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. 2022 Aug 15;12(4):144-155.
eCollection 2022.

A clinicopathologic study of 13 cases of primary lymphoma in soft tissue and review of literature

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A clinicopathologic study of 13 cases of primary lymphoma in soft tissue and review of literature

Jing Duan et al. Am J Blood Res. .

Abstract

Primary lymphoma in soft tissue is very rare. In order to understand the clinicopathological features of primary lymphoma in soft tissue, we found 13 cases (0.3%) of primary lymphoma in soft tissue by reviewing 4303 lymphomas diagnosed in our institution from 2010 to 2019. Tumors were found in the following sites: 8 in lower extremity (2 in leg, 1 in calf, 1 in knee and 4 in buttock), 1 in upper extremity (left shoulder) and 4 in the trunk (3 in waist and 1 in thoracolumbar). The most common histologic type was DLBCL (7/13, 54.8%). 6 cases of which had follow-up information. 25 patients were also selected by screening the English literature search (from Jan 2010 to December 2019) including 1102 studies. Compared to the results of literature review, our results are similar with them. The tumor sites were as follows: 10 in lower extremity, 4 in upper extremity, 9 in the trunk and 2 in masticatory muscle. The most common histological type was also DLBCL (n=11/25, 44%). Overall survival analysis of all 31 patients including our 6 cases with primary lymphoma in soft tissue showed no significant difference between different histological type (Log Rank P=0.120, Breslow P=0.157). The differential diagnosis includes malignant melanoma, rhabdomyosarcoma and metastatic carcinoma in soft tissue.

Keywords: Soft tissue; clinicopathologic feature; differential diagnosis; immunohistochemistry; lymphoma.

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Conflict of interest statement

None.

Figures

Figure 1
Figure 1
Preferred reporting items for systematic reviews and meta-analyses (PRISMA) flow diagram.
Figure 2
Figure 2
HE and immunohistochemistry staining of different types of primary lymphoma in soft tissue. A. DLBCL infiltrated skeletal muscle; B. The diffusely infiltrated small oval blue tumor cells in high grade B-cell lymphoma (Invasive B cell lymphoma between Burkitt lymphoma and DLBCL); C. High grade B-cell lymphoma infiltrated skeletal muscle; D. ALCL tumor cells diffusely distributed and had classical nuclear morphology; E. PTCL tumor cells diffusely distributed. HE ×200; F, G. DLBCL was positive for CD20 and CD79a; H-N. ALCL was positive for CD3, CD4, CD5, TIA-1, Granzyme B, CD30, and ALK; O. Ki-67 index was high. IHC ×200.
Figure 3
Figure 3
Overall survival analysis of 31 primary lymphomas in soft tissues. 1 BCL (B-cell lymphoma); 2 ALCL (anaplastic large cell lymphoma); 3 PTCL (peripheral T cell lymphoma); 4 BL (Burkitt lymphoma); 5 PBL (plasmablastic lymphoma); Log Rank P=0.120, Breslow P=0.157.

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