mother, maternal use of
    potentially teratogenic medications, and
    pathogenic antibodies (anti-Ro-- ) transmitted
    from the mother may present risks to the fetus.

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Ro(SS-A) Foetal risk
  • Neonatal lupus in mothers with circulating
    anti-Ro(SS-A) antibodies
  • Increased risk of prematurity and spontaneous
    abortion
  • Congenital heart block

23
Nonatal lupus
24
Antiphospholipid syndrome(aPLs)in pregnant with
SLE
  • Approximately one third of patients who have SLE
    also have aPLs..
  • aPLs heterogeneous group of autoantibodies that
    bind phospholipids, proteins, or a
    phospholipidprotein complex on platelets and or
    vascular endothelium.
  • Two best characterized the lupus anticoagulant
    (LA) and anticardiolipin antibodies (aCL)
  • .

25
Suggested clinical and laboratory criteria for
the diagnosis of APS
  • Pregnancy Loss
  • Recurrent spontaneous abortion Unexplained
    fetal death
  • Thrombosis Venous thrombosis Arterial
    thrombosis, stroke
  • Autoimmune thrombocytopenia hemolytic anemia
  • Transient ischemic attacks
  • Chorea gravidarum Livedo reticularis
  • Laboratory criteria
  • Lupus anticoagulant, Anticardiolipin
    antibodies , gt1520 IgG binding units activated
    partial thromboplastin time .

26
Conditions Specific to Pregnancy
  • Herpes gestationis (HG) (also known as
    "pemphigoid gestationis") .
  • Pruritic and urticarial papules and plaques of
    pregnancy (PUPPP).
  • Intrahepatic cholestasis of pregnancy (ICP) may
    present with intense pruritus.
  • Prurigo of pregnancy
  • Pruritic folliculitis of pregnancy

27
Herpes Gestationis H G (pemphigoid gestationis)
  • The incidence 1 in 50,000 pregnancies
  • Developing during the second or third trimester
    (mean onset, 21 weeks) reported in the first
    trimester.
  • Intensely pruritic, urticarial lesions on the
    abdomen in half of the cases especially
    periumbilically, with a rapid progression to
    multiple, generalized bullae. Face, mucous
    membranes, palms, and soles spared.

28
  • Improving during the later part of pregnancy,
    only to flare at delivery or postpartum in about
    75 of patients
  • Histopathology a subepidermal vesicle with
    perivascular infiltration (lymphocytes
    eosinophils).
  • Direct immunofluorescence C3 with or without IgG
    in a linear band along the basement membrane zone
    (BMZ). The antibody localizes to the roof of the
    blister.
  • A mismatch of HLA antigens between the mother and
    father, manifested by an immunologic response
    against the paternal class II antigens at the
    placental BMZ with cross-reaction at the skin
    BMZ.

29
Foetal Risk in in HG
  • The newborn shows signs of HG in less than 10 of
    cases.
  • The foetal risk prematurity and low
    birthweight,

30
Urticarial plaques vesiculations
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Pruritic and Urticarial Papules and Plaques of
Pregnancy(PUPPP)
  • Occuring in approximately 1 in 240 pregnant
    women, typically in the third trimester in first
    pregnancy
  • The urticarial papules begin within striae on the
    abdomen and thighs and, sparing the
    periumbilical region, face, palms, and soles.
  • The lesion may be also vesicles or targetoid.
  • Not to recur in subsequent pregnancies

35
  • Biopsy a spongiotic epidermis with a
    perivascular inflammatory infiltrate increased
    numbers of eosinophils.
  • Immunofluorescence negative
  • Poseing no risk to the mother (except pruritus)
    or fetus, resolveing postpartum.
  • Aetiology
  • Abdominal distention eliciting an inflammatory
    response by damaging the connective tissue
  • A substance released from placenta into the
    maternal circulation triggers fibroblast
    proliferation

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Intrahepatic Cholestasis of Pregnancy (ICP)
  • In the third trimester of pregnancy (mean, 31
    weeks) with a mild form of intrahepatic bile
    secretory dysfunction.
  • Features 1-generalized pruritus with or without
    jaundice 2-absence of primary skin lesions, (3)
    biochemical abnormalities consistent with
    cholestasis,(elevated serum bile acids (mean,
    1349 mug/100 mL) and (4) resolution after
    delivery.
  • Recurrence with subsequent pregnancy

39
Pathophysiology
  • Estrogens interfere with the diffusion of fluid
    across the canalicular membrane of the hepatocyte
    and subsequently with hepatic bile acid
    secretion.
  • Inhibition of hepatic glucuronyl-transferase
  • Altered estrogen metabolism in the liver,
    resulting in reduced biliary volume and excretion
    of these compounds

40
Prurigo of pregnancy (PP )
  • The incidence 1 in 300 pregnancies.
  • In all trimesters of pregnancy
  • Erythematous papules and nodules on the extensor
    surfaces of the extremities and occasionally on
    the abdomen
  • Recurrence during subsequent pregnancies is
    variable
  • Related to an atopic background

41
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42
Pruritic folliculitis of pregnancy (PFP)
  • Generalized, pruritic erythematous, follicular
    papules, developing from the fourth to the ninth
    month of gestation .
  • A form of steroid acne, with no evidence of any
    immunologic or hormonal abnormalities.
  • Some authors have suggested that PFP and PP
    should be included within the spectrum of
    "polymorphic eruption of pregnancy.

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44
The Use of Drugs for Dermatologic Conditions in
Pregnancy
45
FDA Pregnancy Categories
  • A Controlled studies show no fetal risk
  • B No risk to human fetus despite possible
    animal risk.
  • C Risk cannot be ruled out human studies are
    lacking.
  • D Positive evidence for risk to human fetus,
    but benefits may outweigh risks of drug
  • X Contraindicated in pregnancy there is no
    reason to risk use of drug in pregnancy
  • Undetermined No pregnancy category yet assigned

46
  • Topical corticosteroids during pregnancy with a
    low risk to the fetus( Category C risk) as the
    risk cannot be ruled out because no human studies
    have been done.
  • Topical povidone-iodine and podophyllin place a
    fetus at risk. not recommended for use during
    pregnancy
  • Analgesics associated with minimal risk to the
    fetus or infant. Indomethacinassociated with
    problems in infants .

47
  • Retinoids and antineoplastic isotretinoin (used
    to treat acne vulgaris) antineoplastic eg
    methotrexate category X.
  • Antipruritic agents. doxepin avoided during
    pregnancy and lactation. Hydroxyzine risk in
    the first trimester of pregnancy and is
    associated with a risk of congenital abnormality.
  • Antibioticsincluding tetracycline
    ciprofloxacin--pose potential risks during
    pregnancy.. Penicillins are considered
    comparatively safe during pregnancy

48
  • THANK YOU
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