7. Increased melanin production
:Café au lait spots-1
A-Multiple neurofibromatosis(Von
(Recklinhausen disease
.B-Polyostotic fibrous dysplasia
8. A-multiple neurofibromatosis
It is an inherited autosomal dominant
neuroectodermal abnormality
,characterized by proliferation of fibrous
element of the nerve
9. Clinical features
Multiple nodules: sessile-1
or pedunculated mostly
affects the trunk
Tongueinvolvement,appears as
multiple nodules,due to
lingual nerve
involvement,scrotal
tongue and enlarged
.fungiform papillae
10. Neurological manifestation: a-centrally- 2
(located lesions (deafness ,pain ,epilepsy
b-mandibular nerve involvement appears as
R.L area associated with lip numbness
11. :Café au lait pigmentation- 3
More than 5mm
(prepubertal
More than 15 mm in
diameter: post
pubertal
14. Albright syndrome- 2
As Jaffe but have
endocrinal
:disturbances
parathyroidThyroid
Pituitary
Gonads (precocious
(puberty
15. smoker melanosis- 2
Diffuse brown flat
macules ,mainly on
anterior labial
gingiva,in cigarette
smokers
On the palate in pipe
smokers
16.
17. Pigmented lichen planus
This increase in
melanogenesis may
be stimulated by the
infilterate of TLynphocytes,through
the cytokines they
produce
Rare in erosive or)
(papular form
22. Melanoma/Malignant melanoma
.Raised ,painless ,sessile or pedunculated
Most commonly found on the palate and
.anterior labial gingiva
:Malignant transformation
Increased pigmentation Bleeding or ulceration
- -
23.
24.
25. Peutz- jegher syndrome
:Clinical picture
A-brown pigmentation: multiple melanotic
(macules )perioral-perinasal-perioccular
Hands and feet also affected
Facial pigmentation may disappear but intra
.oral remain
B-Intestinal polyposis
30. Heamochromatosis
Primary :disorder of newborn ,due to
increased intestinal iron absorption
Secoundry: due to increased iron intake, or
increased RBCs destruction
31. Porphyria
Hereditary disease caused by abnormalities in heme biosynthesis,
results in increased porphyrins
:Types
cutaneous hepatic porphyria:erythema ,then vesicles ,then-1
form bullae,that heal by scar with skin hyperpigmentation
:congenital
erythropoeitic porphyria-2
a-Excessive porphyrin in in bone marrow,causes photosensitivity ,then
.vesicular eruption
b- vesicles contain serous fluid with red fluorescence C-red urine
(D-lavender teeth)both decidious and permanent teeth
32.
33. Pellagra
(:It is Niacin (nicotinic acid deficiency
Dermatitis with melanin pigmentation of skin -1
Dementia-2
Diarrhea-3
Death-4
:Oral manifestation
Stomatitis,glossitis,ANUG,Angular
Cheilosis,Herpes labialis,deminution of taste
sensation
34.
35.
36. Endocrinopathic pigmentation
Bronzing of skin and
patchy melanosis of
oral mucous
membrane due to
Pituitary
hyperfunction or
Addisons
disease(increase in
ACTH( stimulate
melanocytes
41. Lipopigments
A-Lipochrome(Carotene(:yellow or red fat
soluble pigments found in
carrots,tomato ,sweet potato,green leafs
. and egg yolk
Excessive intake of carotene results in
carotenemia
Results in yellow color of skin and mucous
(membrane ,(no eye involvement
53. Kaposis sarcoma
Rare tumour of vascular origin,accompany
HIV infection
Sites: head ,neck ,tip of nose ,intra-orally:
palate
54.
55.
56. Hereditary Hemorrhagic
Telangiectasia
A Genetically transmitted disease ,inherited as an
autosomal dominant trait, about 100 purple
papule on the vermilion and mucosal surfaces of
.the lips and tongue
.Also the facial skin and neck are also involved
:Differential diagnosis
.Petechial hemorrhages with platelet disorders
57.
58. Varix
Pathological dilatation of veins and venules
mostly common intra orally in the ventral
surface of the tongue appear as tortuous
(blue ,red and purple elevation
Degenerative change in adventitia of venous
.walls as result of aging