Title: SKIN and Pregnancy.ppt
1SKINand PREGNANCY
- By
- Dr M. Y.Abd El-Mawla,MD
- Zagazig Faculty of Medicine,Zagazig ,EGYPT
2Introduction
- 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
3Changes 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.
4Melasma
5Changes 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
6Telogen effluvium
7Androgenic aalopecia
8Vascular Changesin Pregnancy
- Erythema (most women)
- Spider telangiectases (66)
- Vagina (Jacquemier-Chadwick sign)Cervix
(Goodell's sign -- bluish)PalmsGingiva - Chest
- Legs
- Face
9Vascular 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
10Pyogenic granuloma
11Glandular 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)
12Connective 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,
13Striae distensae
14Skin 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
16Other 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
17Impetigo herpetiformis
18Impetigo herpetiformis 2
19Pregnancy 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 .
20Systemic 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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22Ro(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
23Nonatal lupus
24Antiphospholipid 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) - .
25Suggested 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 .
26Conditions 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
27Herpes 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.
29Foetal Risk in in HG
- The newborn shows signs of HG in less than 10 of
cases. - The foetal risk prematurity and low
birthweight,
30Urticarial plaques vesiculations
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34Pruritic 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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38Intrahepatic 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
39Pathophysiology
- 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
40Prurigo 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
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42Pruritic 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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44The Use of Drugs for Dermatologic Conditions in
Pregnancy
45FDA 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
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