Conjunctival Intraepithelial Neoplasia With IgG and Complement Deposition: Spurious Association or Biologically Explainable?

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Authors: Daniel D Zhang, Deepak Raja, Wang L. Cheung, Curtis Edward Margo
Cited by: 0
References: 14

Abstract

Conjunctival intraepithelial squamous neoplasia (CIN) is a premalignant ocular surface lesion typically diagnosed by clinical features and confirmed with routine histopathologic examination, rather than immunofluorescence studies. Direct immunofluorescence (DIF) of conjunctival tissue is most commonly used to support the diagnosis of autoimmune blistering diseases, particularly mucous membrane pemphigoid, by identifying immunoreactant deposition along the basement membrane zone (BMZ). However, such findings are not expected in CIN and may complicate interpretation. We report a case of CIN with unexpected positive DIF findings of IgG and C3 in the BMZ. A 63-year-old man with a clinically apparent conjunctival lesion underwent biopsy, which confirmed CIN on routine histopathology. A portion of the specimen was inadvertently submitted for DIF, revealing linear deposition of IgG and C3 along the conjunctival BMZ. The patient had no clinical history or examination findings suggestive of mucous membrane pemphigoid, other autoimmune blistering disease, or systemic inflammatory disorder that could account for these immunoreactant deposits. This association suggests nonspecific deposition of immunoglobulins and complement in the setting of conjunctival neoplasia, a phenomenon rarely reported in the literature. This case highlights the potential for false-positive DIF results in conjunctival lesions and emphasizes the importance of submitting a concomitant biopsy for routine light microscopy when ordering DIF in patients with suspected mucous membrane pemphigoid to ensure accurate diagnosis.

Fields of Study & Subjects

Autoimmune Bullous Skin Diseases Ocular Surface and Contact Lens Oral Health Pathology and Treatment

Publication details

Journal / source
Cureus
Volume
18
Issue
2
Pages
e103709–e103709
Publication date
16 February 2026
Language
EN