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KELOID DISEASE
(Case Presentation)
PRESENTED BY
Antony Mamati.
PACORI- ACCRA 2019
GRAPHIC IMAGES
We see what we want?
Common things are usually very rare to spot.
History
A 23 year old female was referred by
plastic surgeons for radiotherapy to the
posterior ear lobe, following the
development of a Keloid Scar, three
years after an ear piercing
No family history of keloids
Pathology
Keloid is a unique human dermal
fibroproliferative disorder that occurs after injury,
inflammation, surgery,and burn.
Commonly causes of keloids include acne,
folliculitis, chicken pox, vaccinations and trauma
(such as, earlobe piercing, lacerations, or surgical
wounds).
It is a benign growth, well-demarcated area of
fibrous tissue overgrowth that extends beyond the
original defect
Baron Jean-Louis Alibert
(1768-1837)
Described appearance “Chele” (crab-claw)
(also means: to grab as in “chelation”)
Crab-claw-like  Cheloid  Keloid
GRAPHIC IMAGES
Viewer discretion advised
EFFECTS OF KELOIDS
Compromise aesthetic Impairment of
function
Itchy
Pain
Purutic
How best can they be treated?
Treatment Options
Surgery
Intralesional Steroids
Radiation
Laser
Cryotherapy
Pressure
Multimodality Therapy
Still Trying
Surgery Drawbacks
Painful
Difficult reconstruction with large keloids
Utilizes normal surrounding tissue – limiting later
reconstructive options
Low long term success as monotherapy
Steroids
 Triamcinolone
 Hydrocortisone
 Dexamethasone
 Methylprednisone
Laser
1980s in vogue
Proposed Mechanism
No knife  Less tissue trauma
Cryotherapy- cold treatment
Diminishes size and induration (HTS >Keloid) when
used as monotherapy
<10% Recurrence when combined with surgery
Photos Courtesy of Dr. Redett
Pressure Therapy
Radiation
Orthovoltage machine
Produces low energies
Deposits 100% of the dose at 0.5 cm of skin surface.
Effective in treating skin lesions like keloids.
Radiation beam is directed by a cone to the site of
excision.
Beam is Filtered and collimated by copper and lead
shields- peak kilovoltage.
THE TREATMENT UNIT
TREATMENT PROCESS
Cell cycle versus cell death
The cell proliferation cycle is defined by two time
periods: Mitosis M, where division takes place.
The period of DNA synthesis S.
The S and M portions of the cell cycle are separated
by two periods (gaps) G1 and G2.
The time between successive divisions (mitoses)
is called the cell cycle time.
The cell cycle time for mammalian cells is of the
order of 10 - 20 hours:
Treatment process cont….
S phase is usually in the range of 6 - 8 hours.
M phase is less than 1 hour.
G2 is in the range of 2 - 4 hours.
G1 is in the range of 1 - 8 hours.
In general, cells are most radio-sensitive in the M and
G2 phases, and most radio-resistant in the late S
phase.
SXRT has to be delivered within 48 hours for
maximum effect.
Fate of irradiated cells
Irradiation of a cell will result in one of the following nine
possible outcomes:
 No effect
Division delay: The cell is delayed from going
through division.
 Apoptosis: The cell dies before it can divide or
afterwards by fragmentation into smaller bodies,
which are taken up by neighboring cells.
Reproductive failure: The cell dies when
attempting the first or subsequent mitosis.
Genomic instability: There is a delayed form of
reproductive failure as a result of induced
genomic instability.
CONT..
Mutation: The cell survives but contains a
mutation.
Transformation: The cell survives but the
mutation leads to a transformed phenotype and
possibly carcinogenesis.
Bystander effects: An irradiated cell can send
signals to neighboring unirradiated cells and
induce genetic damage in them.
Adaptive responses: The irradiated cell is
stimulated to react and become more resistant to
subsequent irradiation.
RADIATION SAFETY
Three principles of radiation protection:-
TIME, SHIELDING, DISTANCE.
Risk of carcinogenesis attributable to
keloid radiation therapy is very low when
surrounding tissues, including the thyroid
and mammary glands, especially in
children and infants, are adequately
protected
CUSTOMISED S LEAD
MATERIAL
CONES
1. If the technology is safe, then we will be safe.
2. If the human is safe, then we will be safe
3. If the organization is safe, then we will be safe’.
Patient tolerability
Studies indicate that post
excision SXRT is well
tolerated by patients
Non-invasive
Single day treatment
unless otherwise stated
The Other big question ?
After treatment is it acceptable ?- Aesthetically
Patient Distribution at NRC
Female Male
Ear 238 48
Abdomen 13 8
Face 9 40
others 100
360
114
210
In this case…
Plastic surgery was carried out to remove the Keloid
Scar. The patient attended the following day for a
single dose of radiotherapy to the scar, plus a small
margin of 5mm. The pinna was taped forward to
expose the effected posterior section of the lobe.
Radiotherapy prescription
12Gy in single fraction.
HVL 0.2mm Cu
Energy used was:- 100kv.
Actual Field size:- 3.5 x 1.5 cm –margins of
2mm
Cone size used:- 4 X 6cm
Shielding :-A lead cut out was used to
define the field size and protect the
surrounding
tissue.
Conclusion
Challenging cases
A case to think
A 32 year old
female
Para 1+0
No family history
of keloid
Developed keloid
after c-section
Had steroidal
injection 4
courses.
Thank You

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Keloid Disease (Case Presentation)

  • 1. KELOID DISEASE (Case Presentation) PRESENTED BY Antony Mamati. PACORI- ACCRA 2019
  • 3. We see what we want? Common things are usually very rare to spot.
  • 4. History A 23 year old female was referred by plastic surgeons for radiotherapy to the posterior ear lobe, following the development of a Keloid Scar, three years after an ear piercing No family history of keloids
  • 5. Pathology Keloid is a unique human dermal fibroproliferative disorder that occurs after injury, inflammation, surgery,and burn. Commonly causes of keloids include acne, folliculitis, chicken pox, vaccinations and trauma (such as, earlobe piercing, lacerations, or surgical wounds). It is a benign growth, well-demarcated area of fibrous tissue overgrowth that extends beyond the original defect
  • 6. Baron Jean-Louis Alibert (1768-1837) Described appearance “Chele” (crab-claw) (also means: to grab as in “chelation”) Crab-claw-like  Cheloid  Keloid
  • 8. EFFECTS OF KELOIDS Compromise aesthetic Impairment of function
  • 10. How best can they be treated?
  • 13. Surgery Drawbacks Painful Difficult reconstruction with large keloids Utilizes normal surrounding tissue – limiting later reconstructive options Low long term success as monotherapy
  • 14. Steroids  Triamcinolone  Hydrocortisone  Dexamethasone  Methylprednisone
  • 15. Laser 1980s in vogue Proposed Mechanism No knife  Less tissue trauma
  • 17. Diminishes size and induration (HTS >Keloid) when used as monotherapy <10% Recurrence when combined with surgery Photos Courtesy of Dr. Redett Pressure Therapy
  • 19. Orthovoltage machine Produces low energies Deposits 100% of the dose at 0.5 cm of skin surface. Effective in treating skin lesions like keloids. Radiation beam is directed by a cone to the site of excision. Beam is Filtered and collimated by copper and lead shields- peak kilovoltage.
  • 21. TREATMENT PROCESS Cell cycle versus cell death The cell proliferation cycle is defined by two time periods: Mitosis M, where division takes place. The period of DNA synthesis S. The S and M portions of the cell cycle are separated by two periods (gaps) G1 and G2. The time between successive divisions (mitoses) is called the cell cycle time. The cell cycle time for mammalian cells is of the order of 10 - 20 hours:
  • 22. Treatment process cont…. S phase is usually in the range of 6 - 8 hours. M phase is less than 1 hour. G2 is in the range of 2 - 4 hours. G1 is in the range of 1 - 8 hours. In general, cells are most radio-sensitive in the M and G2 phases, and most radio-resistant in the late S phase. SXRT has to be delivered within 48 hours for maximum effect.
  • 23. Fate of irradiated cells Irradiation of a cell will result in one of the following nine possible outcomes:  No effect Division delay: The cell is delayed from going through division.  Apoptosis: The cell dies before it can divide or afterwards by fragmentation into smaller bodies, which are taken up by neighboring cells. Reproductive failure: The cell dies when attempting the first or subsequent mitosis. Genomic instability: There is a delayed form of reproductive failure as a result of induced genomic instability.
  • 24. CONT.. Mutation: The cell survives but contains a mutation. Transformation: The cell survives but the mutation leads to a transformed phenotype and possibly carcinogenesis. Bystander effects: An irradiated cell can send signals to neighboring unirradiated cells and induce genetic damage in them. Adaptive responses: The irradiated cell is stimulated to react and become more resistant to subsequent irradiation.
  • 25. RADIATION SAFETY Three principles of radiation protection:- TIME, SHIELDING, DISTANCE. Risk of carcinogenesis attributable to keloid radiation therapy is very low when surrounding tissues, including the thyroid and mammary glands, especially in children and infants, are adequately protected
  • 27. 1. If the technology is safe, then we will be safe. 2. If the human is safe, then we will be safe 3. If the organization is safe, then we will be safe’.
  • 28. Patient tolerability Studies indicate that post excision SXRT is well tolerated by patients Non-invasive Single day treatment unless otherwise stated The Other big question ? After treatment is it acceptable ?- Aesthetically
  • 29. Patient Distribution at NRC Female Male Ear 238 48 Abdomen 13 8 Face 9 40 others 100 360 114 210
  • 30. In this case… Plastic surgery was carried out to remove the Keloid Scar. The patient attended the following day for a single dose of radiotherapy to the scar, plus a small margin of 5mm. The pinna was taped forward to expose the effected posterior section of the lobe.
  • 31. Radiotherapy prescription 12Gy in single fraction. HVL 0.2mm Cu Energy used was:- 100kv. Actual Field size:- 3.5 x 1.5 cm –margins of 2mm Cone size used:- 4 X 6cm Shielding :-A lead cut out was used to define the field size and protect the surrounding tissue.
  • 34. A case to think A 32 year old female Para 1+0 No family history of keloid Developed keloid after c-section Had steroidal injection 4 courses.