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Klinika Oczna / Acta Ophthalmologica Polonica
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2/2021
vol. 123
 
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Original paper

Benign tumors of the orbit in children and adolescents – clinical and histopathological analysis

Marta Świerczyńska
1, 2
,
Erita Filipek
1, 2

1.
Department of Pediatric Ophthalmology, Faculty of Medical Sciences in Katowice, Medical University of Silesia, Katowice, Poland
2.
Department of Pediatric Ophthalmology, Kornel Gibiński University Clinical Center, Medical University of Silesia, Katowice, Poland
KLINIKA OCZNA 2021, 123, 2:85–89
Online publish date: 2021/07/14
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INTRODUCTION

Benign orbital tumors in children and adolescents are found more often than in adults. They are characterized by a different clinical picture, location and dynamics of development [1-5]. These lesions can be primary, secondary or metastatic [6-8]. Depending on the size and location, tumors may remain asymptomatic or distort the outline of the orbit and as they grow cause subsequent deformation and bone erosion, eyeball displacement and ocular motility disturbance, pressure on the extraocular muscles, double vision, decreased visual acuity, amblyopia, secretory function of the lacrimal gland disturbance, deformation of the shape of the eyelids and their drooping. Lesions in contact with the optic nerve induce symptoms related to its compression. Moreover, a cyst may rupture and cause local inflammation as a result of an injury or spontaneously [2, 4, 7, 9-12]. Imaging tests are especially important in the diagnosis of orbital neoplasms, and removed lesions should be subject to histopathological evaluation [4, 7, 10, 11].
In terms of pathomorphology, non-malignant neoplasms can be divided into: choristomas (growth of normal tissue growing in an inappropriate place, a form of heterotopia; includes dermoid and epidermal cysts), hamartomas (excessive growth of tissue in its anatomical place, e.g. hemangiomas) and pseudotumors (inflammatory and other) [10, 11]. Katowitz et al. [10] published a summary of studies on lesions in developmental age diagnosed as benign orbital tumors. Almost 2,000 analyzed cases show a wide spectrum of diagnoses. The most numerous group included inflammatory, infectious and non-infectious (abscesses and tissue inflammations) disorders. In addition, the following were distinguished: cystic tumors, neurogenic, vascular, bony, histiocytic, and degenerative lesions, as well as those related to injuries.

AIM OF THE STUDY

The aim of the study was a retrospective clinical and histopathological evaluation of benign tumors of the orbit in children and adolescents undergoing surgical treatment based on material of the Clinic of Pediatric Ophthalmology of the Medical University of Silesia in Katowice.

MATERIAL AND METHODS

The analysis included 172 patients, 97 girls (56.4%) and 75 boys (43.6%), aged 6 months to 17 years (mean age 3.7 ±4.9 years), operated in the clinic in 2010-20120 due to the presence of benign orbital tumors. The subjects were divided into 4 age groups: 0-4 years, 5-9 years, 10-14 years and 15-18 years. The removed lesions were submitted to histopathological verification. Tumor-like lesions were excluded from the analysis.

RESULTS

From October 2010 to August 2020, in the clinic, ocular tumors were removed in 1344 patients aged 6 months to 18 years (mean age 7.6 ±5.9 years). Benign neoplasms accounted for 54.1% of diagnoses, and nodular inflammatory processes dominated among the remaining lesions. Tumors were most often located in the conjunctiva (34.1%), on the eyelids (24.7%), in the orbit (23.7%) and less frequently in the corneal limbus (9.5%), the lacrimal caruncle (5.9 %) and the plica semilunaris (2.1%). Benign neoplasms of the orbit were removed in 172 patients. In the age groups 0-4 years, 5-9 years, 10-14 years, 15-18 years, the above-mentioned lesions occurred in 71.5%, 13.4%, 9.3%, and 5.8% of patients, respectively. Single, unilateral tumors dominated. Only two children had coexistence of a dermoid cyst and an orbital lipoma. The results of histopathological examinations showed that in the treated patients the most common were dermoid and epidermal cysts as well as dermolipomas, classified as choristomas (Table I). Children were qualified for surgery because of the gradual enlargement of nodular lesions within the orbital tissues, as well as epibulbar lesions that penetrated deep into them. In older patients, cosmetic reasons prevailed. In most cases, pathological symptoms were observed from the day of birth. However, sometimes parents noticed the lesion later, when the amount of periorbital fat began to decrease as the child grew, allowing better visualization of the tumor. The lesions were also detected accidentally during palpation, e.g. while washing the face of a child. All patients underwent a complete ophthalmological examination, supplemented by an ultrasound examination of the eyes. In selected cases, computed tomography (CT) was performed to assess whether the tumor models the orbital bone or the eyeball. No reduction in visual acuity or abnormalities in the anterior and posterior segments of the eye were found among the examined persons.

DISCUSSION

Among the operated patients, dermoid and epidermal cysts accounted for 68.6% of all excised tumors. According to the literature data [1, 3, 4, 7, 9, 10, 13-15], dermoids are the most common benign lesions within the eyelids, corneal limbus and orbit, which is consistent with the results of our current and previous observations [5]. In terms of pathomorphology, there are 4 types of choristomas: dermoid, dermolipoma, single-tissue choristoma and complex choristoma. Dermoid cysts are the most common among dermoid tumors. To confirm their presence, it is necessary to find elements of the skin adnexa, especially the lacrimal glands. In contrast, epidermal cysts lack these adnexa [4, 8, 10].
Dermoid cysts are formed between the 3rd and 5th week of fetal life as a result of the sequestration of the ectoderm and/or mesoderm from the surface of the embryo and its movement under the skin through the fetal closure lines of the bones. This explains their typical location, most often in the upper temporal part of the orbit, in conjunction with the frontozygomatic suture (60-86%) or, much less often, in the upper nasal part of the orbit, in conjunction with the frontonasal suture (10% to 25%) [3, 4, 8-10, 12, 13, 16, 17]. Dermoid cysts are divided into superficial and deep [18]. The former are more frequent and usually appear up to the age of 3. They are usually smooth, hard, removable and painless nodules in the subcutaneous tissue, near the brow bone, and the skin above them remains unchanged (Fig. 1, 2). They are characterized by slow growth and usually do not cause functional disturbances. [3, 8, 9, 11, 12, 15, 17]. Deep dermoid cysts, on the other hand, often remain undetected for many years, and their first symptom may be exophthalmos or deformation of the orbit. They require detailed imaging diagnostics in order to precisely plan the surgery [7, 9, 10, 13].
Progression of dermoid cysts can be difficult to determine. In the group we analyzed, children were qualified for surgery taking into account presumable complications, including the possibility of a cyst rupture. In some of the operated patients, especially the older ones, fusion of the tumor with the orbital periosteum was found, as well as bone deformities [3, 9, 10, 12, 13, 15-17, 19]. As dermoids grow their wall becomes thinner and the contents of the cyst (mainly lipids and keratin) leak. As a consequence, chronic inflammation and fibrosis begin in adjacent tissues. It is postulated that more than 2/3 of the excised cysts show different degrees of progression of the inflammatory process in histopathological examination. Additionally, the risk of developing inflammatory lesions increases with age [10, 12, 16]. It is worth mentioning that after early excision of tumors, no eyelid or eye dysfunctions were observed among the treated patients and the cosmetic effects were satisfactory.
Teratomas, which contain elements from all three germ cell layers, are another rare type of tumors. They probably arise from a primitive pluripotent germ cell, which then differentiates into mature structures. An orbital teratoma can be cystic or solid and causes exophthalmos, which is usually visible at birth and may gradually increase. Vision loss occurs as a result of chronically increased intraocular pressure, optic nerve atrophy and keratopathy [8, 11]. In CT, teratoma appears as a multi-chambered lesion that may be accompanied by orbital enlargement and intracranial hyperplasia [8, 10]. In such cases, tumor resection is performed in cooperation with neurosurgeons. Complete teratoma removal is mandatory because of possible presence of malignant features in the above tumors and the reports of malignant transformation in an incompletely excised lesion [20, 21]. When vision is present in the affected globe, attempts can be made to separate the tumor from the globe and optic nerve during orbitotomy. However, limited exenteration of the globe and teratoma is undertaken in patients without identifiable visual function and a deformed globe. In such cases, the mentioned procedure aims to preserve uninvolved orbital structures [10]. There was one teratoma among the patients we examined; fortunately its small size allowed for surgical removal without damaging the eyeball.
Epibulbar-orbital dermolipomas and lipomas were the most extensive benign tumors in the analyzed group. They appeared as soft, removable, pale pink or yellow-pink lesions with non-cystic lobular structure, and their surface was often keratinous (Fig. 3). These lesions typically fill the temporal parts of the conjunctival fornices, most often the superior ones. Then they cross the orbital septum and drill into the orbit, in the vicinity of the lateral rectus muscle or the lacrimal gland. Occasionally they induce pressure on the eyeball, develop astigmatism and also cause the dry eye syndrome or strabismus [3, 4, 10, 15]. Dermolipomas are seen more frequently in congenital developmental disorders, mainly involving the craniofacial complex: Goldenhar syndrome, Treacher Collins syndrome, linear nevus sebaceous syndrome, hemifacial microsomia and facial cleft [10, 22-26]. In the case of surgical treatment of non-cystic nodular lesions, without clearly defined boundaries, there is no unequivocal opinion about the need for their early removal. Such an indication exists when the mobility of the eyeball is impaired or there is visual dysfunction. In the case of asymptomatic lesions, the decisive factors are the tumor size and cosmetic considerations. The extent of the surgery is usually limited to excision of the anterior part of the lesion. The close proximity of the lacrimal ductules, the palpebral lobe of the lacrimal gland, the lateral rectus muscle as well as the lateral horn of the levator palpebrae superioris may complicate complete resection [4, 10]. No regrowth of the incompletely removed epibulbar lesions was found in the studied group.
Surgical treatment of the above-mentioned tumors was performed under general anesthesia. Depending on the location, the lesion was removed from the anterior orbital access or from a cutaneous or conjunctival incision. Skin incisions were made directly above the tumor (along the line of Langer) and in the case of lesions in the brow bone area, below the brow hairs. The encysted tumors were completely removed, except for 4 whose walls ruptured during isolation (their sacs were later completely excised). During the surgery, it was possible to say that some of the lesions fused with the periosteum of the orbit, creating cavities. Their walls were separated from the periosteum without damaging the deeper bone structures. When the lesion located in the superior temporal part of the orbit was removed, attention was paid to the vicinity of the lacrimal gland and its protection against damage.
Epibulbar tumors irregularly shaped and occupying the retrobulbar space were excised within the available visual limits. Oculomotor muscles in the operative field were extracted from the surrounding tumor tissue and visualized to prevent their accidental cutting. The operations were uneventful and the wounds healed without complications, leaving smooth, linear, non-discolored scars.

CONCLUSIONS

The spectrum of benign ocular tumors in developmental age is wide, and the orbit remains one of the most comon location of these lesions. The most frequently diagnosed tumors are choristomas, which have typical locations and a characteristic clinical picture. Treatment of these neoplasms involves their excision with subsequent histopathological evaluation. However, the strategy of surgical treatment depends on the location and extent of the lesion and accompanying symptoms.

DISCLOSURE

The authors declare no conflict of interest.

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