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SKIN CHANGES AND
 DERMATOSES OF
   PREGNANCY

Dr. HUSSEIN ABOUL FOTOUH
       Dermatologist
 Al Meeqat General Hospital
    Almadina Almunawara
 During pregnancy immunologic endocrine
  metabolic and vascular changes occur that
  make the pregnant woman susceptible to skin
  changes both physiologic and pathologic.
 They are

 A-Physiologic skin changes

 B-Dermatoses aggravated by pregnancy

 C-Dermatoses of pregnancy
Physiologic skin changes
 Caused by the hormonal changes of
  pregnancy
 1-Pigmentary changes

 (usually regress postpartum)

 -Diffuse hyperpigmentation(90% with
  accentuation of normally hyperpigmented
  areas e.g. areolae axillae linea alba
 -Melasma(70% of pregnant)

 -Darkening of nevi

 -Pigmentation of axillae and inner thighs
 2-Hair changes (hirsutism postpartum
  telogen effluvium postpartum male pattern
  alopecia)
 3-Nail changes (subungual hyperkeratosis
  distal onycholysis transverse grooving and
  brittleness)
 4-Glandular
 -Increased eccrine activity (hyperhidrosis
  miliaria and dyshidrotic eczema)
 -Decreased apocrine activity )(hidradenitis
  suppurativa)
 -Increased sebaceous activity (exacerbation
  of AV enlarged Montgomery follicles of
  areolae)
 5-Striae distensae or atrophicae
Vascular(spider nevi palmar erythema-6
nonpitting facial edema varicosities
(dermographism and haemorrhoides
Gingival hyperemia and gingivitis-7
Prurigo gravidarum due to functional-8
 hepatic disturbance induced by estrogens
Dermatoses aggravated by pregnancy
   1-Infections ( severe seborrhoeic dermatitis or orovulval
  candidiasis should raise suspicion of HIV during pregnancy)
 -Viral (H. simplex- condyloma accuminata ( cs is
  indicated for both)- varicella zoster)
   -Bacterial (leprosy)- protozoan (trichomoniasis)
   -Fungal (Candida -pityrosporum folliculitis)
   .AIDS pregnancy accelerates the development of
    AIDS in an asymptomatic HIV +ve patient.
   2-Inflammatory disorders
   -Atopic dermatitis–acne vulgaris –Hidradenitis
    suppurativa –Chronic plaque psoriasis –Fox
    fordyce disease (all may improve) -urticaria
 3-Autoimmune diseases -SLE –
  Dermatomyositis
 -Pemphigus vulgaris – Systemic sclerosis
 -Rheumatoid arthritis (improve)
 4-Metabolic diseases
 -Porphyria cutanea tarda – Acrodermatitis
  enteropathica
 5- Connective tissue disorders
 -Ehler Danlos syndrome – Pseudoxanthoma
  elasticum
 6- Tumors
 -Pyogenic granuloma –Glomus tumor –
  Hemangioma –Hemangioendothelioma –
  dermatofibroma –neurofibroma -melanoma
 7-Miscellaneus    –Sarcoidosis (may improve
 during pregnancy) –Mycosis fungoides
 -Neurofibromatosis
 Erythrokeratoderma variabilis
 DERMATOSES        OF PREGNANCY(6)


 1-Intrahepatic cholestasis of pregnancy (ICP)
 2-Impetigo herpetiformis (IH)

 3-Herpes gestationis (HG)

 4-Pruritic urticarial papules and plaques of
  pregnancy (PUPPP)
 5-Prurigo of pregnancy (PP)

 6-Pruritic folliculitis of pregnancy (PFP)
Intrahepatic cholestasis of pregnancy
   It is seen in the third trimester ( unlike physiologic
    prurigo gravidarum which occurs in the first
    trimester) . It is characterized by
   -Elevated liver function tests and serum bile acids
   -Generalized pruritus ( high bile salts) and
    excoriations (without primary skin lesions) with jaundice in
    50% of cases that resolves after delivery
   -Malabsorption of fat with weight loss vitamin k
    deficiency------- IU Hge
   -Increased fetal distress and stillbirths
   -50% recurrence with subsequent pregnancies
   TTT emollients cholestyramin UVB evening primrose
    oil.
(IMPETIGO HERPETIFORMIS(IH
   A variant of pustular psoriasis( histopathologically)
    characterized by widespread sheets of
    erythema with pustular margin starting
    in flexures sparing face hands and feet there is
    fever diarrhea and vomiting.
   -It starts usually in the third trimester and resolves
    postpartum but may recur with subsequent
    pregnancies
   -associated with hypocalcaemia high ESR and
    leukocytosis.
   TTT prednisolone 40 mg daily calcium and
    termanination is indicated (stillbirth and placental
    insufficiency).
Herpes gestationis (HG( an autoimmune bullous
     :disorder closely related to Bullous pemphigoid .Onset
   -second or third trimester .Recurrence is common
    with subsequent pregnancies and oral contraceptives
   -Intensely pruritic erythematous plaques on the
    abdomen periumblical----------generalized bullous
    eruption sparing face mucous membranes palms and
    soles
   -Histopathology subepidermal separation basal cell
    necrosis eosinophilic spongiosis.
   Direct Immuno Fluorescence shows linear c3 and IgG
    at BMZ
   HG factor is a circulating IgG Ab. that binds toAg2 in
    BMZ the same antigen is found in the placenta.It
    stimulates complement pathway----c3 deposition at
    BMZ---chemotaxis of eosinophils----proteolytic
    enzymes-----dermoepidermal separation
   TTT mild cases potent topical steroids
    and systemic antihistamines

   -prednisone 20—40mg daily

   -Plasmapheresis

   NB Avoid dapsone-----neonatal
    hemolysis and avoid oral
    contraception-------HG recurrences
PRURITIC URTICARIAL PAPULES AND PLAQUES OF
 PREGNANCY (PUPPP( SYN. POLYMORPHIC ERUPTION
 OF PREGNANCY
 The most common 1to 300 preg.
 -occurs in primigravidas in the third
  trimester and does not usually recur in
  subsequent pregnancies.
 -severely pruritic polymorphous eruptions
  (urticarial-papules-plaques-and erythema
  multiforme like lesions) usually begin in the
  striae on the abdomen and spreading
  peripherally .The face palms and soles are
  commonly spared.It resolves after delivery.
 -HISTOPATHOLOGY mild spongiosis and superficial
    perivascular inflammatory cell infiltrate with many
Pathogenesis

Rapid abdominal distention in     primigravidas in
third trimester may cause damage to
connective tissue in the striae and trigger the
.inflammatory response to PUPPP

.It is harmless to the fetus and mother-
TTT Antihistamines – short course of oral
prednisone –topical steroids and antipruritics-
UVB therapy
   PRURIGO OF PREGNANCY (PP)

   -Onset 2nd or 3rd trimester with no recurrence with
    subsequent pregnancy.

   -Clinically pruritic papules or nodules on extensors of
    limbs or abdomen (similar to nodular prurigo) as
    there may be an atopic background. No
    complications.

   -TTT topical steroids – antihistamines – resolution
    -----weeks after pregnancy
   PRURITIC FOLLICULITIS OF PREGNANCY(PFP)

   -Onset 2nd or 3rd trimester with no recurrence with
    subsequent pregnancy.

   -Clinically similar to steroid acne (pruritic
    erythematous follicular papules on limbs and
    abdomen).

   -No complications

   -TTT Topical steroids – Resolution is postpartum
THANK YOU

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Skin changes and dermatoses of pregnancy

  • 1.
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  • 3. SKIN CHANGES AND DERMATOSES OF PREGNANCY Dr. HUSSEIN ABOUL FOTOUH Dermatologist Al Meeqat General Hospital Almadina Almunawara
  • 4.
  • 5.  During pregnancy immunologic endocrine metabolic and vascular changes occur that make the pregnant woman susceptible to skin changes both physiologic and pathologic.  They are  A-Physiologic skin changes  B-Dermatoses aggravated by pregnancy  C-Dermatoses of pregnancy
  • 6.
  • 7. Physiologic skin changes  Caused by the hormonal changes of pregnancy  1-Pigmentary changes  (usually regress postpartum)  -Diffuse hyperpigmentation(90% with accentuation of normally hyperpigmented areas e.g. areolae axillae linea alba  -Melasma(70% of pregnant)  -Darkening of nevi  -Pigmentation of axillae and inner thighs
  • 8.
  • 9.  2-Hair changes (hirsutism postpartum telogen effluvium postpartum male pattern alopecia)  3-Nail changes (subungual hyperkeratosis distal onycholysis transverse grooving and brittleness)  4-Glandular  -Increased eccrine activity (hyperhidrosis miliaria and dyshidrotic eczema)  -Decreased apocrine activity )(hidradenitis suppurativa)  -Increased sebaceous activity (exacerbation of AV enlarged Montgomery follicles of areolae)  5-Striae distensae or atrophicae
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  • 17. Vascular(spider nevi palmar erythema-6 nonpitting facial edema varicosities (dermographism and haemorrhoides Gingival hyperemia and gingivitis-7 Prurigo gravidarum due to functional-8 hepatic disturbance induced by estrogens
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  • 19.
  • 20.
  • 21.
  • 22.
  • 23. Dermatoses aggravated by pregnancy  1-Infections ( severe seborrhoeic dermatitis or orovulval candidiasis should raise suspicion of HIV during pregnancy)  -Viral (H. simplex- condyloma accuminata ( cs is indicated for both)- varicella zoster)  -Bacterial (leprosy)- protozoan (trichomoniasis)  -Fungal (Candida -pityrosporum folliculitis)  .AIDS pregnancy accelerates the development of AIDS in an asymptomatic HIV +ve patient.  2-Inflammatory disorders  -Atopic dermatitis–acne vulgaris –Hidradenitis suppurativa –Chronic plaque psoriasis –Fox fordyce disease (all may improve) -urticaria
  • 24.
  • 25.
  • 26.  3-Autoimmune diseases -SLE – Dermatomyositis  -Pemphigus vulgaris – Systemic sclerosis  -Rheumatoid arthritis (improve)  4-Metabolic diseases  -Porphyria cutanea tarda – Acrodermatitis enteropathica  5- Connective tissue disorders  -Ehler Danlos syndrome – Pseudoxanthoma elasticum  6- Tumors  -Pyogenic granuloma –Glomus tumor – Hemangioma –Hemangioendothelioma – dermatofibroma –neurofibroma -melanoma
  • 27.
  • 28.
  • 29.  7-Miscellaneus –Sarcoidosis (may improve during pregnancy) –Mycosis fungoides -Neurofibromatosis Erythrokeratoderma variabilis
  • 30.
  • 31.
  • 32.  DERMATOSES OF PREGNANCY(6)  1-Intrahepatic cholestasis of pregnancy (ICP)  2-Impetigo herpetiformis (IH)  3-Herpes gestationis (HG)  4-Pruritic urticarial papules and plaques of pregnancy (PUPPP)  5-Prurigo of pregnancy (PP)  6-Pruritic folliculitis of pregnancy (PFP)
  • 33. Intrahepatic cholestasis of pregnancy  It is seen in the third trimester ( unlike physiologic prurigo gravidarum which occurs in the first trimester) . It is characterized by  -Elevated liver function tests and serum bile acids  -Generalized pruritus ( high bile salts) and excoriations (without primary skin lesions) with jaundice in 50% of cases that resolves after delivery  -Malabsorption of fat with weight loss vitamin k deficiency------- IU Hge  -Increased fetal distress and stillbirths  -50% recurrence with subsequent pregnancies  TTT emollients cholestyramin UVB evening primrose oil.
  • 34. (IMPETIGO HERPETIFORMIS(IH  A variant of pustular psoriasis( histopathologically) characterized by widespread sheets of erythema with pustular margin starting in flexures sparing face hands and feet there is fever diarrhea and vomiting.  -It starts usually in the third trimester and resolves postpartum but may recur with subsequent pregnancies  -associated with hypocalcaemia high ESR and leukocytosis.  TTT prednisolone 40 mg daily calcium and termanination is indicated (stillbirth and placental insufficiency).
  • 35.
  • 36. Herpes gestationis (HG( an autoimmune bullous :disorder closely related to Bullous pemphigoid .Onset  -second or third trimester .Recurrence is common with subsequent pregnancies and oral contraceptives  -Intensely pruritic erythematous plaques on the abdomen periumblical----------generalized bullous eruption sparing face mucous membranes palms and soles  -Histopathology subepidermal separation basal cell necrosis eosinophilic spongiosis.  Direct Immuno Fluorescence shows linear c3 and IgG at BMZ  HG factor is a circulating IgG Ab. that binds toAg2 in BMZ the same antigen is found in the placenta.It stimulates complement pathway----c3 deposition at BMZ---chemotaxis of eosinophils----proteolytic enzymes-----dermoepidermal separation
  • 37. TTT mild cases potent topical steroids and systemic antihistamines  -prednisone 20—40mg daily  -Plasmapheresis  NB Avoid dapsone-----neonatal hemolysis and avoid oral contraception-------HG recurrences
  • 38.
  • 39.
  • 40.
  • 41.
  • 42. PRURITIC URTICARIAL PAPULES AND PLAQUES OF PREGNANCY (PUPPP( SYN. POLYMORPHIC ERUPTION OF PREGNANCY  The most common 1to 300 preg.  -occurs in primigravidas in the third trimester and does not usually recur in subsequent pregnancies.  -severely pruritic polymorphous eruptions (urticarial-papules-plaques-and erythema multiforme like lesions) usually begin in the striae on the abdomen and spreading peripherally .The face palms and soles are commonly spared.It resolves after delivery.  -HISTOPATHOLOGY mild spongiosis and superficial perivascular inflammatory cell infiltrate with many
  • 43. Pathogenesis Rapid abdominal distention in primigravidas in third trimester may cause damage to connective tissue in the striae and trigger the .inflammatory response to PUPPP .It is harmless to the fetus and mother- TTT Antihistamines – short course of oral prednisone –topical steroids and antipruritics- UVB therapy
  • 44.
  • 45.
  • 46.
  • 47. PRURIGO OF PREGNANCY (PP)  -Onset 2nd or 3rd trimester with no recurrence with subsequent pregnancy.  -Clinically pruritic papules or nodules on extensors of limbs or abdomen (similar to nodular prurigo) as there may be an atopic background. No complications.  -TTT topical steroids – antihistamines – resolution -----weeks after pregnancy
  • 48.
  • 49. PRURITIC FOLLICULITIS OF PREGNANCY(PFP)  -Onset 2nd or 3rd trimester with no recurrence with subsequent pregnancy.  -Clinically similar to steroid acne (pruritic erythematous follicular papules on limbs and abdomen).  -No complications  -TTT Topical steroids – Resolution is postpartum
  • 50.
  • 51.