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Table of Content - Volume 11 Issue 2 - August 2018


 

A study of autologous epidermal non-cultured cell suspension in stable vitiligo patients

 

Madhavilatha M1, Thejaswi C2*

 

1Professor, 2Post Graduate Student, Department of Dermatology, Venereology and Leprosy, Santhiram Medical College, Nandyala, Kurnool Andhra Pradesh, INDIA.

Email: prabhakarrao10696@gmail.com

 

Abstract              Background: To study the extent of repigmentation after autologous epidermal non-cultured cell suspension in stable vitiligo patients. Patients and Methods: A prospective, longitudinal study was conducted to study the extent of repigmentation after autologous epidermal non-cultured cell suspension in 30 stable vitiligo patients. Results: By subjective assessment, 10% (3) patients showed poor response, 30% (9) showed good response and 60% (18) patients showed excellent response after follow-up at 6 months with good patient satisfaction. By objective assessment 10% (3) patients showed poor response, 13.3% (4) showed fair response and 23.3% (7) patients showed good response, 53.3% (16) patients showed excellent response after follow-up at 6 months. Extent of repigmentation was evaluated as - 10% (3) showed poor response, 10% (3) showed fair response and 20% (6) patients showed good response, 60% (18) patients showed excellent response after follow-up at 6 months. Conclusion: Autologous non-cultured epidermal cell suspension in stable vitiligo is a safe, effective, simple method, with superior quality of repigmentation.

 Keywords: Vitiligo, vitiligo surgery, grafting, dermabrasion, repigmentation, non-cultured melanocytes.

 

INTRODUCTION

Vitiligo is an autoimmune disorder characterized by asymptomatic, localized and/or generalized depigmentation of the skin and/ or mucous membranes in the form of typical chalky-white or milky macule(s)1 with incidence ranges from 0.1 to > 8.8% across India,1,2 most of the studies showing female preponderance.1 Many treatment modalities are currently used for vitiligo like topical, systemic, phototherapy, lasers and surgical methods. Recent surgical advances include autologous non-cultured epidermal cell suspensions and cultured melanocyte suspensions.3 A study was undertaken to evaluate the extent of repigmentation after autologous epidermal non-cultured cell suspension in stable vitiligo patients. A complete history with precipitating factors, previous medical treatment, any associated diseases, was obtained followed by a complete physical examination. Routine blood investigations were done and tests for thyroid function done where required. Preoperative photographs of donor and recipient area were taken. Postoperative pigmentation was evaluated using scoring system and digital photography.

 

PATIENTS AND METHODS

Patients

Study population:

The study is conducted on a study population of 30 patients presenting with stable vitiligo attending OPD in Department of DVL, Santhiram Medical College and General Hospital, Nandyal.

Inclusion criteria:

1) Stable vitiligo not responding to medical treatment, (stability as defined by IADVL taskforce)

Exclusion criteria:

  1. Age < 12 years, > 50 years
  2. Unstable vitiligo
  3. Koebner’s phenomenon
  4. Keloidal and hypertrophic scar tendency
  5. Patients with platelet disorders, anemia or bleeding disorders.
  6. Immunocompromised patients like HIV, Hepatitis B or C positive
  7. Patients who have active skin disease/infection at treatment area.
  8. Un-cooperative patients or patients unable to understand the protocol or give informed consent

Methods

  1. Ethical clearance from the instituitional ethics committee
  2. Informed written consent
  3. Pre-structured proforma
  4. Preoperatively, patients will be assessed and,
  5. Investigated with routine investigations and special investigations when required.

The data has been collected and analysed in an excel sheet. Proportions are calculated for the data.


 

RESULTS

Criteria for evolution

Score

Factor

Total

0

1

2

3

A.Extent of pigmentation

≤50%

51%-70%

71%-90

>90

X5

 

B. Color match

Poor

Good

Excellent

-

X3

 

C. Complications (Recipient area)**

Minimal cobblestone/variegated appearance

Moderate to marked cobblestone/variegated appearance milia

Thick graft margins, wrinkles over graft ,type patch appearance

Keloid hypertrophic scar

X-3

 

D. Complications (Donor area)**

Minimal hypo/hyperpigmentation, minimal scarring

Moderate hype/hyper pigmentation, moderate scarring

Gross hype/hyperpigmentation, unsightly scarring

Keloid depigmentation

x-2

 

Result: 17-21-Excellent; 12-16-Good;7-11-Fair; 6 or less-Poor

(A+B+C+D)

*Excellent color match-Minimal hypo or hyperpigmentation of grafted area not requiring camouflage.

*Good color match-Moderate hypo or hyperpigmentation amenable to light camouflage.

*Poor color match-Gross hypo or hyperpigmentation difficult to cover up with ordinary make up.

**In presence of complications belonging to more than one score, only the highest score should be multiplied the factor

 

On removal of dressing on the recipient area, crusted scabs were seen partially attached to dermabraded area, along with erythematous achromic areas. Repigmentation usually started by 2- 3 weeks and was complete within 6 months in most of the patients. Earliest onset of pigmentation was observed within 10 days with pin-point pigmentation. In some patients with perifollicular type of repigmentation, initially islands of pigmentation was seen which later coalesced to form uniform repigmentation. Whereas in other patients, diffuse pigmentation was seen in central part of vitiliginous area, then gradually spread to pigment surrounding margins. Repigmentation was rapid and maximum in initial 3-4 months, then slowed in the following months. Repigmentation in donor area was of perifollicular type in all patients and was completed within 1- 6 months.

             Photo 1: Before procedure Photo1b: After dressing removal            Photo 1c: After 10 days of procedur Photo 1d: After 6 months

Photo 2a: Before procedure Photo 2b: After 6 months Photo 3a: Before procedure   Photo 3b: After 6 months

Photo 4a: Before procedure  Photo 4b: After 6 months Photo 5a : Before procedure            Photo 5b: After 6 months

   Photo 6a: Before procedure  Photo 6b: After 6 months

 

DISCUSSION

This procedure is also known by other names like non-culture melanocyte transfer, basal cell suspension technique, non-culture cellular transplant.7 The principle is seeding of melanocytes i.e. introduction of melanocytes from normal skin into a region of depigmented skin 8. The basic principle is to separate the basal cells and the melanocytes by trypsinization, and prepare a suspension which is applied on the dermabraded lesional skin 9. During the initial 7 days of healing, melanocytes and keratinocytes present in the grafted material, multiply and repigment the depigmented area. Further pigmentation can be accelerated by topical psoralen therapy 9, NBUVB and PUVA. However, some authorities use phototherapy only if there is delay in onset of repigmentation 6,10. Pigmentation in the treated areas gradually increases in size due to melanocyte proliferation and migration under the influence of cytokines secreted by surrounding keratinocytes. Hence, melanocytes taken from a small donor can pigment a much larger recipient area 9.A total of 30 patients were included in this prospective longitudinal study and followed up at 1 month, 3 months and 6 months. All patients completed the study.

 

Table 1: Age

STUDY

AGE GROUP

between

PROPORTION

PRESENT STUDY

20 patients

12 – 50 years

Youngest -12 years Oldest - 50 years.

Highest proportion - 40 % (8) patients in

group 21-30 years

11

Sobhy            et al

13 – 33 years

Highest proportion - 60% in age group <15 years

 

Table 2: Sex

STUDY

MALES

FEMALES

Present study

33.3% (10) patients

66.7% (20) patients

11

Sobhy            et al

7 patients

13 patients

12

Rajesh Verma                  et al

52.6% (10)

47.4% (9)

 

 

                                           Figure 1: Duration of stability                                     Figure 2: Associated Diseases

Sobhy13 et al found that the most important variable is the stability of the disease (2 years or more) rather than the duration of the disease. But, in the present study, patients with stability less than 2 years were also included according to IADVL task force guidelines regarding the stability.

In this study, association with only thyroid disease has been noted, 83.3% (25) patients had normal thyroid function tests, whereas 16.7% (5) patients had abnormal thyroid function tests. All 5 patients with abnormal thyroid function tests were females.

 

Figure 3: Subjective Assessment  Figure 4: Objective assessment


Figure 5: Overall EOP

After follow-up at 6 months, 10% (3) showed poor response, 30% (9) showed good response and60% (18) patients showed excellent response.

After follow-up at 6 months, 10% (3) showed poor response, 13.3% (4) showed fair response and% (7) patients showed good response, 53.3% (16) patients showed excellent response.Gauthier14 in study has reported incomplete repigmentation in 20% of patients, probably due to type of vitiligo.

After follow-up at 6 months 10% (3) showed poor response, 10% (3) showed fair response and20% (6) patients showed good response, 60% (18) patients showed excellent response.

 

Table 4:

 

STUDY

COMPARATIVE REPIGMENTATION IN OTHER STUDIES (IN %)

EXCELLENT

GOOD

FAIR

POOR

PRESENT STUDY

60

20

10

10

Munish paul6

65

18

8

8

Sobhy11 et al

35

55

10

NIL

RajeshVerma12 et al

NIL

62

20

18

Pandya15 et al

52.2

_

_

_

 

AGE AT PRESENTATION VERSUS EXTENT OF PIGMENTATION AT 6 MONTHS

At the end of 6 months, excellent repigmentation was seen in 100% (5) patients in age group 11- 20 years and repigmentation observed was better and occurred earlier in younger patients than in older patients.Sobhy11 et al, also reported earlier repigmentation and better prognosis in age group <15 years than in older patients, probably due to younger cell that grows and multiplies rapidly.Czajkowski R9, also has found that the time of proliferation of melanocytes in invitro culture conditions depends on the age of the patient and, younger the patient, faster is the melanocytes proliferation.

ADVERSE EFFECTS IN DONOR AND RECIPIENT AREA

Though initially some patients developed hyperpigmentation and mild textural abnormality at donor site, after few months, they gradually decreased to match with surrounding area. Similarly, hyperpigmentation at recipient area too gradually decreased and they were not a significant causeof distress to the patients. Further, in this study, none of the patients had developed donor site infection, hypopigmentation and scarring.

 

STUDY

DONOR AREA

RECIPIENT AREA

PRESENT STUDY

Hyperpigmentation – 20% (6) patients

Infection/hypopigmentation scarring - NONE

Hyperpigmentation – 33.3% (10) patients

Van geel et al

Minor textural changes - 65%

Color mismatch - 80.4% (54)

Gauthier14

No     hypopigmentation,     scars          or keloid

Imperfect color matching - 20%

Munish paul6

Hyperpigmentation - 5

Hyperpigmentation - 12% (6) patients

 

Hypopigmentation - 8% (4) patients Hypopigmented border -12 patients

Pandya15 et al,

Infection - 7.4%

 

Koebner’s response - 1 patient

_

Sobhy11 et al

_

Hyperpigmentation - 1 patient Hypopigmentation - 1 patient

 


CONCLUSION

In the present study, by subjective assessment, 10% (3) patients showed poor response, 30% (9) showed good response and 60% (18) patients showed excellent response after follow-up at 6 months with good patient satisfaction. By objective assessment 10% (3) patients showed poor response, 13.3% (4) showed fair response and 23.3% (7) patients showed good response, 53.3% (16) patients showed excellent response after follow-up at 6 months. Extent of repigmentation was evaluated as - 10% (3) showed poor response, 10% (3) showed fair response and 20% (6) patients showed good response, 60% (18) patients showed excellent response after follow-up at 6 months. Repigmentation was uniform, matched well with surrounding skin and usually completed within 6 months. Cosmetic acceptability is also superior as there is no cobble-stoning or scarring seen in other methods, giving good patient satisfaction. The study confirms that repigmentation by autologous non-cultured epidermal cell suspension in stable vitiligo is a safe, effective, and simple method, with superior quality of repigmentation, very few adverse effects and high level of patient satisfaction with possibility to repigment vitiliginous skin manifold larger than the donor skin.

 

REFERENCES

  1. Sehgal V Srivastava G. Vitiligo: Compendium of clinico-epidemiological features. Indian J Dermatol Venereol Leprol. 2007;73(3):149-56.
  2. Davinder Parsad, Sendhil M Kumaran. Depigmentary and hypopigmentary disorders. In: Sacchidanand S, editor. IADVL Textbook of Dermatology.4ed.Bhalani Publishing House;2015.P1308-1322.
  3. Nanja van Geel and Reinhart Speeckaert. Acquired pigmentary disorders. In: C Griffiths, J Barker, T Bleiker, R Chalmers D Creamer, editors. Rook’s textbook of dermatology. 9th ed, Wiley-Blackwell publishing; 2016. p88.34-88.40.
  4. Majid I. Efficacy of targeted narrowband ultraviolet B therapy in Vitiligo. Indian Journal of Dermatology. 2014;59(5):485.
  5. Gupta S, Honda S, Kumar B. A novel scoring system for evaluation of results of autologous transplantation methods in vitiligo. Indian J Dermatol Venereal Leprol 2002;68:33-7.
  6.  Paul M. Autologous non-cultured basal cell-enriched epidermal cell suspension transplantation in vitiligo: Indian experience. Journal of Cutaneous and Aesthetic Surgery. 2011;4(1):23.
  7. Majid I. Grafting in vitiligo: How to get better results and how to avoid complications. Journal of Cutaneous and Aesthetic Surgery. 2013;6(2):83.
  8. Picardo M, Boissy R, Dell′Anna M. On the pathophysiology of vitiligo: Possible treatment options. Indian Journal of Dermatology, Venereology, and Leprology. 2012;78(1):24.
  9. Czajkowski R: Comparision of melanocytes transplantation methods for the treatment of vitiligo. Dermatol Surg. 2004;30:1400-5.
  10. Mysore VSalim T. Cellular grafts in management of leucoderma. Indian Journal of Dermatology.2009;54(2):142.
  11. Sobhy N, Atia A, Elramly M. Some modifications in transplantation of autologus non -cultured melanocytes-keratinocytes suspension in treatment of segmental and focal vitiligo (Egyptian Experience in Alexandria University). Our Dermatology Online. 2013;4(1):5-10.
  12. Verma R, Grewal R, Chatterjee M, Pragasam V, Vasudevan B, Mitra D. A comparative study of efficacy of cultured versus non cultured melanocyte transfer in the management of stable vitiligo. Medical Journal Armed Forces India. 2014;70(1):26-31.
  13. Sobhy N, Elbeheiry A, Elramly M, Saber H Kamel L, Soror O: Transplantation of non-cultured melanocytes versus dermabraton and split thickness grafting in cases of non-progressive vitiligo and stable forms of leukoderma. MD thesis Alexandria Dermatology Department 2002.
  14. Gauthier YBenzekri L. Non-cultured epidermal suspension in vitiligo: From laboratory to clinic. Indian Journal of Dermatology, Venereology, and Leprology. 2012;78(1):59-63.
  15. Pandya V, Parmar K, Shah B, Bilimoria F. A study of autologous melanocyte transfer in treatment of stable vitiligo. Indian Journal of Dermatology, Venereology and Leprology. 2005;71(6):393-7.






 





 


 

 



 





 


 

 

 



 




 











 









 


 









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