{Reference Type}: Case Reports
{Title}: Recurrent corneal melting in the paraneoplastic pemphigus associated with Castleman's disease.
{Author}: Gong H;Zhou S;Hu Y;Lan Y;Zeng H;Wang L;Liu Q;Wang M;
{Journal}: BMC Ophthalmol
{Volume}: 16
{Issue}: 0
{Year}: Jul 2016 12
{Factor}: 2.086
{DOI}: 10.1186/s12886-016-0280-7
{Abstract}: BACKGROUND: The ocular presentation of Castleman's disease (CD)-associated paraneoplastic pemphigus (PNP) has rarely been reported. In this report, we describe a young patient with CD-associated PNP who had recurrent corneal ulceration in addition to cicatrizing conjunctivitis.
METHODS: We describe a case of 23-year-old male with mucocutaneous erosion and conjunctival injection and erosion who was found to have PNP. Pelvic hyaline-vascular CD was detected and completely excised. The mucocutaneous lesions improved postoperatively. Two years after pelvic surgery, the patient gradually developed conjunctival symblepharon in both eyes and pterygium in the right eye. The patient then underwent a successful exclusion of the symblepharon, an excision of the pterygium and an amniotic membrane transplantation in the right eye. However, after 6 months, he experienced an aseptic corneal ulcer and recurrent pterygiumin the right eye. After treatment with systemic and local immunosuppressive medications, the corneal ulcer gradually healed and remained stable.
CONCLUSIONS: Corneal ulceration and melting, in addition to conjunctivitis, as a complication of CD-associated PNP, can be successfully managed with systemic and local immunosuppressants.