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Case Reports
. 2023 Dec 11;15(12):e50337.
doi: 10.7759/cureus.50337. eCollection 2023 Dec.

A Rare Case of Primary Follicular Dendritic Cell Sarcoma of the Kidney

Affiliations
Case Reports

A Rare Case of Primary Follicular Dendritic Cell Sarcoma of the Kidney

Amanda E Sion et al. Cureus. .

Abstract

The objective of this case report is to describe a rare case of primary follicular dendritic cell sarcoma (FDCS) of the kidney. FDCS is a rare soft tissue malignancy that most often presents intranodally with lymphadenopathy of the neck, mediastinum, and axilla. One-third of cases present extranodally and most commonly affect the liver, lung, and tonsils. To date, there have been few reports of retroperitoneal FDCS and, to the best of our knowledge, only two other reported cases with primary renal involvement. We present a 56-year-old female with end-stage renal disease on hemodialysis who presented to the hospital with a hypertensive emergency. Computed tomography (CT) of the abdomen was obtained revealing a left-sided renal mass and she subsequently underwent left radical nephrectomy. The pathologic features of the mass revealed oval to spindle cells with eosinophilic cytoplasm, dispersed vesicular chromatin, and small nucleoli found arranged in fascicles, whorls, and storiform patterns with occasional multinucleate forms. The neoplastic cells were immunoreactive to vimentin and expressed cell markers for CD23, CD35, and CD68. These features confirmed a final pathologic diagnosis of primary FDCS of the kidney. To our knowledge, this is the third case of primary renal FDCS reported in the literature. Extranodal FDCS is rare but does occur and needs to be on the differential diagnosis if pathologic features point to its diagnosis.

Keywords: extranodal; fdcs; follicular dendritic cell sarcoma; kidney; primary renal.

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Conflict of interest statement

The authors have declared that no competing interests exist.

Figures

Figure 1
Figure 1. Non-contrast abdominal CT.
Lobulated, heterogenous mass arising from the superior posterolateral aspect of the left kidney with focal hyperdense and hypoattenuating areas.
Figure 2
Figure 2. Histological slides of renal tumor.
(A) Tumor with oval to spindled cells with dispersed chromatin, binucleated (solid arrow) and multinucleated cells (hollow arrow), inflammatory cells (solid arrowhead), and mitotic figures (hollow arrowhead). (B) Spindle cells (hollow arrowhead) and oval cells (solid arrowhead) with dispersed chromatin, inflammatory cells (solid arrow), and mitotic figures (hollow arrow). (C) Immunohistochemical stains for CD 23 show positivity in the dendritic cells (brown stain). (D) Immunohistochemical stains for CD 35 show positivity in the dendritic cells (brown stain). (E) Tumor with multinucleated cells (solid arrow), inflammatory cells (hollow arrow), and intranuclear pseudoinclusion (hollow arrowhead). (F) Normal kidney (lower left) and tumor (upper right).

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