|Year : 2023 | Volume
| Issue : 1 | Page : 103-105
Recurrent solitary fibrous tumor of eyelid: A rare entity
Syed Wajahat Ali Rizvi1, Saifullah Khalid2, Syed Ali Raza Rizvi3, Shagufta Qadri2, Mohammed Azfar Siddiqui4
1 Department of Ophthalmology, Institute of Ophthalmology, Jawaharlal Nehru Medical College, Aligarh Muslim University, Aligarh, Uttar Pradesh, India
2 Department of Radiology, Jawaharlal Nehru Medical College, Aligarh Muslim University, Aligarh, Uttar Pradesh, India
3 Department of Ophthalmology, Al Nahdha Hospital, MOH, Muscat, Oman
4 Department of Radiology, Saint Louis University, MO, USA
|Date of Submission||16-May-2022|
|Date of Decision||07-Nov-2022|
|Date of Acceptance||14-Jan-2023|
|Date of Web Publication||21-Feb-2023|
Syed Wajahat Ali Rizvi
Institute of Ophthalmology, Jawaharlal Nehru Medical College, Aligarh Muslim University, Aligarh, Uttar Pradesh
Source of Support: None, Conflict of Interest: None
| Abstract|| |
Orbital and adnexal solitary fibrous tumors (SFT) are rare entities. The clinico-radiological and histologic features overlap with those of other spindle cell variants, and hence the use of immunohistochemical stains helps in making an accurate diagnosis. Furthermore, a thorough surgical resection is imperative to prevent tumor recurrences. We report a rare case of SFT arising primarily from the eyelid with multiple recurrences.
Keywords: Eyelid, fibrous tumor, immunostains, recurrence
|How to cite this article:|
Ali Rizvi SW, Khalid S, Raza Rizvi SA, Qadri S, Siddiqui MA. Recurrent solitary fibrous tumor of eyelid: A rare entity. Oman J Ophthalmol 2023;16:103-5
|How to cite this URL:|
Ali Rizvi SW, Khalid S, Raza Rizvi SA, Qadri S, Siddiqui MA. Recurrent solitary fibrous tumor of eyelid: A rare entity. Oman J Ophthalmol [serial online] 2023 [cited 2023 Mar 26];16:103-5. Available from: https://www.ojoonline.org/text.asp?2023/16/1/103/370032
| Introduction|| |
Solitary fibrous tumors (SFTs) are rare, benign, mesenchymal neoplasms typically involving the pleura, although meningeal, oral, pericardial, kidney, and liver involvement has also been reported. SFT of the orbit is extremely rare and that of eyelids is even rarer with very few reported cases in the literature., These tumors typically present with painless and progressive proptosis, palpable lid mass, epiphora, etc. On magnetic resonance imaging (MRI), the tumor appears isointense on T1-weighted images and iso- to hyperintense on T2-weighted images. Usually, SFTs run a nonaggressive course; however, recurrences, tissue invasion, and/or metastasis are rare and mostly seen due to the incomplete resection. On histopathology, the features of SFTs often overlap with that of other spindle cell tumors, especially hemangiopericytoma, and therefore, immunohistochemistry plays an important role in correctly identifying the type of tumor. Characteristically, they show positivity for CD34, vimentin, bcl-2, and STAT6 and negative for desmin, cytokeratin, and S-100. Whereas CD34 is fairly sensitive for SFTs, staining for STAT6 shows both high sensitivity and specificity. Therefore, STAT6 has become an important adjunct with CD34 to help differentiate SFT from other histologic variants. We here report a rare presentation of SFTs with predominant eyelid involvement and multiple recurrences.
| Case Report|| |
A 60-year-old female presented with a painless progressive swelling of the left lower lid for the past 7 years with epiphora. She had similar swelling in the left lower lid in 2006 and 2013, for which she has undergone surgery, although it reappears 1–2 years later. There were no records available pertaining to previous surgical interventions. On examination, a firm diffuse left lower lid mass measuring approximately 20 mm across with poorly defined posterior extent and mild medial ectropion was present [Figure 1]a. On lid eversion, conjunctival scarring with the obliteration of fornix medially and punctal stenosis could be seen. MRI orbit showed a well-defined soft-tissue mass (25 mm × 20 mm × 10 mm TD × AP × CC) appearing isointense on T1W and hyperintense on T2W sequence encroaching into the extraconal space with the indentation on the anteroinferior globe; furthermore, nasolacrimal duct seems to be obliterated [Figure 2]a, [Figure 2]b. A total tumor excision through a conjunctival approach was carried out, and a well-defined mass measuring 25 mm × 15 mm adherent to the overlying conjunctiva was identified and retrieved ensuring complete excision [Figure 1]b. The patient recovered well with only mild medial ectropion of the lower lid remaining [Figure 1]c.
|Figure 1: (a) Preoperative clinical photograph showing a large swelling of the lower lid and medial ectropion, also to be noted is the conjunctival scarring present medially. (b) Gross tissue specimen measuring 25 mm × 15 mm. (c) Postoperative appearance at 1 month|
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|Figure 2: (a) Fat saturated T1W sagittal and T2W axial scan showing a well-defined postseptal lesion. (b) Coronal T2W and T1W show a lobular, T2 hyperintense, and T1 isointense lesion in medial aspect of left lower lid. (c) Observe diffusely proliferating tumor cells arranged in fascicles and occasional storiform pattern (H and E, ×40). (d) Oval to spindle tumor cells with vascular spaces (H and E, ×100). (e) Tumor cells avidly staining with CD34 immunostain|
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Histological evaluation revealed a partially capsulated tissue with oval-to-spindle cells arranged in a fascicular and storiform pattern. Tumor also showed epitheloid and hemangiopericytomatous morphology at places; however, no mitosis or necrosis was seen [Figure 2]c, [Figure 2]d. On immunohistochemistry, cells were found positive for CD34 and negative for S-100 [Figure 2]e.
The patient showed no sign of recurrence at the 6-month follow-up with a partial improvement in epiphora.
| Discussion|| |
SFTs are rare and slow-growing benign mesenchymal tumors consisting of spindle cells. They most commonly arise from the pleura, but extrapleural involvement has also been frequently seen; however, their orbital occurrence is extremely rare and that of eyelids is even rarer.,, Although the typical presentation is usually during middle age, the diagnosis should be considered in all age groups. On radiological evaluation, they show isointensity on T1-weighted and heterogenous isointensity to hyperintensity on T2-weighted scans. However, none of these characteristics are diagnostic of SFT, and therefore it may sometimes be difficult to distinguish it from other orbital lesions. Histologically, SFTs display variable morphological patterns that overlap with other spindle cell tumors such as hemangiopericytoma, angiofibromas, and schwanommas. Additional workup with immunohistochemistry is therefore essential to determine the type of spindle cell tumor. SFTs show a strong reactivity to CD34, STAT6, vimentin, and bcl-2; however, they are negative for desmin, S-100, and muscle-specific actin. Although CD34 positivity of SFTs is highly sensitive, it is relatively nonspecific while STAT6 has high sensitivity and specificity. Mostly, SFTs run a benign course, but incomplete resection often leads to recurrences and tissue invasion, and therefore a meticulous tumor excision is imperative. Complete tumor resection rather than histological appearance is the single most important prognostic factor.
In our case, the patient presented with a long-standing eyelid swelling with multiple recurrences following surgical excision. This is an uncommon presentation as eyelid SFTs have rarely been reported and that too with multiple recurrences. We, therefore, emphasize the importance of complete tumor resection and the establishment of accurate diagnosis using appropriate immunohistochemical stains for fibrous tumors. Equally, critical is to keep a long follow-up of such cases as SFTs are known to have malignant transformation.
Statement of ethics
A written informed consent (including the images) has been obtained from the patient. All procedures were carried out in adherence to the tenets of the Declaration of Helsinki.
Declaration of patient consent
The authors certify that they have obtained all appropriate patient consent forms. In the form, the patient has given her consent for her images and other clinical information to be reported in the journal. The patient understands that name and initials will not be published and due efforts will be made to conceal identity, but anonymity cannot be guaranteed.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
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