ArticleCureus2025
Zanubrutinib‑Induced Symmetrical Soft Tissue Forearm Swelling in a Patient With Waldenström Macroglobulinemia.
Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
1 citing paper in PubMed.
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Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Zanubrutinib is a second-generation Bruton tyrosine kinase (BTK) inhibitor approved for the treatment of several indolent B-cell lymphomas. Although it has a more favorable safety profile than its predecessor, ibrutinib, rare adverse effects continue to emerge with broader clinical use. We report the case of an 87-year-old man with Waldenström macroglobulinemia (WM) who developed bilateral, non-pitting, soft tissue swelling of the forearms approximately 16 weeks after initiating zanubrutinib 160 mg orally twice daily. The swelling extended from the elbows to the hands, was symmetrical, non-tender, and not associated with any other symptoms. Doppler ultrasound ruled out deep vein thrombosis, and no alternative causes such as trauma, infection, or hypoalbuminemia were identified. A 50% dose reduction of zanubrutinib led to partial improvement, while complete resolution was observed 12 weeks after drug discontinuation. Unlike previously reported cases of BTK inhibitor-associated edema, which typically involve the lower extremities and present unilaterally or with associated skin changes, this case is unique in its bilateral presentation and upper extremity location without cutaneous involvement. The mechanism remains unclear but may involve vascular endothelial dysfunction or altered lymphatic drainage. Prompt recognition of this atypical presentation is essential for avoiding unnecessary interventions and optimizing therapeutic decisions.
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Registered trials
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