| Literature DB >> 32251268 |
Qais S Dirar1,2, Hebah M Musalem1, Selwa A F Al-Hazzaa1,2, Abdulaziz A Al Zoba2, Amal A Almalki1,2.
Abstract
BACKGROUND Xeroderma pigmentosum (XP) is an autosomal recessive disease caused by mutations in DNA repair genes. Clinical manifestations include extreme sensitivity to ultraviolet (UV) rays, freckle-like pigmentation, ocular abnormalities, and an increased risk of developing neoplasms in sun-exposed areas of the skin, mucous membranes, and eyes. This paper describes the clinical outcome of pegylated interferon alpha 2b (PEG-IFN-alpha-2b) subconjunctival injections and topical mitomycin C (MMC) in the treatment of ocular surface squamous neoplasia (OSSN) in patients with XP. CASE REPORT A series of 3 patients with histopathologically-proven biopsy specimens of XP-associated neoplasia of the eyelids and ocular surface underwent subconjunctival injections of PEG-IFN-alpha-2 band topical cycles of MMC. There was a noticeable decrease in the size and severity of ocular surface squamous neoplasia, with minimal adverse effects of flu-like symptoms with mild fever and generalized malaise. Transient mental depression was reported in 2 of our patients, and only 1 patient developed autoimmune diabetes mellitus, which required insulin therapy after the discontinuation of the PEG-IFN-alpha-2b. CONCLUSIONS The literature on the specifics of ocular care using PEG-IFN-alpha-2b for XP-associated OSSN is sparse. However, according to our clinical experience, the combination of PEG-IFN-alpha-2b subconjunctival injection and the topical cycles of MMC is a promising long-term medical therapy to minimize the development and recurrence of OSSN in XP patients.Entities:
Year: 2020 PMID: 32251268 PMCID: PMC7161929 DOI: 10.12659/AJCR.921301
Source DB: PubMed Journal: Am J Case Rep ISSN: 1941-5923
Figure 1.Three images of the left eye from Case 1, taken 3 years apart. (A) Baseline before current presentation. (B) Left eye at time of presentation, showing vascularized lesion on the corneal surface with pink irregular masses extending to the surrounding conjunctiva. (C) Taken at 18 months of treatment, showing opaque cornea with severe fibrosis and no active lesions.
Figure 2.Four images from Case 2 taken 2 years apart. (A) Right eye before treatment with basal cell carcinoma involving the lateral third of the lower eyelid and extending to the right lateral canthus. (B) Right eye after surgical excision and 21 months of therapy. (C) Left eye before treatment, showing the cornea with the limbal 360-degree involvement by an irregular hazy white growth which was identified as fibrosis with no malignant cells on biopsy. (D) Left eye after surgical excision and 21 months of therapy.
Figure 3.Four images of Case 3 taken 2 years apart. (A) Post-surgical excision on the right eye, showing focal squamous cell carcinomas in situ at 03: 00 limbal area. (B) Right eye after 18 months of therapy. (C) Post-surgical excision on left eye showing focal epithelial dysplasia at limbal conjunctiva with irregular vascularization. (D) Left eye after 18 months of therapy.