Abstract

BackgroundExtranodal marginal zone lymphoma (MZL), also called mucosa-associated lymphoid tissue (MALT) lymphoma accounts for 7–8 % of non-Hodgkin lymphomas (NHLs) and most commonly involves the stomach. However, muscle involvement is very rare.Case descriptionA 57-year-old woman was referred to our orthopaedics and traumatology clinic with a painful lump in the left arm. Physical examination revealed a red-colored mass on the left arm and an enlarged lymph node measuring almost 5 cm in the left axillary region and 3 cm in the right axillary region. Tru-cut biopsy of the mass in the left arm was consistent with MZL. The diagnosis was MALT lymphoma infiltrating the skeletal muscle (stage IIEA). R-CHOP was started. Two additional infusions of rituximab were administered after the sixth cycle of R-CHOP. Then, the patient received radiotherapy to the left arm at a dose of 30 Gy. After 1 year of follow-up, the patient had no evidence of disease.Discussion and evaluationMALT lymphoma arises in a number of epithelial tissues. The clinical presentation of MALT lymphoma varies depending upon the tissue involved. To our knowledge, rare cases of MALT lymphoma of the skeletal muscle have been reported. Although the available literature suggests that primary skeletal muscle NHL with advanced stage is associated with poor prognosis, the case presented here suggests that rituximab based combination therapy followed by radiotherapy can be an effective treatment for primary skeletal MALT lymphoma.ConclusionThere is limited data regarding the prognosis and treatment of MALT lymphoma of the skeletal muscle. This case implies that rituximab based combination therapy followed by radiotherapy should be considered for the treatment of primary skeletal MALT lymphoma.

Highlights

  • Extranodal marginal zone lymphoma (MZL), called mucosa-associated lymphoid tissue (MALT) lymphoma accounts for 7–8 % of non-Hodgkin lymphomas (NHLs) and most commonly involves the stomach

  • The available literature suggests that primary skeletal muscle NHL with advanced stage is associated with poor prognosis, the case presented here suggests that rituximab based combina‐ tion therapy followed by radiotherapy can be an effective treatment for primary skeletal MALT lymphoma

  • There is limited data regarding the prognosis and treatment of MALT lymphoma of the skeletal muscle. This case implies that rituximab based combination therapy followed by radiotherapy should be considered for the treatment of primary skeletal MALT lymphoma

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Summary

Discussion and evaluation

MALT lymphoma arises in a number of epithelial tissues, including the stomach, salivary gland, lung, small bowel and thyroid. Involved field radiation therapy for treatment of stomach MALT has been well established, yielding excellent outcomes with over 90 % local control reported in most studies (Tsang et al 2001; Tsai et al 2007). The aforementioned case suggests that primary skeletal lymphoma shows more aggressive behavior, presents as advanced stage, and is associated with poor outcome (Gill et al 2006). One previous case presented with early stage (IE) and was treated with involved field radiation therapy resulting in complete response (EdwardsBennett et al 2011). The available data is very limited and probably suggests that primary skeletal muscle NHL with advanced stage is associated with poor prognosis, the case presented here suggests that rituximab based combination therapy followed by radiotherapy can be an effective option for treatment of primary skeletal MALT lymphoma. It needs to be mentioned that 1 year-follow up is too short to support the long term effectiveness of this approach for an indolent lymphoma

Conclusion
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