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EXAMINATION
OF THE
SKIN AND MUCOSAE
Dr. Sorin Stamate
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GENERALITIES
TEGUMENTUM = WHAT COVERS
= is the outer covering of living tissue,
with complexes functions:
sensation
adaptive immune system
heat regulation
storage and synthesisexcretion
= semiological map
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GENERALITIES
Thickness= 0,2 - 0,5mm (at the level of the eyelids)
4 - 8mm (at the level of the heels)
Surface =1,5 - 2 m2, with:
folds:
coarsely (inframammary, intergluteal, inguinal)
more discreet (the flexion face of joints)
fine (fingerprints)
palmary and plantar foldsmark the limits of
papillary crests
infundibular depressions (popularly - pores)
correspond to the openings of
sudoriferous glands channels or to
sebaceous follicles
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GENERALITIES
3 layers:
The epidermis:
Superficial, no blood vessels Layers of cells melanocytes produce melanin
The dermis:
Connective tissue (collagenic, elastic and reticular
fibers, fibroblasts, mast cells) Nerves, blood vessels, lymphatic vessels, muscles,
Sebaceous glands, the channels of sebaceous glands
Role: derm is nutr i t ion, skin analyzer
The hypodermis: Adipose lobules separated by fibrous tracts,
Nerves, receptors, blood and lymphatic vessels,
Sudoriferous glands, the deeper portion of bulb of hair
Role: tegum ent support
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SKIN GLANDS
Sudoriferous glands:
= merocrine glandsproduce sweat: water, chloride,
sodium, potassium, lactic acid, urea, fat acids,
mucopolysaccharides, glycoproteins, hydrosoluble
vitamins
Sebaceous glands
= holocrine glands
Open at the level of hair follicle produce sebum (oxycholesterin, cholesterin, unsaturated fat acids, soaps)
androgens increase secretion
estrogens decrease secretion
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hair 1:
1hair shaft
2sebaceous gland
3epidermis
4dermis
5hair follicle
6hair bulb
7papill
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HAIRS AND NAILS
= Annexa of skin
- visible from the outsideNAILS
= corneous thin sheets on the surface of the
distal phalangessource: nail matrix
the lunula is a part of the nail matrix
HAIR
the enlarged basal part of a hair within the skin =
ROOT
the part of a hair projecting beyond the skin =
SHAFT
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CUTANEOUS SYMPTOMS:
PRURITUS
pruritus (latin) = itch
= cutaneous symptom produced by subliminal irritation of
nervous terminations by the mediators (histamine,
acetylcholine) which determines an attenuated pain
In producing pruritus, interfere:
Genetic factors
Psychological factorsemotional pruritus
Secondary lesions:
excoriations
lichenification
cutaneous infections
local pigmentations
degraded nails
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Pruritus Prurigo(Prurigo =
papulous, pruriginous lesions, determining local pruritus)
PRURITUS
SECONDARY(Determined by cutaneous affections)
PRIMITIVE(SINE MATERIA)
GENERALIZE
LOCAL
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SYSTEMIC PRURITUS
Appears in:
Jaundice syndromes(billiary salts retention;appears in pre-jaundice phase
Neoplasia; increases in night or in heat conditions)
Paraneoplasic pruritus(lymphoma, lymphosarcoma, carcinoma)
Diabetes mellitus(! Early signs)
Uremia(calcium deposits in the tegument irritation of nervousterminations)
Gout(teenagers)
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SYSTEMIC PRURITUS
Appears in:
Parasitic infections
Hyperthyroid, hypothyroid, Cushing syndrome,
acromegaly, menopauses)
Senile (elasticity changes; + capillary fragility)
Drugs allergy
(usually along with urticarian eruption)
Scabies - intensive (specially during the night), +
grattage lesions
Other causes: psychological, gastric hypoacidity,
feriprive anemia/pernicious, avitaminose
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LOCAL PRURITUS
Has preferential localization in several affections:
VulvarDiabetes mellitus (associated to candidose)
menopause (widow pruritus)
iron deficiency
lack of vitamins uterin/anexial neoplasia
psychogenic
Scrotal/Penian Diabetes mellitus
Prostate carcinoma
urinary tract infections (frequent urethritis)
psychogenic
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LOCAL PRURITUS
Has preferential localization in several affections:
Abdomen, hips, extremities hepatitis, cirrhosis
Nasal:
asthma allergic rhinitis
lambliase (children)
uremia
morphinomania hyperfoliculinemia
Auricular
diabetes mellitus
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LOCAL PRURITUS
Has preferential localization in several affections:
Scalp: alcohol abuse
pre-/postmenstrual
Anal:
parasitic infections
hemorrhoids
intestinal diseases
nearby infections
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SKIN COLOUR CHANGES
Skin color: results from 4 natural pigments other pathologic ones
melanin (brown) oxyhemoglobin (bright red)mainly within arteries/capillaries
deoxyhemoglobin (more bluish)present in venous blood
carotene (yellow)
Special conditions/pathologic ones:
hemosiderin bilirubin
metals
Depends on: skin thickness light (artifical light distorts colours)
!!! The examination of skin color must be done in
sunlight
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SKIN COLOUR CHANGES
CLASSIFICATION:
PALLOR
CYANOSIS
JAUNDICE
HYPERCAROTENEMIA
CHANGES OF SKIN PIGMENTATION
HYPEREMIA (redness of the skin)
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PALLOR
= lighter color of the skin and visible mucosae, causes by areduced amount of oxyhemoglobin
Main causes: THICKENING OF THE SKIN (myxedema, edema)
LACK OF DEVELOPPMENT OF DERMAL CAPPILARIES
(hypogonadism in men - Egyptian picture aspect)
VASOCONSTRICTION (strong emotions, acutecirculatory failure)
ANAEMIA
(in association with tiredness and fatigue)
!!! Pallor is best appreciated where the epidermis is
thinnest: the fingernails, the lips, tongue, palpebral
conjunctiva, palmar skin
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PALLOR
Different colors associated with pallor could be
correlated with the causes of the anemia+ f lavin ic shadehemolytic anemia
+ yel lowish shade - pernicious anemia
+ verd in ic shadeyoung girls chlorosis (green
sickness) = hypchromic anemia
+ l ighter yel low shadegastric neoplasia
+ cafe au lait shadebacterial endocarditis
+ white like paper shadeacute hemorrhagicanemia
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PALLOR
Pallor is associated with clue signs that could
ascertain the origins of anemia: Koi lonych ia= spoon nails - anemia due to
iron deficiency (the nails are flattened and
have concavities) Hunter gloss i t ispernicious anemia
Inappetence & loss of w eight- neoplasia
Cutaneous hemo rrhagic mani festat ions(petechia, ecchymoses, hematomas)acute
leukemia, loss of blood
C OS S
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CYANOSIS
= bluish color of the skin and mucosal surfaces due to the
presence in the circulating blood of an increased
quantity of reduced Hb (more than 5g/dl) or a different
type of Hb
- Disappears with digital pressure
CYANOSIS FALSE CYANOSIS
= discoloration of the skin induced by deposition of gold
salts (chrys ias is), silver salts (argyr ia), arsenic or othercompounds
N.B.
False cyanosis doesnt disappear with digital pressure
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CYANOSIS
Due to abnormal hemoglobin
or rare type of hemoglobin
-Kansas Hb
- Methemoglobin
- Sulphuretted Hb
Due to an increased
quantity of reduced Hb
Increased quantity of reduced
Hb in the arterial blood
CYANOSIS
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CYANOSIS DUE TO ABNORMAL Hb/rare Hb
Appears in patients without a cardiac and pulmonary
disease. They are rare conditions.METHEMOGLOBINEMIA:
Oxidative substances- intoxication with nitrites, fenacetin,
clorat de potasiu, derivati anilinici
Congenital/genetic- hemoglobin M
IdiopaticMethemoglobinemia nefamiliala
SULPHURETTED HEMOGLOBIN: Hijmans van der Berghtoxic cyanosis
- due to presence of sulphuretted hydrogen in intestine
Administration of drugs like fenacetinor sulphamides
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CYANOSIS DUE TO AN QUANTITY OF
REDUCED Hb
The bluish color appears when the quantity of reduced
Hb in the arterial blood is more than 5 g/dl (Normally:
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CYANOSIS
CYANOSIS
LOCALIZED
GENERALIZED
CENTRAL
PERIPHERAL
CARDIAC
/STASIS
PULMONARY
right-left SHUNT
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PULMONARY CENTRAL CYANOSIS
This is the sign of respiratory insufficiency
Bad oxygenation (low arterial saturation) of arterial bloodin the lungs
Caused by:
Low alveolar oxygen pressure
Disturbances in gas exchange
Ventilation/perfusion mismatch
Characteristics:
Generalized (even the tongue is cyanotic) Warm (hypoxia induces vasodilatation)
Negative Lewis test (rubbing the ear lobe with the fingertips does
not make cyanosis to disappear)
Oxygen supplementation of the inspired air may correct cyanosis
CENTRAL CYANOSIS WITH RIGHT TO
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CENTRAL CYANOSIS WITH RIGHT-TO-
LEFT SHUNT
It is also called the blue syndrome
Causes:- Congenital heart disease (CHD) with right-to-left
shunt (Fallot tetralogy)
Associated with retarded growth and physical
development, dyspnea on exertion, clubbing of the fingers
and toes
Positionsquatting.
Anoxic episodes (spells).
It is not influenced by oxygen administration
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CENTRAL CYANOSIS
CENTRAL GENERALIZED PERIPHERAL
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CENTRAL GENERALIZED PERIPHERAL
CYANOSIS (STASIS)
The sign of right heart failure
Accompanied by gravitational edema
Characters of peripheral cyanosis:
Respects blood peripheral circuits
DOESNT affect the tongue COLD (because of the low velocity of blood: stasis +
vasoconstriction)
Positive Lewis testrubbing the ear lobe with the
fingertips makes cyanosis to disappear becoming red) In CARDIOGENIC SHOCK patient presents pale cyanosis
due to vasoconstriction, marmoreal teguments, which
remain cold and cyanotic when adopting a declive position
LOCALIZED CYANOSIS
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LOCALIZED CYANOSIS
ERYTHROCYANOSIS
Appears in POLYCYTHEMIA VERA
It is also called red cyanosis
Described by Osler in XIX century, as red like
roses in summer and blue like indigo in winter Color changes are more obvious in the areas
exposed to temperature variations (face and
hands) It is associated with pruritus sine materia which
commonly starts after a bath
LOCALIZED CYANOSIS
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LOCALIZED CYANOSIS
It is due to an increased tissue oxygen extraction ofarterial blood produced by 2 mechanisms:
Decreased arterial supply
Slowing down of venous-capillary circulation
LOCALIZED
CYANOSIS
ACUTE
CHRONIC
Thrombophlebitis
(Phlegmatia coerulea)Arterial embolus
Peripheral chronic
ischemia syndrome
Acrocyanosis
LOCALIZED CYANOSIS
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LOCALIZED CYANOSIS
ACROCYANOSIS
= refers to a persistent blue or cyanotic discoloration of thedigits, most commonly occurring in the hands although also
occurring in the face and feet as well
Appears in: cold exposure, phlebitis, chronic venous
failure, Raynaud syndrome
Causes: functional anomalies in capillary circulation
LIVEDO RETICULARIS- a lace-like purplish discoloration
- a particular aspect: RACEMOS LIVEDOpermanent red-violet arborizations??in SLE, PAN
- abdomen: acute pancreatitis
FACE CYANOSIS
venous thrombosis, superior cave vein syndrome
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ACROCYANOSIS
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THROMBOPHLEBITIS
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LIVEDO RETICULARIS