Literature DB >> 23588884

The presenting manifestations of subcutaneous panniculitis-like T-cell lymphoma and T-cell lymphoma and cutaneous γδ T-cell lymphoma may mimic those of rheumatic diseases: a report of 11 cases.

Lin Yi1, Shi Qun, Zheng Wenjie, Zhang Wen, Li Jian, Zhao Yan, Zhang Fengchun.   

Abstract

This study aims to investigate the association between subcutaneous panniculitis-like T-cell lymphoma (SPTCL) or cutaneous gamma/delta T-cell lymphoma (CGDTCL) and a variety of manifestations that mimic autoimmune disorders. A retrospective chart review was made for 11 patients who were initially diagnosed as autoimmune diseases but finally turned out to be SPTCL or CGDTCL. Eleven patients were initially diagnosed with erythema nodosum, nodular panniculitis, lupus erythematosus profundus, systemic vasculitis, dermatomyositis, or pyoderma gangrenosum. The interval between presenting symptoms and the diagnosis of lymphoma was 17.5 (range, 3-84)  months on average. Nearly all cases had multiple subcutaneous nodules or plaques that were most commonly distributed on the extremities and trunk. Fever was the primary accompanying sign (9/10), followed by lymphadenopathy (6/11), splenomegaly (5/11), and hepatomegaly (3/11). Two patients developed hemophagocytic syndrome. A total of 26 biopsies involving multiple anatomic locations were performed. Antirheumatic therapy including steroids and immunosuppressive agents administered before the identification of T-cell lymphoma revealed unsustainable therapeutic effect. In contrast, seven cases gained partial response after chemotherapy, while the remaining four cases died with disease progression and disease-associated severe infections. SPTCL and CGDTCL are rare and heterogeneous which may resemble those rheumatologic diseases that are characterized by inflammation involving the skin or subcutaneous fat tissue. The diagnosis relies on the constellation of disease-specific pathologic, immunophenotypic, and T-cell receptor gene rearrangement tests. In the context of an ambiguous clinical picture demonstrating inconsistency with the initial diagnosis of benign autoimmune diseases, repeated excisional biopsies of the subcutaneous lesions may be required to uncover the underlying lymphoma.

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Year:  2013        PMID: 23588884     DOI: 10.1007/s10067-013-2258-7

Source DB:  PubMed          Journal:  Clin Rheumatol        ISSN: 0770-3198            Impact factor:   2.980


  15 in total

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3.  Fatal subcutaneous panniculitis-like T-cell lymphoma with interface change and dermal mucin, a dead ringer for lupus erythematosus.

Authors:  Linglei Ma; Bizhan Bandarchi; Earl J Glusac
Journal:  J Cutan Pathol       Date:  2005-05       Impact factor: 1.587

Review 4.  Criteria for diagnosis of Behçet's disease. International Study Group for Behçet's Disease.

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5.  Lupus profundus, indeterminate lymphocytic lobular panniculitis and subcutaneous T-cell lymphoma: a spectrum of subcuticular T-cell lymphoid dyscrasia.

Authors:  C M Magro; A N Crowson; A J Kovatich; F Burns
Journal:  J Cutan Pathol       Date:  2001-05       Impact factor: 1.587

Review 6.  Etiology and management of pyoderma gangrenosum: a comprehensive review.

Authors:  Iris Ahronowitz; Joanna Harp; Kanade Shinkai
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7.  Atypical lymphocytic lobular panniculitis.

Authors:  Cynthia M Magro; A Neil Crowson; John C Byrd; A David Soleymani; Igor Shendrik
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Review 8.  Rheumatic disorders as paraneoplastic syndromes.

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Review 9.  Immunophenotypic and molecular features, clinical outcomes, treatments, and prognostic factors associated with subcutaneous panniculitis-like T-cell lymphoma: a systematic analysis of 156 patients reported in the literature.

Authors:  Ronald S Go; Susan M Wester
Journal:  Cancer       Date:  2004-09-15       Impact factor: 6.860

10.  Subcutaneous panniculitis-like T-cell lymphoma: definition, classification, and prognostic factors: an EORTC Cutaneous Lymphoma Group Study of 83 cases.

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Journal:  Blood       Date:  2007-10-12       Impact factor: 22.113

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1.  Role of PET imaging in peritoneal involvement of subcutaneous panniculitis-like T-cell lymphoma.

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2.  Primary Cutaneous Gamma-Delta T-Cell Lymphoma Initially Diagnosed as Subcutaneous Panniculitis-like T-Cell Lymphoma with Dermatomyositis.

Authors:  Chika Hirata; Kozo Nakai; Yusuke Kurasawa; Naoki Maekawa; Shuichi Kuniyuki; Keiko Yamagami; Masahiko Ohsawa; Daisuke Tsuruta
Journal:  Dermatopathology (Basel)       Date:  2022-04-29

3.  Primary cutaneous γδ-T-cell lymphoma (CGD-TCL) with unilateral lower extremity swelling as first-onset symptom: a rare case report.

Authors:  Duo Li; Lijun Huang; Bin Guo; Qiuyuan Wen; Weiyuan Wang; Jiadi Luo; Songqing Fan
Journal:  Int J Clin Exp Pathol       Date:  2014-07-15

4.  Secondary Gamma-Delta T-Cell Lymphoma Not Otherwise Specified (NOS) From Chronic Immunosuppression.

Authors:  Madeleine E Turcotte; Amar H Kelkar; Joanna Chaffin; Nam H Dang
Journal:  Cureus       Date:  2021-05-02

5.  Subcutaneous Panniculitis-like T Cell Lymphoma Mimicking Early-Onset Nodular Panniculitis.

Authors:  Guifen Shen; Lingli Dong; Shengtao Zhang
Journal:  Am J Case Rep       Date:  2016-06-25

6.  The coexistence of lupus erythematosus panniculitis and subcutaneous panniculitis-like T-cell lymphoma in the same patient.

Authors:  Xinyu Wu; Antonio Subtil; Brittany Craiglow; Kalman Watsky; Asher Marks; Christine Ko
Journal:  JAAD Case Rep       Date:  2018-02-04

7.  Primary Cutaneous Gamma-Delta T-Cell Lymphoma With Long-Term Indolent Clinical Course Initially Mimicking Lupus Erythematosus Profundus.

Authors:  Laura von Dücker; Mariella Fleischer; Nathalie Stutz; Markus Thieme; Mareike Witte; Detlef Zillikens; Christian D Sadik; Patrick Terheyden
Journal:  Front Oncol       Date:  2020-02-19       Impact factor: 6.244

  7 in total

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