Case ReportFollicular dendritic cell sarcoma of the liver: unusual presentation of a rare tumor and literature review
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Cited by (27)
Extranodal follicular dendritic cell sarcoma intimately associated with the pancreas
2022, Human Pathology ReportsCitation Excerpt :Extranodal sites are most common (58%), in keeping with the mesenchymal origin, followed by isolated lymph node involvement (31%) and both nodal and extranodal (10%) disease. Virtually any site in the body can be affected; [2] the head and neck [5–10] are most often involved in isolated nodal disease, and the thorax, [11–13] abdomen [14–19] and soft tissue are most commonly involved in extranodal disease. Rare cases have been reported in unusual sites such as the urinary bladder [20] and thigh. [21]
Hepatic Follicular Dendritic Cell Sarcoma with Epithelioid Morphology: Histopathologist's Perspective
2022, Journal of Clinical and Experimental HepatologyCitation Excerpt :The gastrointestinal tract, pancreas, liver, spleen, peritoneum, and different peritoneal attachments, lungs, skin, soft tissue, and oral cavity including palate and tonsil are the common sites of extranodal involvement.7,9 Primary sarcoma of the liver is uncommon and is responsible for only 0.1% of primary liver tumors.2,10 FDC sarcoma is an uncommon primary sarcoma of the liver with only 30 anecdotal reports in the English literature.1–3,6,7,9–24
Epstein-Barr virus-negative inflammatory pseudotumor-like variant of follicular dendritic cell sarcoma of the liver: A case report and literature review
2021, Clinics and Research in Hepatology and GastroenterologyDisorders of Dendritic Cells
2018, Atlas of Hematopathology: Morphology, Immunophenotype, Cytogenetics, and Molecular Approaches, Second EditionDendritic cell sarcoma: A pooled analysis including 462 cases with presentation of our case series
2013, Critical Reviews in Oncology/HematologyCitation Excerpt :Demographic and clinical features of all cases are summarized in Table 3. Carefully and thoroughly reviewing English literature, 343 FDCS cases were found, including ours [10–190] (Table 3). Median age at diagnosis was 50 years (range 9–90 years).