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Concurrence of Ocular Cicatricial Pemphigoid in Chronic Ocular Graft-Versus-Host Disease.
Taketani, Yukako; Dehghani, Shima; Sinha, Shruti; Freitag, Suzanne K; Papaliodis, George; Foster, Stephen; Dohlman, Thomas H; Dana, Reza.
Afiliación
  • Taketani Y; Massachusetts Eye and Ear, Department of Ophthalmology, Harvard Medical School, Boston, MA; and.
  • Dehghani S; Massachusetts Eye and Ear, Department of Ophthalmology, Harvard Medical School, Boston, MA; and.
  • Sinha S; Massachusetts Eye and Ear, Department of Ophthalmology, Harvard Medical School, Boston, MA; and.
  • Freitag SK; Massachusetts Eye and Ear, Department of Ophthalmology, Harvard Medical School, Boston, MA; and.
  • Papaliodis G; Massachusetts Eye and Ear, Department of Ophthalmology, Harvard Medical School, Boston, MA; and.
  • Foster S; Massachusetts Eye and Ear, Department of Ophthalmology, Harvard Medical School, Boston, MA; and.
  • Dohlman TH; Massachusetts Eye Research and Surgery Institution, Waltham, MA.
  • Dana R; Massachusetts Eye and Ear, Department of Ophthalmology, Harvard Medical School, Boston, MA; and.
Cornea ; 43(3): 387-390, 2024 Mar 01.
Article en En | MEDLINE | ID: mdl-38128104
ABSTRACT

PURPOSE:

The aim of this study was to report a series of 3 patients with ocular graft-versus-host disease (oGVHD) with progressive cicatricial conjunctival changes who were diagnosed with ocular cicatricial pemphigoid (OCP) after conjunctival biopsy.

METHODS:

This study was a retrospective case series.

RESULTS:

Three patients who received hematopoietic stem cell transplantation for hematologic malignancies developed oGVHD and subsequently were diagnosed with OCP. Case 1 was a 73-year-old woman with oGVHD who developed symblepharon and showed positive IgA, IgG, and C3 staining of the basement membrane zone (BMZ) on conjunctival biopsy, consistent with OCP. She was systemically treated with tacrolimus and prednisone with resolution of conjunctival inflammation. Case 2 was a 68-year-old man with oGVHD who developed symblepharon, severe dry eye, and corneal epithelial defect. An initial conjunctival biopsy was negative, but a repeat biopsy performed 10 years later showed positive BMZ IgA and IgG staining. Healing of the epithelial defect was achieved after treatment with high-dose systemic cyclosporine. Case 3 was a 75-year-old woman with oGVHD who had a nonhealing corneal epithelial defect and symblepharon with positive IgA BMZ staining on conjunctival biopsy, consistent with OCP. The patient responded well to methotrexate with healing of the epithelial defect.

CONCLUSIONS:

Although low-grade conjunctival fibrotic changes may be observed in chronic oGVHD, development of severe and progressive cicatricial changes, including symblepharon formation, should prompt consideration of biopsy to rule out concurrent OCP, the management of which differs from that of oGVHD.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Penfigoide Benigno de la Membrana Mucosa / Enfermedad Injerto contra Huésped Límite: Aged / Female / Humans / Male Idioma: En Revista: Cornea Año: 2024 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Penfigoide Benigno de la Membrana Mucosa / Enfermedad Injerto contra Huésped Límite: Aged / Female / Humans / Male Idioma: En Revista: Cornea Año: 2024 Tipo del documento: Article
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