Eosinophilic Fasciitis with Hypereosinophilia as the Initial Clinical Manifestation of Peripheral T-Cell Lymphoma, Not Otherwise Specified

A 58-year-old man presented with painful edema of the extremities, and a diagnosis of eosinophilic fasciitis (EF) was confirmed. He also met the criteria for hypereosinophilic syndrome (HES), but there were no findings suggestive of malignancies or hematologic neoplasms despite a close examination....

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Published inInternal Medicine Vol. 61; no. 22; pp. 3425 - 3429
Main Authors Okuyama, Shuhei, Satomi, Hidetoshi, Ishikawa, Ryuto, Shishido, Tsutomu, Sato, Keijiro, Ueki, Toshimitsu, Sumi, Masahiko, Kobayashi, Hikaru
Format Journal Article
LanguageEnglish
Published Japan The Japanese Society of Internal Medicine 15.11.2022
Japan Science and Technology Agency
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Summary:A 58-year-old man presented with painful edema of the extremities, and a diagnosis of eosinophilic fasciitis (EF) was confirmed. He also met the criteria for hypereosinophilic syndrome (HES), but there were no findings suggestive of malignancies or hematologic neoplasms despite a close examination. He was started on steroid therapy but subsequently developed severe liver dysfunction, hemophagocytic lymphohistiocytosis, hepatosplenomegaly, and renal involvement. The diagnosis of peripheral T-cell lymphoma, not otherwise specified was finally established by a bone marrow reexamination and liver biopsy. In cases of eosinophilia, EF, and/or HES, it is important to suspect an intrinsic abnormality, including potential T-cell lymphoma.
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Correspondence to Dr. Shuhei Okuyama, okuyama442@gmail.com
ISSN:0918-2918
1349-7235
1349-7235
DOI:10.2169/internalmedicine.9300-21