Published online Jul 26, 2020. doi: 10.12998/wjcc.v8.i14.3097
Peer-review started: May 18, 2020
First decision: June 4, 2020
Revised: June 9, 2020
Accepted: June 29, 2020
Article in press: June 29, 2020
Published online: July 26, 2020
Processing time: 67 Days and 8.4 Hours
Follicular dendritic cell (FDC) sarcomas are rare neoplasms that occur predominantly in the lymph nodes. They can also occur extranodally. Extranodal FDC sarcomas most commonly present as solitary masses. Inflammatory pseudotumor (IPT)-like FDC sarcomas, a subcategory of FDC sarcomas, are rarer than other sarcoma subtypes. They are composed of spindle or ovoid neoplastic cells and exhibit an admixture of plasma cells and prominent lymphoplasmacytic infiltration. Paraneoplastic pemphigus (PNP), also known as paraneoplastic autoimmune multiorgan syndrome, is a rare autoimmune bullous disease that is associated with underlying neoplasms. PNP has a high mortality, and its early diagnosis is usually difficult.
We describe a 27-year-old woman who presented with stomatitis, conjunctivitis, and skin blisters and erosions as her first symptoms of PNP with an intra-abdominal IPT-like FDC sarcoma. The patient underwent surgical tumor resection and received tapering oral corticosteroid treatment. She showed no recurrence at the 1-year follow-up.
IPT-like FDC sarcomas are rare underlying neoplasms that have an uncommon association with PNP. PNP-associated FDC sarcomas predominantly occur in intra-abdominal sites and suggest a poor prognosis. Surgical resection is an essential and effective treatment for PNP and primary and recurrent FDC sarcomas.
Core tip: To date, 32 cases of paraneoplastic pemphigus (PNP)-associated follicular dendritic cell (FDC) sarcomas have been reported in the English literature. Inflammatory pseudotumor-like FDC sarcoma was described as an underlying neoplasm of PNP in only two cases. Here, we report a case that PNP was the patient’s first symptom of an intra-abdominal inflammatory pseudotumor-like FDC sarcoma, and review the related literature.