Evidence map›Paper›PMID 41877208›Full record

ArticleThrombosis journal2026

Ischemic stroke despite therapeutic anticoagulation in eosinophilic fasciitis with compartment syndrome and deep vein thrombosis: a case report.

Jun He, Wenchao Guo, Haowu Tang, Chuanchong Zong, Xiaorui Jiang

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Article in Thrombosis journal, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

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5 authors.

Jun HeSchool of Clinical Medicine, Shandong Second Medical University, Weifang, China.
Wenchao GuoThe Second School of Clinical Medicine, Binzhou Medical University, Binzhou, China.
Haowu TangSchool of Clinical Medicine, Shandong Second Medical University, Weifang, China.
Chuanchong ZongDepartment of Hand and foot Surgery, The Affiliated Yantai Yuhuangding Hospital of Qingdao University, Yantai, China.
Xiaorui JiangDepartment of Endocrine and Foot and Ankle, The Affiliated Yantai Yuhuangding Hospital of Qingdao University, Yantai, 264000, China. jiang_xr007@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEosinophilic fasciitis is a rare connective tissue disorder characterized by fascial inflammation and eosinophil infiltration. Thromboembolic complications in eosinophilic fasciitis are uncommon and poorly understood. We report a case that highlights the limitations of conventional anticoagulation in preventing eosinophil-mediated thrombosis. CASE PRESENTATION: A 60-year-old Chinese man presented with a 10-day history of progressive bilateral lower extremity swelling and pain. Laboratory investigations revealed severe hypereosinophilia and imaging revealed left lower-extremity deep vein thrombosis complicated by acute compartment syndrome. Despite therapeutic enoxaparin anticoagulation with documented hypocoagulable state on thromboelastography, the patient developed bilateral lacunar infarctions on day 7. Bone marrow aspiration excluded hematological malignancies, and fascial biopsy confirmed eosinophilic fasciitis. Following glucocorticoid therapy initiation, eosinophil levels normalized with complete resolution of symptoms. No recurrence of thrombotic events was observed during one-year follow-up.

conclusionThis case highlights that eosinophilic fasciitis-associated hypereosinophilia can induce a prothrombotic state resistant to conventional anticoagulation, likely through eosinophil granule protein-mediated mechanisms. Early recognition and prompt glucocorticoid therapy, rather than anticoagulation alone, may be critical for preventing life-threatening thromboembolic complications in eosinophilic fasciitis. This report adds to the limited literature on thrombotic manifestations of eosinophilic fasciitis and underscores the need for heightened clinical vigilance and a shift in therapeutic paradigm toward early immunosuppression.

Indexed as

AnticoagulationDeep vein thrombosisEosinophilic fasciitisGlucocorticoidHypereosinophiliaIschemic stroke

Identifiers

PMID41877208
PMCPMC13134330

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