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ABSTRACT
Aims: To determine the efficacy and safety
of using Mitomycin C in the management of pterygium.
Methods: A retrospective study of 37 eyes
(30 patients ), with the mean age of 43 years
(30 -55 years) attending the ophthalmology clinic.17
eyes(17 patients ) were treated by using Mitomycin
C; 14 eyes had primary pterygia and 3 eyes with
recurrent pterygia. 20 eyes (13 patients ) were
treated without use of Mitomycin C; 15 eyes had
primary pterygia and 5 eyes had recurrent pterygia.
All eyes received the same medications postoperatively.
Results: In the Mitomycin C treated eyes,
we noted that only 2 eyes (11.7%) had recurrent
pterygia, after 14 months follow-up, but the recurrence
in the non-Mitomycin C group was higher than that
of the Mitomycin group; with 9 eyes (45%) having
recurrence after the same period of follow-up.
Also we noted that the healing of conjunctiva
was delayed when we used Mitomycin C in comparison
to the other group; which is a known side effect
of Mitomycin C.
Conclusion: From these results we conclude
that the use of Mitomycin C in the management
of pterygium is effective in decreasing the recurrence
of pterygia after excision. So it is a simple,
safe and successfull procedure that we recommend
in all pterygium management.
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INTRODUCTION
A pterygium is an abnormal (non-cancerous)
growth of the conjunctiva; a triangular fibrovascular
sub-epithelial ingrowth of degenerative bulbar conjunctival
tissue over the limbal onto the cornea(1). The conjunctiva
is a thin membrane lining the inside of the eyelid and
part of the eyeball (located between the sclera, or
the "white of the eye") which surrounds the
eyeball.
Excessive growth of the conjunctiva
leads to a pterygium, which appears as a fleshy spot.
Pterygia are nearly always preceded and accompanied
by pingueculae(2).
The exact cause of pterygium is unknown. The most common
factors that contribute to pterygium include:
Excessive exposure to sunlight
Sex: Male
Increasing age
Working outdoors
Excessive exposure to harsh environmental conditions
such as dust, dirt, heat, wind, dryness, and smoke
Excessive exposure to allergens such as industrial solvents
and chemicals.
The symptoms of pterygia include
the following: redness, irritation, tearing, foreign
body sensation, dryness, sometime blurring of vision
especially when it causes corneal astigmatism(11).
Management of pterygium can
be divided into
Observation:
- Periodic eye examination,
usually when the pterygium causes no or minimal symptoms
- If symptoms increase,
additional treatments may include:
- Medications: prescription antibiotics to prevent
infection; corticosteroids to reduce inflammation;
ocular lubricants
- Radiation therapy to stop pterygium cells from reforming(7).
- Mitomycin C to aid in healing and prevent recurrence(8).
Surgery
Indications for pterygium excision include(12): persistent
discomfort, vision distortion, and restricted ocular
motility. Microsurgical excision of a pterygium aims
to achieve a normal, topographically smooth ocular surface(3).
Mitomycin (Mitomycin C; MMC)
is an antibiotic isolated from Streptomyces caespitosus.
The drug is a bioreductive alkylating agent that undergoes
metabolic reductive activation, and has various oxygen
tension-dependent cytotoxic effects on cells, including
the cross-linking of DNA. It is widely used systemically
for the treatment of malignancies, and has gained popularity
as topical adjunctive therapy in ocular and adnexal
surgery over the past 2 decades(6). Its use has been
described in the management of ocular surface neoplasias(4), conjunctival malignant melanoma and primary acquired
melanosis with atypia(5), and in conjunctival intraepithelial
neoplasia(10).
Complications of topical Mitomycin
C have been described in the litreture and include the
following: scleral necrosis and thinning, perforation,
endophthalmitis, endothelial decompensation, glaucoma,
and iritis(9).
MATERIALS AND METHODS
A retrospective study of 37
eyes (30 patients), with the mean age of 43 years (30
-55) years attending the ophthalmology clinic.
We divided the patients into
two main groups; in the first group we use Mitomycin
C, and in the second we only excised the pterygium.
17 eyes (17 patients) were treated
by using Mitomycin C; 14 eyes had primary pterygia and
3 eyes with recurrent pterygia. 20 eyes (13 patients)
were treated without the use of Mitomycin C; 15 eyes
had primary pterygia and 5 eyes had recurrent pterygia.
All eyes received the same medications postoperatively.
The examination included:
- Visual Acuity-a test
to measure the patient's ability to see and read the
smallest letters on an eye chart (by using Topcon
chart projector (vision tester VT-SE; Topcon Co, Japan)
with E letters at a distance of 6 meters.
- Slit Lamp Examination-a
bright light with magnification used to view the eye.
- Photo Documentation-Photography
to record the degree of growth of a pterygium.
The cornea and conjunctiva
were examined by using binocular slit lamp microscope
with magnification, and we chose the patient who had
pterygium indicated for surgical excision (a condition
that causes one of these; visual impairment, persistent
discomfort, and restriction of ocular motility).
We excluded from this
study; pingueculae, simple pterygia that cause no or
minimal symptoms.
In this study we applied
0.4 mg/ml Mitomycin C intra-operatively for 3 minutes
following pterygium excision.
RESULTS
Of the 37 eyes (30 patients);
had Mitomycin C treated eyes (17 eyes). We noted that
only 2 eyes (11.7% ) had recurrent pterygia, after 14
months follow-up (see Table 1), but the recurrence in
the non-Mitomycin C group (20 eyes) was higher than
that of the Mitomycin group 9 eyes (45%) after the same
period of follow-up (see Table 2). Also we noted that
the healing of conjunctiva was delayed when we use Mitomycin
C in comparison to the other group; which is a known
side effect of Mitomycin C; and it is not a significant
complication because we use it in a minimal dose for
a short period of time.
The postoperative recurrent
pterygia in the Mitomycin C group were not from the
primary pterygia, but only from the recurrent pterygia
(preoperative). The recurrent pterygia in the non-Mitomycin
C group were from both primary and recurrent pterygia.
Table
1. Recurrent rate in Mitomycin Group
|
|
Pre-op. |
Post-op. |
| Primary |
Recurrent |
Primary |
Recurrent |
|
Males |
9 |
2 |
0 |
1 |
|
Females |
5 |
1 |
0 |
1 |
|
Total |
14 |
3 |
0 |
2 |
|
Recurrent rate |
|
|
2 eyes (11.7%) |
Table
2. Recurrent rate in Nonmitomycin Group
|
|
Pre-op. |
Post-op. |
| Primary |
Recurrent |
Primary |
Recurrent |
|
Males |
10 |
3 |
2 |
3 |
|
Females |
5 |
2 |
1 |
3 |
|
Total |
15 |
5 |
3 |
6 |
|
Recurrent rate |
|
|
9 eyes (45%) |
DISCUSSION
Pterygium is a common disorder
affecting conjunctiva and cornea especially in hot and
dry environmental areas. It is insignificant when it
is simple and not causing discomfort to the patient
and does not need aggressive management except observation
and some medications such as antibiotics to prevent
the infections; corticosteroids to reduce inflammation;
and ocular lubricants.
Pterygium is significant when
it causes patients discomfort (persistent), visual impairment,
and restriction of ocular motility. These are indications
for excision of pterygium which can be either excision
alone or excision along with adjunctive therapy such
as Mitomycin C, 5 fluorouracil, etc.
The former has had a high recurrence
rate which is annoying for the patient.
In this study we use Mitomycin
C intra-operative with the excision , and we follow-up
these patients, with good results. Recurrence of pterygia
was decreased and there were minimal complications.
From these results we recommend the use of Mitomycin
C in pterygium management because it is a simple, safe,
and successful procedure.
REFERENCE
- Jack J. kanski, Jay
Menon. Clinical Ophthalmology, a systemic approach,
fifth ed. 2003;82-3.
- Thomas J, Lirsegang, Jacksonville,
Florida. American Academy of Ophthalmology. 2002;
section8:339-341.
- Thomas J, Lirsegang, Jacksonville,
Florida. American Academy of Ophthalmology. 2002;
section8:394-396.
- E G Kemp, A N Harnett, and S Chatterjee.
Preoperative topical and intraoperative local mitomycin
C adjuvant therapy in the management of ocular surface
neoplasias, Br J Ophthalmol. 2002 January; 86(1):
31-34.
- Demirci H, McCormick SA, Finger PT.
Topical mitomycin chemotherapy for conjunctival malignant
melanoma and primary acquired melanosis with atypia.
Arch Ophthalmol 2000;118:885-91.
- Abraham, Lekha M.;
Selva, Dinesh; Casson, Robert; Leibovitch, Igal. Mitomycin:
Clinical Applications in Ophthalmic Practice. Drugs,
Volume 66, Number 3, 2006 , pp. 321-340(20).
- Parida DK; Agarwal S; Rath GK, The
role of radiotherapy in the management of Pterygium.The
Indian Practitioner. 1999 Jul; 52(7): 466-8.
- Anduze AL. Pterygium surgery with mitomycin-C:
ten-year results.
Ophthalmic Surg Lasers. 2001 Jul-Aug;32(4):341-5.
- Tsai YY, Lin JM,
Shy JD. Acute scleral thinning after pterygium excision
with intraoperative mitomycin C. Cornea. 2002;21:227-229.
- Rozenman Y, Frucht-Pery
J. Treatment of conjunctival intraepithelial neoplasia
with topical drops of mitomycin C. Cornea 2000;19:1-6.
- Kampitak K.The effect
of pterygium on corneal astigmatism. J Med Assoc Thai.
2003 Jan;86(1):16-23.
- Assia E. Surgical management of pterygium.
Isr Med Assoc J. 2002 Dec;4(12):1138-9.
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