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Case Reports
. 2019 Dec 15;11(12):1231-1239.
doi: 10.4251/wjgo.v11.i12.1231.

Inflammatory pseudotumor-like follicular dendritic cell sarcoma: A brief report of two cases

Affiliations
Case Reports

Inflammatory pseudotumor-like follicular dendritic cell sarcoma: A brief report of two cases

Bi-Xi Zhang et al. World J Gastrointest Oncol. .

Abstract

Background: Follicular dendritic cell (FDC) sarcoma/tumor is a rare malignant tumor of follicular dendritic cells, which is considered a low-grade sarcoma that can involve lymph nodes or extranodal sites. Conventional FDC sarcomas are negative for Epstein-Barr virus (EBV), whereas the inflammatory pseudotumor-like variant consistently shows EBV in the neoplastic cells.

Case summary: We report two cases of inflammatory pseudotumor-like FDC sarcoma in the liver that received 3D laparoscopic right hepatectomy and open right hepatectomy separately.

Conclusion: EBV probe-based in situ hybridization and detection of immunohistochemical markers of FDC play an important role in the diagnosis and differential diagnosis of inflammatory pseudotumor-like FDC sarcoma. Complete surgical excision combined with regional lymphadenectomy may be effective in reducing the postoperative recurrence and metastasis and improving long-term survival rates.

Keywords: Case report; Epstein-Barr virus; Inflammatory pseudotumor-like follicular dendritic cell sarcoma; Liver; Spleen.

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Conflict of interest statement

Conflict-of-interest statement: The authors have no conflicts of interest to declare.

Figures

Figure 1
Figure 1
Magnetic resonance imaging. Two well-circumscribed lesions with long T1 and long or equal T2 signal (arrows). The multiple lesions with long T1 and long T2 signal are hepatic cysts verified by pathological examination later.
Figure 2
Figure 2
Abdominal computed tomography examination. The images show an ill-defined and low-density 10 cm mass (arrows) in the right lobe of the liver, accompanied with enlargement of hepatic portal lymph nodes.
Figure 3
Figure 3
Epstein-Barr virus-positive inflammatory pseudotumor-like follicular dendritic cell sarcoma in the liver. A: Gross picture of an inflammatory pseudotumor-like follicular dendritic cell sarcoma of the liver. A well-circumscribed solid nodule was found in the liver. Note the grayish-white colored and soft cut surface with focal hemorrhage (arrow); B: Haematoxylin and eosin stained image showing that the tumor tissue had a meshwork-like architecture (× 200); C: On high-power field, the tumor was composed of oval to spindle cells with vesicular chromatin and distinct nucleoli. There was less degree of atypia. The background showed abundant lymphocytes and plasma cells (× 400); D: CD21 was detected on the membrane of almost all of tumor cells by immunohistochemistry (× 100); E: Smooth muscle actin was detected in the cytoplasm of a part of tumor cells by immunohistochemistry (× 100); F: Epstein-Barr virus-encoded small RNA-based in situ hybridization demonstrated positive nuclei of the neoplastic dendritic cells (× 200); G: Ki-67 was detected in the nuclei of almost all of tumor cells by immunohistochemistry (30%; × 100).
Figure 4
Figure 4
Epstein-Barr virus positive inflammatory pseudotumor-like follicular dendritic cell sarcoma in the liver with hepatoduodenal ligament lymph node involvement. A: Gross picture of an inflammatory pseudotumor-like follicular dendritic cell sarcoma of the liver. A large and multinodular confluent tumor was found in the liver (arrow); B: Histologic sections of follicular dendritic cell sarcoma showing an unencapsulated tumor (left) with a sharp margin from the adjacent liver parenchyma (right). The tumor tissue was arranged in whorls (× 40); C: On high-power field, the tumor was composed of oval to spindle cells with vesicular chromatin and distinct nucleoli. There was less degree of atypia. The background showed abundant lymphocytes and plasma cells (× 400); D: In the hepatoduodenal ligament lymph node, lymphoid follicles were pushed aside by tumor tissue (× 100); E: CD21 was detected on the membrane of almost all of tumor cells by immunohistochemistry (× 100); F: S100 was detected in the membrance and cytoplasm of almost all of tumor cells by immunohistochemistry (× 100); G: Epstein-Barr virus-encoded small RNA in situ hybridization demonstrated positive nuclei of the neoplastic dendritic cells (× 100); H: Ki-67 was detected in the nuclei of almost all of tumor cells (20%; × 100).

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References

    1. Monda L, Warnke R, Rosai J. A primary lymph node malignancy with features suggestive of dendritic reticulum cell differentiation. A report of 4 cases. Am J Pathol. 1986;122:562–572. - PMC - PubMed
    1. Chan JK, Fletcher CD, Nayler SJ, Cooper K. Follicular dendritic cell sarcoma. Clinicopathologic analysis of 17 cases suggesting a malignant potential higher than currently recognized. Cancer. 1997;79:294–313. - PubMed
    1. Steven HS, Elias C, Nancy LH, Elaine SJ, Stefano AP, Harald S, Jurgen T, Daniel AA, Robert PH, Michelle MLB, Attilio O, Reiner S. WHO classification of tumours of haematopoietic and lymphoid tissues. Lyon: IARC press. 2017:476–479.
    1. Duan GJ, Wu F, Zhu J, Guo DY, Zhang R, Shen LL, Wang SH, Li Q, Xiao HL, Mou JH, Yan XC. Extranodal follicular dendritic cell sarcoma of the pharyngeal region: a potential diagnostic pitfall, with literature review. Am J Clin Pathol. 2010;133:49–58. - PubMed
    1. Saygin C, Uzunaslan D, Ozguroglu M, Senocak M, Tuzuner N. Dendritic cell sarcoma: a pooled analysis including 462 cases with presentation of our case series. Crit Rev Oncol Hematol. 2013;88:253–271. - PubMed

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