Eosinophilic Fasciitis with Hypereosinophilia as the Initial Clinical Manifestation of Peripheral T-Cell Lymphoma, Not Otherwise Specified
Author:
Affiliation:
1. Department of Hematology, Nagano Red Cross Hospital, Japan
2. Department of Pathology, Nagano Red Cross Hospital, Japan
Publisher
Japanese Society of Internal Medicine
Subject
General Medicine,Internal Medicine
Link
https://www.jstage.jst.go.jp/article/internalmedicine/61/22/61_9300-21/_pdf
Reference16 articles.
1. 1. Greer JP, York JC, Cousar JB, et al. Peripheral T-cell lymphoma: a clinicopathologic study of 42 cases. J Clin Oncol 2: 788-798, 1984.
2. 2. Kitano K, Ichikawa N, Shimodaira S, Ito T, Ishida F, Kiyosawa K. Eosinophilia associated with clonal T-cell proliferation. Leuk Lymphoma 27: 335-342, 1997.
3. 3. Swerdlow SH, Campo E, Pileri SA, et al. The 2016 revision of the World Health Organization classification of lymphoid neoplasms. Blood 127: 2375-2390, 2016.
4. 4. Lebeaux D, Sène D. Eosinophilic fasciitis (Shulman disease). Best Pract Res Clin Rheumatol 26: 449-458, 2012.
5. 5. Moulton SJ, Kransdorf MJ, Ginsburg WW, Abril A, Persellin S. Eosinophilic fasciitis: spectrum of MRI findings. AJR Am J Roentgenol 184: 975-978, 2005.
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1. Eosinophilic Fasciitis: Clinical Signs Leading to Diagnosis;Annals of Internal Medicine: Clinical Cases;2022-10-01
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