Medicine · 2021
Intra-muscular follicular dendritic cell sarcoma in the thigh: A case report.
Клинический случайСтатьяНазвание и аннотация: Перевод в очереди
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Cho Yong Jin, Han Song Iy, Lim Sung-Chul
Аннотация
RATIONALE: Follicular dendritic cell sarcoma (FDCS) is an intermediate-grade malignancy originating from follicular dendritic cells. Nodal FDCS is the most common type, meaning that the extranodal type may not be recognized and could be easily misdiagnosed. Reported extranodal sites include the head and neck, retroperitoneum, spleen, liver, and gastrointestinal tract. FDCS in the soft tissue is extremely rare.
PATIENT CONCERNS: A 75-year-old male presented with complaints of a localized swelling and intra-muscular soft tissue mass in the left upper thigh.
DIAGNOSIS: The present tumor consisted of fascicular or vague storiform-arranged spindle cells with less pleomorphism and many lymphoid aggregates. Tumor cells were positive for CD21, CD35, CD68, vimentin, and EGFR. Intra-muscular FDCS was confirmed by immunohistochemical studies.
INTERVENTIONS: The patient received a wide marginal excision, followed by adjuvant radiotherapy.
OUTCOMES: Symptomatic improvements were achieved and no subsequent relapses were observed.
LESSONS: If the tumor arises in the extranodal sites, especially in the soft tissue, it is difficult to include FDCS in the differential diagnosis. When the immunoprofile is not consistent with that of common spindle cell tumors, immunostaining for follicular dendritic cell markers such as CD21, CD23, and CD35, as well as further immunohistochemistry for D2-40, CD68, EGFR, Epstein-Barr virus, and BRAF can be helpful for the diagnosis and subtyping of FDCS. To the best of our knowledge, the present case is the first case of intramuscular FDCS.
PATIENT CONCERNS: A 75-year-old male presented with complaints of a localized swelling and intra-muscular soft tissue mass in the left upper thigh.
DIAGNOSIS: The present tumor consisted of fascicular or vague storiform-arranged spindle cells with less pleomorphism and many lymphoid aggregates. Tumor cells were positive for CD21, CD35, CD68, vimentin, and EGFR. Intra-muscular FDCS was confirmed by immunohistochemical studies.
INTERVENTIONS: The patient received a wide marginal excision, followed by adjuvant radiotherapy.
OUTCOMES: Symptomatic improvements were achieved and no subsequent relapses were observed.
LESSONS: If the tumor arises in the extranodal sites, especially in the soft tissue, it is difficult to include FDCS in the differential diagnosis. When the immunoprofile is not consistent with that of common spindle cell tumors, immunostaining for follicular dendritic cell markers such as CD21, CD23, and CD35, as well as further immunohistochemistry for D2-40, CD68, EGFR, Epstein-Barr virus, and BRAF can be helpful for the diagnosis and subtyping of FDCS. To the best of our knowledge, the present case is the first case of intramuscular FDCS.