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Pyogenic Granuloma of the Cornea in an Infant With Unilateral Microphthalmia
Arch Ophthalmol. 2003;121:1197-1200.
Pyogenic granuloma is an exuberant proliferation of granulation tissue that typically develops after minor trauma or surgery. This well-known, common inflammatory entity occurs most often on the skin of the face and extremities.1-2 Ocular pyogenic granulomas are usually found on the external surface of the eyelid or the palpebral conjunctiva.1-2 They can also occur at the limbus or on the bulbar conjunctiva, simulating a pterygium or a squamous cell carcinoma.3-4 Few have been reported on the cornea, probably because of its avascularity.1-2,4-9 A constant clinical finding of these reported corneal lesions is either an epithelial defect in the presence of corneal neovascularization and ocular surface disease or chronic chemical and/or mechanical irritation. Abnormal corneal vessels are the source of the newly formed proliferating capillaries.
We report an unusual case of a pyogenic granuloma of the cornea in an infant secondary to mechanical ocular trauma induced by prosthetic fitting for microphthalmia. The granuloma initially was thought to be a sporadic event, but the histopathologic findings implicate an in utero perforation, presumably the result of early midtrimester amniocentesis.
Report of a Case
A healthy 1-week-old girl was referred because, at birth, her left eye was noted to be small and a spot was noted on the left cornea. She had no family history of ocular abnormalities. A transabdominal amniocentesis was performed in the 19th week of gestation because of an elevated  -fetoprotein level. The procedure was performed by an experienced gynecologist in a single attempt under ultrasonographic guidance. It was reported to us that the tap was not bloody, and therefore the procedure was considered to be nontraumatic. It is not known whether the ultrasonographer had the amniocentesis needle in constant ultrasonic view or whether the fetus shifted during the procedure.
Examination at age 1 week showed that the left orbit was slightly shallow. The left palpebral fissure was estimated to be two thirds the size of the right. The left cornea was estimated to be 5 mm in diameter compared with 9 mm for the right eye. There was a small tan corneal opacity, about 2 mm in diameter, just above the pupil. The anterior segment appeared otherwise normal, except for a small pupil that could not dilate well and precluded examination of the left fundus. The right eye was anatomically normal.
The child was referred to an ocularist to be fitted with a scleral shell to expand the size of the smaller left fissure. A scleral shell composed of polymethylmethacrylate that measured 12.8 x 12.3 x 3.7 mm was fitted at age 3 weeks. One month later, a larger scleral shell (16.1 x 14.4 x 4.5 mm) was fitted. Each scleral shell had a stem to aid in its removal. The scleral shell was worn constantly and removed and cleaned on a weekly basis.
Shortly afterward, the mother noted that the child's left eye was red with mucous discharge and swelling of the eyelids. Examination by an ophthalmologist revealed a corneal ulcer with a white infiltrate in the left eye. The patient was treated with topical and intravenous antibiotics. A culture was not obtained. The eyelid swelling and ocular hyperemia resolved, although the mother noted a lump on the left cornea that gradually grew during a 1-week period. Examination at that point revealed no eyelid swelling and a white conjunctiva. A smooth-surfaced, pink, elevated mass occupied the central four fifths of the cornea, covering the previously existing tan opacity. The central part of the lesion was tan. The lesion moved with the eyeball, which precluded detailed examination of the other intraocular structures. The fellow eye was normal.
The following week, the mother reported that the lesion had increased markedly in size. An examination under anesthesia was performed to define further the extent and nature of the lesion. The palpebral fissures measured horizontally 17 mm OD and 14 mm OS. The corneas measured horizontally 10 mm OD and 6.5 mm OS. The conjunctiva of the left eye was hyperemic. On the central cornea there was a well-circumscribed, elevated, sessile, smooth, vascular mass measuring 6 x 4.5 mm (Figure 1). Ultrasound biomicroscopy revealed a corneal mass sealing a site of what appeared to be a corneal perforation (Figure 2). The right eye was normal. An excisional biopsy of the corneal lesion was performed. After excision, exposed uveal tissue was noted in the central part of the cornea, so a Gunderson conjunctival flap was used to cover the defect. Because there was concern about sympathetic ophthalmia, the left eye was enucleated 1 month later, and a Medpor (Porex Surgical Inc, Newnan, Ga) implant was placed in the left socket.
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Figure 1. The anterior segment of the left eye shows microphthalmia with pyogenic granuloma of the cornea.
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Figure 2. Ultrasound biomicroscopy reveals a round, pedunculated mass (top arrow) arising from the cornea and sealing the site of perforation (bottom arrow).
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Histopathologic Findings
Macroscopically, the excisional biopsy specimen consisted of a smooth mass of pink soft tissue measuring 6 x 4 x 2 mm. Microscopic examination revealed a multilobed mass whose anterior part was composed of an exuberant proliferation of granulation tissue (Figure 3 A and B). Peripherally the surface of the granuloma was partially covered by thickened conjunctival epithelium. Large folds and pseudorosettes of retina adhered to and were incorporated within the base of the granuloma (Figure 3C). The findings were consistent with a mass of granulation tissue (pyogenic granuloma) incorporating neurosensory retina.
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Figure 3. Histopathologic findings from the resected corneal lesion are consistent with a mass of granulation tissue (pyogenic granuloma) incorporating neurosensory retina. A, Microscopic examination reveals a multilobed mass whose anterior part is composed of an exuberant proliferation of granulation tissue (top arrow). Peripherally the surface of the granuloma is partially covered by thickened conjunctival epithelium. Large folds and pseudorosettes of retina (bottom arrow) are adherent to and incorporated within the base of the granuloma (hematoxylin-eosin, original magnification x10). B, Granulation tissue (pyogenic granuloma) composed of radially oriented proliferating capillaries (arrow) and inflammatory cells (hematoxylin-eosin, original magnification x50). C, Incorporated retinal tissue (arrow) (hematoxylin-eosin, original magnification x25).
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Gross examination of the enucleated eye revealed a markedly microphthalmic globe measuring 12 x 10 x 11 mm, with a corneal perforation and a totally detached retina. Microscopic examination revealed lens material and neurosensory retina prolapsing and incorporated within a perforation of the central cornea. Extensive anterior synechiae were noted.
Comment
Since the first description in 1897, pyogenic granulomas have been reported in many sites, including the eyelid skin, conjunctiva, limbus, lacrimal puncta, acquired anophthalmic orbits, and veins of ocular adnexa.1-2 The occurrence of pyogenic granuloma on the cornea is relatively rare. Googe et al1 reviewed the topic in 1984, and a few cases have been reported since then.2, 5-7,9 Of the previously reported corneal pyogenic granulomas, the youngest patient was aged 10 years.7 Pyogenic granuloma in the cornea has been reported to occur between 1 month to 18 years after the injury.7 There are some morphologic differences between pyogenic granulomas of the cornea and those of other locations. Corneal lesions appear to be more often sessile.2 The lack of a vascular stalk may be responsible for the more sessile form, primarily because the cornea is an avascular tissue. The morphological appearance of pyogenic granulomas of the cornea may be also influenced by chronic mechanical stress from blinking, which may limit the exophytic growth. These 2 factors may be responsible for a typically more intense inflammatory response compared with pyogenic granulomas in other locations.2 Despite its rarity, pyogenic granuloma should be considered in any child with a fleshy, vascular, elevated, rapidly growing corneal mass, especially in the setting of ocular trauma. Such lesions might be misdiagnosed as an anterior segment choristoma, a vascular hamartoma, a teratoma, a viral papilloma, or a squamous cell carcinoma. The age of onset, history of prior trauma, and rapid growth will often point to the correct diagnosis. In our patient we suspected that the lesion was a pyogenic granuloma because it was acquired and grew rapidly. An excisional biopsy was performed to make a definite diagnosis.
The possibility that the diagnostic amniocentesis and constellation of findings in our patient may be related is also worthy of consideration. The use of transabdominal amniocentesis as a means for prenatal diagnostic evaluation of genetic and other congenital diseases has become common in recent years. It has been assumed to be safe for both the mother and the fetus. Despite the recognized safety of the procedure, fetal injuries occur in 3% to 4% of cases.10 Most are innocuous injuries to the skin, which leave only small cutaneous scars.10 Ocular injuries by amniocentesis are rare. We found 6 reports of ocular perforation.11-16 All of them describe trauma to the anterior segment and 2 to the posterior segment. A corneal leukoma may also be a sign of an "old" perforation caused by diagnostic amniocentesis. In our case, the procedure was performed by an experienced gynecologist immediately after ultrasonography, and the tap was considered nontraumatic. The findings of an underdeveloped eye together with evidence of a healed corneal perforation in the presence of a chronically detached retina suggest a perforation during amniocentesis. The partial sealing of the cornea prevented extreme hypotonia and probably allowed further development and differentiation of the ocular structures, including the retina.
In our case, the scleral shell presumably abraded the in utero perforation site. This may have led to an irritated eye and an epithelial defect that appeared to be an ulcer. Corneal infection and ulceration resulted in corneal perforation. To our knowledge, pyogenic granuloma of the cornea in response to perforation from mechanical trauma secondary to the use of a prosthetic scleral shell has not been reported.
Microphthalmia was the initial sign in our patient. Our clinical impression originally was congenital, unilateral, isolated microphthalmia of the left eye. It was not felt that any additional evaluation was warranted. This case report adds support to the notion that microphthalmia can be a rare complication of amniocentesis. We speculate that what had originally been interpreted as a sporadic event may have been caused by unrecognized ocular trauma. It is possible that the previously healed anterior segment injury resulted in a cornea predisposed to another perforation. Perhaps one insult alone is not sufficient to produce a corneal pyogenic granuloma, and the reason that these granulomas are rare, but found in this case, is that in this case the cornea sustained 2 different insults. We are unaware of any similar reports. The presence of a common entity in an unusual site was precipitated by mechanical trauma from the use of an ocular prosthesis for unilateral microphthalmia following midtrimester amniocentesis.
AUTHOR INFORMATION
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The authors have no relevant financial interest in this article.
This study was supported in part by Fight for Sight, Inc, New York, NY.
Ekaterini C. Karatza, MD;
Joseph H. Calhoun, MD;
Ralph C. Eagle, Jr, MD
Philadelphia, Pa
Corresponding author and reprints: Joseph H. Calhoun, MD, Pediatric Ophthalmology Service, Wills Eye Hospital, 840 Walnut St, Philadelphia, PA 19107.
REFERENCES
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1. Googe JM, Mackman G, Peterson MR, et al. Pyogenic granulomas of the cornea. Surv Ophthalmol. 1984;29:188-192.
PUBMED
2. Mietz H, Arnold G, Kirchhof B, Krieglstein GK. Pyogenic granuloma of the cornea: report of a case and review of the literature. Graefes Arch Clin Exp Ophthalmol. 1996;234:131-136.
PUBMED
3. Ferry AP, Zimmerman LE. Granuloma pyogenicum of limbus. Am J Ophthalmol. 1965;74:229-230.
4. Minckler D. Pyogenic granuloma of the cornea simulating squamous cell carcinoma. Arch Ophthalmol. 1979;97:516-517.
ABSTRACT
5. De Potter P, Tardio DJ, Shields CL, Shields JA. Pyogenic granuloma of the cornea after penetrating keratoplasty. Cornea. 1992;11:589-591.
PUBMED
6. Proia AD, Small KW. Pyogenic granuloma of the cornea induced by "snake oil." Cornea. 1994;13:284-286.
PUBMED
7. Cameron JA, Mahmood MA. Pyogenic granulomas of the cornea. Ophthalmology. 1995;102:1681-1687.
ISI
| PUBMED
8. Spraul CW, Grossniklaus HE. Tumors of the cornea and conjunctiva. Curr Opin Ophthalmol. 1996;7:28-34.
PUBMED
9. Papadopoulos M, Snibson GR, McKelvie PA. Pyogenic granuloma of the cornea. Aust N Z J Ophthalmol. 1998;26:185-188.
PUBMED
10. Karp LE, Hayden PW. Fetal puncture during midtrimester amniocentesis. Obstet Gynecol. 1977;49:115-117.
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11. Cross HE, Maumenee AE. Ocular trauma during amniocentesis. Arch Ophthalmol. 1973;90:303-304.
PUBMED
12. Fortin JG, Lemire J. Une complication oculaire de l'amniocentese. Can J Ophthalmol. 1975;10:511-513.
PUBMED
13. Merin S, Beyth Y. Uniocular congenital blindness as a complication of midtrimester amniocentesis. Am J Ophthalmol. 1980;89:299-301.
PUBMED
14. Isenberg SJ, Heckenlively JR. Traumatized eye with retinal damage from amniocentesis. J Pediatr Ophthalmol Strabismus. 1985;22:65-67.
PUBMED
15. Admoni MM, BenEzra D. Ocular trauma following amniocentesis as the cause of leukocoria. J Pediatr Ophthalmol Strabismus. 1988;25:196-197.
PUBMED
16. BenEzra D, Sela M, Peer J. Bilateral anophthalmia and unilateral microphthalmia in two siblings. Ophthalmologica. 1989;198:140-144.
PUBMED
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