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Skin associated systemic disease in elderly

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Seborrheic keratosis : focal epidermal homeostasis loss ... Acromegaly. Addison. Cushing. Dermatomyositis. Down. Cirrhosis. Hypothyroid. SLE. scleroderma ... – PowerPoint PPT presentation

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Title: Skin associated systemic disease in elderly


1
Skin associated systemic disease in elderly
  • Monsawan miniphan M.D.
  • 3/02/2005

2
Scope of diseases
  • Skin associated common systemic disease
  • Diabetes
  • Hyperlipidemia
  • Endocrine disease
  • Others

3
  • Malignancy of skin
  • Bacal cell carcinoma
  • Squamous cell carcinoma
  • Malignant melanoma

4
Skin and aging
  • Two basic theories of aging
  • Programmatic theory
  • Inherent genetic program
  • Stochastic theory
  • Cumulative environmental damage

5
Skin aging
  • Intrinsic aging
  • Universal
  • Inevitable change
  • Attribute to the passage of time alone
  • Photoaging
  • Superimpose on intrinsic aging
  • Attribute to the chronic sun exposure

6
Histologic features of aging skin
  • Epidermis
  • Flatted dermo-epidermal junction
  • Variable thickness
  • Variable cell size and shape
  • Occasional nuclear atypia
  • Fewer melanocyte
  • Fewer Langerhans cell

7
  • Dermis
  • Atrophy
  • Fewer fibroblast
  • Fewer mast cells
  • Fewer blood vessels
  • Abnormal nerve ending

8
  • Appendage
  • Depigmented hair
  • Loss of hair
  • Fewer glands
  • Abnormal nail plates

9
Histology of skin
10
Histology of aging skin
11
Functions of skin decline with age
  • Cell replacement Thermoregulation
  • Barrier function Sweatproduction
  • Chemical clearance Sebumproduction
  • Sensory perception Vit production
  • Mechanical protection DNA repair
  • Wound healing
  • Immune responsesive

12
Common skin disease in elderly
  • Benign neoplasia
  • Seborrheic keratosis focal epidermal
    homeostasis loss leading to increase endothelin1

13
  • Variants of seborrhoeic keratoses include
  • Solar lentigos flat brown marks in sun exposed
    areas
  • Stucco keratoses numerous small dry grey
    stuck-on lesions usually found on lower legs and
    feet
  • Dermatosis papulosa nigra numerous brown warty
    papules on face and neck of dark-skinned
    individuals

14
Solar lentigene
15
Stucco keratoses
16
  • Treatment
  • Removed wish, uncertainty of the correct
    diagnosis.
  • Methods used to remove seborrhoeic keratoses
    include
  • Cryotherapy. (liquid nitrogen)
  • Curettage cautery.
  • Laser surgery
  • Shave biopsy (shaving off with a scalpel)

17
  • Malignant neoplasia
  • Squamous cell carcinoma
  • Basal cell carcinoma
  • Malignant melanoma
  • UV induce DNA damage
  • Decrease DNA damage repair capacity

18
Basal cell carcinoma
  • the most common type of cancer in humans
  • Affect adults, more common in elderly
  • Sun exposure
  • Grow slowly over months or years

19
  • Types of basal cell carcinoma
  • Nodular BCC
  • Superficial BCC
  • Morpgoeic BCC

20
  • Nodular BCC
  • Small translucent growth, rolled edges
  • May be pigmented
  • Ofte smaall blood vessels on surface, bleeding
    spontaneous

21
NODULAR BCC
22
  • Superficial BCC
  • Multiple lesions
  • Upper trunks or shoulders
  • Slow growing patches, shiny pink, slightly scaly,
    bleeding easy

23
SUPEFICIAL BCC
24
  • Morphoeic BCC
  • Skin-color, waxy, thicken scar
  • Most difficult to diagnosis
  • Prone to recurrent

25
MORPHOIC BCC
26
  • Treatment
  • depends on its type, size and location, the
    number to be treated
  • Excision. The lesion is cut out and the skin
    stitched up. This is the most appropriate
    treatment for nodular, infiltrative and morphoeic
    BCCs. Very large lesions may require a flap or
    graft to repair the defect after excision

27
Squamous cell carcinoma
  • Common type of skin cancer
  • Type of squamous cell carcinoma
  • In situ SCC
  • Invasive SCC

28
  • In situ SCC
  • One or more flat red scaly patches up to several
    centimetres wide, often found in large numbers on
    the lower legs. These patches are also known as
    Bowen's disease
  • Malignant cell confine in epidermis

29
  • Causes of in situ SCC
  • Sun exposure
  • Immunosuppression
  • HPV
  • Arsenic ingestion
  • Ionizing radiation

30
BOWEN DISEASE
31
  • Invasive SCC
  • Develop in solar keratosis
  • Solar or actinic keratoses are common small scaly
    lesions arising on the face, ears and hands of
    white skinned people who have spent many years
    outdoors
  • Thickened or tender keratosis may be developing
    into invasive SCC. SCCs are often crusty and may
    bleed easily
  • On the lips, SCC is more common in smokers

32
  • Develop in thermal burn scars and longstanding
    leg ulcers
  • In genital areas, SCC are usually related to
    infection with papillomavirus (genital warts) or
    skin disease such as lichen sclerosus or lichen
    planus vulvar cancer
  • Not usually a threat to life as secondary spread
    (metastasis) is uncommon
  • SCC on the lip or ear appear to be the sites most
    likely to metastasise, so ulcers or lumps in
    these areas should be taken particularly
    seriously

33
SQUAMOUS CELL CARCINOMA
34
SQUAMOUS CELL CARCINIMA OF LIPS
35
  • Treatment
  • Excision the most common treatment of invasive
    SCC
  • Cryotherapy
  • Radiation

36
Malignant melanoma
  • serious skin cancer which is curable if detected
    early
  • Growth from melanocyte in epidermis or mucous
    membrane
  • Common in 50-70 yr

37
  • Causes of melanoma
  • Sun exposure particularly during childhood
  • Serious sunburn, especially when young - however,
    melanoma sometimes occurs on areas of the body
    not normally exposed to the sun
  • Family history of melanoma
  • Fair skin that burns easily - melanoma is common
    in people with Northern European ancestry, and is
    not common among dark-skinned people
  • A large number of abnormal moles (called atypical
    naevi). These moles are usually larger than 6mm,
    with an irregular shape and multicolours

38
  • The ABCDs of melanoma
  • A asymmetry
  • B border irregularity
  • C colour variation
  • D diameter gt 6 mm

39
Superficial melanoma
40
Nodular melanoma
41
  • Treatment
  • Surgical removal
  • Sentinel node biopsy

42
Papulosquamous disorders
  • Psoriasis change in patient environment leading
    to koebnerization
  • systemic medication
  • Atypical presentation flexural psoriasis
  • Drugs aggravated b-blocker, NSAIDs, ACEi
  • Trigger factors urinary incontinence, hearing
    aids, braces

43
Flexural psoriasis
44
Xerosis
  • Disturbance of epidermal maturation
  • Decrease water content in outer layers of stratum
    corneum
  • Dry , rough, skin

45
xerosis
46
Pruritus
  • Penetration of irritants through the damage
    stratum corneum
  • Alter sensory threshold
  • Metabolic disorder
  • Endocrine disorder
  • Adversr drug reaction
  • Parasitic infestation scabies

47
Infection
  • Compromised local cutaneous health predispose to
    growth of infective organism
  • Age-associated decreased immune response
  • Underlying systemic disorder associated with
    decreased immune response

48
scabies
49
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50
  • Metabolic and endocrine disorder
  • DM
  • Renal failure
  • Thyroid disease
  • Hepatic disease
  • Lymphoma, leukemia, PV

51
Skin problems associated with diabetes mellitus
  • Necrobiosis lipoidica
  • Rare, insulin dependent DM
  • One or more tender yellowish brown patches
    develop slowly on the lower legs over several
    months
  • Round, oval or an irregular shape
  • The centre of the patch becomes shiny, pale,
    thinned
  • Prominent blood vessels (telangiectasia)
  • Often painless

52

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54
Treatment
  • Tropical steroid, usually under a plastic
    occlusive dressing
  • Intralesional steroid injections or steroid
    tablet
  • Aspirin and dipyridamol combination
  • Pentoxifylline tablets
  • Oral cyclosporin
  • Photochemotherapy (PUVA)

55
  • Diabetic dermopathy
  • Their cause is unknown
  • Round brown or purple slightly thinned patches
    seen on the shins of diabetic patients
  • Similar lesions are sometimes seen in
    non-diabetics
  • Treatment is not necessary or useful

56
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57
Hyperlipidemia
  • Xanthomata
  • 4 forms tendinous subcutaneous nodule
    found in fascia, ligament and extensor tendon of
    hand, knee and elbow
  • Planar yellow, soft, macule or plaque found on
    the upper eyelids
  • Tuberous yellow to reddish nodule at extensor
    surface of elbows, knees and knuckles
  • Eruptive sudden, multiple reddish yellow papule
    extensor of extremities, buttock

58
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59
PLANAR XANTHOMA
60
ERUPTIVE XANTHOMA
61
Acantosis nigricans
  • Hyperpigmentation, hyperkeratosis,velvety
    distribuion at intertriginous area
  • Most common area axilla, genitaria, groin,
    popliteal fossa, anticubital and neck

62
  • Associated condition
  • Insulin resistant related
  • Obesity
  • Pseudoacromegaly
  • DM
  • Polycystic ovarian disease

63
  • Malignancy related
  • Adenocarcinoma gastric
  • Melanoma
  • Sarcroma
  • Lung carcinoma small cell, squamous,
    bronchoalveolar
  • Lymphoma
  • Endocrine malignancy carcinoid,
    pheochromocytoma, thyroid,testicular
  • Wilm tumor

64
  • Drug induce
  • Somatotrophin
  • Testosterone
  • Nicotinic acid
  • OC
  • Corticosteroid
  • Idiopathic

65
  • Syndromes
  • Acromegaly
  • Addison
  • Cushing
  • Dermatomyositis
  • Down
  • Cirrhosis
  • Hypothyroid
  • SLE
  • scleroderma

66
Acanthosis nigrican
67
Vitiligo
  • Autoimmune disease, pigment cell are destroyed
  • Irregular white patches on the skin
  • Any part of the body may be affect

68
  • Who is prone to vitiligo
  • At least 1 of all population
  • In general good health
  • Greater risk DM, thyroid, B-12 def., Addison,
    alopecia areata

69
  • Cause of vitiligo
  • Unknown
  • Autoimmune against the pigment cell
  • Treatment
  • Topical steroid
  • PUVA

70
vitiligo
71
  • Associated with cancers of the esophagus, lung,
    breast, bladder, stomach, and cutaneous T-cell
    lymphoma

72
Erythroderma
73
  • Diffuse erythema of the skin usually associated
    with induration and scaling
  • Associated with the leukemic phase of cutaneous
    T-cell lymphoma (Sezary syndrome)
  • Other malignancy associations lung, liver,
    prostate, thyroid, colon, pancreas, stomach

74
Collagen Vascular DiseaseDermatomyositis
75
Heliotrope erythema
76
Gottrons papules
77
Dermatomyositis
  • Malignancy risk may be as high as 15 in women
  • No increase in malignancy risk with polymyositis
    or childhood dermatomyositis
  • Females over age 40 have a 32-fold increase risk
    of ovarian cancer

78
Other disorders associated with malignant disease
  • Pruritus
  • Sister Mary Joseph nodule
  • Erythema gyratum repens
  • Subcutaneous fat necrosis
  • Sweets syndrome

79
  • Hypertrichosis lanuginosa acquisita
  • Necrolytic migratory erythema
  • Leukoderma
  • Sign of Leser-Trelat

80
Sister Mary Joseph Nodule
81
Sister Mary Joseph nodule
  • Collective term for a metastatic deposit at the
    umbilicus originating from any primary malignancy
  • Appearance of this lesion usually heralds
    advanced disease and has a poor prognosis.
  • Attributed to Sister Mary Joseph Dempsey who was
    the first surgical assistant to William Mayo
  • Associated malignancies stomach, colon, ovary,
    pancreas

82
Sweets Syndrome (Acute Febrile Neutrophilic
Dermatosis)
83
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84
Sweets SyndromeSubtypes
  • Classic (71)
  • Neoplasia (11) hematologic malignancies,
    usually AML
  • Inflammatory Disease (16)
  • Pregnancy (2)

85
Sweets Syndrome
  • Major Criteria (both required)
  • Abrupt onset of tender or painful erythematous
    plaques or nodules occasionally with vesicles,
    pustules or bullae
  • Predominantly neutrophilic infiltration in the
    dermis without leukocytoclastic vasculitis
  • Minor criteria (2 of 4)
  • Preceded by an nonspecific respiratory or
    gastrointestinary tract infection or vaccination
    or associated with
  • Inflammatory diseases as chronic autoimmune
    disorders, infections etc.
  • Hemoproliferative disorders or solid malignant
    tumors
  • Pregnancy
  • Accompanied by periods of general malaise and
    fever (gt38C)
  • Laboratory values during onset (three out of four
    necessary)
  • ESR gt 20mm n.W.,
  • C-reactive Protein positive,
  • segmented-nuclear neutrophils and stabs gt 70 in
    peripheral blood smear,
  • leukocytosis gt 8.000
  • Excellent response to treatment with systemic
    corticosteroids or potassium iodide

86
Necrolytic Migratory Erythema(Glucagonoma
Syndrome )
87
Necrolytic Migratory Erythema
  • Rare syndrome associated with a glucagon
    producing alpha cell tumour of the pancreas
  • Associated findings glossitis, stomatitis,
    weight loss, hyperglycemia, anemia, alopecia,
    diabetes
  • Diagnosis angiography, octreotide scan
  • Resection of the tumor clears the eruption
  • Similar eruption may be seen with cirrhosis,
    pancreatitis, celiac sprue, and zinc deficiency

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90
Hypertrichosis Lanuginosa Acquisita
  • Acquired excessive growth of lanugo (velus) hairs
  • Initially covers face and ears may involve all
    hair-bearing skin
  • Malignancy associations include colon, rectum,
    bladder, lung, pancreas, breast.

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92
Sign of Leser-Trelat
  • Sudden appearance of multiple seborrheic
    keratoses
  • Association with internal malignancy is unproven

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94
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