3. Classification
a) Skin appendages or skin adnexa, such as:
• Hair follicles, sebaceous and sweat glands
b) Common cyst – sebaceous cyst, dermoid cyst
c) Soft tissue tumor – lipoma, fibroma, neurofibromatosis
a) Epidermal tumor as will be explained in precancerous lesion
e) Moles (naevi)
5. Sebaceous cyst (epidermoid cyst)
It is a retention cyst that is caused by the
blockage of sebaceous gland duct.
• The cyst lined with stratified squamous
epithelium contain a grayish white material
• Often found on scalp, trunk, face, any hairy
areas of the body except the palm and the
sole
6.
7. Clinical features:
• Slowly growing cyst and often painless
• If infected or inflamed, it becomes red, painful
and tender to touch
• Cyst forms a small, well defined cystic swelling
usually fixed to overlying skin at one point,
freely movable, central punctum may be seen
• Lesion may be solitary or multiple
• Sometimes it attains a large size
8.
9. Treatment depends on its clinical state;
• Incision and drainage
• Complete excision of the cyst
10. Dermoid cyst
• Dermoid cyst is lined by stratified squamous
epithelium filled with sebaceous material
• Could occur anywhere in the body. If in the
skin, mostly on the face, neck or scalp
sc
13. Clinical features:
Sequestration dermoid: presents at birth but not
appear clinically except after few years when cyst
begins to extend (slowly growing), usually occur at
fusion lines, painless mass, intense inflammation
may occur if cyst rupture spontaneously or because
of trauma
Implantation dermoid: occurs secondary to
punctured wounds which displace some epithelial
cells into sc tissues. Mainly in the fingers, palm and
sole. Cyst usually small and tense and sometimes
scarred overlying skin
17. Lipoma
Lipomas are benign aggregates of slowly
growing adipocytes
• most common subcutaneous soft tissue tumor
• Incidence 1:1000 persons, > in young males
18. Clinical features:
• Most common as a painless slowly growing
solitary swelling
• Multiple lipomatosis could occur
• Present anywhere on the body (subcutaneous,
subfascial, intermuscular, submucosa,
retroperitoneal)
• May contain other tissue as fibrolipoma or
angiolipoma
• O/E : well circumscribed mass of variable sizes,
soft in consistency, lobulated surface, slippery
edges, non tender (unless they grow compressing
an underlying nerve)
20. Dercum’s disease (adiposis dolorosa) is
tender fat deposits especially on trunk
Complications are rare include:
1. Degenerative changes lead to
liquefaction and calcification
2. Malignant transformation (liposarcoma)
can occur in retropertoneal lipoma
21. Treatment:
• Small, asymptomatic lipomas
require no treatment
• Definitive treatment is surgical
excision
Indication to excise lipomas:
1. Mostly for cosmetic reasons
2. To evaluate their histology
when liposarcomas must be
ruled out
3. When they cause symptoms
4. Become larger than 5cm,
exhibit malignant behavior,
located mainly of thigh,
shoulder, retroperitoneum
22. Fibroma
Benign tumor composed of fibrous or
connective tissue
• Can grow in all organs, arising from
mesenchyme tissue
23. Hard fibroma (fibroma durum)
• In skin it is called dermatofibroma
(mc painful skin tumor)
• Common cutaneous nodule of
unknown etiology, > in females
• Firm pigmented nodule usually
on the lower legs, arms
• Special form is keloid
Soft fibroma (fibroma molle)
• Fibroma with a shaft
(acrochordon, skin tag)
• Represents as hyperplastic dermis
either pedunculated or sessile
• Most common sites are axilla,
neck, inguinal region
• No malignant threat
24. Treatment:
- No treatment unless for cosmesis or liability to
trauma
- Surgical excision under local anaesthesia or by
laser/radiowave/electrocoagulation/cryothera
py
Elliptical excision of a
dermatofibroma on the arm
Removal of acrochordon
25. Neurofibroma
Neurofibromatosis is a proliferative condition of
the endoneurium of nerves associated with
tumor formation. These tumors occur under the
skin and throughout the nervous system.
26. a) Solitary neurofibroma – between the age 20-
50 yrs. Usually found in sc tissue affecting
nerves of upper limb, mobile sideways,
forming a small elongated firm tender
swelling. Cystic degeneration may occur
Rx: tumor should be completely excised
27. b) Generalized neurofibromatosis (Von Recklinghausen’s
disease)
• Autosomal dominant disorder with widespread
affection of nerves
• Preceded with multiple café-au-lait spots, increase in
size and number over time
• Freckling in the arm pit/groin region during childhood
adolescence
• Subcutaneous or cutaneous neurofibromas all over the
body surface (small, slowly growing, painless,rubbery
skin lesions, movable sideways but not in line of nerve)
Rx: Excision of all tumors is impossible. Complete
resection indicated only for very large tumors, painful or
tumors producing pressure symptoms.
28. Melanocytes migrate from neural crest to the basal epidermis
during embryogenesis.
When this melanocytes layer in epidermis they form a simple
mole. Melanocytes that aggregate in the dermis or at
dermoepidermal junction are called nevus cells.
Classifications :
- Lentigo
- Junctional
- Compound
- Intradermal
29.
30. • Lentigos: small, sharply
circumscribed pigmented
macules which are marker for
sun damage and some systemic
syndromes. Solar lentigenes
>common in fairer skin
• Junctional naevus: deeply
pigmented macule or papule
occurs commonly in childhood
and adolescence. Represents
dermoepidermal proliferation of
naevus cells usually progress to
form compound or intradermal
with advancing age. No
malignant potential.
31. • Compound naevus:
maculopapular pigmented
lesion becomes prominent
during adolescence.
Represent a junctional
proliferation of naevus cells
with nest and columns in
dermis.
• Intradermal naevus: faintly
pigmented papules in adults
showing no junctional
proliferation but a cluster of
dermal melanocytes.
32. • Blue naevus: benign skin lesion
4x > common in children
typically affecting face and
extremities
• Halo naevus: halo of
depigmentation around any
benign nevus represents an
antibody response to
melanocyte. Depigmentation is
important as it may also be a
feature of MM. It is assoc. with
vitiligo.
33. Treatment of nevi:
- Nevi are virtually always benign before
puberty
- Indicated for cosmetic reasons, subject to
trauma or if there are alerting signs of change
Mode of inheritance
Dercum disease (adiposis dolorosa) is believed to be transmitted in an autosomal dominant manner with incomplete penetrance[12, 13] ; it is particularly strong in the line of great grandmother-mother-daughter; however, most reported cases of adiposis dolorosa appear to be sporadic.[14]
diagnosis : generalized obesity, chronic pain in adipose tissue more than 3 months, no treatment
Complications:
- Sarcomatous changes
- Myxomatous degeneration
- Saponification
- Calcification
Liposuction has been used to remove large lipomas in anatomically sensitive locations
Dermatofibroma causes theory: reactive process to traumatic insults
Keloid extend beyond the boundaries of original wound, growths can be several cm thick, extremely hard, smooth, mirror like surface
Surgical removal of fibroma skin infiltrational is performed under local anesthesia, usually in a clinic. Holding this surgery is possible in several ways: traditional conventional surgical excision with a scalpel, by laser, radiowave or electrocoagulation. The most modern and preferred methods now are laser and radio wave removal of the fibroid, as they give the opportunity to perform this surgery is almost bloodless, which is achieved by simultaneously sealing small blood vessels on the cut. In addition, there is sterilization of the surgical wound by using a laser beam or a radio wave, the wound surface is covered with a delicate film of fibrin which protects the wound from infection and prevents development of inflammatory complications. This ensures fast and optimal postoperative wound healing, and in the case of small fibromas of the skin is possible, with no visible signs of the surgery. This procedure takes 15-20 minutes. Minor trauma of the surgery allows the patient to quickly return to normal life.
Neurofibromas are tumors of the nerve fibers. The term neurofibromatosis refers to two different genetic diseases characterized by skin abnormalities and nervous system tumors:
Neurofibromatosis type 1: Also called NF-1 or Von Recklinghausen’s disease.
Neurofibromatosis type 2: Also known as NF-2.
two types of neurofibromatosis.
Type NF 1 : A mutation of the NF1 gene causes a loss of neurofibromin allows cells to grow uncontrolled and the cells are cancer cells.
Type NF 2: A mutation of the NF2 gene causes loss of merlin, which also leads to uncontrolled cell growth
Symptoms
The symptoms of NF-1 and NF-2 present themselves in very different ways. One of the most common early signs of NF-1 are the skin discolorations referred to as “café-au-lait” spots. Because NF-2 tumors may involve the hearing nerve, unexplained hearing loss or ringing in the ears might be an early symptom.
Incidence
NF-1 is the more common form of neurofibroma, appearing in one of every 3000 or 4000 people worldwide. NF-2 is a little more rare, occurring in one of every 35,000-40,000.
Cause
The predisposition to tumor formation in both disorders is related to genetic abnormalities which interfere with a protein that normal regulates and prevents tumor formation.
Treatment
Surgery is the most common form of treatment for neurofibroma. However, removal of the tumor can be tricky because these growths are often woven through the nerve structure.
Malignant change is assoc with pain
Blue naevus is a tumor of melanocytes , rarely change to malignant, shiny blue color